Recent Advancements in Mesoporous Nanomaterials: Synthesis, Characterization and Catalytic Applications

A special issue of Nanomaterials (ISSN 2079-4991). This special issue belongs to the section "Synthesis, Interfaces and Nanostructures".

Deadline for manuscript submissions: closed (31 December 2023) | Viewed by 6500

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Guest Editor
Department Chemistry of Surface and Catalysis, “Ilie Murgulescu” Institute of Physical Chemistry, Romanian Academy, 060021 Bucharest, Romania
Interests: catalysts and catalytic processes; synthesis of nanomaterials and mesoporous oxide, composite and hybrid materials; immobilization on support of transitional metals, enzymes and organometallic complexes; characterization of materials (scanning electron microscopy-SEM, UV-Vis spectroscopy, IR coupled adsorption-desorption, gas permeation); catalytic oxidation in gas and liquid phase; photocatalysis; phase transfer catalysis; catalysis on membranes
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Special Issue Information

Dear Colleagues,

Recent advancements in nanomaterials synthesis are outstandingas they allow size, morphology and structure to be controlled more effectively. Due to these properties, nanomaterials have led to many interesting applications in catalysis because of their special physical and chemical properties compared with bulk materials. The introduction of mesopores with well-defined structures to improve mass-transfer efficiency widened the range of the applications in terms of nanocatalysis. Thus, a wide variety of new nanomaterials (semiconductors, oxides, carbon and other compounds) with large pore sizes, high surface areas and tunable architectures of mesopores have been obtained as supports or active materials in catalysis. Additionally, significant attention has been paid to the development of mesoporous nanocatalysts using greener chemistry (environmentally friendly materials as surfactants and precursors).

This Special Issue will focus on recent advancements in mesoporous nanomaterials: synthesis, characterization and catalytic applications. A special emphasis will be given to new mesoporous nanomaterials such as modified oxide supports, metal-incorporated oxide supports, transition metals oxides, composites and hybrid materials. A variety of novel synthetic strategies, advanced characterization techniques and new catalytically active species that may modify and justify the activity and selectivity of mesoporous oxides in catalytic reactions of interest performed in gas or liquid phase can be directions of interest. The addition of some synergistic components on mesoporous supports (mixed oxides, composite or hybrid materials) is desirable to accurately tune the interactions with the local environment, leading to improved catalytic performance. The interaction between active sites and support with their electronic structure modulation and a significant promoting effect on activity and selectivity can be another topic of interest that can be approached, along with the others, by the researchers interested in the synthesis, characterization and the use of the mesoporous nanoparticles as catalysts.

Dr. Viorica Pârvulescu
Guest Editor

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Keywords

  • mesoporous nanomaterials
  • nanomaterials synthesis
  • mesoporous catalysts
  • modified supports
  • composite catalysts
  • mixed nanooxides
  • nanocatalysis
  • synergetic effect
  • metal-support interaction
  • hybrid catalysts

Published Papers (5 papers)

