蒽醌
过氧化氢
光催化
光化学
氧化还原
化学
共轭体系
催化作用
聚合物
可见光谱
有机化学
材料科学
光电子学
作者
Xiahong Xu,Rongjian Sa,Wei Huang,Yan Sui,Wen‐Tong Chen,Gangyong Zhou,Xiaodan Li,Yuntong Li,Hong Zhong
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-10-11
卷期号:12 (20): 12954-12963
被引量:156
标识
DOI:10.1021/acscatal.2c04085
摘要
The photocatalytic generation of hydrogen peroxide (H2O2) from H2O and O2 under visible light irradiation is a hopeful approach to achieve solar-to-chemical energy transformation. While the lack of specific redox reaction centers is still the main reason for low photocatalytic H2O2 production efficiency, herein, we present a conjugated organic polymer (AQTEE-COP) containing anthraquinone redox centers by Sonogashira cross-coupling reaction between 2,6-dibromoanthraquinone (AQ) and 1,1,2,2-tetrakis(4-ethynylphenyl)ethene. The extended π-conjugated framework with an electron push–pull effect between electron-donating tetraphenylethene moieties and electron-withdrawing anthraquinone moieties not only broadened the visible light absorption range but also promoted the separation and migration of photo-induced charge carriers. Meanwhile, the anthraquinone moieties can serve as redox centers to accept photo-induced electrons and transfer them to adsorbed O2 molecules for subsequent H2O2 production. The well-defined structure of AQTEE-COP with task-specific anthracene redox centers provides molecular-level insights into the mechanistic understanding of the photocatalytic H2O2 generation from H2O and O2. The AQTEE-COP exhibits efficient photocatalytic H2O2 production with an initial rate of 3204 μmol g–1 h–1 under visible light (λ ≥ 400 nm) irradiation without any additional photosensitizers, organic scavengers, or co-catalysts. This article provides a protocol for the rational design of pre-functionalized conjugated organic polymer-based materials for solar-to-chemical energy transformation.
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