过电位
分解水
析氧
催化作用
双金属片
三元运算
阳极
材料科学
阴极
电解水
电催化剂
化学工程
无机化学
化学
电解
电化学
物理化学
电极
光催化
电解质
工程类
生物化学
计算机科学
程序设计语言
作者
Hanfeng Liang,Appala Naidu Gandi,Dalaver H. Anjum,Xianbin Wang,Udo Schwingenschlögl,Husam N. Alshareef
出处
期刊:Nano Letters
[American Chemical Society]
日期:2016-11-09
卷期号:16 (12): 7718-7725
被引量:1103
标识
DOI:10.1021/acs.nanolett.6b03803
摘要
Efficient water splitting requires highly active, earth-abundant, and robust catalysts. Monometallic phosphides such as Ni2P have been shown to be active toward water splitting. Our theoretical analysis has suggested that their performance can be further enhanced by substitution with extrinsic metals, though very little work has been conducted in this area. Here we present for the first time a novel PH3 plasma-assisted approach to convert NiCo hydroxides into ternary NiCoP. The obtained NiCoP nanostructure supported on Ni foam shows superior catalytic activity toward the hydrogen evolution reaction (HER) with a low overpotential of 32 mV at −10 mA cm–2 in alkaline media. Moreover, it is also capable of catalyzing the oxygen evolution reaction (OER) with high efficiency though the real active sites are surface oxides in situ formed during the catalysis. Specifically, a current density of 10 mA cm–2 is achieved at overpotential of 280 mV. These overpotentials are among the best reported values for non-noble metal catalysts. Most importantly, when used as both the cathode and anode for overall water splitting, a current density of 10 mA cm–2 is achieved at a cell voltage as low as 1.58 V, making NiCoP among the most efficient earth-abundant catalysts for water splitting. Moreover, our new synthetic approach can serve as a versatile route to synthesize various bimetallic or even more complex phosphides for various applications.
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