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Research

23 pages, 4675 KiB  
Article
Highly Efficient Ru-Based Catalysts for Lactic Acid Conversion to Alanine
by Iunia Podolean, Mara Dogaru, Nicolae Cristian Guzo, Oana Adriana Petcuta, Elisabeth E. Jacobsen, Adela Nicolaev, Bogdan Cojocaru, Madalina Tudorache, Vasile I. Parvulescu and Simona M. Coman
Nanomaterials 2024, 14(3), 277; https://doi.org/10.3390/nano14030277 - 29 Jan 2024
Viewed by 938
Abstract
The primary objective of this research was to develop efficient solid catalysts that can directly convert the lactic acid (LA) obtained from lignocellulosic biomass into alanine (AL) through a reductive amination process. To achieve this, various catalysts based on ruthenium were synthesized using [...] Read more.
The primary objective of this research was to develop efficient solid catalysts that can directly convert the lactic acid (LA) obtained from lignocellulosic biomass into alanine (AL) through a reductive amination process. To achieve this, various catalysts based on ruthenium were synthesized using different carriers such as multi-walled carbon nanotubes (MWCNTs), beta-zeolite, and magnetic nanoparticles (MNPs). Among these catalysts, Ru/MNP demonstrated a remarkable yield of 74.0% for alanine at a temperature of 200 °C. This yield was found to be superior not only to the Ru/CNT (55.7%) and Ru/BEA (6.6%) catalysts but also to most of the previously reported catalysts. The characterization of the catalysts and their catalytic results revealed that metallic ruthenium nanoparticles, which were highly dispersed on the external surface of the magnetic carrier, significantly enhanced the catalyst’s ability for dehydrogenation. Additionally, the -NH2 basic sites on the catalyst further facilitated the formation of alanine by promoting the adsorption of acidic reactants. Furthermore, the catalyst could be easily separated using an external magnetic field and exhibited the potential for multiple reuses without any significant loss in its catalytic performance. These practical advantages further enhance its appeal for applications in the reductive amination of lactic acid to alanine. Full article
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13 pages, 5956 KiB  
Article
One-Pot Synthesis of Ultra-Small Pt Nanoparticles-Loaded Nitrogen-Doped Mesoporous Carbon Nanotube for Efficient Catalytic Reaction
by Qian Zhang, Minying Wu, Yuanyuan Fang, Chao Deng, Hsin-Hui Shen, Yi Tang and Yajun Wang
Nanomaterials 2023, 13(19), 2633; https://doi.org/10.3390/nano13192633 - 25 Sep 2023
Viewed by 1129
Abstract
In this study, Pt nanoparticles-loaded nitrogen-doped mesoporous carbon nanotube (Pt/NMCT) was successfully synthesized through a polydopamine-mediated “one-pot” co-deposition strategy. The Pt source was introduced during the co-deposition of polydopamine and silica on the surface of SiO2 nanowire (SiO2 NW), and Pt [...] Read more.
In this study, Pt nanoparticles-loaded nitrogen-doped mesoporous carbon nanotube (Pt/NMCT) was successfully synthesized through a polydopamine-mediated “one-pot” co-deposition strategy. The Pt source was introduced during the co-deposition of polydopamine and silica on the surface of SiO2 nanowire (SiO2 NW), and Pt atoms were fixed in the skeleton by the chelation of polydopamine. Thus, in the subsequent calcination process in nitrogen atmosphere, the growth and agglomeration of Pt nanoparticles were effectively restricted, achieving the in situ loading of uniformly dispersed, ultra-small (~2 nm) Pt nanoparticles. The method is mild, convenient, and does not require additional surfactants, reducing agents, or stabilizers. At the same time, the use of the dual silica templates (SiO2 NW and the co-deposited silica nanoclusters) brought about a hierarchical pore structure with a high specific surface area (620 m2 g−1) and a large pore volume (1.46 cm3 g−1). The loading process of Pt was studied by analyzing the electron microscope and X-ray photoelectron spectroscopy of the intermediate products. The catalytic performance of Pt/NMCT was investigated in the reduction of 4-nitrophenol. The Pt/NMCT with a hierarchical pore structure had an apparent reaction rate constant of 0.184 min−1, significantly higher than that of the sample, without the removal of the silica templates to generate the hierarchical porosity (0.017 min−1). This work provides an outstanding contribution to the design of supported noble metal catalysts and also highlights the importance of the hierarchical pore structure for catalytic activity. Full article
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19 pages, 6507 KiB  
Article
Co- and Ni-Doped TiO2 Nanoparticles Supported on Zeolite Y with Photocatalytic Properties
by Gabriela Petcu, Florica Papa, Irina Atkinson, Adriana Baran, Nicoleta G. Apostol, Simona Petrescu, Lionel Richaudeau, Jean-Luc Blin and Viorica Parvulescu
Nanomaterials 2023, 13(15), 2200; https://doi.org/10.3390/nano13152200 - 28 Jul 2023
Cited by 4 | Viewed by 1263
Abstract
Zeolite Y samples with microporous and hierarchical structures containing Ti–Ni and Ti–Co oxides were obtained as active photocatalysts. Different Ti amounts (5, 10% TiO2) were supported, followed by the loading of Ni or Co oxides (5%). X-ray diffraction evidenced the presence [...] Read more.
