材料科学
非阻塞I/O
析氧
氮化物
催化作用
无机化学
X射线光电子能谱
过渡金属
化学工程
氧化物
镍
纳米技术
电化学
电极
冶金
图层(电子)
有机化学
物理化学
工程类
化学
作者
Chengan Liao,Baopeng Yang,Ning Zhang,Min Liu,Guoxin Chen,Xiao‐Ming Jiang,Gen Chen,Junliang Yang,Xiaohe Liu,Ting‐Shan Chan,Ying‐Jui Lu,Renzhi Ma,Wei Zhou
标识
DOI:10.1002/adfm.201904020
摘要
Abstract Combining transition metal oxide catalysts with conductive carbonaceous material is a feasible way to improve the conductivity. However, the electrocatalytic performance is usually not distinctly improved because the interfacial resistance between metal oxides and carbon is still large and thereby hinders the charge transport in catalysis. Herein, the conductive interface between poorly conductive NiO nanoparticles and semi‐conductive carbon nitride (CN) is constructed. The NiO/CN exhibits much‐enhanced oxygen evolution reaction (OER) performance than corresponding NiO and CN in electrolytes of KOH solution and phosphate buffer saline, which is also remarkably superior over NiO/C, commercial RuO 2 , and mostly reported NiO‐based catalysts. X‐ray photoelectron spectroscopy and extended X‐ray absorption fine structure spectrum reveal that a metallic Ni–N bond is formed between NiO and CN. Density functional theory calculations suggest that NiO and CN linked by a Ni–N bond possess a low Gibbs energy for OER intermediate adsorptions, which not only improves the transfer of charge but also promotes the transmission of mass in OER. The metal–nitrogen bonded conductive and highly active interface pervasively exists between CN and other transition metal oxides including Co 3 O 4 , CuO, and Fe 2 O 3 , making it promising as an inexpensive catalyst for efficient water splitting.
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