过电位
材料科学
氢氧化物
纳米晶材料
析氧
氧化物
电极
化学工程
电合成
石墨烯
水滑石
电化学
镍
金属氢氧化物
电催化剂
无机化学
化学
催化作用
纳米技术
冶金
物理化学
工程类
生物化学
作者
Zhenhua Yan,Hongming Sun,Xiang Chen,Huanhuan Liu,Yaran Zhao,Haixia Li,Wei Xie,Fangyi Cheng,Jun Chen
标识
DOI:10.1038/s41467-018-04788-3
摘要
Abstract Electrochemical deposition is a facile strategy to prepare functional materials but suffers from limitation in thin films and uncontrollable interface engineering. Here we report a universal electrosynthesis of metal hydroxides/oxides on varied substrates via reduction of oxyacid anions. On graphitic substrates, we find that the insertion of nitrate ion in graphene layers significantly enhances the electrodeposit–support interface, resulting in high mass loading and super hydrophilic/aerophobic properties. For the electrocatalytic oxygen evolution reaction, the nanocrystalline cerium dioxide and amorphous nickel hydroxide co-electrodeposited on graphite exhibits low overpotential (177 mV@10 mA cm −2 ) and sustains long-term durability (over 300 h) at a large current density of 1000 mA cm −2 . In situ Raman and operando X-ray diffraction unravel that the integration of cerium promotes the formation of electrocatalytically active gamma-phase nickel oxyhydroxide with exposed (003) facets. Therefore, combining anion intercalation with cathodic electrodeposition allows building robust electrodes with high electrochemical performance.
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