Composite of lead-free halide perovskite Cs3Bi2Br9 with TiO2 as an efficient photocatalyst for C(sp3)-H bond activation

被引:27
|
作者
Cui, Zihao [1 ,2 ]
Zhang, Qianqian [1 ]
Fu, Hui [1 ]
Liu, Qihao [2 ]
Liu, Xiaolei [1 ]
Wu, Yaqiang [1 ]
Gao, Peng [1 ]
Wang, Zeyan [1 ]
Zheng, Zhaoke [1 ]
Cheng, Hefeng [1 ]
Liu, Yuanyuan [1 ]
Dai, Ying [3 ]
Huang, Baibiao [1 ]
Wang, Peng [1 ]
机构
[1] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
[2] Shandong Yunhai Guochuang Innovat Technol Co Ltd, Jinan 250101, Peoples R China
[3] Shandong Univ, Sch Phys, Jinan 250100, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Lead-free perovskite; Cs3Bi2Br9; TiO2; C-H bonds activation; Photocayalysis; PHOTON-ABSORPTION; BENZYL ALCOHOL; NANOCRYSTALS; OXIDATION; BANDGAP;
D O I
10.1016/j.apcatb.2023.122812
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
Herein, a facile anti-solvent preparation strategy is proposed to fabricate lead-free halide perovskite Cs3Bi2Br9 with TiO2, which boosts photocatalytic activation of C(sp3)-H bonds in toluene oxidation. TiO2 not only works as nucleation center to reduce the particle size of perovskite, but could form type II heterojunction with Cs3Bi2Br9, thus improving the photocatalytic performance of the TiO2/Cs3Bi2Br9 composite. Under AM 1.5 G simulated sunlight irradiation, the optimal TiO2/Cs3Bi2Br9 composite exhibits both high production rate (9692.5 mu mol g- 1 h-1) and selectivity (91 %) of benzaldehyde product. As verified by in-situ ESR, in-situ FT-IR and DFT calculations, center dot O2- and h+ are demonstrated to be the main active species in this process. This work provides a new insight into the design of high-performance lead-free perovskite photocatalysts for organic synthesis.
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页数:10
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