Next Article in Journal
Effects of the Water Matrix on the Degradation of Micropollutants by a Photocatalytic Ceramic Membrane
Next Article in Special Issue
Magnesium-Doped Sr2(Fe,Mo)O6−δ Double Perovskites with Excellent Redox Stability as Stable Electrode Materials for Symmetrical Solid Oxide Fuel Cells
Previous Article in Journal
Application and Visualization of Fluorescent-Tagged Antiscalants in Electrodialysis Processing of Aqueous Solutions Prone to Gypsum Scale Deposition
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Identifying Characteristic Frequencies in the Electrochemical Impedance of Ion-Exchange Membrane Systems

by
Antonio Angel Moya
Department of Physics, University of Jaén, 23071 Jaén, Spain
Membranes 2022, 12(10), 1003; https://doi.org/10.3390/membranes12101003
Submission received: 29 September 2022 / Revised: 11 October 2022 / Accepted: 13 October 2022 / Published: 16 October 2022
(This article belongs to the Special Issue Membranes for Energy Conversion (Volume II))

Abstract

:
In this study, the characteristic frequencies of the electrochemical impedance of ion-exchange membrane systems constituted by the membrane and two diffusion boundary layers adjacent to the membrane were investigated. Approximations of the impedance of the Randles equivalent electric circuit in multiple frequency ranges were considered, and the characteristic frequencies of the zeros and poles of orders ½ and 1 were derived. The characteristic geometric frequencies, those associated with the interfacial charge transfer and the diffusive transport processes, as well as those associated with the transitions between processes, were identified by means of analytical expressions.

1. Introduction

Studies on electrochemical properties of ion-exchange membrane systems are currently receiving considerable attention due to the potential environmental applications of such systems in various fields of science and technology, such as electrodialysis for brackish water or seawater desalination [1] and renewable energy harvesting, such as pressure-retarded osmosis or reverse electrodialysis [2]. In addition, such membranes are often used as separators in electrochemical energy storage devices, such as rechargeable lithium-ion batteries [3], redox flux batteries [4] and fuel cells [5], or as elements joined to the porous electrodes in systems for capacitive deionization desalination [6] or blue energy production from salinity differences [7].
Electrochemical impedance spectroscopy is a powerful method for characterizing many of the electrical properties of a wide variety of electrochemical systems, including membrane systems [8]. Since the work of Sistat et al. [9], a number of papers dealing with the electrochemical impedance of systems constituted by an ion-exchange membrane and two diffusion boundary layers (DBLs) adjacent to the membrane have appeared in the literature [10,11,12,13,14,15,16,17]. These works include the identification of specific topics in the field of ion exchange, such as diffusion coefficients dependent on ionic concentrations [10], the inhomogeneity of the membrane fixed charge [11], asymmetry of the bathing concentrations [12], geometry of the fluidic channels [13], competitive transport of counter ions [14], water splitting [15], interfacial resistances [16] and fouling [17]. Impedance functions can also be applied in the small-signal dynamic modelling of electrochemical power sources, such as Li-ion batteries and fuel cells, including ion-exchange membranes, which are of particular importance due to the increasing incorporation of such devices into sophisticated electric and electronic systems [18,19]. Multiple studies on the dynamic response of ion-exchange membrane systems have been published in fields related to proton-exchange membrane fuel cells [20,21,22,23].
Impedance experimental data are usually interpreted on the basis of the Randles equivalent electric circuit; the relationship between the circuit elements and the physical and chemical parameters of the system are determined by the Nernst–Planck–Donnan equations under electroneutrality on the basis of the Teorell–Mayer–Sievers model. The differential capacitances of the electric double layers (EDLs) at the membrane–solution interfaces as given by the Gouy–Chapman theory are also included [24]. Although the properties of the Randles circuit model of the electrochemical interface are well-known [25], the characteristic frequencies of the impedance basic function of ion-exchange membrane systems, particularly in the absence of interfacial resistances, have not been investigated in detail.
The main purpose of this paper is to contribute to this area by conducting a novel theoretical study on the identification of the characteristic frequencies of the electrochemical impedance of ion-exchange membrane systems constituted by the membrane and two DBLs adjacent to the membrane on the basis of the zero-pole representation of the approximations of the impedance in multiple frequency ranges. The characteristic frequencies of the zeros and poles of orders ½ and 1 in the impedance of the Randles equivalent electric circuit were derived in this study. The characteristic geometric frequencies, those associated with the interfacial charge transfer and the diffusional transport processes and those associated with the transitions between processes were theoretically identified by means of analytical expressions. The values of these frequencies enabled evaluation of the role played by the capacitances of the EDLs in the impedance model and by the characteristic frequencies within the usual range of experimentation in the characterization of electrical properties of membrane systems.