Zeolite Y samples with microporous and hierarchical structures containing Ti–Ni and Ti–Co oxides were obtained as active photocatalysts. Different Ti amounts (5, 10% TiO2) were supported, followed by the loading of Ni or Co oxides (5%). X-ray diffraction evidenced the presence of TiO2 as an anatase. N2 adsorption–desorption results showed type IV isotherms for hierarchical zeolite Y samples, and a combination of type IV and I isotherms for zeolite Y samples. UV–Vis diffuse reflectance spectra showed a shift in the absorption band to visible with increasing Ti loading and especially after Co and Ni addition. A significant effect of the support was evidenced for Ti and its interaction with Co/Ni species. The zeolite Y support stabilized Ti in the 4+ oxidation state while hierarchical zeolite Y support favored the formation of Ti3+ species, Ni0 and Ni2+ and the oxidation of Co to 3+ oxidation state. Photocatalytic activity, under UV and visible light irradiation, was evaluated by the degradation of amoxicillin, used as a model test. The photocatalytic mechanism was investigated using ethanol, p-benzoquinone and KI as ·OH and ·O2 radicals and hole (h+) scavengers. The best results were obtained for the immobilized Ni-Ti species on the hierarchical zeolite Y support. Full article
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22 pages, 13493 KiB  
Article
Cu(II) and Mn(II) Anchored on Functionalized Mesoporous Silica with Schiff Bases: Effects of Supports and Metal–Ligand Interactions on Catalytic Activity
by Mihaela Mureseanu, Mihaela Filip, Irina Bleotu, Cezar Ionut Spinu, Alexandru Horia Marin, Iulia Matei and Viorica Parvulescu
Nanomaterials 2023, 13(12), 1884; https://doi.org/10.3390/nano13121884 - 19 Jun 2023
Cited by 3 | Viewed by 1210
Abstract
New series of Cu(II) and Mn(II) complexes with Schiff base ligands derived from 2-furylmethylketone (Met), 2-furaldehyde (Fur), and 2-hydroxyacetopheneone (Hyd) have been synthesized in situ on SBA-15-NH2, MCM-48-NH2, and MCM-41-NH2 functionalized supports. The hybrid materials were characterized by [...] Read more.
New series of Cu(II) and Mn(II) complexes with Schiff base ligands derived from 2-furylmethylketone (Met), 2-furaldehyde (Fur), and 2-hydroxyacetopheneone (Hyd) have been synthesized in situ on SBA-15-NH2, MCM-48-NH2, and MCM-41-NH2 functionalized supports. The hybrid materials were characterized by X-ray diffraction, nitrogen adsorption–desorption, SEM and TEM microscopy, TG analysis, and AAS, FTIR, EPR, and XPS spectroscopies. Catalytic performances were tested in oxidation with the hydrogen peroxide of cyclohexene and of different aromatic and aliphatic alcohols (benzyl alcohol, 2-methylpropan-1-ol, and 1-buten-3-ol). The catalytic activity was correlated with the type of mesoporous silica support, ligand, and metal–ligand interactions. The best catalytic activity of all tested hybrid materials was obtained in the oxidation of cyclohexene on SBA-15-NH2-MetMn as a heterogeneous catalyst. No leaching was evidenced for Cu and Mn complexes, and the Cu catalysts were more stable due to a more covalent interaction of the metallic ions with the immobilized ligands. Full article
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18 pages, 9066 KiB  
Article
Variation in Metal–Support Interaction with TiO2 Loading and Synthesis Conditions for Pt-Ti/SBA-15 Active Catalysts in Methane Combustion
by Mihaela Filip, Elena Maria Anghel, Vasile Rednic, Florica Papa, Simona Somacescu, Cornel Munteanu, Nicolae Aldea, Jing Zhang and Viorica Parvulescu
Nanomaterials 2023, 13(10), 1647; https://doi.org/10.3390/nano13101647 - 15 May 2023
Cited by 1 | Viewed by 1263
Abstract
The control of catalytic performance using synthesis conditions is one of the main goals of catalytic research. Two series of Pt-Ti/SBA-15 catalysts with different TiO2 percentages (n = 1, 5, 10, 30 wt.%) were obtained from tetrabutylorthotitanate (TBOT) and peroxotitanate (PT), [...] Read more.
The control of catalytic performance using synthesis conditions is one of the main goals of catalytic research. Two series of Pt-Ti/SBA-15 catalysts with different TiO2 percentages (n = 1, 5, 10, 30 wt.%) were obtained from tetrabutylorthotitanate (TBOT) and peroxotitanate (PT), as titania precursors and Pt impregnation. The obtained catalysts were characterized using X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM), N2 sorption, Raman, X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS), hydrogen temperature-programmed reduction (H2-TPR) and H2-chemisorption measurements. Raman spectroscopy showed framework titanium species in low TiO2 loading samples. The anatase phase was evidenced for samples with higher titania loading, obtained from TBOT, and a mixture of rutile and anatase for those synthesized by PT. The rutile phase prevails in rich TiO2 catalysts obtained from PT. Variable concentrations of Pt0 as a result of the stronger interaction of PtO with anatase and the weaker interaction with rutile were depicted using XPS. TiO2 loading and precursors influenced the concentration of Pt species, while the effect on Pt nanoparticles’ size and uniform distribution on support was insignificant. The Pt/PtO ratio and their concentration on the surface were the result of strong metal–support interaction, and this influenced catalytic performance in the complete oxidation of methane at a low temperature. The highest conversion was obtained for sample prepared from PT with 30% TiO2. Full article
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