Effects of Group IB Metals of Au/Ag/Cu on Boosting Oxygen Evolution Reaction of Cobalt Hydroxide

被引:3
|
作者
Wang, Xianchao [1 ]
Zang, Zehao [1 ]
Fan, Chunyan [1 ]
Zhang, Yintao [1 ]
Li, Xiang [2 ]
Li, Lanlan [1 ]
Yu, Xiaofei [1 ]
Yang, Xiaojing [1 ]
Lu, Zunming [1 ]
Zhang, Xinghua [1 ]
机构
[1] Hebei Univ Technol, Sch Mat Sci & Engn, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Grad Sch, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt hydroxide; Electrons transfer; Heterostructure catalyst; Interface engineering; Oxygen evolution reaction; NANOSHEETS; ELECTROCATALYST; WATER; NANOPARTICLES; FABRICATION; HYDROGEN; CNTS; OER;
D O I
10.1002/cctc.202300033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing high-activity, good-stability oxygen evolution reaction (OER) catalysts is the key to solving the problem of hydrogen production from electrolytic water. Cobalt hydroxide (Co(OH)(2)) is a hopeful OER catalyst, but its poor conductivity and low inherent activity limit its OER performance. Herein, we used group IB metals of Au, Ag, and Cu to increase the OER performance of Co(OH)(2) via the electrodeposition method. All three metals can increase the carrier concentration and proportion of high-valence cobalt ions. The analysis results disclose that the construction of Ag-Co(OH)(2) heterostructure can optimize the electronic structure through interfacial interactions, produce a moderate proportion of high-valence cobalt centers, enhance the charge transport capacity and the adsorption of hydroxyl species, thus accelerating the OER kinetics and effectively improving the inherent catalytic activity. This work not only develops effective and steady catalysts but also provides a facile method to enhance the OER performance through interface engineering.
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页数:10
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