Electrochem doi: 10.3390/electrochem5010008
Authors: Anastasia Leonova Natalia Leonova Lyudmila Minchenko Andrey Suzdaltsev
The possibility of using Si-based anodes in lithium-ion batteries is actively investigated due to the increased lithium capacity of silicon. The paper reports the preparation of submicron silicon fibers on glassy carbon in the KI–KF–KCl–K2SiF6 melt at 720 °C. For this purpose, the parameters of silicon electrodeposition in the form of fibers were determined using cyclic voltammetry, and experimental samples of ordered silicon fibers with an average diameter from 0.1 to 0.3 μm were obtained under galvanostatic electrolysis conditions. Using the obtained silicon fibers, anode half-cells of a lithium-ion battery were fabricated, and its electrochemical performance under multiple lithiations and delithiations was studied. By means of voltametric studies, it is observed that charging and discharging the anode based on the obtained silicon fibers occurs at potentials from 0.2 to 0.05 V and from 0.2 to 0.5 V, respectively. A change in discharge capacity from 520 to 200 mAh g−1 during the first 50 charge/discharge cycles at a charge current of 0.1 C and a Coulombic efficiency of 98–100% was shown. The possibility of charging silicon-based anode samples at charging currents up to 2 C was also noted; the discharge capacity ranged from 25 to 250 mAh g−1.
]]>Electrochem doi: 10.3390/electrochem5010007
Authors: Elizaveta Y. Evshchik Sophia S. Borisevich Margarita G. Ilyina Edward M. Khamitov Alexander V. Chernyak Tatiana A. Pugacheva Valery G. Kolmakov Olga V. Bushkova Yuri A. Dobrovolsky
Determining the oxidation potential (OP) of lithium-ion battery (LIB) electrolytes using theoretical methods will significantly speed up and simplify the process of creating a new generation high-voltage battery. The algorithm for calculating OP should be not only accurate but also fast. Our work proposes theoretical principles for evaluating the OP of LIB electrolytes by considering LiDFOB solutions with different salt concentrations in EC/DMC solvent mixtures. The advantage of the new algorithm compared to previous versions of the theoretical determination of the oxidation potential of electrolyte solutions used in lithium-ion batteries for calculations of statistically significant complexes, the structure of which was determined by the molecular dynamics method. This approach significantly reduces the number of atomic–molecular systems whose geometric parameters need to be optimized using quantum chemical methods. Due to this, it is possible to increase the speed of calculations and reduce the power requirements of the computer performing the calculations. The theoretical calculations included a set of approaches based on the methods of classical molecular mechanics and quantum chemistry. To select statistically significant complexes that can make a significant contribution to the stability of the electrochemical system, a thorough analysis of molecular dynamics simulation trajectories was performed. Their geometric parameters (including oxidized forms) were optimized by QM methods. As a result, oxidation potentials were assessed, and their dependence on salt concentration was described. Here, we once again emphasize that it is difficult to obtain, by calculation methods, the absolute OP values that would be equal (or close) to the OP values estimated by experimental methods. Nevertheless, a trend can be identified. The results of theoretical calculations are in full agreement with the experimental ones.
]]>Electrochem doi: 10.3390/electrochem5010006
Authors: Aslan Achoh Denis Bondarev Elena Nosova Stanislav Melnikov
This study focuses on the modification of ion-exchange membranes by incorporating a phosphorylated dendrimer into sulfonated polytetrafluoroethylene membranes to enhance the specific selectivity between mono-/divalent ions, using the Ca2+/Na+ pair as an example. This research employs mechanical, physicochemical, and electrochemical analyses to explore the effects of P-H20 incorporation on membrane properties. Bulk modification significantly increases membrane selectivity towards calcium ions (the specific permselectivity coefficient rises from 1.5 to 7.2), while maintaining the same level of the limiting current density. Other findings indicate that bulk modification significantly changes the transport-channel structure of the membrane and alters the mechanism of over-limiting mass transfer. The over-limiting current for the pristine membrane is mainly due to non-equilibrium electroconvection, while modified membranes actively participate in the water-splitting reaction, leading to the suppression of the electroconvection. Despite this drawback, the decrease of the over-limiting potential drop results in a decrease in specific energy consumption from 0.11 to 0.07 kWh/mol. In the underlimiting current mode, the specific energy consumption for all studied membranes remains within the same limits of 0.02–0.03 kWh/mol.
]]>Electrochem doi: 10.3390/electrochem5010005
Authors: Vivek Kumar Singh Bibhudatta Malik Rajashree Konar Efrat Shawat Avraham Gilbert Daniel Nessim
The electrocatalytic oxygen evolution reaction (OER) is an arduous step in water splitting due to its slow reaction rate and large overpotential. Herein, we synthesized glycerate-anion-intercalated nickel–iron glycerates (NiFeGs) using a one-step solvothermal reaction. We designed various NiFeGs by tuning the molar ratio between Ni and Fe to obtain Ni4Fe1G, Ni3Fe1G, Ni3Fe2G, and Ni1Fe1G, which we tested for their OER performance. We initially analyzed the catalytic performance of powder samples immobilized on glassy carbon electrodes using a binder. Ni3Fe2G outperformed the other NiFeG compositions, including NiFe layered double hydroxide (LDH). It exhibited an overpotential of 320 mV at a current density of 10 mA cm–2 in an electrolytic solution of pH 14. We then synthesized carbon paper (CP)-modified Ni3Fe2G as a self-supported electrode (Ni3Fe2G/CP), and it exhibited a high current density (100 mA cm−2) at a low overpotential of 300 mV. The redox peak analysis for the NiFeGs revealed that the initial step of the OER is the formation of γ-NiOOH, which was further confirmed by a post-Raman analysis. We extensively analyzed the catalyst’s stability and lifetime, the nature of the active sites, and the role of the Fe content to enhance the OER performance. This work may provide the motivation to study metal-alkoxide-based efficient OER electrocatalysts that can be used for alkaline water electrolyzer applications.
]]>Electrochem doi: 10.3390/electrochem5010004
Authors: Zaheer Masood Haji Muhammad Iftikhar Ahmed Tahiri
Understanding electrochemical reactions at the surface of electrodes requires the accurate calculation of key parameters—the transfer coefficient (α), diffusion coefficient (D0), and heterogeneous electron transfer rate constant (k0). The choice of method to calculate these parameters requires careful consideration based on the nature of the electrochemical reaction. In this study, we conducted the cyclic voltammetry of paracetamol to calculate the values of these parameters using different methods and present a comparative analysis. Our results demonstrate that the Ep − Ep/2 equation for α and the modified Randles–Ševčík equation for D0 is particularly effective for the calculations of these two parameters. The Kochi and Gileadi methods are reliable alternatives for the calculation of k0. Nicholson and Shain’s method using the equation k0 = Ψ(πnD0Fν/RT)1/2 gives the overestimated values of k0. However, the value of k0 calculated using the plot of ν−1/2 versus Ψ (from the Nicholson and Shain equation, where ν is scan rate) agrees well with the values calculated from the Kochi and Gilaedi methods. This study not only identifies optimal methodologies for quasi-reversible reactions but also contributes to a deeper understanding of electrochemical reactions involving complex electron transfer and coupled chemical reactions, which can be broadly applicable in various electrochemical studies.
]]>Electrochem doi: 10.3390/electrochem5010003
Authors: Tijana Mutić Dalibor Stanković Dragan Manojlović Djordje Petrić Ferenc Pastor Vyacheslav V. Avdin Miloš Ognjanović Vesna Stanković
In this work, we successfully prepared a modified cobalt oxide (Co3O4) carbon paste electrode to detect Levofloxacin (LEV). By synthesizing Co3O4 nanoparticles through the chemical coprecipitation method, the electrochemical properties of the electrode and LEV were thoroughly investigated using CV, SWV, and EIS, while material properties were scrutinized using ICP-OES, TEM, SEM, and XRD. The results showed that the prepared electrode displayed a better electrocatalytic response than the bare carbon paste electrode. After optimizing SWV, the electrode exhibited a wide linear working range from 1 to 85 μM at pH 5 of BRBS as the supporting electrolyte. The selectivity of the proposed method was satisfactory, with good repeatability and reproducibility, strongly suggesting a potential application for determining LEV in real samples, particularly in pharmaceutical formulations. The practicality of the approach was demonstrated through good recoveries, and the morphology of the materials was found to be closely related to other parameters, indicating that the developed method can provide a cost-effective, rapid, selective, and sensitive means for LEV monitoring. Overall, this project has made significant progress towards developing a reliable method for detecting LEV and has opened up new opportunities for future research in this field.
]]>Electrochem doi: 10.3390/electrochem5010002
Authors: Adam Cherni Kamel Halouani
At present, direct carbon fuel cells constitute an emerging energy technology that electrochemically converts solid carbon to electricity with high efficiency. The recent trend of DCFCs fueled with biochar from biomass carbonization as green fuel has reinforced the environmental benefits of DCFCs as a clean and sustainable technology. However, there remain new challenges related to some complex unknown kinetic parameters, X=(αa,αc,σg,i0,a,i0,c,ilO2,ilCO2,c,ilCO2,a,ilCO), of the electrochemical conversion of biochar in DCFCs and there is a need for intelligent techniques for prediction and optimization, refering to the available experimental data. The differential evolution (DE) algorithm, which ranked as one of the top performers in optimization competitions with competitive accuracy and convergence speed, was used here for providing the optimized values of these parameters by minimizing the root mean squared errors (RMSE). The proposed technique was then applied to DCFCs fueled by activated pure carbon (APC) using CO2 and CO/CO2 electrochemical models with RMSE around 10−2 and 10−3, respectively. Then, the CO/CO2 model was applied to a DCFC fueled with almond shell biochar (ASB), which displayed a slight increase in RMSE (of the order of 10−2) due to the complex porous structure of ASB and the content of additional chemical elements that affect the electrochemistry of the DCFC and are not considered in the model.
]]>Electrochem doi: 10.3390/electrochem5010001
Authors: Ioannis Christakis Elena Sarri Odysseas Tsakiridis Ilias Stavrakas
Nowadays, the study of air quality has become an increasingly prominent field of research, particularly in large urban centers, given its significant impact on human health. In many countries, government departments and research centers use official high-cost scientific instruments to monitor air quality in their regions. Meanwhile, concerned citizens interested in studying the air quality of their local areas often employ low-cost air quality sensors for monitoring purposes. The optimization and evaluation of low-cost sensors have been a field of research by many research groups. This paper presents an extensive study to identify the safe percentage change limits that low-cost electrochemical air quality sensors can have, in order to optimize their measurements. For this work, three low-cost air quality monitoring stations were used, which include an electrochemical sensor for nitrogen dioxide (NO2) (Alphasense NO2-B43F) and an electrochemical sensor for ozone (O3) (Alphasense OX-B431). The aim of this work is to explore the variance of the aforementioned sensors and how this variability can be used to optimize the measurements of low-cost electrochemical sensors, closer to real ones. The analysis is conducted by employing diagrams, boxplot and violin curves of the groups of sensors used, with satisfactory results.
]]>Electrochem doi: 10.3390/electrochem4040035
Authors: Daniela Nunes da Silva Arnaldo César Pereira
Aptamers are three-dimensional structures of DNA or RNA that present high affinity and selectivity to specific targets, obtained through in vitro screening. Aptamers are used as biological recognizers in electrochemical biosensors, the so-called aptasensors, providing greater specificity in recognizing the most diverse analytes. Electrochemical aptasensors have extremely relevant characteristics, such as high sensitivity, low cost compared to other biorecognizers such as antibodies, and excellent compatibility, being considered one of the most promising alternative methods in several areas, such as biomedical diagnosis and monitoring environmental contaminants. In this sense, the present work reviews the relevant aspects of methodologies based on electrochemical aptasensors and their applications in determining antibiotics, seeking to foster innovation in electrochemical biosensors.
]]>Electrochem doi: 10.3390/electrochem4040034
Authors: Mohana Marimuthu Vinoth Krishnan Shailendra Sudhakaran Sevakumaran Vigneswari Shanmugam Senthilkumar Murugan Veerapandian
The global hazardous waste management market is expected to reach USD 987.51 million by 2027 at a CAGR of 14.48%. The early detection of corrosive, flammable, and infectious toxicants from natural sources or manmade contaminants from different environments is crucial to ensure the safety and security of the global living system. Even though the emergence of advanced science and technology continuously offers a more comfortable lifestyle, there are two sides of the coin in terms of opportunities and challenges, demanding solutions for greener applications and waste-to-wealth strategies. A modern analytical technique based on an electrochemical approach and microfluidics is one such emerging advanced solution for the early and effective detection of toxicants. This review attempts to highlight the different studies performed in the field of toxicant analysis, especially the fusion of electrochemistry and lab-chip model systems, promising for point-of-need analysis. The contents of this report are organised by classifying the types of toxicants and trends in electrochemical-integrated lab-chip assays that test for heavy-metal ions, food-borne pathogens, pesticides, physiological reactive oxygen/nitrogen species, and microbial metabolites. Future demands in toxicant analysis and possible suggestions in the field of microanalysis-mediated electrochemical (bio)sensing are summarised.
]]>Electrochem doi: 10.3390/electrochem4040033
Authors: Wiviane E. R. de Melo Karoline S. Nantes Ana L. H. K. Ferreira Márcio C. Pereira Luiz H. C. Mattoso Ronaldo C. Faria André S. Afonso
Hydrogen peroxide (H2O2) is an essential analyte for detecting neurodegenerative diseases and inflammatory processes and plays a crucial role in pharmaceuticals, the food industry, and environmental monitoring. However, conventional H2O2 detection methods have drawbacks such as lengthy analysis times, high costs, and bulky equipment. Non-enzymatic sensors have emerged as promising alternatives to overcome these limitations. In this research, we introduce a simple, portable, and cost-effective non-enzymatic sensor that uses carbon black (CB) and silver nanoparticle-modified δ-FeOOH (Ag/δ-FeOOH) integrated into a disposable electrochemical cell (DCell). Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and electrochemical impedance spectroscopy (EIS) confirmed successful CB and Ag/δ-FeOOH immobilization on the DCell working electrode. Electrochemical investigations revealed that the DCell-CB//Ag/δ-FeOOH sensor exhibited an approximately twofold higher apparent heterogeneous electron transfer rate constant than the DCell-Ag/δ-FeOOH sensor, capitalizing on CB’s advantages. Moreover, the sensor displayed an excellent electrochemical response for H2O2 reduction, boasting a low detection limit of 22 µM and a high analytical sensitivity of 214 μA mM−1 cm−2. Notably, the DCell-CB//Ag/δ-FeOOH sensor exhibited outstanding selectivity for H2O2 detection, even in potential interferents such as dopamine, uric acid, and ascorbic acid. Furthermore, the sensor has the right qualities for monitoring H2O2 in complex biological samples, as evidenced by H2O2 recoveries ranging from 92% to 103% in 10% fetal bovine serum. These findings underscore the considerable potential of the DCell-CB//Ag/δ-FeOOH sensor for precise and reliable H2O2 monitoring in various biomedical and environmental applications.
