Electrochemical Preparation of Nanocatalysts and Their Application in Electrocatalysis

In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codo...

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Published inInternational journal of analytical chemistry Vol. 2022; pp. 1 - 6
Main Author Zhou, Hao
Format Journal Article
LanguageEnglish
Published New York Hindawi 27.08.2022
John Wiley & Sons, Inc
Wiley
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Abstract In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure (η-MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159 mV, which is slightly higher than 67 mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68 mV·dec−1, which is slightly higher than that of the commercial Pt/C catalyst (40 mV·dec−1) and the reference value (58 mV·dec−1), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion. This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.
AbstractList In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure (η-MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159 mV, which is slightly higher than 67 mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68 mV·dec−1, which is slightly higher than that of the commercial Pt/C catalyst (40 mV·dec−1) and the reference value (58 mV·dec−1), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion. This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.
In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure ( η -MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159 mV, which is slightly higher than 67 mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68 mV·dec −1 , which is slightly higher than that of the commercial Pt/C catalyst (40 mV·dec −1 ) and the reference value (58 mV·dec −1 ), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion . This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.
In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure (η-MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159 mV, which is slightly higher than 67 mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68 mV·dec-1, which is slightly higher than that of the commercial Pt/C catalyst (40 mV·dec-1) and the reference value (58 mV·dec-1), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion. This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure (η-MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159 mV, which is slightly higher than 67 mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68 mV·dec-1, which is slightly higher than that of the commercial Pt/C catalyst (40 mV·dec-1) and the reference value (58 mV·dec-1), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion. This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.
In order to solve the basic problem of high-temperature sintering of molybdenum carbide restricting the efficient construction of molybdenum carbide nanostructures and the full play of hydrogen evolution performance, this article studies the preparation of nano molybdenum carbide/boron nitrogen codoped two-dimensional carbon composite structure catalysts and the electrochemical hydrogen evolution reaction performance. Based on the self-assembly process of gelatin molecules on the surface of a two-dimensional layered boric acid crystal template, a new strategy for constructing a high-performance electrochemical hydrogen evolution reaction catalyst based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure (η -MoC@ BN-CSs) was established. The experimental results show that the overpotential of hydrogen evolution reaction based on molybdenum carbide/boron nitrogen codoped two-dimensional nanocarbon composite structure catalyst is 159mV, which is slightly higher than 67mV of commercial Pt/C catalyst, but lower than the reported literature value in the list. The Tafel slope is 68mV·dec[sup.-1], which is slightly higher than that of the commercial Pt/C catalyst (40mV·dec[sup.-1]) and the reference value (58mV·dec[sup.-1]), but lower than those of other reported literature values in the list, indicating that the molybdenum carbide/boron nitrogen codoped two-dimensional carbon nanocomposites have excellent catalytic performance under alkaline conditions. Conclusion. This kind of two-dimensional nanocomposite structure shows platinum-like catalytic activity when used as an electrochemical hydrogen evolution catalyst in alkaline electrolyte. It has better reaction kinetics and better stability.
Audience Academic
Author Zhou, Hao
AuthorAffiliation JiangSu Vocational College of Business, NanTong 226011, JiangSu, China
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ContentType Journal Article
Copyright Copyright © 2022 Hao Zhou.
COPYRIGHT 2022 John Wiley & Sons, Inc.
Copyright © 2022 Hao Zhou. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0
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SubjectTerms Alternative energy sources
Amino acids
Analytical chemistry
Boric acid
Boron
Carbon
Catalysts
Catalytic activity
Chemical reaction, Rate of
Clean technology
Composite structures
Electric properties
Electrodes
Electrolytes
Electron microscopes
Gelatin
High temperature
Hydrogen
Hydrogen evolution reactions
Molybdenum
Molybdenum carbide
Nanocomposites
Nanoparticles
Nanowires
Nitrogen
Platinum
Precious metals
Reaction kinetics
Self-assembly
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Title Electrochemical Preparation of Nanocatalysts and Their Application in Electrocatalysis
URI https://dx.doi.org/10.1155/2022/9884302
https://www.proquest.com/docview/2709592167
https://www.proquest.com/docview/2710972410
https://pubmed.ncbi.nlm.nih.gov/PMC9440798
https://doaj.org/article/b9b4e8313d9740c9b6f7576b9e62d96f
Volume 2022
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