电催化剂
催化作用
磷化物
材料科学
双功能
分解水
化学工程
析氧
钴
电解质
钒
镍
氢
无机化学
电化学
电极
纳米技术
化学
物理化学
冶金
有机化学
工程类
光催化
生物化学
作者
Hongyao Xue,Alan Meng,Haiqin Zhang,Yu‐Sheng Lin,Zhenjiang Li,Chuansheng Wang
出处
期刊:Nano Research
[Springer Nature]
日期:2021-02-22
卷期号:14 (11): 4173-4181
被引量:66
标识
DOI:10.1007/s12274-021-3359-2
摘要
Cobalt phosphide (CoP) is considered to be a potential candidate in the field of electrocatalysis due to its low-cost, abundant resources and high electrochemical stability. However, there is a great space for further improvement of its electrocatalytic performance since its charge transfer rate and catalytic activity have not reached a satisfactory level. Herein, we design and fabricate a three dimensional urchins like V-doped CoP with different amounts of V-doping on nickel foam electrode. The V-doped CoP/NF electrode with optimized amounts of V-doping (10%) exhibits outstanding hydrogen evolution reaction (HER) performance under universal-pH conditions and preeminent oxygen evolution reaction (OER) performance in alkaline media. Notably, the assembled water-splitting cell displays a cell voltage of only 1.53 V at 10 mA·cm−2 and has excellent durability, much better than many reported related bifunctional catalysts. The experiment results and theoretical analysis revealed that vanadium atoms replace cobalt atoms in CoP lattice. Vanadium doping can not only raise the density of electronic states near the Fermi level enhancing the conductivity of the catalyst, but can also optimize the free energy of hydrogen and oxygen-containing intermediates adsorption over CoP, thus promoting its catalytic activity. Moreover, the unique nanostructure of the catalyst provides the various shortened channels for charge transfer and reactant/electrolyte diffusion, which accelerates the electrocatalytic process. Also, the in situ growth strategy can improve the conductivity and stability of the catalyst.
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