]]>Electrochem doi: 10.3390/electrochem4040032
Authors: Ryohei Mori
In the recent rechargeable battery industry, lithium sulfur batteries (LSBs) have demonstrated to be a promising candidate battery to serve as the next-generation secondary battery, owing to its enhanced theoretical specific energy, economy, and environmental friendliness. Its inferior cyclability, however, which is primarily due to electrode deterioration caused by the lithium polysulfide shuttle effect, is still a major problem for the real industrial usage of LSBs. The optimization of the separator and functional barrier layer is an effective strategy for remedying these issues. In this article, the current progress based on the classification and modification of functional separators is summarized. We will also describe their working mechanisms as well as the resulting LSB electrochemical properties. In addition, necessary performance for separators will also be mentioned in order to gain optimized LSB performance.
]]>Electrochem doi: 10.3390/electrochem4040031
Authors: Wei Zhang Hangxuan Xie Zirui Dou Zhentao Hao Qianhui Huang Ziqi Guo Chao Wang Kanghua Miao Xiongwu Kang
Cobalt diphosphides (CoP2) show a high theoretical capacity and hold great promise as anode materials for lithium-ion batteries (LIBs). However, the large variation in the volume and structure of CoP2 caused during lithium-ion insertion and extraction results in electrode fragmentation and a compromised solid electrolyte interface, ultimately leading to poor cycling performance. Herein, a composite of CoP2 nanoparticles encapsulated in carbon matrix has been successfully synthesized by carbonization of Co-MOF-based zeolitic imidazolate frameworks (ZIF-67) and sequential phosphorization and further wrapped in graphene oxide (CoP2@C@GO). The formation of CoP2 was confirmed by X-ray diffraction, high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The morphology of CoP2@C with and without GO wrapping was examined by scanning electron microscopy and transmission electron spectroscopy. It was demonstrated that the decoration of GO significantly reduces the polarization of CoP2@C electrodes, enhancing their charge capacity and cycling stability as an anode material for LIBs. After 200 cycles, they deliver a capacity of 450 mAh·g−1.
]]>Electrochem doi: 10.3390/electrochem4040030
Authors: Yuanyuan Liu Koichi Jeremiah Aoki Jingyuan Chen
Diffusion-controlled cyclic voltammograms at fast scan rates show peak shifts, as well as decreases in the peak currents from predicted diffusion-controlled currents, especially when the currents are large in a low concentration of supporting electrolytes. This has been conventionally recognized as an IR-drop effect due to solution resistance on the peaks, as well as a heterogeneously kinetic effect. It is also brought about by the negatively capacitive currents associated with charge transfer reactions. The reaction product generates dipoles with counterions to yield a capacitance, the current of which flows oppositely to that of the double-layer capacitance. The three effects are specified here in the oxidation of a ferrocenyl derivative using fast scan voltammetry. The expression for voltammograms complicated with IR-drop is derived analytically and yields deformed voltammograms. The peak shift is approximately linear with the IR-voltage, but exhibits a convex variation. The dependence of some parameters on the peaks due to the IR-drop is compared with those due to the negative capacitance. The latter is more conspicuous than the former under conventional conditions. The two effects cannot be distinguished specifically except for variations in the conductance of the solution.
]]>Electrochem doi: 10.3390/electrochem4040029
Authors: Ponraj Jeyabarathi Marwan Abukhaled Murugesan Kannan Lakshmanan Rajendran Michael E. G. Lyons
An electrochemical photobioreactor with a packed bed containing transparent gel granules and immobilized photosynthetic bacterial cells is shown with a one-dimensional two-phase flow and transport model. We consider the biological/chemical events in the electrochemical photobioreactor, the intrinsically connected two-phase flow and mass transport, and other factors. This model is based on a system of nonlinear equations. This paper applies Akbari-Ganji’s and Taylor series methods to find analytical solutions to nonlinear differential equations that arise in an immobilized-cell electrochemical photobioreactor. Approximate analytical expressions of the concentration of glucose and hydrogen are obtained in liquid and gas phases for different parameter values. Numerical simulations are presented to validate the theoretical investigations.
]]>Electrochem doi: 10.3390/electrochem4040028
Authors: Pranaya Charkravarthula Amos Mugweru
This work was aimed at the development of a sensitive electrochemical detection method for oxycodone in water. Molecularly imprinted electrodes were formed by electro-polymerization process using o-phenylenediamine as a monomer. The electro-polymerization was performed on glassy carbon electrodes in the presence of oxycodone before the extraction of entrapped oxycodone molecules. Various electrochemical techniques were employed to monitor the polymerization and response of the fabricated electrodes toward oxycodone. These techniques included cyclic voltammetry (CV), square wave voltammetry (SWV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). The oxycodone concentration was determined using SWV by measuring the change in the oxidation peak current of [Fe(CN)6]3−/4− in a 0.1 mM acetate buffer solution. At the optimal electro-polymerization conditions, a calibration curve of the current versus the concentration of oxycodone indicated a linear response at a region from 0.4 nM to 5.0 nM with a detection limit of 1.8 ± 0.239 nM. The MIP-modified electrode’s binding isotherm was fitted using a Langmuir model and showed an association constant, KA, of 1.12 × 106, indicating a high affinity of oxycodone molecules to binding sites. This sensor has the potential to act as an alternative method suitable for the on-site analysis of oxycodone.
]]>Electrochem doi: 10.3390/electrochem4030027
Authors: Ramalingam Vanaja Ponraj Jeyabarathi Lakshmanan Rajendran Michael Edward Gerard Lyons
A device that transforms chemical energy into electrical energy is an electrochemical cell. The reaction type inside the cell determines whether it is exothermic or endothermic. This paper discusses the mathematical modelling of exothermic explosions in a slab. This model is based on a nonlinear equation containing a nonlinear term related to Arrhenius, bimolecular, and sensitised laws of reaction kinetics. The absolute temperature can be derived by solving the nonlinear equation using the Akbari–Ganji technique. The mathematical model also numerically solved and simulated in the MATLAB® v2016b software. The new simple theoretical result is validated with previously identified analytical and numerical findings. The influence of the parameters of Frank-Kamenetskii number, activation energy and the numerical exponent on temperature is discussed. The Frank-Kamenetskii number is observed to drop as the temperature is found to decrease, while the activation energy parameter is shown to increase. The numerical exponent has little or no effect on the temperature. An extension of this model to cylinder and sphere geometry is also provided.
]]>Electrochem doi: 10.3390/electrochem4030026
Authors: Mansi Gandhi
Plants have a remarkable position among renewable materials because of their abundance, and nearly thousands of tons are consumed worldwide every day. Most unexploited plants and agricultural waste can be a real potential resource system. With increasing environmental awareness and the growing importance of friendly agricultural waste, crops and fruit waste can be used for efficient conversion into bio-fertilizers, biocarbons, bio-polymers, biosensors and bio-fibers. Global challenges based on limited natural resources and fossil energy reserves simulated keen interest in the development of various electrochemical systems inspired by food and plant scraps, which aid in curbing pollution. The successful adoption of a renewable energy roadmap is dependent on the availability of a cheaper means of storage. In order to cut down the cost of storage units, an improvement on energy storage devices having better stability, power, and energy density with low post-maintenance cost is the vital key. Although food and plant scraps have a huge need for energy storage, it has been extended to various sensing platform fabrications, which are eco-friendly and comparable to organic molecule-based sensors. Current research proclivity has witnessed a huge surge in the development of phyto-chemical-based sensors. The state-of-the-art progresses on the subsequent use of plant-waste systems as nano-engineered electrochemical platforms for numerous environmental science and renewable energy applications. Moreover, the relevant rationale behind the use of waste in a well-developed, sustainable future device is also presented in this review.
]]>Electrochem doi: 10.3390/electrochem4030025
Authors: R. Joseph Mathews Emil Jovanov
Recent advances in commercially available integrated complex impedance spectroscopy controllers have brought rapid increases in the quality of systems available to researchers for wearable and remote patient monitoring applications. As a result, novel sensing methods and electrode configurations are increasingly viable, particularly for low-power embedded sensors and controllers for general electrochemical analysis. This study evaluates a case study of the four electrode locations suitable for wearable monitoring of respiratory and heart activity monitoring using complex impedance spectroscopy. We use tetrapolar electrode configurations with ten stimulation frequencies to characterize the relative differences in measurement sensitivity. Measurements are performed and compared for the magnitude, phase, resistive, and reactive components of the bioimpedance using two COTS-based controllers, the TI AFE4300 and MAX30009. We identify the highest percent relative changes in the magnitude of the impedance corresponding to deep breathing and heart activity across the chest (17% at 64 kHz, 0.5% at 256 kHz, respectively), on the forearm (0.098% at 16 kHz, 0.04% at 8 kHz), wrist-to-wrist across the body (0.28% at 256 kHz, 0.04% at 256 kHz, respectively), and wrist-to-finger across the body (0.35% at 4 kHz, 0.05% at 4 kHz, respectively). We demonstrate that the wrist-to-wrist and wrist-to-finger configurations are most promising and may enable new wearable bioimpedance applications. Additionally, this paper demonstrates that deep respiration and heart activity influence bioimpedance measurements in whole-body measurement configurations, with variations of nearly 1% in measured impedance due to the phase of the breathing cycle.
]]>Electrochem doi: 10.3390/electrochem4030024
Authors: Mansi Gandhi Khairunnisa Amreen
Comprehending the interfacial interaction of nanomaterials (NMs) and biological systems is a significant research interest. NMs comprise various nanoparticles (NPs) like carbon nanotubes, graphene oxides, carbon dots, graphite nanopowders, etc. These NPs show a variety of interactions with biological interfaces via organic layers, therapeutic molecules, proteins, DNA, and cellular matrices. A number of biophysical and colloidal forces act at the morphological surface to regulate the biological responses of bio-nanoconjugates, imparting distinct physical properties to the NMs. The design of future-generation nano-tools is primarily based on the basic properties of NMs, such as shape, size, compositional, functionality, etc., with studies being carried out extensively. Understanding their properties promotes research in the medical and biological sciences and improves their applicability in the health management sector. In this review article, in-depth and critical analysis of the theoretical and experimental aspects involving nanoscale material, which have inspired various biological systems, is the area of focus. The main analysis involves different self-assembled synthetic materials, bio-functionalized NMs, and their probing techniques. The present review article focuses on recent emerging trends in the synthesis and applications of nanomaterials with respect to various biomedical applications. This article provides value to the literature as it summarizes the state-of-the-art nanomaterials reported, especially within the health sector. It has been observed that nanomaterial applications in drug design, diagnosis, testing, and in the research arena, as well as many fatal disease conditions like cancer and sepsis, have explored alongwith drug therapies and other options for the delivery of nanomaterials. Even the day-to-day life of the synthesis and purification of these materials is changing to provide us with a simplified process. This review article can be useful in the research sector as a single platform wherein all types of nanomaterials for biomedical aspects can be understood in detail.
]]>Electrochem doi: 10.3390/electrochem4030023
Authors: Bitan Chakraborty
A chronically stable electrode material with a low impedance for recording neural activity, and a high charge-injection capacity for functional electro-stimulation is desirable for the fabrication of implantable microelectrode arrays that aim to restore impaired or lost neurological functions in humans. For this purpose, we have investigated the electrochemical properties of sputtered ruthenium oxide (RuOx) electrode coatings deposited on planar microelectrode arrays, using an inorganic model of interstitial fluid (model-ISF) at 37 °C as the electrolyte. Through a combination of cyclic voltammetry (CV) and an electrochemical impedance spectroscopy (EIS) modelling study, we have established the contribution of the faradaic reaction as the major charge-injection contributor within the safe neural stimulation potential window of ±0.6 V vs. Ag|AgCl. We have also established the reversibility of the charge-injection process for sputtered RuOx film, by applying constant charge-per-phase current stimulations at different pulse widths, and by comparing the magnitudes of the leading and trailing access voltages during voltage transient measurements. Finally, the impedance of the sputtered RuOx film was found to be reasonably comparable in both its oxidized and reduced states, although the electronic contribution from the capacitive double-layer was found to be slightly higher for the completely oxidized film around 0.6 V than for its reduced counterpart around −0.6 V.
]]>Electrochem doi: 10.3390/electrochem4030022
Authors: John F. Cassidy Rafaela C. de Carvalho Anthony J. Betts
Salts of hexacyanoferrate II/III anions have been widely used as redox couple probe molecules to determine the characteristics of electrode surfaces. Examples include the assessment of electrocatalysts for energy applications and electrocatalysts for the detection of biological or chemical species, as well as the determination of electrochemically active surface areas. An examination of the electrochemical literature, based largely on cyclic voltammetric investigations, reveals a wide range of peak separation and/or heterogeneous electron transfer rate constants, classified sometimes as inner or outer sphere electron transfer processes. Originally developed for the mechanistic interpretation of inorganic transition metal compounds in solution, this terminology has since been extended to account for heterogeneous electron transfer occurring at electrodes. In the case of the hexacyanoferrate II/III anions, there can be a number of reasons why it sometimes behaves as an outer sphere probe and at other times displays inner sphere electron transfer characteristics. After examining some of the structural and chemical properties of the hexacyanoferrate II/III species, the methods used to determine such classifications are described. The most common method involves measuring peak-to-peak separation in a cyclic voltammogram to ascertain a heterogeneous rate constant, but it has inherent flaws. This paper reviews the reasons for the classification disparity, including the effects of various oxygen surface species, the influence of organic surface films, the nature of the cation counter-ion, surface adsorption and surface hydrophilicity/hydrophobicity. Other surface interactions may also take place, such as those occurring with Au corrosion or pH effects. These can impact the electrical double layer and thus may affect the electron transfer process. Consequently, it is recommended that hexacyanoferrate II/III should be considered a multi-sphere or alternatively a surface-sensitive electron transfer species.
