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解锁共价有机框架中的拓扑效应以实现高效过氧化氢光合作用

Unlocking Topological Effects in Covalent Organic Frameworks for High-Performance Photosynthesis of Hydrogen Peroxide.

作者信息

Cheng Jun, Wu Yuting, Zhang Wan, Wang Lei, Wu Xiaojun, Xu Hangxun

机构信息

Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Key Laboratory of Precision and Intelligent Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.

Key Laboratory of Precision and Intelligent Chemistry, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.

出版信息

Adv Mater. 2025 Jan;37(1):e2410247. doi: 10.1002/adma.202410247. Epub 2024 Nov 7.

Abstract

Covalent organic frameworks (COFs) offer a compelling platform for the efficient photosynthesis of hydrogen peroxide (HO). Constructed with diverse topologies from various molecular building units, COFs can exhibit unique photocatalytic properties. In this study, three π-conjugated 2D sp carbon-linked COFs with distinctly different topologies (hcb, sql, and hxl) are designed to investigate the topological effect on the overall photosynthesis of HO from water and oxygen. Despite their similar chemical and band structures, the QP-HPTP-COF with hxl topology outperformed other COFs in the photosynthesis of HO, demonstrating a remarkable solar-to-chemical conversion efficiency of 1.41%. Comprehensive characterizations confirmed that the hxl topology can substantially improve charge separation and transfer, thereby significantly enhancing photocatalytic performance. This study not only unravels the topology-directed charge carrier dynamics in COFs but also establishes a molecular engineering framework for developing high-performance photocatalysts for sustainable HO production.

摘要

共价有机框架(COFs)为高效光催化合成过氧化氢(HO)提供了一个极具吸引力的平台。由各种分子构建单元构建而成的具有不同拓扑结构的COFs,能够展现出独特的光催化性能。在本研究中,设计了三种具有明显不同拓扑结构(hcb、sql和hxl)的π共轭二维sp碳连接COFs,以研究拓扑结构对水和氧气光催化合成HO的整体影响。尽管它们具有相似的化学和能带结构,但具有hxl拓扑结构的QP-HPTP-COF在HO的光催化合成中表现优于其他COFs,展现出1.41%的显著太阳能到化学能的转换效率。综合表征证实,hxl拓扑结构能够大幅改善电荷分离和转移,从而显著提高光催化性能。本研究不仅揭示了COFs中拓扑结构导向的电荷载流子动力学,还建立了一个分子工程框架,用于开发用于可持续生产HO的高性能光催化剂。

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