化学
苯甲醛
甲苯
吸附
选择性
钙钛矿(结构)
卤化物
嫁接
催化作用
光化学
烷基
无机化学
化学稳定性
盐(化学)
光催化
化学工程
离子
能量转换效率
激进的
多相催化
电子转移
羰基化
作者
Jin-Xin Li,Sheng Tian,Xiong Wang,Wei-Fan Shao,Bing‐Hao Wang,Chao Peng,Lang Chen,Shuang‐Feng Yin
出处
期刊:Chemsuschem
[Wiley]
日期:2026-05-28
卷期号:19 (11): e70762-e70762
摘要
Perovskite halides, a promising class of photocatalysts for the selective oxidation of C(sp 3 )H bonds, face critical challenges for practical implementation. Their inherent chemical instability under illumination and humid conditions, primarily driven by halide ion migration, remains a major obstacle to real‐world application. In this work, dodecylphosphonic acid (DDPA)‐grafted Cs 3 SbBiBr 9 (CSBB) photocatalysts were achieved as an efficient and stable aerobic oxidation photocatalyst. The formation of strong MOP bonds between DDPA and CSBB directs charge transfer and suppress Br – migration. Concurrently, the long alkyl chain (C 12 ) creates a hydrophobic surface, enhancing toluene adsorption while effectively repelling water and preventing perovskite hydrolysis. Remarkable toluene conversion rate of 21.648 mmol g −1 and 85% selectivity towards benzaldehyde is realized, which is 3.8 times that of pristine CSBB. Moreover, the stability of CSBB was significantly enhanced after DDPA modification.
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