钴
材料科学
氧化钴
煅烧
析氧
无机化学
化学工程
电催化剂
氧化物
氧气
催化作用
物理化学
电极
电化学
化学
有机化学
冶金
工程类
作者
Xinran Li,Jilei Wei,Qing Li,Shasha Zheng,Yuxia Xu,Pan Du,Changyun Chen,Jiyang Zhao,Huaiguo Xue,Qiang Xu,Huan Pang
标识
DOI:10.1002/adfm.201800886
摘要
Abstract Taking advantage of the self‐assembling function of amino acids, cobalt–alanine complexes are synthesized by straightforward process of chemical precipitation. Through a controllable calcination of the cobalt–alanine complexes, N‐doped Co 3 O 4 nanostructures (N‐Co 3 O 4 ) and N‐doped CoO composites with amorphous carbon (N‐CoO/C) are obtained. These N‐doped cobalt oxide materials with novel porous nanostructures and minimal oxygen vacancies show a high and stable activity for the oxygen evolution reaction. Moreover, the influence of calcination temperature, electrolyte concentration, and electrode substrate to the reaction are compared and analyzed. The results of experiments and density functional theory calculations demonstrate that N‐doping promotes the catalytic activity through improving electronic conductivity, increasing OH − adsorption strength, and accelerating reaction kinetics. Using a simple synthetic strategy, N‐Co 3 O 4 reserves the structural advantages of micro/nanostructured complexes, showing exciting potential as a catalyst for the oxygen evolution reaction with good stability.
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