]]>Electrochem doi: 10.3390/electrochem4020021
Authors: Yuanyuan Liu Koichi Jeremiah Aoki Jingyuan Chen
Chronoamperometric curves for the oxidation of a ferrocenyl derivative via a potential step, calculated using the Cottrell equation, showed less diffusion-controlled currents on a platinum wire electrode. This lower deviation cannot be explained via Butler–Volmer heterogeneous kinetics, but was ascribed to the negatively capacitive current associated with a redox reaction. The deviation in fully oxidized electrical potential corresponds to the non-zero concentration at the electrode surface, which cannot be predicted using the Nernst equation. This equation expresses the relationship between the electrical potential and activity at the electrode surface rather than the concentration. The diffusion equation determines the relationship between the current and surface concentration rather than activity. Negative capacitance or a non-zero concentration may arise from structure formation on the electrode owing to dipole–dipole interactions, which are similar to the generation of double-layer capacitance, including frequency dispersion. Following this concept, we derive expressions for a lowered diffusion-controlled current and time-dependent surface concentration. The negatively capacitive current shows the time dependence of t−0.9, which is similar to the decay of double-layer capacitive currents. The surface concentration decays with t−0.4-dependence.
]]>Electrochem doi: 10.3390/electrochem4020020
Authors: Jayaprakash Sushmitha Subramanian Nellaiappan
The present study focuses on the electrochemical sensing of amoxicillin (AMX, as a model antibiotic drug) and its interaction with Uropathogenic E. coli (UPEC) bacteria (as a model pathogen) under physiological conditions. The electrochemical sensor probe is formulated by nanostructured gold wires (AuNWs) embedded in a carbon nanofiber–chitosan (CNF-CHIT) matrix. The synthesis of AuNWs is characterized by scanning electron microscopy (SEM), UV-Visible spectrophotometry, and X-ray photoelectron spectroscopy (XPS). The CNF-CHIT/AuNW-modified system is characterized by SEM and XPS. Initially, the CNF-CHIT/AuNW electrode was utilized for the sensing of AMX; later, in the antibiotic drug-assisted sensing of UPEC, i.e., in the presence of AMX, the interaction of UPEC was studied. The modified electrode showed appreciable sensitivity for AMX sensing; also, the interaction of AMX with UPEC is studied at two different conditions. One, at a fixed concentration of AMX (100 µM) and different concentrations of UPEC bacteria (0.6–1.2 × 106 CFU/mL), and another with incubation time (1 h–1 h 35 min) for bacterial reaction. The electrochemical antimicrobial resistance developed by UPEC, which is inherent in the sensing of AMX, is the key concept for the detection of pathogens.
]]>Electrochem doi: 10.3390/electrochem4020019
Authors: Aurel Ottlakan Gyorgy Lazar Judit Olah Andras Nagy Gabor Vass Marton Vas Raissa Pereira Erika Kis
Electrochemotherapy (ECT) has evolved significantly during the last decade, expanding treatment indications from superficial skin lesions to advanced-stage, deep-seated tumors in hard-to-reach areas. Electrodes have also shown steady technological improvement throughout the years. Besides standard and VEG (variable geometry electrode) electrodes, the introduction of laparoscopic electrodes has brought on a new era in ECT treatment, making the minimally invasive approach a reality. The exact role of ECT in the oncological dashboard is yet to be determined; however, increased tumor response, pain relief, and a low number of adverse events may yield the way for more widespread application of the technique with possible further inclusion of ECT in international oncological guidelines. The aim of this review is to give an overview on the current status of ECT in deep-seated tumor treatment and shed light on its emerging role in local anticancer therapy.
]]>Electrochem doi: 10.3390/electrochem4020018
Authors: Emad F. Newair Aboelhasan G. Shehata Menna Essam
A study of keracyanin chloride (KC) electrochemical behavior in an aqueous buffer solution using screen-printed carbon electrodes (SPCEs) and glassy carbon electrodes (GCEs) was performed. Cyclic voltammetry (CV) and square-wave voltammetry (SWV) were used to analyze the electrochemical response of KC under studied conditions. A clear redox wave was observed for KC, primarily due to the oxidation of the catechol 3′,4′-dihydroxyl group of its ring B, with a minor redox wave from oxidation of the hydroxyl groups in ring A. Compared to GCEs, using modified SPCEs resulted in two-fold amplification in the electrochemical oxidation signal of KC. Using SPCEs as a working electrode could provide high sensitivity in the quantification of KC and the ability to gauge KC quantification to significantly lower detection limits.
]]>Electrochem doi: 10.3390/electrochem4020017
Authors: Shruti Patle Dinesh Rotake Kishor Rewatkar
Ammonium dihydrogen phosphate (ADP) single crystals along with the incorporated 0.5 and 1% L-lysine, an organic molecule which possesses a good nonlinear response, were grown with the vision to meet the requirements of the optoelectronic industry. The inclusion of the L-lysine molecule in the crystal was confirmed by the XRD and EDX. The experiment not only confirms the inclusion level of the impurity but also the capability of the amino acid molecule to bond hydrogen within the crystal facet. A minor decrease in lattice parameters was reported for all ADP: L-lysine crystals compared with pure ADP. The structures of the grown crystals were identified as tetragonal with the space group I42d by the single-crystal XRD analysis. Vibrational signatures and functional groups were confirmed using FTIR spectroscopy. The thermal stability and decomposition temperatures of 0.5 and 1% L-lysine-added crystals were measured by TG/DTA and found to be 203 °C and 207 °C, respectively. The UV–visible transmission spectra prove a higher transparency for doped crystals as compared to pure crystals; therefore, these doped crystals can be considered the best option for the frequency doubling process in a broad range of visible and near-IR spectra. The improved hardness of the doped crystals was confirmed by the Vickers hardness data. The nonlinear optical (NLO) behaviour investigated using a second-harmonic generation (SHG) technique, indicating an efficient quadratic nonlinear coefficient of ADP: Lysine crystals at a 1064 nm initial wavelength, shows about 1.5-fold higher efficiency compared with undoped ADP.
]]>Electrochem doi: 10.3390/electrochem4020016
Authors: Lorenzo Damiani Roberto Revetria Pietro Giribone
This paper focuses on an industrial application where renewable power produced by photovoltaic panels is exploited to feed a pneumatic transport plant. The proposed system requires the careful management of the energy flows involved since it includes the interaction with the electric grid and with an electrochemical storage (battery) rather than the correct choice of the photovoltaic panel and battery itself. A dedicated control system needs to be developed in order to accord together these energetic flows, also providing a degree of flexibility to implement different control logics. The methodology employed in the research is simulation, which through the construction of a model in Matlab Simulink is able to reproduce the behavior of the system components and their energetic interactions for a long time period. The aim of the research is to provide a tool for assessing the energetic convenience of different battery–PV panel combinations. Moreover, an economical assessment of the proposed system is provided and compared to the traditional setup. Simulation results show that the proposed system provides energy savings with respect to a traditional grid-powered plant. The economic assessment shows that the system becomes convenient over the traditional setup within a time frame compatible with an average PV panel’s useful life.
]]>Electrochem doi: 10.3390/electrochem4020015
Authors: Perumal Pandurangan
Polysaccharide-based natural polymer electrolyte membranes have had tremendous consideration for the various energy storage operations including wearable electronic and hybrid vehicle industries, due to their unique and predominant qualities. Furthermore, they have fascinating oxygen functionality results of a higher flexible nature and help to form easier coordination of metal ions thus improving the conducting profiles of polymer electrolytes. Mixed operations of the various alkali and alkaline metal–salt-incorporated biopolymer electrolytes based on different polysaccharide materials and their charge transportation mechanisms are detailly explained in the review. Furthermore, recent developments in polysaccharide electrolyte separators and their important electrochemical findings are discussed and highlighted. Notably, the characteristics and ion-conducting mechanisms of different biopolymer electrolytes are reviewed in depth here. Finally, the overall conclusion and mandatory conditions that are required to implement biopolymer electrolytes as a potential candidate for the next generation of clean/green flexible bio-energy devices with enhanced safety; several future perspectives are also discussed and suggested.
]]>Electrochem doi: 10.3390/electrochem4020014
Authors: Misael Bessa Sales José Gadelha Lima Neto Ana Kátia De Sousa Braz Paulo Gonçalves De Sousa Junior Rafael Leandro Fernandes Melo Roberta Bussons Rodrigues Valério Juliana de França Serpa Ana Michele Da Silva Lima Rita Karolinny Chaves De Lima Artemis Pessoa Guimarães Maria Cristiane Martins de Souza Ada Amélia Sanders Lopes Maria Alexsandra de Sousa Rios Leonardo Farias Serafim José Cleiton Sousa dos Santos
The unique properties of metal-organic frameworks (MOFs) such as their large surface area and high porosity have attracted considerable attention in recent decades. The MOFs are a promising class of materials for developing highly efficient biosensors due to these same properties. This bibliometric analysis focused on the use of MOFs as enzyme-coupled materials in biosensor construction and aimed to provide a comprehensive overview of the research field by analyzing a collected database. The analysis included identifying the countries that have published the most, the most prominent applications, and trends for future directions in the field. The study used three databases with different numbers of documents, differentiated by research areas, with refinements made to the search as needed. The results suggest that MOF-derived biosensors are a growing field, with the Republic of China emerging as a significant contributor to research in this area. The study also used computational processing of trend analysis and geocoding to reveal these findings.
]]>Electrochem doi: 10.3390/electrochem4020013
Authors: Jinghui Miao
With the surge of electric vehicles, fast charging has become one of the major challenges for the development of Li-ion and Li metal batteries. The degradation of battery electrodes at fast charging has been identified as among the gating factors. While there have been extensive studies on anode and cathode degradation modes, not sufficient efforts have been made to dive deep into the kinetics of battery charging and its influence on electrode degradation, especially during fast charging. This review presents a comprehensive yet concentrated perspective into such issues. By tracing back to the kinetic origins of battery charging, it is revealed that the intrinsic properties of electrode active materials and the microstructures of electrode are of great importance in determining electrode kinetics. Most of the electrode degradation modes are closely related to the high overpotentials and the spatial inhomogeneity in Li concentration and pertinent characteristics, which are results of the sluggish electrode kinetics during fast charging. Approaches to mitigate electrode degradation are summarized from the aspect of improving electrode kinetics and circumventing detrimental side reactions.
]]>Electrochem doi: 10.3390/electrochem4020012
Authors: Munira Siddika Md. Mahmudul Hasan Tahamida A. Oyshi Mohammad A. Hasnat
Water pollution has badly affected human health, aquatic life, and the ecosystem. The purity of surface water can be measured in terms of dissolved oxygen (DO) measurements. Hence, it is desirable to have a portable and simple-to-use dissolved oxygen sensor. One possible remedy is an electrochemical sensor. Thus, we proposed an ITO-IrOx electrocatalyst for an effective and interference-free DO sensor utilizing the principle of oxygen reduction reaction (ORR). The ITO-IrOx was characterized using cyclic voltammetry (CV), scanning electron microscopy (SEM), electrochemical impedance spectrometry (EIS), X-ray photoelectron spectroscopy (XPS), and reflectance spectroscopy-based techniques. Reflectance spectra of the ITO-IrOx electrode showed the photoresist capability. The EIS spectra revealed lower charge transfer resistance for the ITO-IrOx electrode in ORR. The IrOx film on ITO exhibited a quick (one electron, α = 1.00), and reversible electron transfer mechanism. The electrode demonstrated high stability for oxygen sensing, having a limit of detection (LOD) of 0.49 ppm and interference-free from some common ions (nitrate, sulphate, chloride etc.) found in water.
]]>Electrochem doi: 10.3390/electrochem4010011
Authors: Rossarin Ampairojanawong Ajalaya Boripun Sayan Ruankon Thanapong Suwanasri Kraipat Cheenkachorn Tawiwan Kangsadan
Electrically driven separation (EDS) technology with a high voltage (HV) alternating current source (AC) was used to remove glycerol and other contaminants from biodiesel in order to meet the ASTM D6751 and EN 14214 standards. Biodiesel was produced from a transesterification of refined palm oil and methanol using sodium methylate as a homogeneous catalyst. The effects of an Iron (Fe) electrode, including types of electrode configurations, vertical distance between electrodes, applied voltage, and separation time, were studied. Furthermore, the effects of the remaining catalyst and soap content in biodiesel phase were also investigated to improve the separating performance using the EDS technique. The EDS using HVAC and low amperage with a point-to-point electrode configuration showed the highest separation efficiency of 99.8%. The optimum vertical distance between electrodes was 3 cm, while the optimum applied voltage was 3 kV. The separation time of 240 s yielded the best separating performance, completely eliminating the unreacted catalyst, and the lowest of the normalized remaining soap value content was obtained. Considering all of this, the EDS technique had higher efficiency to remove glycerol and other contaminants than a conventional separation of gravitation settling. The final biodiesel product was produced with the high purity of 98.0 wt% after purification and met all standard specifications.
]]>Electrochem doi: 10.3390/electrochem4010010
Authors: Meryem Zouarhi
Iron is a widely used metal due to its low cost and availability, but it is susceptible to corrosion in many circumstances. This corrosion can result in economic and environmental losses, and negatively affect the physical and chemical properties of the metal. This chapter provides a background on iron corrosion in archaeology and introduces various inhibitors used for its protection. It starts with a general overview of corrosion and metallurgy of iron, followed by an in-depth explanation of the mechanisms of iron corrosion in water and air. The chapter concludes with a review of different corrosion inhibitors, focusing on those made from natural plant extracts.
]]>Electrochem doi: 10.3390/electrochem4010009
Authors: Jamuna Thapa Magar Indra Kumari Budhathoki Anil Rajaure Hari Bhakta Oli Deval Prasad Bhattarai
Green corrosion inhibitors are of great interest due to their exciting and environmentally friendly behavior in mild steel corrosion control during and after the acid cleaning process. Herein, alkaloids were extracted from the stem of Ageratina adenophora and were ensured by qualitative chemical tests as well as spectroscopic test methods. The corrosion inhibition efficacy of the alkaloids against mild steel corrosion was evaluated by gravimetric, electrochemical and EIS measurement methods. In addition, the adsorption isotherm, free energy of adsorption and thermodynamic parameters of the process were evaluated. The investigations indicated the most promising inhibition efficacy of the alkaloids for mild steel corrosion. The adsorption isotherm study revealed that the adsorption of inhibitor molecules on the MS interface was manifested by dominant physisorption followed by chemisorption. Free energy and thermodynamic parameters are well suited to endothermic processes.
]]>Electrochem doi: 10.3390/electrochem4010008
Authors: Van Tu Nguyen Hung Tran Nguyen Nu Huong Tran
In this paper, ZnO nanorods were synthesized by the hydrothermal method and used as anodes for zinc-silver batteries. The Tafel and EIS curve analysis results show that ZnO nanorods have better anti-corrosion and charge transport properties than ZnO powders. At 0.1 C discharge conditions, the ZnO electrode exhibits more stable cycle efficiency than the powder electrode; after 25 cycles, the capacity is higher by 95%. The superior electrochemical performance is due to the ZnO nanorods having the ability to conduct electrons and increase the surface area. Therefore, the possible growth mechanism of ZnO nanorods has been investigated.
