Highly Active Nodules on Concave–Convex Channel Walls of Covalent Organic Frameworks for Photocatalytic Hydroperoxide Production

X Xinhe Ye (Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Guangdong-Hongkong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices and Department of Chemistry) B Bingxian Chu (Department of Chemistry) Q Quan Zuo (Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Guangdong-Hongkong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices and Department of Chemistry) H Hao Nian (Department of Chemistry Shenzhen Key Laboratory of Micro/Nano‐Porous Functional Materials (SKLPM) SUSTech‐Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM‐JIL) Guangdong‐Hongkong‐Macao Joint Laboratory for Photonic‐Thermal‐Electrical Energy Materials and Devices, and Advanced Institute for Ocean Research Southern University of Science and Technology Shenzhen China) L Lei Li Q Qiang Xu (Key Laboratory of Material Simulation Methods & Software of Ministry of Education, College of Physics)

Abstract

ABSTRACT Covalent organic frameworks (COFs) are promising photocatalysts for hydrogen peroxide (H 2 O 2 ) production. However, the smooth channels of traditional COFs exhibit weak charge density gradients and lack highly electron‐localized sites for O 2 adsorption, thereby showing unsatisfactory photocatalytic performances. Herein, we present a channel wall engineering strategy to introduce nodules with high electron localization into COF channels by topological regulation. In contrast with the smooth channel walls within the traditional COFs, the nodules on the concave–convex channel walls of COFs served as active sites with an electron‐rich structure and enhanced charge separation ability for the photocatalytic H 2 O 2 production. Grafting polar carboxylic groups to the nodules further resulted in a strong built‐in electric field and hydrogen bond network inside the channels, accelerating the transport of electrons and protons. The carboxylic group‐grafted COF (DFH‐COF) achieved a H 2 O 2 production rate of 6075 µmol h −1 g −1 in pure water and an apparent quantum yield as high as 14.6% at 475 nm. This study provides a powerful strategy of channel wall engineering of COFs to enhance the photocatalytic performances.

Article Details

Volume / Issue Vol. 65, Issue 16
Published April 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

X

Xinhe Ye

Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Guangdong-Hongkong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices and Department of Chemistry

B

Bingxian Chu

Department of Chemistry

Q

Quan Zuo

Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Guangdong-Hongkong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices and Department of Chemistry

H

Hao Nian

Department of Chemistry Shenzhen Key Laboratory of Micro/Nano‐Porous Functional Materials (SKLPM) SUSTech‐Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM‐JIL) Guangdong‐Hongkong‐Macao Joint Laboratory for Photonic‐Thermal‐Electrical Energy Materials and Devices, and Advanced Institute for Ocean Research Southern University of Science and Technology Shenzhen China

L

Lei Li

Q

Qiang Xu

Key Laboratory of Material Simulation Methods & Software of Ministry of Education, College of Physics