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2D MXene Nanomaterials as Electrocatalysts for Hydrogen Evolution Reaction (HER): A Review

期刊

MICROMACHINES
卷 13, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/mi13091499

关键词

2D MXene; Ti3C2Tx; water splitting; hydrogen evolution reaction; Tafel slope

资金

  1. National Research Foundation of Korea (NRF) - Korean government, Ministry of Science and ICT (MSIT), Republic of Korea [2021R1F1A1046648]
  2. Science and Engineering Research Board (SERB), Department of Science and Technology (DST), India [SRG/2021/001028]
  3. Natural Science Foundation of Jiangxi Province [20212BCJL23053, 20212BAB203015]
  4. Research Foundation of the Education, Department of Jiangxi Province [GJJ200808]

向作者/读者索取更多资源

MXenes, a novel family of 2D transition metal carbide, nitride and carbonitride materials, have gained tremendous interest as potential electrocatalysts for hydrogen evolution reaction (HER). This review article summarizes recent developments in MXene-based electrocatalysts synthesis and HER performance, and evaluates the superiority of MXene-based catalysts over traditional Pt/C catalysts.
MXenes, a novel family of 2D transition metal carbide, nitride and carbonitride materials, have been gaining tremendous interest in recent days as potential electrocatalysts for various electrochemical reactions, including hydrogen evolution reaction (HER). MXenes are characterized by their etchable metal layers, excellent structural stability, versatility for heteroatoms doping, excellent electronic conductivity, unique surface functional groups and admirable surface area, suitable for the role of electrocatalyst/support in electrochemical reactions, such as HER. In this review article, we summarized recent developments in MXene-based electrocatalysts synthesis and HER performance in terms of the theoretical and experimental point of view. We systematically evaluated the superiority of the MXene-based catalysts over traditional Pt/C catalysts in terms of HER kinetics, Tafel slope, overpotential and stability, both in acidic and alkaline electrolytic environments. We also pointed out the motives behind the electro catalytic enhancements, the effect of synthesis conditions, heteroatom doping, the effect of surface terminations on the electrocatalytic active sites of various MXenes families. At the end, various possible approaches were recommended for a deeper understanding of the active sites and catalytic improvement of MXenes catalysts for HER.

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