Fe Enhanced Visible-Light-Driven Nitrogen Fixation on BiOBr Nanosheets

被引:147
作者
Liu, Yang [2 ]
Hu, Zhuofeng [1 ]
Yu, Jimmy C. [2 ]
机构
[1] Sun Yat Sen Univ, Guangzhou, Peoples R China
[2] Chinese Univ Hong Kong, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLECULAR-OXYGEN ACTIVATION; DOPED TIO2; PHOTOCATALYTIC PROPERTIES; SOLAR-ENERGY; AMMONIA; CONVERSION; VACANCIES; WATER; PHOTOREDUCTION; HYDROGENATION;
D O I
10.1021/acs.chemmater.9b04448
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
Photocatalytic conversion of nitrogen (N-2) to ammonia (NH3) requires strong binding of N-2 onto the catalyst surface and the generation of photoexcited electrons to activate the N equivalent to N bond. In this study, Fe is doped into BiOBr nanosheets, where the photoexcited electrons have enough energy to break the N equivalent to N bond. The presence of Fe induces the formation of oxygen vacancies (OVs) in its vicinity, making it a photoexcited electron-rich region. The reduced Fe species effectively donates its available 3d orbital electron into the pi N-N antibonding orbital to activate the adsorbed N-2. With Fe as the active site, the N-2 fixation rate of Fe-doped BiOBr is enhanced by eight times. This work provides a sustainable alternative for N-2 photofixation and strategies for the catalyst design.
引用
收藏
页码:1488 / 1494
页数:7
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