Article Enhanced photocatalytic activity and mechanism insight of copper-modulated lead-free Cs2AgSbCl6 double perovskite microcrystals

被引:2
|
作者
Wu, Daofu [1 ]
Liu, Xiaoqing [1 ]
Tian, Changqing [2 ]
Zhou, Jinchen [2 ]
Lai, Junan [1 ]
Ran, Hongmei [2 ]
Gao, Bo [2 ]
Zhou, Miao [1 ]
Huang, Qiang [2 ]
Tang, Xiaosheng [1 ,2 ,3 ]
机构
[1] Chongqing Univ, Coll Optoelect Engn, Key Lab Optoelect Technol & Syst, Minist Educ, Chongqing 400044, Peoples R China
[2] Chongqing Univ Posts & Telecommun, Coll Optoelect Engn, Chongqing 400065, Peoples R China
[3] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
HALIDE DOUBLE PEROVSKITE; CO2; REDUCTION; SOLAR-CELLS; EFFICIENT; PHOTOREDUCTION; GENERATION; CATALYSTS; SITES;
D O I
10.1016/j.isci.2023.107355
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lead halide perovskites are prospective candidates for CO2 photoconversion. Herein, we report copper-doped lead-free Cs2AgSbCl6 double perovskite microcrystals (MCs) for gas-solid phase photocatalytic CO2 reduction. The 0.2Cu@Cs2AgSbCl6 double perovskite MCs display unprecedented CO2 photo -reduction capability with CO and CH4 yields of 412 and 128 mmol g(-1) , respec-tively. The ultrafast transient absorption spectroscopy reveals the enhanced separation of photoexcited carriers in copper-doped Cs2AgSbCl6 MCs. The active sites and reaction intermediates on the surface of the doped Cs2AgSbCl6 are dynamically monitored and precisely unraveled based on the in-situ Fourier transform infrared spectroscopy investigation. In combination with density functional theory calculations, it is revealed that the copper-doped Cs2AgSbCl6 MCs facilitate sturdy CO2 adsorption and activation and strikingly enhance the photocatalytic performance. This work offers an in-depth interpretation of the photocatalytic mechanism of Cs2AgSbCl6 doped with copper, which may provide guidance for future design of high-performance photocata-lysts for solar fuel production.
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页数:16
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