]]>Electrochem doi: 10.3390/electrochem4010007
Authors: Electrochem Editorial Office Electrochem Editorial Office
High-quality academic publishing is built on rigorous peer review [...]
]]>Electrochem doi: 10.3390/electrochem4010006
Authors: Bongiwe Silwana Mangaka Matoetoe
High levels of H2O2 in food can lead to oxidative stress. Which has been linked to a number of neurological diseases. Hence, its detection in beverages is essential. However, a complicated structure of the reaction medium of H2O2 makes the detection procedure very difficult. For this reason, sensitive strategic methods are required. In this study, quantification of H2O2 in milk and apple juice has been obtained via the electrochemical sensing platform based on GCE/SiO-CeONPs. Scanning Electron Microscopy (SEM), Cyclic voltammetry(CV), and electron impedance spectroscopy(EIS) were employed to characterize the composite. The kinetics investigation of the sensor with H2O2 revealed an a quasi-reversible one -electron adsorption process. Under optimized conditions, the Differential Pulse Voltammetry (DPV) in 0.1 M Phosphate buffer (PB) pH 5.5 of the H2O2 displayed a peak at 0.13 V vs. Ag/AgCl with the detection limits of 0.0004 µM, linearity range of 0.01–0.08 µM. The observed LOD values of this method for real samples were calculated to be 0.006 µM and 0.007 µM with LOQ of 0.02 µM for milk and apple juice, respectively. The recovery of the analyte was from 92 to 99%. Furthermore, due to good selectivity and stability, the benefit of this sensor is its applicability in multiple fields.
]]>Electrochem doi: 10.3390/electrochem4010005
Authors: Yaniv Shlosberg Kimi C. Rubino Nathan S. Nasseri Andrea S. Carlini
In recent years, clean energy technologies that meet ever-increasing energy demands without the risk of environmental contamination has been a major interest. One approach is the utilization of plant leaves, which release redox-active NADPH as a result of photosynthesis, to generate photocurrent. In this work, we show for the first time that photocurrent can be harvested directly from the fruit of a cherry tree when associated with a bio-electrochemical cell. Furthermore, we apply electrochemical and spectroscopic methods to show that NADH in the fruit plays a major role in electric current production.
]]>Electrochem doi: 10.3390/electrochem4010004
Authors: Ítala M. G. Marx
Food quality and safety pose an increasing threat to human health worldwide [...]
]]>Electrochem doi: 10.3390/electrochem4010003
Authors: Md. Mahmudul Hasan
Recently, ascorbic acid (AA) has been studied as an environment-friendly fuel for energy conversion devices. This review article has deliberated an overview of ascorbic acid electrooxidation and diverse ion exchange types of AA-based fuel cells for the first time. Metal and carbon-based catalysts generated remarkable energy from environment-friendly AA fuel. The possibility of using AA in a direct liquid fuel cell (DLFC) without emitting any hazardous pollutants is discussed. AA fuel cells have been reviewed based on carbon nanomaterials, alloys/bimetallic nanoparticles, and precious and nonprecious metal nanoparticles. Finally, the obstacles and opportunities for using AA-based fuel cells in practical applications have also been incorporated.
]]>Electrochem doi: 10.3390/electrochem4010002
Authors: Gongshin Qi Jiazhi Hu Michael Balogh Lei Wang Devendrasinh Darbar Wei Li
Li and Mn-rich layered cathode (LLC) materials show great potential as the next generation cathode materials because of their high, practical and achievable specific capacity of ~250 mAh/g, thermal stability and lower raw material cost. However, LLC materials suffer from degradation of specific capacity, voltage fading due to phase transformation upon cycling and transition-metal dissolution, which presents a significant barrier for commercialization. Here, we report the effects of Ni content on the electrochemical performance, structural and thermal stability of a series of Co-free, LLC materials (Li1.2NixMn0.8-xO2, x = 0.12, 0.18, 0.24, 0.30 and 0.36) synthesized via a sol-gel method. Our study shows that the structure of the material as well as the electrochemical and thermal stability properties of the LLC materials are strongly dependent on the Ni or Mn content. An increase in the Ni to Mn ratio results in an increase in the average discharge voltage and capacity, as well as improved structural stability but decreased thermal stability.
]]>Electrochem doi: 10.3390/electrochem4010001
Authors: Muneendra Prasad Arcot Magnus Cronin Michael Fowler Mark Pritzker
Catalyst layer defects and irregularities in catalyst-coated membrane (CCM) electrodes affect the lifetime of polymer electrolyte membrane fuel cells (PEMFCs) during their operation. Thus, catalyst layer defects are important concerns for fuel cell manufacturers and prompt the development of quality control systems with the aim of fabricating defect-free electrodes. Consequently, the objective of this study is to gain a fundamental understanding of the morphological changes of real catalyst layer defects that have developed during CCM production. In this paper, missing catalyst layer defects (MCLD) formed during the decal transfer process are investigated through a nondestructive method using reflected light microscopy. The geometric features of the defects are quantified, and their growth is measured at regular time intervals from beginning-of-life (BOL) to end-of-life (EOL) until the OCV has dropped by 20% of its initial value as per a DOE-designed protocol. Overall, two types of degradation are observed: surface degradation caused by catalyst erosion and crack degradation caused by membrane mechanical deformation. Furthermore, catalyst layer defects formed during the decal transfer process were found to exhibit a higher growth rate at middle-of-life (MOL-1) and stabilize by EOL. This type of study will provide manufacturers with baseline information to allow them to select and reject CCMs, ultimately increasing the lifetime of fuel cell stacks.
]]>Electrochem doi: 10.3390/electrochem3040055
Authors: Khaja Wahab Ahmed Myeong Je Jang Saeed Habibpour Zhongwei Chen Michael Fowler
Hydrogen production using an Anion exchange membrane (AEM) electrolyzer allows the use of non-platinum group metal catalysts for oxygen evolution reaction (OER). Nickel and Cobalt-based oxides are active in an alkaline environment for OER and are relatively inexpensive compared to IrO2 catalysts used in Polymer electrolyte membrane (PEM) electrolysis. Mixed metal oxide catalysts NiFeOx and NiFeCoOx catalysts were synthesized by the coprecipitation method using NaOH. X-ray diffraction results showed mainly NiO diffraction peaks for the NiFeOx catalyst due to the low concentration of Fe, for the NiFeCoOx catalyst, NiCo2O4 diffraction peaks were observed. NiFeCoOx catalysts showed a higher Anion exchange membrane water electrolysis (AEMWE) performance compared to NiFeOx and commercial NiO, the highest current density at 2 V was 802 mA cm−2 at 70 °C using 1 M KOH as an electrolyte. The effect of electrolyte concentration was studied by using 0.01 M, 0.1 M and 1 M KOH concentrations in an electrolysis operation. Electrochemical Impedance spectroscopy was performed along with the equivalent circuit fitting to calculate ohmic and activation resistances, the results showed a decrease in ohmic and activation resistances with the increase in electrolyte concentration. Commercially available AEM (Fumasep FAA-3-50 and Sustainion dioxide membrane X-37-50 grade T) were tested at similar conditions and their performance was compared. EIS results showed that X-37-50 offered lower ohmic resistance than the FAA-3-50 membrane.
]]>Electrochem doi: 10.3390/electrochem3040054
Authors: Onisha Thapa Jamuna Thapa Magar Hari Bhakta Oli Anil Rajaure Durga Nepali Deval Prasad Bhattarai Tanka Mukhiya
The residual ions of the acid cleaning processes induce the further corrosion of the metals, and this could be minimized using green inhibitors. Alkaloids extracted from plant parts could be cost effective and efficient inhibitors. In this work, alkaloids from Solanum xanthocarpum stem were successfully extracted, and they were characterized by qualitative chemical tests and spectroscopic measurements. As-extracted alkaloids were employed as green corrosion inhibitors for mild steel. The effectiveness of the inhibitor was determined by the weight loss and electrochemical measurement methods. From the weight loss measurement, the maximum inhibition efficiency of 93.14% was achieved. The temperature effect study revealed that the inhibitor can work up to a temperature of 58 °C. This could be one of the highest working temperatures among the reported green inhibitors. The electrochemical measurement reveals that the alkaloids could inhibit effectively up to 98.14% of the corrosion and serve as a mixed-type green inhibitor. A study on the kinetic parameters reflects that the inhibitor forms a potential barrier for the protection of a mild steel surface against corrosion. The values obtained from the thermodynamic parameters study reflect that the process is a spontaneous endothermic process. Based on the findings, it is revealed that the alkaloids extracted from S. xanthocarpum can serve as an excellent, eco-friendly and a promising green inhibitor against mild steel corrosion.
]]>Electrochem doi: 10.3390/electrochem3040053
Authors: Daniela Nunes da Silva Arnaldo César Pereira
The present work consisted of the development of an electrode based on carbon paste modified with magnetic molecularly imprinted polymer (CPE-MagMIP) for 17-β-estradiol (E2) detection. The incorporation of magnetic material (MagMIP) improved sensor performance, an increase of over 317%. The proposed method resulted in a linear response range from 0.5 to 14.0 μM, and the detection limit (LOD) and quantification limit (LOQ) were equal to 0.13 and 0.44 μM, respectively. Under optimized conditions, the developed sensor obtained satisfactory parameters in E2 determination in water samples, demonstrating selectivity, accuracy, and precision, making it a promising method for monitoring E2 in environmental samples.
]]>Electrochem doi: 10.3390/electrochem3040052
Authors: André H. B. Dourado
The electric double layer (EDL) is the most important region for electrochemical and heterogeneous catalysis. Because of it, its modeling and investigation are something that can be found in the literature for a long time. However, nowadays, it is still a hot topic of investigation, mainly because of the improvement in simulation and experimental techniques. The present review aims to present the classical models for the EDL, as well as presenting how this region affects electrochemical data in everyday experimentation, how to obtain and interpret information about EDL, and, finally, how to obtain some molecular point of view insights on it.
]]>Electrochem doi: 10.3390/electrochem3040051
Authors: Mehrnaz Javadipour Toshan Wickramanayake Seyed Amir Alavi Kamyar Mehran
Lithium-ion batteries (LiBs) are used as the main power source in electric vehicles (EVs). Despite their high energy density and commercial availability, LiBs chronically suffer from non-uniform cell ageing, leading to early capacity fade in the battery packs. In this paper, a non-invasive, online characterisation method based on deep learning models is proposed for cell-level SoH estimation. For an accurate measurement of the state of health (SoH), we need to characterize electrochemical capacity fade scenarios carefully. Then, with the help of real-time monitoring, the control systems can reduce the LiB’s degradation. The proposed method, which is based on convolutional neural networks (CNN), characterises the changes in current density distributions originating from the positive electrodes in different SoH states. For training and classification by the deep learning model, current density images (CDIs) were experimentally acquired in different ageing conditions. The results confirm the efficiency of the proposed approach in online SoH estimation and the prediction of the capacity fade scenarios.
]]>Electrochem doi: 10.3390/electrochem3040050
Authors: Andrey Suzdaltsev
Due to its prevalence in nature and its particular properties, silicon is one of the most popular materials in various industries. Currently, metallurgical silicon is obtained by carbothermal reduction of quartz, which is then subjected to hydrochlorination and multiple chlorination in order to obtain solar silicon. This mini-review provides a brief analysis of alternative methods for obtaining silicon by electrolysis of molten salts. The review covers factors determining the choice of composition of molten salts, typical silicon precipitates obtained by electrolysis of molten salts, assessment of the possibility of using electrolytic silicon in microelectronics, representative test results for the use of electrolytic silicon in the composition of lithium-ion current sources, and representative test results for the use of electrolytic silicon for solar energy conversion. This paper concludes by noting the tasks that need to be solved for the practical implementation of methods for the electrolytic production of silicon, for the development of new devices and materials for energy distribution and microelectronic application.
]]>Electrochem doi: 10.3390/electrochem3040049
Authors: Maria Zaib Umar Farooq Muhammad Makshoof Athar
In this study, an electrochemical sensor for the monitoring of Hg (II) at trace levels by using differential pulse anodic stripping voltammetry has been reported. Basically the electrochemical sensor is a Phanerochaete chrysosporium-based carbon paste electrode. Here, Phanerochaete chrysosporium has played a new vital role in electrochemical detection of heavy metal apart from its known contribution in their removal. Optimal voltammetric response was observed at −0.7 V deposition potential l, 5% biomass concentration ratio (w/w), and neutral pH conditions with 12 min as the accumulation time. Selectivity was evaluated in the presence of different interfering cations. Linear range was observed for 5–50 µgL−1 of metal concentration with a detection limit of 4.4 µgL−1. The equivalence of new and reference analytical methods was statistically assessed in mercury samples collected from chlor-alkali industrial effluent by correlation of results (Pearson’s product-moment correlation), weighted Deming regression analysis, paired comparison test, relative standard deviation (RSD), median relative error (MRE), root mean square error (RMSE), and predicted residual sum of square (PRESS). This work presented a simple, efficient, and promising analytical tool in trace level detection of Hg (II), as compared to previously reported carbon paste electrodes based on biological material.
]]>Electrochem doi: 10.3390/electrochem3040048
Authors: Lena Birkner Maik Eichelbaum
Platinum dissolution in PEM fuel cells is an increasingly important indicator for the state-of-health and lifetime prediction of fuel cells in real applications. For this reason, portable online analysis tools are needed that can detect and quantify platinum with high sensitivity, selectivity, and accuracy in the product water of fuel cells. We validated the hanging mercury drop electrode (HMDE) and non-toxic bismuth film electrodes for the voltammetric determination of platinum for this purpose. Bismuth films were prepared by reductive deposition on both a glassy carbon solid state electrode and on a screen-printed electrode (film on-chip electrode). Both bismuth film electrodes could be successfully validated for the determination of platinum by adsorptive stripping voltammetry. An LOD of 7.9 μg/L and an LOQ of 29.1 μg/L were determined for the bismuth film solid state electrode, values of 22.5 μg/L for the LOD and of 79.0 μg/L for the LOQ were obtained for the bismuth film on-chip electrode. These numbers are still much higher than the results measured with the HMDE (LOD: 0.76 ng/L; LOQ: 2.8 ng/L) and are not sufficient to detect platinum in the product water of a fuel cell run in different load tests. The amount of dissolved platinum produced by a 100 W fuel cell stack upon dynamic and continuous high load cycling, respectively, was in the range of 2.9–4.1 ng/L, which could only be detected by the HMDE.
