材料科学
光催化
共轭体系
聚合物
能量转换效率
光化学
物理化学
化学工程
无机化学
光电子学
催化作用
有机化学
化学
工程类
复合材料
作者
Xinyu Sun,Tingyu Yang,Yuming Dong,Rong Ji,Hui Zhao,Jiawei Zhang,Yongfa Zhu
标识
DOI:10.1002/aenm.202405687
摘要
Abstract The photocatalytic O 2 reduction reaction offers a promising approach to synthesizing H 2 O 2 . Nevertheless, the low conversion efficiency of O 2 − constrains the efficiency of photocatalytic H 2 O 2 production. This is because O 2 can readily obtain electrons to generate O 2 − , but it is challenging to reacquire electrons after generating O 2 − . Accordingly, this study proposes the improvement of the conversion efficiency of O 2 − through the directional enrichment of photogenerated charges at sites of O 2 − reduction and stabilization of O 2 − . This study introduces a phenanthrenequinone group with adjacent carbonyl groups as the O 2 − reduction reaction site. The directional enrichment of photogenerated charges at the O 2 − reduction site enhances the probability of O 2 − obtaining electrons. Concurrently, the special adsorption configuration enhances the adsorption, and stabilizes·O 2 − on the catalyst surface, accelerating the conversion of O 2 − to H 2 O 2 and achieving an H 2 O 2 generation rate of 3400 µmol g −1 h −1 . This work presents an innovative tactic regarding the efficient reduction of O 2 − to H 2 O 2 , which informs the structural design of advanced photocatalytic systems for the production of H 2 O 2 .
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