光催化
催化作用
共价键
过氧化氢
化学
光合作用
可见光谱
人工光合作用
光化学
氧气
分解水
制氢
结晶度
接受者
材料科学
化学工程
纳米技术
组合化学
有机化学
工程类
物理
生物化学
光电子学
凝聚态物理
结晶学
作者
Mingjie Liu,Peipei He,Hantao Gong,Zheng‐Hua Zhao,Yueming Li,Kai Zhou,Yuemin Lin,Jing Li,Zongbi Bao,Qiwei Yang,Yiwen Yang,Qilong Ren,Zhiguo Zhang
标识
DOI:10.1016/j.cej.2024.148922
摘要
Direct synthesis of hydrogen peroxide (H2O2) using oxygen and water through the photocatalytic route is a prospective approach for the on-site production of H2O2. However, the limited varieties of photocatalytic sites and ambiguous structure-active relationship impede the development of environmentally friendly technology. Herein, we report a active compound (benzotrithiophene, BTT) for the photosynthesis of H2O2 using oxygen and water, and design four benzotrithiophene-based 2D covalent organic frameworks (BTT-COFs) linked with aromatic amines linkers. Significant enhancement in photocatalytic activity has been observed via the introduction of BTT struct into 2D COFs. The high crystallinity of COFs increases the visible light absorption ability and photostability of BTT. The suitable distance of BTT struct in COFs and the construction of donor–acceptor (D-A) structure further promote the carrier generation and transfer. The COF-BTT-TAPT exhibited the highest H2O2 production rate of 620 μmol g−1 h−1. Mechanism investigation experiments have given the validation that BTT-COFs efficiently reduce oxygen in pure water to form H2O2 under visible-light irradiation. This work paves a revolutionary way for designing and fabricating high-performance metal-free photocatalysts for visible-light-driven H2O2 production.
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