]]>Electrochem doi: 10.3390/electrochem3040047
Authors: Hari Bhakta Oli Jamuna Thapa Magar Nawaraj Khadka Anup Subedee Deval Prasad Bhattarai Bishweshwar Pant
Using natural plant extracts on metallic substances is the most frequently studied green corrosion inhibition approach in corrosion science. In this work, Coriaria nepalensis Stem Alkaloid (CNSA) has been successfully extracted and characterized by qualitative chemical (Mayer’s and Dragendroff’s) test and spectroscopic (UV and FTIR) measurement. CNSA has been employed as a green inhibitor for Mild Steel (MS) corrosion subjected to 1 M H2SO4 solution. The corrosion inhibition efficacy has been assessed by weight loss and polarization measurement methods. The effect of inhibitor concentration, immersion period, and temperature on the inhibition efficiency for the MS immersed in both acid and inhibitor solutions of different concentrations have been investigated. The maximum inhibition effect observed for CNSA is 96.4% for MS immersed in 1000 ppm inhibitor solution for 6 h at 18 °C by the weight loss measurement method. Similarly, the polarization measurement method observed a 97.03% inhibition efficiency for MS immersed for 3 h. The adsorption of inhibitor molecules on the MS surface aligns with the Langmuir model. The free energy of adsorption obtained is −28.75 kJ/mol indicating physical adsorption dominance over chemical adsorption. These findings suggested that CNSA has greater potential as an efficient green inhibitor.
]]>Electrochem doi: 10.3390/electrochem3040046
Authors: Ponraj Jeyabarathi Lakshmanan Rajendran Michael E. G. Lyons Marwan Abukhaled
The theoretical model for a packed porous catalytic particle of the slab, cylindrical, and spherical geometries shape in fixed-bed electrochemical reactors is discussed. These particles have internal mass concentration and temperature gradients in endothermic or exothermic reactions. The model is based on a nonlinear reaction–diffusion equation containing a nonlinear term with an exponential relationship between intrinsic reaction rate and temperature. The porous catalyst particle’s concentration is obtained by solving the nonlinear equation using Akbari-Ganji’s method. A simple and closed-form analytical expression of the effectiveness factor for slab, cylindrical, and spherical geometries was also reported for all values of Thiele modulus, activation energy, and heat reaction. The accordance with results of a reliable numerical method shows the good accuracy that their approximate solution yields.
]]>Electrochem doi: 10.3390/electrochem3040045
Authors: Aijuan Li Yuanshuai Jiang Xinnian Sun Huajun Chi Chuanhu Niu Gang Liu
Electrochemical energy storage technology has the characteristics of convenient use, fast response, and flexible configuration. At present, the energy storage technology used in smart electric vehicles is mainly electrochemical energy storage technology. In particular, the promotion of electrochemical energy storage technology in the field of smart electric vehicles is an effective way to achieve the goal of carbon neutrality. One of the most critical issues limiting the development and popularity of intelligent electric vehicles is the performance and range of power batteries; vehicle path planning is very important to the performance of power batteries and the driving range. Improved path planning algorithms can obviously shorten the path length and reduce the time of searching and planning a path under the condition of the same starting point and end point, that is, to increase the range of the power battery. On the premise of the comprehensive analysis of the intelligent electric vehicle’s grasp of environmental information, trajectory planning methods are divided into local trajectory planning and global trajectory planning methods. The main content of the trajectory planning method is given, the key technologies involved in the research are discussed, and its advantages and disadvantages are analyzed. Finally, the main development trends of intelligent electric vehicle trajectory planning technology in the future are proposed.
]]>Electrochem doi: 10.3390/electrochem3040044
Authors: Rajaram Karki Ajay Kumar Bajgai Nawaraj Khadka Onisha Thapa Tanka Mukhiya Hari Bhakta Oli Deval Prasad Bhattarai
In situ corrosion inhibition in acid cleaning processes by using green inhibitors is at the forefront of corrosion chemistry. Plant extracts, especially alkaloids, are known to be good corrosion inhibitors against mild steel corrosion. In this research, alkaloids extracted from Acacia catechu have been used as green corrosion inhibitors for mild steel corrosion in a 1 M H2SO4 solution. Qualitative chemical tests and FTIR measurements have been performed to confirm the alkaloids in the extract. The inhibition efficiency of the extract has been studied by using weight-loss and potentiodynamic polarization methods. A weight-loss measurement has been adopted for the study of inhibitor’s concentration effect, with a variation employed to measure the inhibition efficiency for time and temperature. The weight-loss measurement revealed a maximum efficiency of 93.96% after 3 h at 28 °C for a 1000 ppm alkaloid solution. The 1000 ppm inhibitor is effective up to a temperature of 48 °C, with 84.39% efficiency. The electrochemical measurement results revealed that the alkaloids act as a mixed type of inhibitor. Inhibition efficiencies of 98.91% and 98.54% in the 1000 ppm inhibitor concentration solution for the as-immersed and immersed conditions, respectively, have been achieved. The adsorption isotherm has indicated the physical adsorption of alkaloids. Further, the spontaneous and endothermic adsorption processes have been indicated by the thermodynamic parameters. The results show that alkaloids extracted from the bark of Acacia catechu can be a promising green inhibitors for mild steel corrosion.
]]>Electrochem doi: 10.3390/electrochem3040043
Authors: Sergey V. Sokolkov
Digital medicine based on the integration of all medical data from a particular patient has become a reality today, thanks to information technology. Traditional medical examinations can be supplemented by assessment results of the oxidative-anti-oxidative (OAO) status of the body. Electrochemical sensors are able to not only determine the integral indicators of the OAO system of the body but also to depict details of the processes occurring in the system. The main obstacle to the widespread use of electrochemical sensors in medical diagnostics is the extremely small amount of received information in comparison to the tens of thousands of known human diseases. The problem can be eliminated only by rethinking the purpose of electrochemical measurement within the framework of thermodynamics of information processes and information theory. In the information paradigm of electrochemical analysis of biological fluids, a sample is considered an electrochemical message created by a sensor. The purpose of electrochemical measurement is to obtain information in a volume sufficient to identify the sample composition within the range of possible concentrations of its components. The fundamentals of the thermodynamics of information processes are considered and conclusions that are of practical importance for the development of electrochemical sensors and analyzers are derived. It is shown that the potentiostatic control of the sensor is physically impacted by the electromechanical instability of the electrical double layer, which is the main source of sensor signal noise. Estimates of a minimum amount of analytical signal information required for the identification of a sample of known composition, such as a biological fluid, are provided. Examples of highly informative analytical signals for flowing and stationary samples are presented. Problems related to the visualization of such signals are noted.
]]>Electrochem doi: 10.3390/electrochem3040042
Authors: Etienne Dijoux Nadia Yousfi Steiner Michel Benne Marie-Cécile Péra Brigitte Grondin-Perez
Reliability of proton exchange membrane fuel cells (PEMFCs) is a major issue for large industrialization and commercialization. Indeed, performance can be degraded due to abnormal operating conditions, namely, faults, which lead either to a transient decay of the fuel cell performance or to permanent damage that cannot be recovered. The literature shows that long-time exposure to faults leads to fuel cell degradation. Therefore, it is necessary to use tools that can not only diagnose these faulty conditions, but also modify the fuel cell operations to recover a healthy operating point. For that purpose, one approach is the Active Fault Tolerant Control (AFTC) strategy which is composed of three functions. First, a diagnosis part allows fault detection and identification. Then a decision part, which is an algorithm aiming at finding a new operating point that mitigates the occurring fault. Finally, a control part applies the mitigation strategy established by the decision algorithm. The present work focuses on the decision part. and aims to bring a new contribution to PEMFCs reliability improvement and address water management issues, namely, the cell flooding and membrane drying out with the developed AFTC tool. The strategy is tested and validated on a single PEMFC cell and results are presented, analyzed, and discussed.
]]>Electrochem doi: 10.3390/electrochem3040041
Authors: Mansi Gandhi Khairunnisa Amreen Brahm Kumar Tiwari
Naturally occurring phytonutrients/phyto-components are likely to have therapeutic values. These phyto-derived naturally occurring components, such as polyphenols, phenolics, flavonoids and phenolic acids have a hydrocarbon background with a polyphenolic ring, an ester bond with a polyphenolic ring, etc. Their structures play a critical role in determining the chemical and physical attributes that define their activity/functions and roles. Owing to their chemical structure, most of them are electroactive. Thus, these phytochemicals can be used in the preparation of electrochemical sensors. Gaining an understanding of functional genotypical units using electrochemistry is a unique study. The feasibility of incorporating an array of biosensors into a fully-automated micro-electrochemical system is further explored. This review is intended to provide in-depth knowledge of biosensors’ applications based on/for Plantae kingdom and varieties. The discussion focuses primarily on the fields associated with the fully-automated micro-electrochemical system and appropriate methods for its advancement. The intended approach is to provide a selective outlook including the setbacks/shortcomings and usefulness of opting for the concerned technique.
]]>Electrochem doi: 10.3390/electrochem3040040
Authors: Khaja Wahab Ahmed Myeong Je Jang Moon Gyu Park Zhongwei Chen Michael Fowler
Hydrogen is considered to be the fuel of the future and with the advancement of fuel cell technology, there is a renewed interest in hydrogen production by the electrolysis of water. Among low-temperature water electrolysis options, polymer electrolyte membrane (PEM) electrolyzer is the preferred choice due to its compact size, intermittent use, and connectivity with renewable energy. In addition, it is possible to generate compressed hydrogen directly in the PEM electrolyzer, thereby reducing the additional pressurization cost for hydrogen storage. The development of electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is a major focus of electrolysis research. Other components, such as PEMs, gas diffusion layers (GDL), and bipolar plates (BPs) have also received significant attention to enhance the overall efficiency of PEM electrolyzers. Improvements in each component or process of the PEM electrolyzer have a significant impact on increasing the energy efficiency of the electrolyzer. This work discusses various synthesis techniques to improve the dispersion of OER electrocatalyst and reducing catalyst loading for the PEM electrolyzer. Various techniques are discussed for the development of electrocatalysts, including nanostructured, core shell, and electrodeposition to deposit catalysts on GDL. The design and methodology of new and improved GDL are discussed along with the fabrication of gas diffusion electrodes and passivation techniques to reduce the oxidation of GDL. The passivation technique of BPs using Au and Pt is summarized for its effect on electrolysis efficiency. Finally, the optimization of various operating conditions for PEM electrolyzer are reviewed to improve the efficiency of the electrolyzer.
]]>Electrochem doi: 10.3390/electrochem3040039
Authors: Shifa Felemban Patricia Vazquez Thanih Balbaied Eric Moore
Lab-on-a-chip has recently become an alternative for in situ monitoring for its portability and simple integration with an electrochemical immunoassay. Here, we present an electrochemical cell-on-a-chip configured in a three-electrode system to detect benzo(a)pyrene (BaP) in water. 11-Mercaptoundecanoic acid (MUA), a self-assembled monolayer (SAM), was used to modify a gold chip surface to reduce the randomness of antibody binding. A carboxylic acid group was activated with -ethyl-3-(3-dimethylaminopropyl) (EDC) in combination with N-hyrodsuccinimide (NHS) before antibody immobilisation. The mechanism of the electrochemical reactions on a gold surface and SAM formation were investigated by cyclic voltammetry and contact angle measurements. The data revealed a lower contact angle in the modified chip and a scan rate of 50 mV/s. Through the addition of modification layers and thiol end groups to the SAM, our design allowed the chip surface to became more insulated. All were tested by amperometric detection using the developed Q-sense system. This novel technique detected multiple samples, and completed the analysis reasonably quickly. While the integrated system proved successful in a lab setting, the aim of the research is to use this system for in situ analysis, which can be brought into a water environment to carry out tests with existing processes. In this way, any issues that may arise from an environmental setting can be rectified in an efficient manner.
]]>Electrochem doi: 10.3390/electrochem3030038
Authors: Selvaraj Chinnathambi Mahinder Ramdin Thijs J. H. Vlugt
Mass transport of different species plays a crucial role in electrochemical conversion of CO2 due to the solubility limit of CO2 in aqueous electrolytes. In this study, we investigate the transport of CO2 and other ionic species through the electrolyte and the membrane, and its impact on the scale-up process of HCOO−/HCOOH formation. The mass transport of ions to the electrode and the membrane is modelled at constant current density. The mass transport limitations of CO2 on the formation of HCOO−/HCOOH is investigated at different pressures ranges from 5–40 bar. The maximum achievable partial current density of formate/formic acid is increased with increasing CO2 pressure. We use an ion exchange membrane model to understand the ion transport behaviour for both the monopolar and bipolar membranes. The cation exchange (CEM) and anion exchange membrane (AEM) model show that ion transport is limited by the electrolyte salt concentrations. For 0.1 M KHCO3, the AEM reaches the limiting current density more quickly than the CEM. For the BPM model, ion transport across the diffusion layer on either side of the BPM is also included to understand the concentration polarization across the BPM. The model revealed that the polarization losses across the bipolar membrane depend on the pH of the electrolyte used for the CO2 reduction reaction (CO2RR). The polarization loss on the anolyte side decreases with an increasing pH, while, on the cathode side, it increases with increasing catholyte pH. With this combined model for the electrode reactions and the membrane transport, we are able to account for the various factors influencing the polarization losses in the CO2 electrolyzer. To complete the analysis, we simulated the full cell polarization curve and fitted with the experimental data.
]]>Electrochem doi: 10.3390/electrochem3030037
Authors: Douglas Vieira Thomaz Riccardo Goldoni Gianluca Martino Tartaglia Cosimino Malitesta Elisabetta Mazzotta
Electrochemical immunosensors are often described as innovative strategies to tackle urgent epidemiological needs, such as the detection of SARS-CoV-2 main biomarker, the spike glycoprotein. Nevertheless, there is a great variety of receptors, especially recombinant antibodies, that can be used to develop these biosensing platforms, and very few reports compare their suitability in analytical device design and their sensing performances. Therefore, this short report targeted a brief and straightforward investigation of the performance of different impedimetric biorecognition surfaces (BioS) for SARS-CoV-2, which were crafted from three commonly reported recombinant antibodies and molecularly-imprinted polymer (MIP) nanoparticles (nanoMIP). The selected NanoMIP were chosen due to their reported selectivity to the receptor binding domain (RBD) of SARS-CoV-2 spike glycoprotein. Results showed that the surface modification protocol based on MUDA and crosslinking with EDC/NHS was successful for the anchoring of each tested receptor, as the semicircle diameter of the Nyquist plots of EIS increased upon each modification, which suggests the increase of Rct due to the binding of dielectric materials on the conductive surface. Furthermore, the type of monoclonal antibody used to craft the BioS and the artificial receptors led to very distinct responses, being the RBD5305 and the NanoMIP-based BioS the ones that showcased the highest increment of signal in the conditions herein reported, which suggests their adequacy in the development of impedimetric immunosensors for SARS-CoV-2 spike glycoprotein.
