Co-Constructing Interfaces of Multiheterostructure on MXene (Ti3C2Tx)-Modified 3D Self-Supporting Electrode for Ultraefficient Electrocatalytic HER in Alkaline Media

被引:179
作者
Lv, Zepeng [1 ,2 ]
Ma, Wansen [1 ,2 ]
Wang, Meng [1 ,2 ]
Dang, Jie [1 ,2 ]
Jian, Kailiang [1 ,2 ]
Liu, Dong [1 ,2 ]
Huang, Dejun [3 ]
机构
[1] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Chongqing Key Lab Vanadium Titanium Met & New Mat, Chongqing 400044, Peoples R China
[3] Spectris Instrumentat & Syst Shanghai Ltd, Shanghai 200233, Peoples R China
基金
中国国家自然科学基金;
关键词
cobalt nitride; cobalt phosphide; electrocatalysts; electrodeposition; MXene; HYDROGEN EVOLUTION; TI3C2; MXENE; EFFICIENT; PERFORMANCE; NANOSHEETS; NI2P;
D O I
10.1002/adfm.202102576
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalysis is a potential method for sustainable hydrogen production, and the development of non-noble metal-based effective electrocatalysts for electrochemical water splitting is the core of exploiting and utilizing renewable energy. Herein, a stupendous electrocatalyst with multiheterostructure interfaces and 3D porous structure is synthesized, and the mechanisms of enhanced electrocatalytic activity combining multicharacterizations and density functional calculations are clarified. Especially, the fabricated Co2P/N@Ti3C2Tx@NF (denoted as CPN@TC) exhibits an ultralow overpotential of 15 mV to arrive at a current density of 10 mA cm(-2) with the long-term durability and a small Tafel slope of 30 mV dec(-1) in 1 m KOH, which even compares with noble metal catalysts favorably. The outstanding HER activity is ascribed to multiheterointerfaces for adsorbing H2O and H*, fine conductivity for the electronic transmission, and well-designed structure for rapid transport of ions and gases. It is reasonable to think that the synthetic strategy of CPN@TC can be extended to the preparation of transition-metal-based phosphides for enhanced catalytic performance.
引用
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页数:8
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