Tuning hydrogen binding modes within RuO2 lattice by proton and electron co-doping for active and stable acidic oxygen evolution

被引:47
作者
He, Junying [1 ]
Chen, Weixin [2 ]
Gao, Hongmei [1 ]
Chen, Yuxiang [1 ]
Zhou, Ling [1 ]
Zou, Yuqin [1 ]
Chen, Ru [1 ]
Tao, Li [1 ]
Lu, Xia [2 ]
Wang, Shuangyin [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chem Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Sun Yat Sen Univ, Sch Mat, Guangzhou 510275, Peoples R China
来源
CHEM CATALYSIS | 2022年 / 2卷 / 03期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
DISSOLUTION; STABILITY; DIOXIDE; TRENDS; REDOX;
D O I
10.1016/j.checat.2022.01.012
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
Solid polymer electrolyzer (SPE), which directly uses pure water as electrolyte, holds great promise for green hydrogen production, yet developing a durable and active electrocatalyst for a protonrich anode remains a bottleneck issue owing to the high catalyst dissolution under polarization potential. Here, proton and electron co-doping was employed to construct an Ru-O-H sec sec sec O bond within RuO2 lattice, and the hydrogen binding modes not only engineered the electronic interaction between Ru and O atoms but also formed a hydrogen bond, which was demonstrated to be an effective way to increase the electrocatalytic activity and stabilize the lattice oxygen. The intrinsic activity of representative 75-HRuO2 loaded on a glassy carbon electrode was almost ten times that of the pristine one, only requiring an overpotential of 200 mV (@10 mA cm(-2)). Moreover, it demonstrated ideal stability (@0.5 A cm(-2)) in the SPE device.
引用
收藏
页码:578 / 594
页数:17
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