]]>Electrochem doi: 10.3390/electrochem3030036
Authors: Boyang Li Lihua Zhang Jianrui Zhang Yaqiong Su
The design and preparation of novel, high-efficiency, and low-cost heterogeneous catalysts are important topics in academic and industry research. In the past, inorganic materials, metal oxide, and carbon materials were used as supports for the development of heterogeneous catalysts due to their excellent properties, such as high specific surface areas and tunable porous structures. However, the properties of traditional pristine carbon materials cannot keep up with the sustained growth and requirements of industry and scientific research, since the introduction of nitrogen atoms into carbon materials may significantly enhance a variety of their physicochemical characteristics, which gradually become appropriate support for synthesizing supported transition metal catalysts. In the past several decades, the transition metal anchored on nitrogen-doped carbon catalysts has attracted a tremendous amount of interest as potentially useful catalysts for diverse chemical reactions. Compared with original carbon support, the doping of nitrogen atoms can significantly regulate the physicochemical properties of carbon materials and allow active metal species uniformly dispersed on the support. The various N species in support also play a critical role in accelerating the catalytic performance in some reactions. Besides, the interaction between support and transition metal active sites can offer an anchor site to stabilize metal species during the preparation process and then improve reaction performance, atomic utilization, and stability. In this review, we highlight the recent advances and the remaining challenges in the preparation and application of transition metal anchored on nitrogen-doped carbon catalysts.
]]>Electrochem doi: 10.3390/electrochem3030035
Authors: Bin Zhao
A three-dimensional (3D) hybrid nanostructure of Fe3O4 nanoparticles uniformly anchored on vertically-aligned carbon nanotubes (VACNTs) was fabricated by a facile two-step method. Assisted by supercritical carbon dioxide (SCCO2), the Fe precursor was firstly absorbed on CNT surface and then transformed into Fe3O4 nanoparticles by vacuum thermal annealing. Owing to the synergetic effects of well-distributed Fe3O4 nanoparticles (~7 nm) and highly conductive VACNTs, the hybrid electrode exhibits a high specific capacitance of 364.2 F g−1 at 0.5 A g−1 within the potential range from −0.9 to +0.1 V in Na2SO3 electrolyte and an excellent cycling stability of 84.8% capacitance retention after 2000 cycles at a current density of 4 A/g. This 3D hybrid architecture consisting of aligned CNTs and pseudocapacitive metal oxide may be a promising electrode for high-performance supercapacitors.
]]>Electrochem doi: 10.3390/electrochem3030034
Authors: Gerardo Salinas Bernardo A. Frontana-Uribe
Conducting polymers (CPs) are highly conjugated organic macromolecules, where the electrical charge is transported in intra- and inter-chain pathways. Polyacetylene, polythiophene and its derivatives, polypyrrole and its derivatives, and polyaniline are among the best-known examples. These compounds have been used as electrode modifiers to gain sensitivity and selectivity in a large variety of analytical applications. This review, after a brief introduction to the electrochemistry of CPs, summarizes the application of CPs’ electrode interfaces towards heavy metals’ detection using potentiometry, pulse anodic stripping voltammetry, and alternative non-classical electrochemical methods.
]]>Electrochem doi: 10.3390/electrochem3030033
Authors: Singaravel Anandhar Salai Sivasundari Rathinam Senthamarai Mohan Chitra Devi Lakshmanan Rajendran Michael E. G. Lyons
The mathematical model proposed by Chapman and Antano (Electrochimica Acta, 56 (2010), 128–132) for the catalytic electrochemical–chemical (EC’) processes in an irreversible second-order homogeneous reaction in a microelectrode is discussed. The mass-transfer boundary layer neighbouring an electrode can contribute to the electrode’s measured AC impedance. This model can be used to analyse membrane-transport studies and other instances of ionic transport in semiconductors and other materials. Two efficient and easily accessible analytical techniques, AGM and DTM, were used to solve the steady-state non-linear diffusion equation’s infinite layers. Herein, we present the generalized approximate analytical solution for the solute, product, and reactant concentrations and current for the small experimental values of kinetic and diffusion parameters. Using the Matlab/Scilab program, we also derive the numerical solution to this problem. The comparison of the analytical and numerical/computational results reveals a satisfactory level of agreement.
]]>Electrochem doi: 10.3390/electrochem3030032
Authors: Maedeh Najafi Sebastiano Bellani Valerio Galli Marilena Isabella Zappia Ahmad Bagheri Milad Safarpour Hossein Beydaghi Matilde Eredia Lea Pasquale Riccardo Carzino Simone Lauciello Jaya-Kumar Panda Rosaria Brescia Luca Gabatel Vittorio Pellegrini Francesco Bonaccorso
In this work, we report the synthesis of an active material for supercapacitors (SCs), namely α-Fe2O3/carbon composite (C-Fe2O3) made of elongated nanoparticles linearly connected into a worm-like morphology, by means of electrospinning followed by a calcination/carbonization process. The resulting active material powder can be directly processed in the form of slurry to produce SC electrodes with mass loadings higher than 1 mg cm−2 on practical flat current collectors, avoiding the need for bulky porous substrate, as often reported in the literature. In aqueous electrolyte (6 M KOH), the so-produced C-Fe2O3 electrodes display capacity as high as ~140 mAh g−1 at a scan rate of 2 mV s−1, while showing an optimal rate capability (capacity of 32.4 mAh g−1 at a scan rate of 400 mV s−1). Thanks to their poor catalytic activity towards water splitting reactions, the electrode can operate in a wide potential range (−1.6 V–0.3 V vs. Hg/HgO), enabling the realization of performant quasi-symmetric SCs based on electrodes with the same chemical composition (but different active material mass loadings), achieving energy density approaching 10 Wh kg−1 in aqueous electrolytes.
]]>Electrochem doi: 10.3390/electrochem3030031
Authors: Samia Alsefri Thanih Balbaied Ibtihaj Albalawi Hanan Alatawi Eric Moore
PCBs (polychlorinated biphenyls) are a very large group of organic compounds that have between two and ten chlorine atoms attached to the biphenyl. These compounds have an acute impact as environmental pollutants, causing cancer and other adverse health effects in humans. It is therefore imperative to develop techniques for the cost-effective detection of PCBs at very low concentrations in ecosystems. In this paper, a novel label-free, indirect, competitive electrochemical immunosensor was first developed with a PCB-BSA conjugate. It is shown herein to compete with free PCBs for binding to the anti-PCB polyclonal primary antibody (IgY). Then, we used a secondary antibody to enhance the sensitivity of the sensor for the detection of PCB in a sample. It has been successfully immobilized on an 11-mercaptoundecanoic acid (11-MUA)-modified gold electrode via a carbodiimide-coupling reaction using cross-linking 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS) on the electrode surface. The immunosensor was investigated by cyclic voltammetry and differential pulse voltammetry in a standard solution of [Fe(CN)6]3−/4−. A linear range of 0.011–220 ng/mL−1 and a limit of detection (LOD) of 0.11 ng/mL−1 for PCBs detection were achieved by the developed immunosensor, showing advantages over conventional assays. The novel label-free electrochemical immunosensor discussed in this paper is a solution for simple, rapid, cost-effective sample screening in a portable, disposable format. The proposed immunosensor has good sensitivity, and it can prove to be an adequate real-time monitoring solution for PCBs in soil samples or other samples.
]]>Electrochem doi: 10.3390/electrochem3030030
Authors: Mansi Gandhi Khairunnisa Amreen
The profiling, or fingerprinting, of distinct varieties of the Plantae kingdom is based on the bioactive ingredients, which are systematically segregated to perform their detailed analysis. The secondary products portray a pivotal role in defining the ecophysiology of distinct plant species. There is a crucial role of the profiling domain in understanding the various features, characteristics, and conditions related to plants. Advancements in variable technologies have contributed to the development of highly specific sensors for the non-invasive detection of molecules. Furthermore, many hyphenated techniques have led to the development of highly specific integrated systems that allow multiplexed detection, such as high-performance liquid chromatography, gas chromatography, etc., which are quite cumbersome and un-economical. In contrast, electrochemical sensors are a promising alternative which are capable of performing the precise recognition of compounds due to efficient signal transduction. However, due to a few bottlenecks in understanding the principles and non-redox features of minimal metabolites, the area has not been explored. This review article provides an insight to the electrochemical basis of plants in comparison with other traditional approaches and with necessary positive and negative outlooks. Studies consisting of the idea of merging the fields are limited; hence, relevant non-phytochemical reports are included for a better comparison of reports to broaden the scope of this work.
]]>Electrochem doi: 10.3390/electrochem3030029
Authors: Davilal Parajuli Srijana Sharma Hari Oli Dilip Bohara Deval Bhattarai Arjun Tiwari Amar Yadav
Two different types of alkaloids are successfully extracted from two plants Artemisia vulgaris (AV) and Solanum tuberosum (ST) in the laboratory and used as corrosion inhibitors for mild steel samples. The corrosion inhibition potential of these alkaloids is determined by weight loss and potentiodynamic polarization measurement methods. Based on the weight loss measurement study of a sample immersed for 6 h in 1000 ppm inhibitor solution of AV and ST alkaloids, the corrosion inhibition efficiency is found to be 92.58% and 90.79%, respectively. The potentiodynamic polarization measurement shows 88.06% and 83.22% corrosion inhibition efficiency for AV and ST alkaloids, respectively, for the sample immersed for 1 h in 1000 ppm inhibitor solution. These promising efficiency and suitable immersion time effect can lead to the development of good green inhibitors.
]]>Electrochem doi: 10.3390/electrochem3030028
Authors: D. Parajuli Deb Kumar Shah Devendra KC Subhash Kumar Mira Park Bishweshwar Pant
The impact of doping concentration and thickness of n-InGaN and p-InGaN regions on the power conversion efficiency of single junction-based InGaN solar cells was studied by the Silvaco ATLAS simulation software. The doping concentration 5 × 1019 cm−3 and 1 × 1015 cm−3 were optimized for n-InGaN and p-InGaN regions, respectively. The thickness of 300 nm was optimized for both n-InGaN and p-InGaN regions. The highest efficiency of 22.17% with Jsc = 37.68 mA/cm2, Voc = 0.729 V, and FF = 80.61% was achieved at optimized values of doping concentration and thickness of n-InGaN and p-InGaN regions of InGaN solar cells. The simulation study shows the relevance of the Silvaco ATLAS simulation tool, as well as the optimization of doping concentration and thickness of n- and p-InGaN regions for solar cells, which would make the development of high-performance InGaN solar cells low-cost and efficient.
]]>Electrochem doi: 10.3390/electrochem3030027
Authors: Ru Wang Koichi Jeremiah Aoki Jingyuan Chen
The amount of anodically dissolved charge of silver by linear sweep stripping voltammetry has been observed to be smaller than that of the potentiostatically deposited charge. The imbalance in the charge is opposite to the participation in the double-layer capacitance. This can be explained in terms of the negative capacitive current, which is caused by dipoles of generated redox charge (Ag+) with counterions (NO3−). Lower concentrations of counterions may suppress the capacitance to retain the equality of the charge. This prediction is examined in this work by the oxidation of silver film at various concentrations of NO3− by anodic stripping voltammetry. The capacitance decreased with a decrease in the salt concentrations less than 0.05 mol dm−3. Low concentrations of salts prevent loss of the anodic charge in electroanalysis. This dependence was related with the lifespan of generated silver nitrate dipoles and is described theoretically.
]]>Electrochem doi: 10.3390/electrochem3030026
Authors: Kirti Rajeev Gupta Divesh N. Srivastava
Here, we report the performance of a biodegradable polymer-based Plastic chip Electrode (PCE) as a current collector in supercapacitor applications. Its production was evaluated using two redox materials (conducting polymers polyaniline and poly(3,4-ethylene dioxythiophene)) and a layered material, rGO. The conducting polymers were directly deposited over the Eco-friendly PCE (EPCE) using the galvanostatic method. The rGO was prepared in the conventional way and loaded over the EPCE using a binder. Both conducting polymers and rGO showed proper specific capacitance compared to previous studies with regular current collectors. Electrodes were found highly stable during experiments in high acidic medium. The supercapacitive performance was evaluated with cyclic voltammetry, charge–discharge measurements, and impedance spectroscopy. The supercapacitive materials were also characterized for their electrical and microscopic properties. Polyaniline and PEDOT were deposited over EPCEs showing >150 Fg−1 and >120 Fg−1 specific capacitance, respectively, at 0.5 Ag−1. rGO continued to show higher particular capacitance of >250 Fg−1 with excellent charge–discharge cyclic stability. The study concludes that EPCs can be used as promising electrodes for electrical energy storage applications.
]]>Electrochem doi: 10.3390/electrochem3030025
Authors: Ramasamy Umadevi Ponraj Jeyabarathi Kothandapani Venugopal Michael E. G. Lyons Lakshmanan Rajendran
A mathematical model of an ideal biotrickling filter (BF) system that inoculates a recently identified strain of Chelatococcus daeguensis TAD1 and brings about efficient nitrogen oxide treatment is discussed. The proposed model is based on nonlinear mass transport equations at the gas–biofilm interface. Using Akbari–Ganji’s technique, approximate analytical expressions for the nitric oxide concentration in the gaseous and biofilm phases were developed for all feasible system parameters. In addition, to investigate the dynamic behaviour of the system, a numerical analysis of the problem is provided using MATLAB tools. To demonstrate this new approach, graphical data are provided and quantitatively discussed. This theoretical result has good agreement with the numerical simulation (MATLAB) results for the experimental values of parameters.
]]>Electrochem doi: 10.3390/electrochem3030024
Authors: Tatsushi Nakayama Bunji Uno
Reactivity of (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid (caffeic acid), classified as a hydroxycinnamic acid (HCA) derivative, toward electrogenerated superoxide radical anion (O2•−) was investigated through cyclic voltammetry, in situ electrolytic electron spin resonance spectrometry, and in situ electrolytic ultraviolet–visible spectrometry in N,N-dimethylformamide (DMF), aided by density functional theory (DFT) calculations. The quasi-reversible redox of dioxygen/O2•− is modified in the presence of caffeic acid, suggesting that O2•− is scavenged by caffeic acid through proton-coupled electron transfer. The reactivities of caffeic acid toward O2•− are mediated by the ortho-diphenol (catechol) moiety rather than by the acryloyl group, as experimentally confirmed in comparative analyses with other HCAs. The electrochemical and DFT results in DMF suggested that a concerted two-proton-coupled electron transfer mechanism proceeds via the catechol moiety. This mechanism embodies the superior kinetics of O2•− scavenging by caffeic acid.
