Boosting electrocatalytic hydrogen evolution over the wide pH range for CoP3 nanowire arrays via Ni doping

被引:6
作者
Pi, Mingyu [1 ,2 ]
Luo, Yue [1 ]
Chen, Yujia [1 ]
Chen, Feiyu [1 ]
Liu, Jun [3 ]
Zhang, Dingke [1 ]
Yang, Jie [1 ]
机构
[1] Chongqing Normal Univ, Coll Phys & Elect Engn, Chongqing 401331, Peoples R China
[2] Nanjing Univ, Coll Engn & Appl Sci, Nanjing 210093, Peoples R China
[3] Chongqing Yunkang Zhilian Technol Co Ltd, Chongqing 401331, Peoples R China
基金
中国博士后科学基金;
关键词
Ni-doped CoP3; Electrocatalyst; Hydrogen evolution; Wide pH range; CARBON CLOTH; PERFORMANCE; NANOARRAY; ELECTRODE;
D O I
10.1016/j.jallcom.2022.165440
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CoP3 is a promising electrocatalyst for the hydrogen evolution reaction, however it is still challenging for CoP3-based catalyst to deliver excellent activities in a wide pH range. In this work, the self-standing Ni-doped CoP3 nanowire arrays (Ni-CoP3 NWs) on carbon fiber paper were synthesized by hydrothermal method followed with an in situ phosphating process. The results show that the Ni doping effectively boosts the electrocatalytic hydrogen evolution for CoP3 NWs over the wide pH range with good stability. The Ni doped CoP3 NWs sample with the Ni: Co mole ratio of 10% (Ni-CoP3-10%) shows a low overpotential of 66 mV to afford the current density of 10 mA cm(-2) in 0.5 M H2SO4, which is the optimal catalytic performance in this work. Furthermore, Ni-CoP3-10% sample also shows excellent electrocatalytic performance in alkaline and neutral conditions, which needs the overpotential of 114 and 131 mV to afford the current density of 10 mA cm(-2) in 1 M KOH and 1 M PBS, respectively. The enhanced electrocatalytic activity can be ascribed to that the Ni doping improves the electron transport, increases the electrochemical active surface area and optimizes the Gibbs free energy of hydrogen adsorption for the CoP3 NWs, which develops it as a promising electrochemical catalyst for hydrogen evolution. (C) 2022 Published by Elsevier B.V.
引用
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页数:7
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