卤化物
钙钛矿(结构)
复合数
光催化
甲苯
成核
选择性
材料科学
异质结
化学工程
化学
光化学
无机化学
复合材料
催化作用
有机化学
光电子学
工程类
作者
Zihao Cui,Qianqian Zhang,Hui Fu,Qihao Liu,Xiaolei Liu,Yaqiang Wu,Peng Gao,Zeyan Wang,Zhaoke Zheng,Hefeng Cheng,Yuanyuan Liu,Ying Dai,Baibiao Huang,Peng Wang
标识
DOI:10.1016/j.apcatb.2023.122812
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 μmol g−1 h−1) and selectivity (91 %) of benzaldehyde product. As verified by in-situ ESR, in-situ FT-IR and DFT calculations, •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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