Hu Xunliang, Tan Bien
Key Laboratory of Optoelectronic Chemical Materials and Devices (Ministry of Education), School of Optoelectronic Materials & Technology, Jianghan University, Wuhan, 430056, China.
Key Laboratory of Material Chemistry for Energy Conversion and Storage Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Luoyu Road No. 1037, Wuhan, 430074, China.
Chemistry. 2025 Aug 1;31(43):e202501902. doi: 10.1002/chem.202501902. Epub 2025 Jul 10.
Hydrogen peroxide (HO) plays a pivotal role in energy and environmental applications, but its industrial synthesis remains hampered by high energy consumption, environmental concerns, and safety risks. Artificial photosynthesis offers a sustainable alternative by leveraging solar energy to catalyze HO production from oxygen and water. Covalent organic frameworks (COFs) have emerged as promising photocatalysts due to their well-defined structures and customizable active sites, enabling efficient solar-to-chemical conversion (SCC). This review comprehensively explores recent progress in COF-mediated photocatalytic HO synthesis. It begins with an overview of photocatalytic principles, followed by a detailed analysis of reaction mechanisms and performance metrics for HO generation. Emphasis is placed on tailored COF design strategies-such as electronic structure optimization and redox-active site engineering-to improve catalytic efficiency. Finally, we identify key challenges hindering the development of high-performance COFs photocatalysts tailored for sustainable H₂O₂ synthesis.
过氧化氢(HO)在能源和环境应用中起着关键作用,但其工业合成仍然受到高能耗、环境问题和安全风险的阻碍。人工光合作用通过利用太阳能催化由氧气和水生产HO,提供了一种可持续的替代方法。共价有机框架(COF)因其结构明确和活性位点可定制,已成为有前景的光催化剂,能够实现高效的太阳能到化学能的转换(SCC)。本综述全面探讨了COF介导的光催化HO合成的最新进展。首先概述了光催化原理,接着详细分析了HO生成的反应机制和性能指标。重点关注定制的COF设计策略,如电子结构优化和氧化还原活性位点工程,以提高催化效率。最后,我们确定了阻碍开发用于可持续H₂O₂合成的高性能COF光催化剂的关键挑战。