Engineering Amorphous/Crystalline Rod-like Core-Shell Electrocatalysts for Overall Water Splitting

被引:18
|
作者
Li, Linfeng [1 ]
Sun, Huachuan [1 ]
Xu, Xuefei [1 ]
Humayun, Muhammad [1 ]
Ao, Xiang [1 ]
Yuen, Muk Fung [2 ]
Xue, Xinying [3 ]
Wu, Ying [4 ]
Yang, Yang [5 ]
Wang, Chundong [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Opt & Elect Informat, Wuhan Natl Lab Optoelect, Opt Valley Lab, Wuhan 430074, Peoples R China
[2] Chinese Univ Hong Kong, Shenzhen 518172, Guangdong, Peoples R China
[3] Shihezi Univ, Coll Sci, Dept Phys, Shihezi 832003, Peoples R China
[4] Tarim Univ, Coll Chem & Chem Engn, Alaer 843300, Peoples R China
[5] Chinese Acad Sci, Shenzhen Inst Adv Technol, Adv Energy Storage Technol Res Ctr, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
amorphous; crystalline coupling; rod-like core-shell; overall water splitting; electron redistribution; active site identification; EFFICIENT OXYGEN EVOLUTION; HIGHLY-EFFICIENT; CATALYSTS; ELECTRODE; FOAM;
D O I
10.1021/acsami.2c13417
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The design of bifunctional electrocatalysts for hydrogen and oxygen evolution reactions delivering excellent catalytic activity and stability is highly desirable, yet challenged. Herein, we report an amorphous RuO2-encapsulated crystalline Ni0.85Se nanorod structure (termed as a/c-RuO2/Ni0.85Se) for enhanced HER and OER activities. The as-prepared a/c-RuO2/Ni0.85Se nanorods not only demonstrate splendid HER activity (58 mV@10 mA cm-2 vs RHE), OER activity (233 mV@10 mA cm-2 vs RHE), and electrolyzer activity (1.488 V@10 mA cm-2 vs RHE for overall water splitting) but also exhibit long-term stability with negligible performance decay after 50 h continuous test for overall water splitting. In addition, the variation of the d-band center (from the perspective of bonding and antibonding states) is unveiled theoretically by density functional theory calculations upon amorphous RuO2 layers coupling to clarify the increased hydrogen species adsorption for HER activity enhancement. This work represents a new pathway for the fabrication of bifunctional electrocatalysts toward green hydrogen
引用
收藏
页码:50783 / 50793
页数:11
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