光催化
卤化物
化学
纳米晶
催化作用
氧化还原
钙钛矿(结构)
光化学
可见光谱
偶联反应
介孔材料
辐照
金属
化学工程
纳米技术
纳米颗粒
联轴节(管道)
反应条件
原位
营业额
无机化学
降级(电信)
作者
Jianyao Kou,Ji Li,Yan Cao,Chun Li,Yingxuan Xu,Yuxing Huang,Xin Zhuo
标识
DOI:10.1021/acs.inorgchem.6c02071
摘要
Abstract In recent years, metal halide perovskite materials have emerged as potential tools for photocatalytic redox reactions owing to their low cost, tunable band gaps, and other excellent optoelectronic properties. However, their applications are limited by poor stability. Here, we prepared a novel CsPbBr3/SBA-15 photocatalyst, in which CsPbBr3 nanocrystals (CsPbBr3 NCs) were in situ grown and confined in mesoporous SBA-15. The CsPbBr3/SBA-15 catalyst demonstrated remarkable reactivity, with turnover number (TON) and turnover frequency (TOF) reaching as high as 9604.8 and 1600.8 h–1 in the α-alkylation of aldehydes, respectively. To the best of our knowledge, these values are the highest ever achieved in a batch reaction system. Moreover, the CsPbBr3 NCs confined in SBA-15 exhibited excellent stability, which survived in a water environment for more than 8 months. Overall, these results demonstrate the successful construction of a highly efficient and stable CsPbBr3/SBA-15 photocatalyst, offering a promising and robust platform for organic synthesis toward photocatalytic C–C bond formation.
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