]]>Electrochem doi: 10.3390/electrochem3030023
Authors: Hao Ma Wenhui Pei Qi Zhang
In the field of automated technology research and development, trajectory tracking plays a crucial role in the energy consumption of the vehicle’s power battery. Reducing the deviation between the actual trajectory and the reference trajectory is the focus of trajectory tracking research. This paper proposes the use of the model predictive control (MPC) method to reduce the deviation of lateral and longitudinal position between the actual driving trajectory and the reference trajectory. First, the driving conditions of the vehicle are reflected by establishing the vehicle dynamics model. Then, the MPC trajectory tracking controller is built by designing the objective function with constraints; Finally, the feasibility of this approach was verified by a joint Carsim-Simulink simulation. The simulation results show that the MPC controller designed in this paper can track the trajectory better, and reduce the lateral and longitudinal position deviation. To a certain extent, the battery energy consumption is reduced and the accuracy of the tracking trajectory and the safety of vehicle driving are improved.
]]>Electrochem doi: 10.3390/electrochem3020022
Authors: Sophie Lakard Emmanuel Contal Karine Mougin Boris Lakard
Electrochemical oxidation of electrolyte solutions containing carbazole (Cz) and 2-(9H-carbazol-9-yl)acetic acid (CzA) monomers was performed in acetonitrile solutions. Different Cz and CzA feed ratios were used to electrodeposit solid polymer films of various compositions, and to study the influence of the monomer ratio on the physicochemical properties (electroactivity, topography, adhesion, stiffness, wettability) of the polymer films. Thus, electrochemical oxidation led to the deposition of a solid film of micrometric thickness, but only for the solutions containing at least 30% of Cz. The proportion of Cz and CzA in the electrodeposited polymer films has little impact on the adhesion strength values measured by AFM. On the contrary, this proportion significantly modifies the stiffness of the films. Indeed, the stiffness of the polymer films varies from 9 to 24 GPa depending on the monomer ratio, which is much lower than the value obtained for unmodified polycarbazole (64 GPa). This leads to the absence of cracks in the films, which all have a fairly homogeneous globular structure. Moreover, among the different polymer films obtained, those prepared from 70:30 and 50:50 ratios in Cz:CzA monomer solutions seem to be the most interesting because these green films are conductive, thick, low in stiffness, do not show cracks and are resistant to prolonged immersion in water.
]]>Electrochem doi: 10.3390/electrochem3020021
Authors: Pandy Pirabaharan M. Chitra Devi Rajagopal Swaminathan Lakshmanan Rajendran Michael E. G. Lyons
Biosensor behaviour is characterised by non-linear differential equations that describe well-defined physical, chemical, and biological processes. Mathematical modelling of these biosensors is highly desirable since they have many applications. These models enable the prediction of a variety of their properties. In this study, the cyclic conversion of the substrate in an amperometric biosensor with an oxidase enzyme membrane electrode is studied using a mathematical model. The governing parameters for the Michaelis–Menten kinetics of enzymatic reactions are the enzyme kinetic and diffusion rates across the enzymatic layer. In this paper, we solved the non-linear equations analytically and numerically for all experimental values of parameters. This problem is simulated in MATLAB® v2016b software using the PDE solver. Our analytical solutions are compared to simulation results to validate the proposed model.
]]>Electrochem doi: 10.3390/electrochem3020020
Authors: Mustafa Khan Xuli Ding Hongda Zhao Yuxin Wang Ning Zhang Xiaojing Chen Jiahao Xu
Selenium (Se)-based cathode materials have garnered considerable interest for lithium-ion batteries due to their numerous advantages, including low cost, high volumetric capacity (3268 mAh cm−3), high density (4.82 g cm−3), ability to be cycled to high voltage (4.2 V) without failure, and environmental friendliness. However, they have low electrical conductivity, low coulombic efficiency, and polyselenide solubility in electrolytes (shuttle effect). These factors have an adverse effect on the electrochemical performance of Li-Se batteries, rendering them unsuitable for real-world use. In this study, we briefly examined numerous approaches to overcoming these obstacles, including selecting an adequate electrolyte, the composition of Se with carbonaceous materials, and the usage of metal selenide base electrodes. Furthermore, we examined the effect of introducing interlayers between the cathode and the separator. Finally, the remaining hurdles and potential study prospects in this expanding field are proposed to inspire further insightful work.
]]>Electrochem doi: 10.3390/electrochem3020019
Authors: Harriet Whiley Thilini P. Keerthirathne Emma J. Kuhn Muhammad Atif Nisar Alex Sibley Peter Speck Kirstin E. Ross
Airborne microorganisms play a significant role in the transmission of infectious diseases. As such, improving indoor microbial air quality can enhance infection control in numerous settings. This study examined the efficacy of the PlasmaShield® air purification device to remove airborne microorganisms under laboratory conditions. Pure cultures of model microorganisms at varying concentrations were aerosolized using a 1-jet Collison nebulizer through stainless-steel removable piping prior to reaching the PlasmaShield® device. The surviving microorganisms were captured using the Staplex® MBS-6 Six Stage Microbial Air Sampler and enumerated via culture on agar plates. The positive-hole-corrected colony/plaque-forming units were compared with the negative control (microorganisms aerosolized through an empty PlasmaShield® casing). The PlasmaShield® statistically significantly (p < 0.05) reduced airborne Escherichia coli, Staphylococcus epidermidis, Bacteriophage MS2 and Cladosporium sp. compared with the negative control. The maximum removal achieved was estimated to be 4 × log10E. coli (99.99% removal), 4 × log10S. epidermidis (99.97% removal), 7 × log10 MS2 (99.99998% removal) and 5 × log10Cladosporium sp. (99.999% removal). Scanning electron microscope images of the surviving microorganisms showed that the PlasmaShield® damaged the cell membrane of these model microorganisms. This study provides proof-of-concept evidence to support the use of this technology to improve indoor microbial air quality.
]]>Electrochem doi: 10.3390/electrochem3020018
Authors: Jeevan Jaidi Sandeep Dattu Chitta Chaithanya Akkaldevi Satyam Panchal Michael Fowler Roydon Fraser
Rechargeable Li-ion batteries are widely used in renewable energy storage and automotive powertrain systems, and therefore, an efficient thermal management system is imperative for maximum battery life and safety. Battery heat generation and dissipation rates primarily depend on the battery surface temperatures, which are affected by the coolant system design and coolant inlet conditions. In this paper, a two-way coupled electrochemical-thermal simulation with selected experimental validation has been performed and analyzed the effect of water coolant inlet conditions on the effectiveness of commercial mini-channel cold-plates for 20 Ah LiFePO4 prismatic batteries. Three coolant inlet temperatures (25–45 °C) and four flow rates (150–600 mL/min) are tested at three different discharge rates (2–4 C) and the performance of coolant system design has been analyzed in terms of battery peak (maximum) temperature and temperature difference (i.e., non-uniformity) across the battery. The predicted results indicate that the coolant flow rate has a profound effect on the battery temperature non-uniformity, while the coolant inlet temperature has a significant effect on the battery peak temperature. At high coolant flow rates, the battery surface temperature difference is within the acceptable range (ΔT < 5 °C), but the maximum temperatures are high at all discharge rates. Further, at the low coolant inlet temperature of 25 °C and the high coolant flow rate of 600 mL/min, the battery temperature rise at the top and bottom locations during the constant current discharge process is high, indicating that the battery heat generation rate is high at a low coolant inlet temperature.
]]>Electrochem doi: 10.3390/electrochem3020017
Authors: Nibedita Swain Isha Soni Pankaj Kumar Gururaj Kudur Jayaprakash
In the agricultural field, pesticides are used tremendously to shield our crops from insects, weeds, and diseases. Only a small percentage of pesticides employed reach their intended target, and the remainder passes through the soil, contaminating ground and surface-water supplies, damaging the crop fields, and ultimately harming the crop, including humans and other creatures. Alternative approaches for pesticide measurement have recently received a lot of attention, thanks to the growing interest in the on-site detection of analytes using electrochemical techniques that can replace standard chromatographic procedures. Among all organochlorine pesticides such as gamma-lindane are hazardous, toxic, and omnipresent contaminants in the environment. Here, in this review, we summarize the different ways of the gamma-lindane detection, performing the electrochemical techniques viz cyclic, differential, square wave voltammetry, and amperometry using various bare and surface-modified glassy carbon and pencil carbon electrodes. The analytical performances are reported as the limit of detection 18.8 nM (GCE–AONP–PANI–SWCNT), 37,000 nM (GCE), 38.1 nM (Bare HBPE), 21.3 nM (Nyl-MHBPE); percentage recovery is 103%.
]]>Electrochem doi: 10.3390/electrochem3020016
Authors: Leandro A. Almeida Bruno V. M. Rodrigues Debora T. Balogh Rafaela C. Sanfelice Luiza A. Mercante Amanda F. Frade-Barros Adriana Pavinatto
Bisphenol A (BPA) is considered an endocrine-disrupting compound and can cause toxicological effects, even at low doses. The development of sensitive and reliable sensors that would allow the detection of such contaminant is highly pursued. Herein, we report an electrochemical sensing strategy based on a simple and low-cost nanocomposite film sensor platform for BPA detection. The platform was developed by modifying a fluorine-doped tin oxide (FTO) electrode with layer-by-layer (LbL) films of chitosan (Chi) and gold nanoparticles functionalized with a polythiophene derivative (AuNPs:PTS). The growth of the Chi/AuNPs:PTS LbL films was monitored by UV–Vis spectroscopy. Electrochemical characterization revealed that the three-bilayer film exhibited the highest electrocatalytic performance and differential-pulse voltammetry (DPV) measurements demonstrated that the modified electrode was suitable for BPA detection through a quasi-reversible and adsorption-controlled electrochemical oxidation and reduction process. The developed sensor exhibited a linear response range from 0.4 to 20 μmol L−1, with a detection limit of 0.32 μmol L−1. The sensor showed good reproducibility with relative standard deviations of 2.12% and 3.73% to intra- and inter-electrode, respectively. Furthermore, the platform demonstrated to be suitable to detect BPA in real water samples, as well as selective for BPA detection in solutions with 100-fold excess of common interfering compounds.
]]>Electrochem doi: 10.3390/electrochem3020015
Authors: Peteris Lesnicenoks Ainars Knoks Sergei Piskunov Laimonis Jekabsons Janis Kleperis
Renewable energy resources (wind, solar) are unpredictable, so it is wise to store the electricity they generate in an energy carrier X. Various PtX (power to useful energy-intensive raw material such as hydrogen, synthetic natural gas, fuel) applications have been proposed. At the heart of our work is widely used idea to convert residual CO2 from biogas plant into higher hydrocarbons using electricity from renewables (e.g., sun, wind, hydro). The specific goal is to produce ethylene-highly demanded hydrocarbon in plastics industry. The process itself is realised on electrocatalytic carbon/copper cathode which must be selective to reaction: 2CO2 + 12e− + 12H+→C2H4 + 4H2O. We propose a bottom-up approach to build catalyst from the smallest particles-graphene sheet stacks (GSS) coated with metallic copper nanocrystals. Composite GSS-Cu structure functions as a CO2 and proton absorber, facilitating hydrogenation and carbon–carbon coupling reactions on Cu-nanocluster/GSS for the formation of C2H4. In our design electrocatalytic electrode is made from nitrogen-doped graphene sheet stacks coated with copper nanostructures. The N-GSSitself can be drop-casted or electrophoretically incorporated onto the carbon paper and gas diffusion electrode. Electrochemical deposition method was recognized as successful and most promising to grow Cu nanocrystals on N-GSS incorporated in conducting carbon substrate. Gaseous products from CO2 electro-catalytic reformation on the cathode were investigated by mass-spectrometer but the electrode surface was analysed by SEM/EDS and XRD methods.
]]>Electrochem doi: 10.3390/electrochem3020014
Authors: Qi Zhang Wenhui Pei Xudong Liu
The large-scale development of new energy and energy storage systems is a key way to ensure energy security and solve the environmental crisis, as well as a key way to achieve the goal of “carbon peaking and carbon neutrality” [...]
]]>Electrochem doi: 10.3390/electrochem3020013
Authors: Amrita Chapagain Debendra Acharya Anju Kumari Das Kisan Chhetri Hari Bhakta Oli Amar Prasad Yadav
Alkaloids are aromatic hydrocarbons with nitrogen as heteroelements in the ring structure that are responsible for bonding with the metal surface and help to reduce corrosion of metals such as mild steel (MS) in an acidic medium. In this study, the alkaloid of Rhynchostylis retusa (RR) was extracted by solvent extraction method and confirmed by chemical test as well as FTIR spectroscopic test. Extracted alkaloids were tested as green inhibitors for the MS corrosion in a 1.0 M H2SO4 solution. The inhibition efficiency (IE) of alkaloid extracts of RR was studied by the weight loss measurement method and electrochemical polarization method. Results showed that the maximum IE in the gravimetric method was 87.51% in 1000 ppm solution at 6 h immersion time. Open circuit potential (OCP) and potentiodynamic polarization results indicated that the extracted alkaloids acted as a mixed type of inhibitor. IE by polarization method was found to be 93.24% for the sample immersed for 6 h. The temperature effect study reveals that inhibitors can work only below 35 °C. Alkaloids of RR can be successfully extracted and used as corrosion inhibitors for MS in an acidic medium below 35 °C.
]]>Electrochem doi: 10.3390/electrochem3020012
Authors: Yiming Jiang Chun-Yi Chen Xun Luo Daisuke Yamane Masanori Mizoguchi Osamu Kudo Ryu Maeda Masato Sone Tso-Fu Mark Chang
Nickel–cobalt alloys were prepared by alloy electrodeposition with a sulfamate bath, and the mechanical properties on the micro-scale were evaluated for the application as micro-components in miniaturized electronic devices. Nickel bromide and a commercially available surface brightener were used as the additives. The cobalt content increased from 21.5 to 60.1 at.% after addition of nickel bromide into the bath, and the grain size refined from 21.1 to 13.2 nm when the surface brightener was used. The mechanical properties on the micro-scale were evaluated by micro-compression test using micro-pillar type specimens fabricated by a focused ion beam system to take the sample size effect into consideration. The yield strength of the nickel–cobalt alloy having an average grain size at 13.9 nm and cobalt content of 66.6 at.% reached 2.37 GPa, revealing influences from the sample size, grain boundary strengthening, and solid solution strengthening effects.
