Enhancing hydrogen evolution reaction performance of transition metal doped two-dimensional electride Ca 2 N

被引:10
作者
Liu, Baoyu [1 ,2 ]
Chen, Ziqiang [2 ]
Xiong, Rui [1 ,2 ]
Yang, Xuhui [3 ]
Zhang, Yinggan [4 ]
Xie, Teng [1 ,2 ]
Wen, Cuilian [1 ,2 ]
Sa, Baisheng [1 ,2 ]
机构
[1] Fuzhou Univ, Multiscale Computat Mat Facil, Fuzhou 350100, Peoples R China
[2] Fuzhou Univ, Coll Mat Sci & Engn, Key Lab Ecomat Adv Technol, Fuzhou 350100, Peoples R China
[3] Fujian Normal Univ, Coll Environm Sci & Engn, Fujian Key Lab Pollut Control & Resource Reuse, Fuzhou 350007, Peoples R China
[4] Xiamen Univ, Coll Mat, Fujian Prov Key Lab Theoret & Computat Chem, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Two-dimensional electride; Density functional theory calculations; Hydrogen evolution reaction; Transition metal doping; Ca; 2; N; OXYGEN REDUCTION; MOS2; EDGES; CATALYST;
D O I
10.1016/j.cclet.2022.06.066
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two-dimensional electride Ca2N has strong electron transfer ability and low work function, which is a po-tential candidate for hydrogen evolution reaction (HER) catalyst. In this work, based on density functional theory calculations, we adopt two strategies to improve the HER catalytic activity of Ca2N monolayer: in-troducing Ca or N vacancy and doping transition metal atoms (TM, refers to Ti, V, Cr, Mn, Fe, Zr, Nb, Mo, Ru, Hf, Ta and W). Interestingly, the Gibbs free energy AGH * of Ca2N monolayer after introducing N vacancy is reduced to-0.146 eV, showing good HER catalytic activity. It is highlighted that, the HER cat-alytic activity of Ca2N monolayer can be further enhanced with TM doping, the Gibbs free energy AGH * of single Mo and double Mn doped Ca2N are predicted to be 0.119 and 0.139 eV, respectively. The present results will provide good theoretical guidance for the HER catalysis applications of two-dimensional elec-tride Ca2N monolayer.(c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:5
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