Toward enhanced alkaline hydrogen electrocatalysis with transition metal-functionalized nitrogen-doped carbon supports

被引:11
作者
Li, Peng [1 ]
Zhao, Guoqiang [1 ,2 ]
Cheng, Ningyan [1 ]
Xia, Lixue [3 ]
Li, Xiaoning [1 ]
Chen, Yaping [2 ]
Lao, Mengmeng [1 ]
Cheng, Zhenxiang [1 ]
Zhao, Yan [3 ,4 ]
Xu, Xun [1 ]
Jiang, Yinzhu [2 ]
Pan, Hongge [2 ,5 ]
Dou, Shi Xue [1 ]
Sun, Wenping [2 ]
机构
[1] Univ Wollongong, Australian Inst Innovat Mat, Inst Superconducting & Elect Mat, Wollongong, NSW 2522, Australia
[2] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China
[3] Wuhan Univ Technol, Int Sch Mat Sci & Engn, State Key Lab Silicate Mat Architectures, Wuhan 430070, Hubei, Peoples R China
[4] Wuhan Univ, Inst Technol Sci, Wuhan 430072, Hubei, Peoples R China
[5] Xian Technol Univ, Inst Sci & Technol New Energy, Xian 710021, Shaanxi, Peoples R China
基金
澳大利亚研究理事会; 中国博士后科学基金;
关键词
Multifunctional support; Hydrogen oxidation reaction; Hydrogen evolution reaction; Metal-support interaction; Electrocatalysis; OXYGEN REDUCTION CATALYSIS; ELECTROLYTE FUEL-CELLS; WATER ELECTROLYSIS; POROUS CARBONS; EVOLUTION; EFFICIENT; OXIDE; SALTS;
D O I
10.1016/S1872-2067(21)63935-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Superior catalyst supports are crucial to developing advanced electrocatalysts toward heterogeneous catalytic reactions. Herein, we systematically investigate the role of transition metal-functionalized N-doped carbon nanosheets (M-N-C, M = Mn, Fe, Co, Ni, Cu, Mo, and Ag) as the multifunctional electrocatalyst supports toward hydrogen evolution/oxidation reactions (HER/HOR) in alkaline media. The results demonstrate that all the M-N-C nanosheets, except Cu-N-C and Ag-N-C, can promote the alkaline HER/HOR electrocatalytic activity of Pt by accelerating the sluggish Volmer step, among which Mn plays a more significant role. Analyses reveal that the promotion effect of M-N-C support is closely associated with the electronegativity of the metal dopants and the relative filling degree of their d-orbitals. For one, the metal dopant in M-N-C with smaller electronegativity would provide more electrons to oxygen and hence tune the electronic structure of Pt via the M-O-Pt bonds at the interface. For another, the transition metal in M-N4 moieties with more empty d orbitals would hybridize with O 2p orbitals more strongly that promotes the adsorption of water/hydroxyl species. The results demonstrate the conceptual significance of multifunctional supports and would inspire the future development of advanced electrocatalysts.
引用
收藏
页码:1351 / 1359
页数:9
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