Suppr超能文献

用于促进光催化产过氧化氢的乙烯基锚定共价有机框架

Vinyl-Group-Anchored Covalent Organic Framework for Promoting the Photocatalytic Generation of Hydrogen Peroxide.

作者信息

Yu Hong, Zhang Fengtao, Chen Qian, Zhou Pan-Ke, Xing Wandong, Wang Sibo, Zhang Guigang, Jiang Yi, Chen Xiong

机构信息

State Key Laboratory of Photocatalysis on Energy and Environment, and Key Laboratory of Molecular Synthesis and Function Discovery, College of Chemistry, Fuzhou University, Fuzhou, 350116, P. R. China.

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai, 201620, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2024 May 21;63(21):e202402297. doi: 10.1002/anie.202402297. Epub 2024 Apr 15.

Abstract

The artificial photosynthesis of HO from water and oxygen using semiconductor photocatalysts is attracting increasing levels of attention owing to its green, environmentally friendly, and energy-saving characteristics. Although covalent organic frameworks (COFs) are promising materials for promoting photocatalytic HO production owing to their structural and functional diversity, they typically suffer from low charge-generation and -transfer efficiencies as well as rapid charge recombination, which restricts their use as catalysts for photocatalytic HO production. Herein, we report a strategy for anchoring vinyl moieties to a COF skeleton to facilitate charge separation and migration, thereby promoting photocatalytic HO generation. This vinyl-group-bearing COF photocatalyst exhibits a HO-production rate of 84.5 μmol h (per 10 mg), which is ten-times higher than that of the analog devoid of vinyl functionality and superior to most reported COF photocatalysts. Both experimental and theoretical studies provide deep insight into the origin of the improved photocatalytic performance. These findings are expected to facilitate the rational design and modification of organic semiconductors for use in photocatalytic applications.

摘要

利用半导体光催化剂从水和氧气中人工合成过氧化氢因其绿色、环保和节能的特性而受到越来越多的关注。尽管共价有机框架(COF)因其结构和功能的多样性而成为促进光催化过氧化氢生成的有前景的材料,但它们通常存在电荷产生和转移效率低以及电荷快速复合的问题,这限制了它们作为光催化过氧化氢生成催化剂的应用。在此,我们报道了一种将乙烯基部分锚定到COF骨架上以促进电荷分离和迁移从而促进光催化过氧化氢生成的策略。这种含乙烯基的COF光催化剂表现出84.5 μmol·h(每10 mg)的过氧化氢生成速率,这比不含乙烯基官能团的类似物高十倍,并且优于大多数报道的COF光催化剂。实验和理论研究都深入洞察了光催化性能提高的根源。这些发现有望促进用于光催化应用的有机半导体的合理设计和改性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验