Facile synthesis of V-doped CoP nanoparticles as bifunctional electrocatalyst for efficient water splitting

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 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,Baoyu Guo,Lei Wang,Yong‐Ming Chai,Bin Dong
出处
期刊:Journal of Energy Chemistry [Elsevier BV]
卷期号:39: 182-187 被引量:92
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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