]]>Electrochem doi: 10.3390/electrochem3010011
Authors: Željko Petrovski Mateus P. Moreira Andreia F. M. Santos Sunny K. S. Freitas Noémi Jordão Renata A. Maia Ana V. M. Nunes Luis C. Branco Hugo Cruz Pierre M. Esteves
Ferrocene-based porous organic polymers (FPOPs) were prepared from phenol-formaldehyde polymer (Bakelite) and phenol as starting materials; and two possible mechanisms for polymerization were discussed. Solid-state 13C CP-MAS NMR, FTIR, powder XRD, elemental analysis and ICP (Fe, Na, B) were performed to characterize the prepared materials. The two synthetic approaches produced polymers with different pore sizes: the FPOP synthesized through Bakelite presented a higher surface area (52 m2 g−1) when compared to the one obtained by the bottom-up polymerization from phenol (only 5 m2 g−1). Thermogravimetric analysis confirmed the thermal stability of the material, which decomposed at 350 °C. Furthermore, cyclic voltammetry (CV) of the new FPOP on modified electrodes, in ACN and 0.1 M TBAP as an electrolyte, showed fully reversible electron transfer, which is similar to that observed for the ferrocene probe dissolved in the same electrolyte. As a proof-of-concept for an electrochromic device, this novel material was also tested, with a color change detected between yellow/brownish coloration (reduced form) and green/blue coloration (oxidized form). The new hybrid FPOP seems very promising for material science, energy storage and electrochromic applications, as well as for plastic degradation.
]]>Electrochem doi: 10.3390/electrochem3010010
Authors: Roshny Joy Neethu T. M Balakrishnan Akhila Das Shimna Shafeek Vijay Kumar Thakur Karim Zaghib Jabeen Fatima Manamkeri Jaffarali Mogalahalli Venkatesh Venkatashamy Reddy Prasanth Raghavan
In the present era, different allotropes of carbon have been discovered, and graphene is the one among them that has contributed to many breakthroughs in research. It has been considered a promising candidate in the research and academic fields, as well as in industries, over the last decade. It has many properties to be explored, such as an enhanced specific surface area and beneficial thermal and electrical conductivities. Graphene is arranged as a 2D structure by organizing sp2 hybridized C with alternative single and double bonds, providing an extended conjugation combining hexagonal ring structures to form a honeycomb structure. The precious structure and outstanding characteristics are the major reason that modern industry relies heavily on graphene, and it is predominantly applied in electronic devices. Nowadays, lithium-ion batteries (LIBs) foremostly utilize graphene as an anode or a cathode, and are combined with polymers to use them as polymer electrolytes. After three decades of commercialization of the lithium-ion battery, it still leads in consumer electronic society due to its higher energy density, wider operating voltages, low self-discharge, noble high-temperature performance, and fewer maintenance requirements. In this review, we aim to give a brief review of the domination of graphene and its applications in LIBs.
]]>Electrochem doi: 10.3390/electrochem3010009
Authors: Ana T. S. C. Brandão Renata Costa A. Fernando Silva Carlos M. Pereira
The development of energy storage devices with better performance relies on the use of innovative materials and electrolytes, aiming to reduce the carbon footprint through the screening of low toxicity electrolytes and solvent-free electrode design protocols. The application of nanostructured carbon materials with high specific surface area, to prepare composite electrodes, is being considered as a promising starting point towards improving the power and energy efficiency of energy storage devices. Non-aqueous electrolytes synthesized using greener approaches with lower environmental impact make deep eutectic solvents (DES) promising alternatives for electrochemical energy storage and conversion applications. Accordingly, this work proposes a systematic study on the effect of the composition of DES containing a diol and an amide as HBD (hydrogen bond donor: 1,2-propylene glycol and urea), on the electrochemical performance of graphene and graphite composite electrodes/DES electrolyte interface. Glassy carbon (GC) was selected as the bare electrode material substrate to prepare the composite formulations since it provides an electrochemically reproducible surface. Gravimetric capacitance was measured for commercial graphene and commercial graphite/GC composite electrodes in contact with choline chloride, complexed with 1,2-propylene glycol, and urea as the HBD in 1:2 molar ratio. The electrochemical stability was followed by assessing the charge/discharge curves at 1, 2, and 4 A g−1. For comparison purposes, a parallel study was performed using commercial graphite. A four-fold increase in gravimetric capacitance was obtained when replacing commercial graphite (1.70 F g−1) by commercial graphene (6.19 F g−1) in contact with 1,2-propylene glycol-based DES. When using urea based DES no significant change in gravimetric capacitance was observed when commercial graphite is replaced by commercial graphene.
]]>Electrochem doi: 10.3390/electrochem3010008
Authors: Tatsushi Nakayama Ryo Honda Kazuo Kuwata Shigeyuki Usui Bunji Uno
Scavenging of electrogenerated superoxide radical anion (O2•−) by pyrogallol (PyH3) was investigated on the basis of cyclic voltammetry and in situ electrolytic electron spin resonance spectrum in N,N-dimethylformamide with the aid of density functional theory (DFT) calculations. Quasi-reversible dioxygen/O2•− redox couple was modified by the presence of PyH3, suggesting that O2•− was scavenged by PyH3 through proton-coupled electron transfer (PCET) involving two proton transfer and one electron transfer. DFT calculation suggested that the pre-reactive formation of a hydrogen-bond (HB) complex and the subsequent concerted two-proton-coupled electron transfer characterized by catechol moiety in PyH3 is plausible mechanism that embodies the superior kinetics of the O2•− scavenging by PyH3 as shown in the electrochemical results. Furthermore, it was clarified that the three hydroxyl groups of PyH3 promote the formation of HB complex, in comparative analyses using related compounds, resulting in the promotion of the O2•− scavenging.
]]>Electrochem doi: 10.3390/electrochem3010007
Authors: Electrochem Editorial Office Electrochem Editorial Office
Rigorous peer-reviews are the basis of high-quality academic publishing [...]
]]>Electrochem doi: 10.3390/electrochem3010006
Authors: José E. da S. Souza Gabriel P. de Oliveira Jeferson Y. N. H. Alexandre José G. L. Neto Misael B. Sales Paulo G. de S. Junior André L. B. de Oliveira Maria C. M. de Souza José C. S. dos Santos
Several studies have shown the development of electrochemical biosensors based on enzymes immobilized in metal–organic frameworks (MOFs). Although enzymes have unique properties, such as efficiency, selectivity, and environmental sustainability, when immobilized, these properties are improved, presenting significant potential for several biotechnological applications. Using MOFs as matrices for enzyme immobilization has been considered a promising strategy due to their many advantages compared to other supporting materials, such as larger surface areas, higher porosity rates, and better stability. Biosensors are analytical tools that use a bioactive element and a transducer for the detection/quantification of biochemical substances in the most varied applications and areas, in particular, food, agriculture, pharmaceutical, and medical. This review will present novel insights on the construction of biosensors with materials based on MOFs. Herein, we have been highlighted the use of MOF for biosensing for biomedical, food safety, and environmental monitoring areas. Additionally, different methods by which immobilizations are performed in MOFs and their main advantages and disadvantages are presented.
]]>Electrochem doi: 10.3390/electrochem3010005
Authors: Vinolyn Sylvia Rajendran Joy Salomi Lakshmanan Rajendran Michael E. G. Lyons
A theoretical model of amperometric enzyme electrodes has been developed in which chemical amplification occurs in a single enzyme membrane via cyclic substrate conversion. The system is based on non-stationary diffusion equations with a nonlinear factor related to the Michaelis–Menten kinetics of the enzymatic reaction. By solving the nonlinear equations using the AGM technique, simple analytical expressions of concentration substrate, product, and amperometric current response are derived. Further, biosensor sensitivity, resistance, and gain are obtained from the current. MATLAB programming was used to carry out the digital simulation. The analytical results are validated with the numerical results. The effect of substrate concentration, maximum enzymatic rate, and membrane thickness on biosensor response was evaluated.
]]>Electrochem doi: 10.3390/electrochem3010004
Authors: Valbonë Mehmeti Fetah Podvorica
Alkylphosphonic acids are well known for their ability to form self-assembled monolayers on hydroxide surfaces. A crucial step to understanding fundamentally how these surfaces are created is the elucidation of the interaction process that leads to such interface creation. In this study, we employed electrochemical impedance spectroscopy (EIS), Monte Carlo and molecular dynamics to understand this process. The interaction with the Cu(111) surface of three different alkylphosphonic acids (hexyl-, octyl- and decylphosphonic acids) is evaluated in an aqueous acidic and in an ethanol solution by Monte Carlo and molecular dynamics simulations, while EIS measurements are used to put in evidence the impact of the layer made in ethanol on copper protection. Nyquist diagrams of copper samples modified with an alkylphosphonic monolayer showed a higher polarization resistance that mitigates the copper corrosion in an aqueous acid medium. The phase–frequency Bode plots had higher and broader phase maxima for a modified copper surface with phosphonic moieties, which confirmed the ability of this organic layer to prevent copper corrosion.
]]>Electrochem doi: 10.3390/electrochem3010003
Authors: Devendrasinh Darbar Indranil Bhattacharya
Estimating the accurate State of Charge (SOC) of a battery is important to avoid the over/undercharging and protect the battery pack from low cycle life. Current methods of SOC estimation use complex equations in the Extended Kalman Filter (EKF) and the equivalent circuit model. In this paper, we used a Feed Forward Neural Network (FNN) to estimate the SOC value accurately where battery parameters such as current, voltage, and charge are mapped directly to the SOC value at the output. A FNN could self-learn the weights with each training data point and update the model parameters such as weights and bias using a combination of two gradient descents (Adam). This model comprises the Dropout technique, which can have many neural network architectures by dropping the neuron/mode at each epoch/training cycle using the same weights and biases. Our FNN model was trained with data comprising different current rates and tested for different cycling data, for example, 5th, 10th, 20th, and 50th cycles and at a different cutoff voltage (4.5 V). The battery used for estimating the SOC value was a Na-ion based battery, which is highly non-linear, and it was fabricated in a house using Na0.67Fe0.5Mn0.5O2 (NFM) as a cathode and Na metal as a reference electrode. The FNN successfully estimated the SOC value for the highly non-linear nature of the Na-ion battery at different current rates (0.05 C, 0.1 C, 0.5 C, 1 C, 2 C), for different cycling data, and at higher cut-off voltage of –4.5 V Na+, reaching the R2 value of ~0.97–~0.99, ~0.99, and ~0.98, respectively.
]]>Electrochem doi: 10.3390/electrochem3010002
Authors: Avni Berisha
The corrosion behavior of mild steel in a 1 M aqueous sulfuric acid medium in the presence and absence of the drug Pantoprazole was investigated using potentiodynamic polarization and quantum chemical calculations as well as Monte Carlo and molecular dynamic simulations. The potentiodynamic experiments indicated that this molecule, as a result of its adsorption on a mild steel surface, functioned as a mixed inhibitor. The goal of the study was to use theoretical calculations to acquire a better understanding of how inhibition works. The adsorption behavior of the examined compounds on the Fe (1 1 0) surface was calculated using a Monte Carlo simulation. Furthermore, the molecules were studied using density functional theory (DFT), especially the PBE functional, to determine the relationship between the molecular structure and the corrosion inhibition behavior of the chemical under research. The adsorption energies of Pantoprazole (in its three different protonation states) iron were calculated more precisely using molecular mechanics with periodic boundary conditions (PBC). The predicted theoretical parameters were found to be in agreement with the experimental data, which was a considerable help in understanding the corrosion inhibition mechanism displayed by this chemical.
]]>Electrochem doi: 10.3390/electrochem3010001
Authors: Samantha Macchi Iris Denmark Thuy Le Mavis Forson Mujeebat Bashiru Amanda Jalihal Noureen Siraj
Fuel cells are a promising alternative to non-renewable energy production industries such as petroleum and natural gas. The cathodic oxygen reduction reaction (ORR), which makes fuel cell technology possible, is sluggish under normal conditions. Thus, catalysts must be used to allow fuel cells to operate efficiently. Traditionally, platinum (Pt) catalysts are often utilized as they exhibit a highly efficient ORR with low overpotential values. However, Pt is an expensive and precious metal, posing economic problems for commercialization. Herein, advances in carbon-based catalysts are reviewed for their application in ORRs due to their abundance and low-cost syntheses. Various synthetic methods from different renewable sources are presented, and their catalytic properties are compared. Likewise, the effects of heteroatom and non-precious metal doping, surface area, and porosity on their performance are investigated. Carbon-based support materials are discussed in relation to their physical properties and the subsequent effect on Pt ORR performance. Lastly, advances in fuel cell electrolytes for various fuel cell types are presented. This review aims to provide valuable insight into current challenges in fuel cell performance and how they can be overcome using carbon-based materials and next generation electrolytes.
]]>Electrochem doi: 10.3390/electrochem2040042
Authors: M’hamed Chahma
π-conducting materials such as chiral polythiophenes exhibit excellent electrochemical stability in doped and undoped states on electrode surfaces (chiral electrodes), which help tune their physical and electronic properties for a wide range of uses. To overcome the limitations of traditional surface immobilization methods, an alternative pathway for the detection of organic and bioorganic targets using chiral electrodes has been developed. Moreover, chiral electrodes have the ability to carry functionalities, which helps the immobilization and recognition of bioorganic molecules. In this review, we describe the use of polythiophenes for the design of chiral electrodes and their applications as electrochemical biosensors.
]]>Electrochem doi: 10.3390/electrochem2040041
Authors: Chen Fang Gao Liu
Silicon (Si) is a promising anode material to realize many-fold higher anode capacity in next-generation lithium-ion batteries (LIBs). Si electrochemistry has strong dependence on the property of the Si interface, and therefore, Si surface engineering has attracted considerable research interest to address the challenges of Si electrodes such as dramatic volume changes and the high reactivity of Si surface. Molecular nanostructures, including metal–organic frameworks (MOFs), covalent–organic frameworks (COFs) and monolayers, have been employed in recent years to decorate or functionalize Si anode surfaces to improve their electrochemical performance. These materials have the advantages of facile preparation, nanoscale controllability and structural diversity, and thus could be utilized as versatile platforms for Si surface modification. This review aims to summarize the recent applications of MOFs, COFs and monolayers for Si anode development. The functionalities and common design strategies of these molecular structures are demonstrated.
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