2. Theoretical Basis

In this study, we considered a membrane with a thickness of d and two identical DBLs adjacent to the membrane, each with a thickness of δ, as shown in the sketch in Figure 1. The ionic transport is one-dimensional and perpendicular to the membrane–solution interface. The membrane is bathed by two bulk solutions of a 1:1 symmetric binary electrolyte; c0 is the salt concentration in the solutions, and a cation-exchange membrane with a negative fixed charge of concentration X is assumed. The membrane is assumed to be ideal and fully impermeable to co-ions and without interfacial resistance; counter-ion transport is described by means of resistance and geometric capacitance. The diffusion coefficients of the cation and anion in the solution phase are denoted by D1 and D2, respectively, and DS = 2D1D2/(D1 + D2) is the salt diffusion coefficient. The electric permittivity of the solution phase is denoted by ε.
According to the Randles model and previous studies by Nikonenko and Kozmai [24], the impedance of the ion-exchange membrane system, Z, can be written as:
Z   =   Z g   +   1 s   C D L   +   1 Z d L   +   1 s   C D R   +   1 Z d R
where Zg is the geometric impedance given by:
Z g   =   R a c L 1   +   s   R a c L   C g L   +   R M 1   +   s   R M   C g M   +   R a c R 1   +   s   R a c R   C g R
Here, s (s = ) is the Laplace variable; j is the imaginary unit; and ω is the angular frequency, which is 2π times the conventional frequency, f (ω = 2πf). RM and CgM are the resistance and geometric capacitance of the membrane, respectively. CgL and CgR are the geometric capacitances of the DBLs, expressed as:
C g L   =   C g R   =   ε δ
The ohmic resistances of the left and right DBLs, respectively, are:
R a c L   =     R   T F 2   δ ( D 1   +   D 2 )   c 0   ln   ( 1     β L ) β L
R a c R   =   R   T F 2   δ ( D 1   +   D 2 )   c 0   ln   ( 1   +   β L ) β L
In these expressions, the constants F, R and T represent Faraday constant, ideal gas constant and absolute temperature, respectively. The dimensionless parameter βL is:
β L   =   I D C I L
i.e., it is the quotient between the dc component of the electric current, IDC, and the limiting electric current density through the system, IL, which is obtained when the concentration gradient reaches its maximum value in a DBL or on one of the surfaces of the membrane, expressed as:
I L   =   2   F   D 1   c 0 δ
The capacitances of the EDLs at the interfaces are:
C D L   =   ε L D   cosh   ( F   ϕ D C d L 2   R   T )
C D R   =   ε L D   cosh   ( F   ϕ D C d R 2   R   T )
where LD is the Debye length in the solution phases and is expressed as:
L D   =   ε   R   T 2   F 2   c 0
The Donnan electric potential differences at the solution/membrane interfaces are:
ϕ D C d L   =   R   T F ln   [ X c 0   ( 1     β L ) ]  
ϕ D C d R   =   R   T F ln   [ c 0   ( 1   +   β L ) X ]
The Warburg diffusion impedances are expressed as:
Z d L R d L   =   Z d R R d R   =   tanh   s   τ s   τ
where:
R d L   =   2   R   T F   I L   ( 1 1     β L )     R a c L
R d R   =   2   R   T F   I L   ( 1 1   +   β L )     R a c R
and
τ   =   δ 2 D S
At the highest frequencies, the limit of the impedance function (Z) is zero. At intermediate frequencies, the geometric, ohmic or ac resistance of the system (Rac) is the limit of the impedance at the highest frequencies:
R a c   =   R a c L   +   R M   +   R a c R
The DC resistance of the system (RDC) is the limit of the impedance at the lowest frequencies:
R D C   =   R M   +   2   R   T F   I L   ( 1 1   +   β L   +   1 1     β L )
The total diffusion resistance is:
R d   =   R d L   +   R d R   =   R D C     R a c
The electrochemical impedance of an ion-exchange membrane system is represented by the electric circuit shown in Figure 2. In the high-frequency range, the impedance is governed by the geometric terms. In the low-frequency range, the Randles circuit at each interface is constituted by the parallel combination of the EDL capacitance and the finite-length Warburg diffusion impedance. The conductive term of the impedance for the non-zero dc component of the electric current, which was originally described by Sistat et al. [9] and included in the model by Nikonenko and Kozmai [24], is ignored. This term appears for dc current values close to the limiting current and does not admit analytical expression, so it is not used to derive the characteristic frequencies. Also, unlike this model [24], the capacitances of the EDLs include the dependence with the Donnan electric potentials.

