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
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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