Atomic-level surface modification of ultrathin Bi2WO6 nanosheets for boosting photocatalytic CO2 reduction

被引:18
|
作者
Zhao, Lulu [1 ,2 ,3 ]
Hou, Huilin [3 ]
Wang, Lin [3 ]
Bowen, Chris R. [4 ]
Wang, Jinguo [1 ,2 ]
Yan, Ruifang [1 ,2 ]
Zhan, Xiaoqiang [3 ]
Yang, Hongli [3 ]
Yang, Man [3 ]
Yang, Weiyou [3 ]
机构
[1] Jilin Univ, Key Lab Automobile Mat, Minist Educ, Changchun 130025, Peoples R China
[2] Jilin Univ, Dept Mat Sci & Engn, Changchun 130025, Peoples R China
[3] Ningbo Univ Technol, Inst Micro Nano Mat & Devices, Ningbo 315211, Peoples R China
[4] Univ Bath, Dept Mech Engn, Bath BA2 7AK, England
基金
中国国家自然科学基金;
关键词
Bi2WO6; Cation exchange; CO2; photoreduction; Photocatalysts; TOTAL-ENERGY CALCULATIONS; OXYGEN VACANCY; HETEROJUNCTION PHOTOCATALYSTS; EFFICIENT; TRANSFORMATION; ABSORPTION; CHALLENGES; SPECTRA; COBALT;
D O I
10.1016/j.cej.2023.148033
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Creating useful chemicals based on artificial CO2 photoreduction is considered to be an attractive approach to address the environmental and energy crises. Currently, its selectivity with high conversion efficiency is still a grand challenge. Here, we report the refined substitution of Bi3+ with Ag+ in ultrathin Bi2WO6 nanosheets through a liquid-phase cation exchange process, favoring a high selectivity towards the photocatalytic produc-tion of CO from CO2. The incorporation of Ag+ could not only significantly promote the adsorption of both CO2 and H2O molecules, but also facilitate the transfer of photogenerated carriers. The as-fabricated photocatalyst achieves a high CO generation rate of 116.96 mu mol g-1 with a superb selectivity of 95.7 % after 6 h reaction without any sacrificial agent, approximate 4.2 times higher than that of pure Bi2WO6. The mechanism for photocatalytic CO2 reduction is proposed, based on in-situ Fourier Transform Infrared spectrometry analyses and Density Functional Theory calculations.
引用
收藏
页数:12
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