3. Results and Discussion

3.1. Impedance Plots

In this study, the electrochemical impedance of an ion-exchange membrane system was numerically obtained from the electric circuit shown in Figure 2 using the electric circuit simulation program PSpice 9.1 (Cadence Design Systems, San Jose, CA, USA) [26]. Simulations were performed for systems with ε = 708 pF/m, δ = 250 μm, c0 = 50 mM, D1 = 1.32·10−9 m2/s and D2 = 1.96·10−9 m2/s. Then, the salt diffusion coefficient is DS = 1.578·10−9 m2/s, the Debye length in the solution is LD = 1.373 nm at T = 298 K and the limiting current density is 50.88 A/m2. For the membrane, the fixed-charge concentration is X = 0.5 M = 100c0, the resistance is RM = 0.2 mΩ·m2 and the geometric capacitance is CgM = 2.5 μF/m2. The chosen values for the parameters could correspond to typical membranes used in electrodialysis when they are immersed in NaCl-diluted solutions.
Figure 3 shows the complex-plane impedance plots in a system for IDC = 0, 0.25IL and 0.5IL. The values of the electric parameters corresponding to the circuit shown in Figure 2 are shown in Table 1. In Figure 3, −Zi(ω) is plotted against Zr(ω) with the angular frequency (ω) as a parameter increasing from the right to the left of the plot (Nyquist-type plot). This figure shows two regions: a geometric arc at high frequencies in the left of the plot and a diffusion arc at low frequencies in the right of the plot, which is a Warburg-type impedance, as it presents a −45° slope straight line at high frequencies and a semicircle at low frequencies. The geometric arc resembles a distorted semicircle and arises from the superposition of the three semicircles corresponding to the geometric impedances of the membrane and of the two DBLs. The usual experimental Nyquist plots of the impedance of ion-exchange membranes show one arc, in addition to the uncompensated resistance of the system [27], because the geometric arc is only experimentally observed when the measurement instruments operate in the range of very high frequency with values outside the usual range of experimentation from 1 mHz to 1 MHz. Then, the electrical conductivity of ion-exchange membranes system is experimentally determined according to the real part of the impedance at the highest frequencies [28,29].
Figure 4 shows the imaginary part with a minus sign of the impedance (−Zi) as a function of frequency (f) in logarithm scale (Bode-type plot). Two peaks are clearly observed in this figure: a geometric peak at high frequencies and a diffusional peak at low frequencies. Furthermore, the frequency at which the diffusional peak is reached is not a function of the dc component of the electric current as expected [30].

