化学
光催化
铀酰
多孔性
光化学
化学工程
无机化学
环境化学
有机化学
催化作用
离子
工程类
作者
Bowen Hu,Wei Jin,Zhi‐wei Huang,Zhiheng Zhou,Kong‐Qiu Hu,Li‐Yong Yuan,Huibing He,Wei‐Qun Shi,Lei Mei
标识
DOI:10.1002/ejic.202500153
摘要
In this work, a new kind of uranyl‐based photocatalysts, i.e., uranyl‐modified porous organic cages, U@HPOCs, are prepared for the first time via a post‐synthetic modification (PSM) of preassembled porous organic cages (POCs) by uranyl sources. The successful integration of uranyl into U@HPOCs, as well as coordination environments of uranyl centers, are well characterized by a combination of analysis techniques, and the catalytic performance of these uranyl compounds as photocatalysts is further evaluated. The results show that all U@HPOCs working as stable heterogeneous catalysts exhibit enhanced photocatalytic activity compared with the corresponding molecular uranyl complex for the oxidation of a mustard gas mimetic 2‐chloroethyl ethyl sulfide (CEES), among which U 20 @HPOC with the highest amount of uranyl loading exhibits the highest catalytic oxidation efficiency. The enhanced catalytic effect of U@HPOCs demonstrates the important role of POCs with restrained nanotraps, which can expedite mass transfer of catalytic substrates effectively and help to improve the chemical stability. This work not only provides a promising uranyl photocatalyst for effective detoxification of toxic contaminants, but also paves the way to acquiring new catalysts by integrating molecular complexes with POCs, which is expected to inspire more systems with improved catalytic activities in the future.
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