材料科学
光电效应
纳米技术
光电子学
电子结构
合理设计
单体
共价键
分子工程
电荷(物理)
联动装置(软件)
光催化
设计要素和原则
载流子
电子元件
调制(音乐)
激光器
不对称
数码产品
半导体
作者
Zhongping Li,Yuqiang Huang,Yucheng Jin,Yanhua Shao,Changqing Li,Jikuan Qiu,Jong-Beom Baek,Xiaoming Liu
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-03-06
标识
DOI:10.1021/acs.nanolett.6c00477
摘要
Covalent organic frameworks (COFs) have emerged as highly promising platforms for optoelectronic applications due to their tunable architecture, extended π-conjugation, and adjustable electronic properties. Introducing asymmetric electronic structures has proven effective in promoting charge separation and transport, thereby enhancing photoelectric conversion efficiency. However, existing strategies to amplify such asymmetry largely rely on the design of new monomers or modification of linkage types. In this work, we present a terminal-group engineering strategy to amplify the intrinsically weak asymmetric interactions in sp2 carbon-conjugated COFs. This approach enables precise modulation of electronic structure and photophysical behavior, resulting in enhanced charge mobility and significantly improved photocatalytic performance. The engineered COFs demonstrate nearly a 4-fold increase in hydrogen peroxide production relative to their unmodified counterparts, while exhibiting excellent structural stability and long-term operational durability. These findings establish terminal-group engineering as a powerful and generalizable design strategy for developing high-performance COF-based optoelectronic and photocatalytic materials.
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