3.2. High-Frequency Geometric Impedance

At the highest frequencies, the Warburg diffusion impedance can be approximated by that in semi-infinite space:
Z d L R d L   =   Z d R R d R   =   tanh   s   τ s   τ     1 s   τ
Then, the impedance of the ion-exchange membrane system at the highest frequencies is:
Z H   =   Z g   +   R d L s   R d L   C D L   +   s   τ     +   R d R s   R d R   C D R   +   s   τ
The geometric impedance function (Zg) is a distribution function with three relaxation times. ZH presents three poles of order 1 at the characteristic frequencies:
ω g L   =   2   π   f g L   =   1 R a c L   C g L
ω g R   =   2   π   f g R   =   1 R a c R   C g R
ω g M   =   2   π   f g M   =   1 R M   C g M
Moreover, ZH presents a pole of order ½ at s = 0 and two other poles of order ½ with the characteristic frequencies:
ω H 1   =   2   π   f H 1   =   1 τ H 1   =   τ R d L 2   C D L 2
ω H R   =   2   π   f H R   =   1 τ H R   =   τ R d R 2   C D R 2
Therefore, the impedance at the highest frequencies present five characteristic frequencies corresponding to the membrane, the left and right solutions and the left and right interfaces according to the Teorell–Meyer–Sievers model [31]. Equations (25) and (26) could be considered as the interfacial characteristic frequencies in the absence of interfacial charge transfer resistances [32]. However, the usual values for the EDL capacitances are very small, and the two interfacial frequencies take an extremely high value (of the order of 1018 Hz), and they cannot be identified in the impedance plots. By neglecting the EDL capacitances, the impedance of an ion-exchange membrane system at high frequencies is more appropriately expressed as:
Z H   =   Z g   +   R d s   τ
The three geometric frequencies cannot be individually identified. The frequency at which the imaginary part with minus sign of the impedance reaches a maximum in the high-frequency region of the Nyquist (Figure 3) and Bode-type (Figure 4) plots must be numerically obtained based on the expression of Zg.
On the other hand, the characteristic frequency (fC) at the intersection point between the geometric and the diffusion arcs in the Nyquist plot or the point at which the imaginary part of the impedance with minus sign reaches a minimum in the overlapped regions of the Nyquist and Bode-type plots can be approximately obtained as follows [33]. Based on a Taylor series at the lowest frequencies for the geometric term and the highest frequencies for the diffusional term, the imaginary part of ZH in Equation (27) can be expressed as:
  Z H i   =   R d 2   ω   τ   +   ( R a c L 2   C g L   +   R M 2   C g M   +   R a c R 2   C g R )   ω
Deriving this function with respect to ω and equaling zero, this function reaches a minimum at the frequency (fC) expressed by the following relation:
ω C   =   2   π   f C   =   ( R d 2   ( R a c L 2   C g L   +   R M 2   C g M   +   R a c R 2   C g R )   2   τ )   2 / 3

