Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution

被引:473
作者
Yan, Zhenhua [1 ]
Sun, Hongming [1 ]
Chen, Xiang [1 ]
Liu, Huanhuan [1 ]
Zhao, Yaran [1 ]
Li, Haixia [1 ]
Xie, Wei [1 ]
Cheng, Fangyi [1 ]
Chen, Jun [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
[2] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China
关键词
WATER OXIDATION; ELECTROCATALYSTS; PERFORMANCE; NUCLEATION; REDUCTION; CATALYSIS; GROWTH; OXIDES; FILMS; IRON;
D O I
10.1038/s41467-018-04788-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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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页数:9
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