Polarized Ultrathin BN Induced Dynamic Electron Interactions for Enhancing Acidic Oxygen Evolution

被引:50
作者
Hao, Yixin [1 ]
Hung, Sung-Fu [2 ]
Tian, Cheng [1 ]
Wang, Luqi [1 ]
Chen, Yi-Yu [2 ]
Zhao, Sheng [1 ]
Peng, Kang-Shun [2 ]
Zhang, Chenchen [3 ]
Zhang, Ying [3 ]
Kuo, Chun-Han [4 ]
Chen, Han-Yi [4 ]
Peng, Shengjie [1 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Peoples R China
[2] Natl Yang Ming Chiao Tung Univ, Dept Appl Chem, Hsinchu 300, Taiwan
[3] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[4] Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu 30013, Taiwan
基金
中国国家自然科学基金;
关键词
Acidic oxygen evolution reaction; RuO2; BN nanosheets; Defect; Electronic back-donation; HEXAGONAL BORON-NITRIDE; WATER OXIDATION; CATALYST; IDENTIFICATION; TEMPERATURE; PERFORMANCE; SITES; OXIDE;
D O I
10.1002/anie.202402018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing ruthenium-based heterogeneous catalysts with an efficient and stable interface is essential for enhanced acidic oxygen evolution reaction (OER). Herein, we report a defect-rich ultrathin boron nitride nanosheet support with relatively independent electron donor and acceptor sites, which serves as an electron reservoir and receiving station for RuO2, realizing the rapid supply and reception of electrons. Through precisely controlling the reaction interface, a low OER overpotential of only 180 mV (at 10 mA cm(-2)) and long-term operational stability (350 h) are achieved, suggesting potential practical applications. In situ characterization and theoretical calculations have validated the existence of a localized electronic recycling between RuO2 and ultrathin BN nanosheets (BNNS). The electron-rich Ru sites accelerate the adsorption of water molecules and the dissociation of intermediates, while the interconnection between the O-terminal and B-terminal edge establishes electronic back-donation, effectively suppressing the over-oxidation of lattice oxygen. This study provides a new perspective for constructing a stable and highly active catalytic interface.
引用
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页数:9
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