3.3. Low Frequency Diffusion Impedance

For intermediate frequencies, the impedance corresponding to the Cottrell behavior, which is that obeying a diffusion transport in semi-infinite space, is expressed as:
Z I   =   R a c   +   R d s   τ
This impedance function presents a pole of order ½ at zero frequency. It also presents a zero of order ½ with the following characteristic frequency:
ω Z   =   2   π   f Z   =   R d R a c   τ
Table 2 shows the numerical values of the main identified characteristic frequencies. The characteristic frequency above zero is significant in plots related to admittance, i.e., the inverse function of the impedance, but it can be considered the characteristic frequency of the Cottrell behavior in the impedance.
For low frequencies, by ignoring the capacitances of the EDLs, the impedance can be written as:
Z L   =   R a c   +   R d   tanh   s   τ s   τ
According to numerical calculation, the imaginary part with minus sign of ZL reaches a maximum of value 0.417227Rd at the following frequency:
ω d   =   2   π   f d   =   2.54065   1 τ ,
which implies the real part, i.e., 0.581634Rd. This frequency is that at which the imaginary part with minus sign of the impedance reaches a maximum in the low-frequency region of the Nyquist (Figure 3) and Bode-type (Figure 4) plots, and it is considered the characteristic frequency of the diffusive transport process in the DBLs. It is also the frequency used to characterize, from an experimental viewpoint, the diffusional behavior in different ion-exchange membrane systems [34].
On the other hand, the frequencies corresponding to the impedance values where the real part, by subtracting Rac, is equal to minus the imaginary part, i.e., values of the Warburg impedance with a phase of −45°, are expressed as:
  ω d n   =   2 π   f d n   =   n 2   π 2 2   τ   , n   =   1 ,   2 ,   3 ,   ..
The transmissive Warburg impedance is constituted by an infinite set of poles corresponding to the Laplace variable values zeroing the denominator. The characteristic frequencies of these poles are expressed as [35]:
ω P n   =   2   π   f P n   =   [ π   ( 2   n     1 ) 2 ] 2 1 τ   , n   =   1 ,   2 ,   3 ,   ..
Then, ZL can be developed into partial fractions by means of Foster series as [35]:
Z L   =   R a c   +   2   R d τ   n   =   1   τ P n 1   +   s   τ P n
The Taylor series around s = 0 of the transmissive Warburg impedance is:
Z L   =   R D C     R d 3   s   τ   +   2   R d 15   ( s   τ ) 2     17   R d 315   ( s   τ ) 3   +   O   ( s 4 )
Operating with the inverse function of the admittance with successive continued fractions yields [35]:
Z L   =   R a c   +   1 1 R d   +   1 3   R d s   τ   +   1 5 R d   +  
At very low frequencies, by considering only the first pole of the transmissive Warburg impedance, the impedance can be expressed as:
Z F 1   =   R a c   +   R d 1   +   s   4   τ π 2 ,
which presents the characteristic frequency corresponding to the first pole of the Warburg impedance:
ω P 1   =   2   π   f P 1   =   π 2 4   τ
Moreover, at the lowest frequencies, the Taylor series with two terms yields:
Z T 1   =   R a c   +   R d 1   +   s   τ 3 ,
which yields the characteristic frequency:
ω T 1   =   2   π   f T 1   =   3   1 τ
At very low frequencies, the Foster series of the impedance can be expressed as:
Z F   =   R a c   +   ( 1     8 π 2 )   R d   +   8 π 2   R d 1   +   s   4   τ π 2 ,
which presents the frequency of the first pole of the Warburg impedance given by Equation (40) as the characteristic frequency. Finally, at the lowest frequencies, the Taylor series with three elements [36] is expressed as:
Z T   =   R a c   +   R d 6   +   5 6   R d 1   +   s   2   τ 5
which yields the characteristic frequency:
ω T   =   2   π   f T   =   2.5   1 τ
The Nyquist plot of the low-frequency impedance of ion-exchange membrane systems (ZL) and those of the different approximations corresponding to the lowest frequencies (ZF1, ZT1, ZF and ZT) are shown in Figure 5 for IDC = 0. The approximation obtained using continued fractions with three terms from the Taylor series around zero frequency of the Warburg impedance appropriately models the impedance of ion-exchange membrane systems at low frequencies [36]. The corresponding characteristic frequency expressed by Equation (45) is very close to the characteristic frequency of the diffusive transport process expressed by Equation (33).

