双功能
过电位
电催化剂
催化作用
析氧
分解水
无机化学
材料科学
化学工程
氧化物
纳米技术
电解质
钴
纳米颗粒
化学
电化学
电极
冶金
物理化学
有机化学
工程类
光催化
作者
Jun‐Feng Qin,Jiahui Lin,Tianshu Chen,Dapeng Liu,Jingyi Xie,Bao-Yu Guo,Lei Wang,Yong‐Ming Chai,Bin Dong
标识
DOI:10.1016/j.jechem.2019.01.022
摘要
Abstract Adjusting the intrinsic activity and conductivity of electrocatalysts may be a crucial way for excellent performance for water splitting. Herein, the rational design of vanadium element doped cobalt phosphide (V-doped CoP) nanoparticles has been investigated through a facile gaseous phosphorization using cobalt vanadium oxide or hydroxide (Co-V hydr(oxy)oxide) as precursor. The physical characterization shows that the homogeneous dispersion of V element on V-doped CoP nanoparticles have obtained, which may imply the enhanced electrocatalytic activity for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The electrochemical measurements of the prepared V-doped CoP in alkaline electrolyte demonstrate the superior electrocatalytic activity for both HER (overpotential of 235 mV@10 mA cm−2) and OER (overpotential of 340 mV @10 mA cm−2). Further, V-doped CoP nanoparticles used as anode and cathode simultaneously in a cell require only 370 mV to achieve a current density of 10 mA cm−2. The outstanding electrocatalytic activity may be ascribed to the improved conductivity and intrinsic activity owing to phosphating and the doping of V element. In addition, the long-term stability of V-doped CoP has been obtained. Therefore, metal doping into transition metal-based phosphides may be a promising strategy for the remarkable bifunctional electrocatalyst for water splitting.
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