Nitrogen-Doped Cobalt Phosphide for Enhanced Hydrogen Evolution Activity

被引:54
作者
Wang, Ling [1 ]
Wu, Haijun [1 ]
Xi, Shibo [2 ]
Chua, Sing Teng [1 ]
Wang, Fenghe [1 ]
Pennycook, Stephen J. [1 ]
Yu, Zhi Gen [3 ]
Du, Yonghua [2 ]
Xue, Junmin [1 ]
机构
[1] Natl Univ Singapore, Fac Engn, Dept Mat Sci & Engn, 9 Engn Dr 1, Singapore 117576, Singapore
[2] ASTAR, Inst Chem & Engn Sci, 1 Pesek Rd, Singapore 627833, Singapore
[3] ASTAR, Inst High Performance Comp, Singapore 138632, Singapore
关键词
N doping; CoP2; porous carbon cloth; Gibbs free energy; enhanced HER activity; GENERALIZED GRADIENT APPROXIMATION; TRANSITION-METAL PHOSPHIDES; WIDE-RANGE; EFFICIENT; WATER; CATALYSTS; OXYGEN; ELECTROCATALYSTS; PERFORMANCE; ELECTRODE;
D O I
10.1021/acsami.9b01235
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Development of highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts has a direct impact on water splitting efficiency and cost-effectiveness. In this work, N-doped CoP2 is successfully synthesized for efficient HER in an alkaline electrolyte, which needs an overpotential of only 64 mV to drive a current density of 10 mA cm(-2), with a small Tafel slope of 47.4 mV dec(-1) and excellent stability for 15 h without any performance loss in 1 M KOH. This represents one of the best HER catalysts in the alkaline electrolyte so far. The successful doping of N into CoP2 is confirmed using X-ray photoelectron spectroscopy, X-ray absorption near-edge structure, and scanning transmission electron microscopy characterizations. It is revealed by first-principle calculations that the partial replacement of P with N not only facilitates electron transfer but also optimizes the Gibbs free energies of H*, H2O, and OH* adsorption on the P active sites, thus facilitating the HER process. This work highlights that anion modification of transition metal phosphides would be an effective and feasible method to enhance their HER activities and provide new insights for the design of novel HER electrocatalysts.
引用
收藏
页码:17359 / 17367
页数:9
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