4. Conclusions

A set of characteristic frequencies of the electrochemical impedance of ion-exchange membrane systems were identified from the zero-pole representation of the approximations of high and low frequencies. This approach allows us to use the values of these frequencies within the range of experimentation for the characterization of electrical properties of ion-exchange membrane systems. In addition to the characteristic geometric frequencies in the membrane and the two DBLs adjacent to the membrane, we identified two new characteristic interfacial frequencies. These frequencies correspond to poles of order ½ of the impedance associated with the contributions of the EDLs, and their numerical values allow us to evaluate the role played by the capacitances of the EDLs in the impedance of ion-exchange membrane systems without interfacial resistances. In the intermediate frequency range, a new characteristic frequency associated with the Cottrell behavior of the system obeying a diffusion transport in semi-infinite space was identified, which would be relevant in studies associated to admittance. In the low frequency range, multiple frequencies were identified, in addition to the characteristic diffusional frequency, i.e., that corresponding to the maximum of the imaginary part with minus sign of the impedance. These are the characteristic frequencies of the infinite poles of the hyperbolic tangent function and those at which the phase of this function is −45°. At very low frequencies, the impedance can be modelled by a function with a single frequency. The expansion into partial fractions of the Warburg impedance exhibits the frequency of the first pole as the characteristic frequency, whereas two additional expressions for the characteristic frequency associated with the expansions in Taylor series can also be identified.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Strathmann, H. Electrodialysis, a mature technology with a multitude of new applications. Desalination 2010, 264, 268–288. [Google Scholar] [CrossRef]
  2. Logan, B.E.; Elimelech, M. Membrane-based processes for sustainable power generation using water. Nature 2012, 488, 313–319. [Google Scholar] [CrossRef] [PubMed]
  3. Lee, H.; Yanilmaz, M.; Toprakçi, O.; Fu, K.; Zhang, X. A review of recent developments in membrane separators for rechargeable lithium-ion batteries. Energy Environ. Sci. 2014, 7, 3857–3886. [Google Scholar] [CrossRef]
  4. Wang, W.; Luo, Q.; Li, B.; Wei, X.; Li, L.; Yang, Z. Recent progress in redox flow battery research and development. Adv. Funct. Mater. 2013, 23, 970–986. [Google Scholar] [CrossRef]
  5. Merle, G.; Wessling, M.; Nijmeijer, K. Anion exchange membranes for alkaline fuel cells: A review. J. Membr. Sci. 2011, 377, 1–35. [Google Scholar] [CrossRef]
  6. Zhao, R.; Biesheuvel, P.M.; van der Wal, A. Energy consumption and constant current operation in membrane capacitive deionization. Energy Environ. Sci. 2012, 5, 9520–9527. [Google Scholar] [CrossRef] [Green Version]
  7. Ahualli, S.; Fernández, M.M.; Iglesias, G.; Jiménez, M.L.; Liu, F.; Wagterveld, M.; Delgado, A.V. Effect of Solution Composition on the Energy Production by Capacitive Mixing in Membrane-Electrode Assembly. J. Phys. Chem. C 2014, 118, 15590–15599. [Google Scholar] [CrossRef]
  8. Barsoukov, E.; Macdonald, J.R. Impedance Spectroscopy: Theory, Experiment and Applications; Wiley: New York, NY, USA, 2005. [Google Scholar]
  9. Sistat, P.; Kozmai, A.; Pismenskaya, N.; Larchet, C.; Pourcelly, G.; Nikonenko, V. Low-frequency impedance of an ion-exchange membrane system. Electrochim. Acta 2008, 53, 6380–6390. [Google Scholar] [CrossRef]
  10. Mareev, S.; Nikonenko, V. A numerical appoach to modeling impedance: Application to study a Warburg-type spectrum in a membrane system with diffusion coefficients depending on concentration. Electrochim. Acta 2012, 81, 268–274. [Google Scholar] [CrossRef]
  11. Moya, A.A. Study of the electrochemical impedance and the linearity of the current–voltage relationship in inhomogeneous ion-exchange membranes. Electrochim. Acta 2012, 55, 2087–2092. [Google Scholar] [CrossRef]
  12. Moya, A.A. Electrochemical impedance of ion-exchange membranes in asymmetric arrangements. J. Electroanal. Chem. 2011, 660, 153–162. [Google Scholar] [CrossRef]
  13. Nandigana, V.V.; Aluru, N. Characterization of electrochemical properties of a micro–nanochannel integrated system using computational impedance spectroscopy (CIS). Electrochim. Acta 2013, 105, 514–523. [Google Scholar] [CrossRef]
  14. Moya, A.A. Electrochemical impedance of ion-exchange membranes in ternary solutions with two counter-ions. J. Phys. Chem. C 2014, 118, 2539–2553. [Google Scholar] [CrossRef]
  15. Kniaginicheva, E.; Pismenskaya, N.; Melnikov, S.; Belashova, E.; Sistat, P.; Cretin, M.; Nikonenko, V. Water splitting at an anion-exchange membrane as studied by impedance spectroscopy. J. Membr. Sci. 2015, 496, 78–83. [Google Scholar] [CrossRef]
  16. Moya, A.A. Electrochemical Impedance of Ion-Exchange Membranes with Interfacial Charge Transfer Resistances. J. Phys. Chem. C 2016, 120, 6543–6552. [Google Scholar] [CrossRef]
  17. Pintossi, D.; Saakes, M.; Borneman, Z.; Nijmeijer, K. Electrochemical impedance spectroscopy of a reverse electrodialysis stack: A new approach to monitoring fouling and cleaning. J. Power Sources 2019, 444, 227302. [Google Scholar] [CrossRef]
  18. Kim, S.-H.; Choi, W.; Lee, K.-B.; Choi, S. Advanced Dynamic Simulation of Supercapacitors Considering Parameter Variation and Self-Discharge. IEEE Trans. Power Electron. 2011, 26, 3377–3385. [Google Scholar] [CrossRef]
  19. German, R.; Hammar, A.; Lallemand, R.; Sari, A.; Venet, P. Novel Experimental Identification Method for a Supercapacitor Multipore Model in Order to Monitor the State of Health. IEEE Trans. Power Electron. 2016, 31, 548–559. [Google Scholar] [CrossRef]
  20. Yuan, X.; Wang, H.; Sun, J.C.; Zhang, J. AC impedance technique in PEM fuel cell diagnosis—A review. Int. J. Hydrogen Energy 2007, 32, 4365–4380. [Google Scholar] [CrossRef]
  21. Loo, K.; Wong, K.; Tan, S.; Lai, Y.; Tse, C.K. Characterization of the dynamic response of proton exchange membrane fuel cells—A numerical study. Int. J. Hydrogen Energy 2010, 35, 11861–11877. [Google Scholar] [CrossRef]
  22. Vijayaraghavan, K.; DeVaal, J.; Narimani, M. Dynamic model of oxygen starved proton exchange membrane fuel-cell using hybrid analytical-numerical method. J. Power Sources 2015, 285, 291–302. [Google Scholar] [CrossRef]
  23. Iftikhar, M.U.; Riu, D.; Druart, F.; Rosini, S.; Bultel, Y.; Retière, N. Dynamic modeling of proton exchange membrane fuel cell using non-integer derivatives. J. Power Sources 2016, 160, 1170–1182. [Google Scholar] [CrossRef]
  24. Nikonenko, V.V.; Kozmai, A.E. Electrical equivalent circuit of an ion-exchange membrane system. Electrochim. Acta 2011, 56, 1262–1269. [Google Scholar] [CrossRef]
  25. Moya, A.A. Identification of characteristic time constants in the initial dynamic response of electric double layer capacitors from high-frequency electrochemical impedance. J. Power Sources 2018, 397, 124–133. [Google Scholar] [CrossRef]
  26. What Is OrCAD PSpice Designer? Available online: https://www.orcad.com/products/orcad-pspice-designer/overview (accessed on 1 October 2022).
  27. Długołęcki, P.; Ogonowski, P.; Metz, S.J.; Saakes, M.; Nijmeijer, K.; Wessling, M. On the resistances of membrane, diffusion boundary layer and double layer in ion exchange membrane transport. J. Membr. Sci. 2010, 349, 369–379. [Google Scholar] [CrossRef]
  28. Berezina, N.P.; Kononenko, N.A.; Dyomina, O.A.; Gnusin, N.P. Characterization of ion-exchange membrane materials: Properties vs structure. Adv. Colloid Interface Sci. 2008, 139, 3–28. [Google Scholar] [CrossRef] [PubMed]
  29. Dzyazko, Y.S.; Rozhdestvenska, L.M.; Vasilyuk, S.; Kudelko, K.; Belyakov, V.N. Composite Membranes Containing Nanoparticles of Inorganic Ion Exchangers for Electrodialytic Desalination of Glycerol. Nanoscale Res. Lett. 2017, 12, 438. [Google Scholar] [CrossRef] [PubMed]
  30. Moya, A.A. Influence of dc electric current on the electrochemical impedance of ion-exchange membrane systems. Electrochim. Acta 2011, 56, 3015–3022. [Google Scholar] [CrossRef]
  31. Konturri, K.; Murtomäki, L.; Manzanares, J.A. Ionic Transport Processes in Electrochemistry and Membrane Science; Oxford University Press: New York, NY, USA, 2008. [Google Scholar]
  32. Moya, A.A. The differential capacitance of the electric double layer in the diffusion boundary layer of ion-exchange membrane systems. Electrochim. Acta 2015, 178, 249–258. [Google Scholar] [CrossRef]
  33. Rubinstein, I.; Zaltzman, B.; Futerman, A.; Gitis, V.; Nikonenko, V. Reexamination of electrodiffusion time scales. Phys. Rev. E 2009, 79, 021506. [Google Scholar] [CrossRef]
  34. Kozmai, A.; Sarapulova, V.; Sharafan, M.; Melkonian, K.; Rusinova, T.; Kozmai, Y.; Pismenskaya, N.; Dammak, L.; Nikonenko, V. Electrochemical Impedance Spectroscopy of Anion-Exchange Membrane AMX-Sb Fouled by Red Wine Components. Membranes 2020, 11, 2. [Google Scholar] [CrossRef] [PubMed]
  35. Kuhn, E.; Forgez, C.; Lagonotte, P.; Friedrich, G. Modelling Ni-mH battery using Cauer and Foster structures. J. Power Sources 2006, 158, 1490–1497. [Google Scholar] [CrossRef]
  36. Moya, A.A. Low-frequency development approximations to the transmissive Warburg diffusion impedance. J. Energy Storage 2022, 55, 105632. [Google Scholar] [CrossRef]
Figure 1. Sketch of the ion-exchange membrane system.
Figure 1. Sketch of the ion-exchange membrane system.
Membranes 12 01003 g001
Figure 2. Equivalent electric circuit model of the impedance of an ion-exchange membrane system.
Figure 2. Equivalent electric circuit model of the impedance of an ion-exchange membrane system.
Membranes 12 01003 g002
Figure 3. Nyquist plot of the impedance of ion-exchange membrane systems for IDC/IL = 0, 0.25 and 0.5. The arrow indicates increasing values of IDC.
Figure 3. Nyquist plot of the impedance of ion-exchange membrane systems for IDC/IL = 0, 0.25 and 0.5. The arrow indicates increasing values of IDC.
Membranes 12 01003 g003
Figure 4. Bode-type plot of the imaginary part of the impedance of ion-exchange membrane systems for IDC/IL = 0, 0.25 and 0.5. The arrow indicates increasing values of IDC.
Figure 4. Bode-type plot of the imaginary part of the impedance of ion-exchange membrane systems for IDC/IL = 0, 0.25 and 0.5. The arrow indicates increasing values of IDC.
Membranes 12 01003 g004
Figure 5. Nyquist plots of the impedance of ion-exchange membrane systems at low frequencies for IDC = 0 and the approximated impedances obtained according to developments of the Warburg impedance.
Figure 5. Nyquist plots of the impedance of ion-exchange membrane systems at low frequencies for IDC = 0 and the approximated impedances obtained according to developments of the Warburg impedance.
Membranes 12 01003 g005
Table 1. Parameters of the electric circuit shown in Figure 2.
Table 1. Parameters of the electric circuit shown in Figure 2.
IDC = 0IDC = 0.25 ILIDC = 0.5 IL
RacL (mΩ·m2)0.40670.46030.5638
RacR (mΩ·m2)0.40670.35700.3298
RM (mΩ·m2)0.2
CgL (μF/m2)2.832
CgR (μF/m2)2.832
CgM (μF/m2)2.5
RdL (mΩ·m2)0.610.94071.4573
RdR (mΩ·m2)0.610.40170.3439
CDL (μF/m2)2.6022.9973.6618
CDR (μF/m2)2.6022.3332.1352
τ (s)39.617
Table 2. Numerical values of the main characteristic frequencies in an ion-exchange membrane system.
Table 2. Numerical values of the main characteristic frequencies in an ion-exchange membrane system.
IDC = 0IDC = 0.25 ILIDC = 0.5 IL
fgL (Hz)140.5 × 106122.1 × 10699.68 × 106
fgR (Hz)140.5 × 106157.4 × 106170.4 × 106
fgM (Hz)318.3 × 106
fHL (Hz)2.51 × 10180.793 × 10180.221 × 1018
fHR (Hz)2.51 × 10187.18 × 101811.69 × 1018
fC (Hz)25.9 × 10327.3 × 10328.9 × 103
fZ (Hz)0.030440.033370.04165
fd (Hz)0.01021
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Moya, A.A. Identifying Characteristic Frequencies in the Electrochemical Impedance of Ion-Exchange Membrane Systems. Membranes 2022, 12, 1003. https://doi.org/10.3390/membranes12101003

AMA Style

Moya AA. Identifying Characteristic Frequencies in the Electrochemical Impedance of Ion-Exchange Membrane Systems. Membranes. 2022; 12(10):1003. https://doi.org/10.3390/membranes12101003

Chicago/Turabian Style

Moya, Antonio Angel. 2022. "Identifying Characteristic Frequencies in the Electrochemical Impedance of Ion-Exchange Membrane Systems" Membranes 12, no. 10: 1003. https://doi.org/10.3390/membranes12101003

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop