Diphenoquinone‐Based Covalent Organic Frameworks for Efficient H <sub>2</sub> O <sub>2</sub> Production via Photothermal Synergistic Catalysis

H Haiyang Liu (Shenzhen Key Laboratory of Biomolecular Assembling and Regulation, Department of Neuroscience, School of Life Sciences, Southern University of Science and Technology) Y Yuxin Hou (The State Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Institute of Ecology, Peking University) X Xianghong Niu (School of Science) S Shanshan Zhu L Liuliu Yang (College of Chemistry Jilin University Changchun People's Republic of China) H Hong Xia S Shuo‐Wang Yang (Institute of High Performance Computing Agency for Science, Technology and Research Singapore Singapore) X Xiaoming Liu (Key Laboratory of Biomimetic Robots and Systems, Ministry of Education, State Key Laboratory of Intelligent Control and Decision of Complex System, and School of Mechatronics Engineering, Beijing Institute of Technology)

Abstract

ABSTRACT Covalent organic frameworks (COFs) have recently attracted tremendous attention as advanced photocatalytic platforms for H 2 O 2 production from oxygen and water. However, their intrinsic catalytic activity and solar‐to‐chemical energy conversion efficiency are unsatisfactory for practical applications. In this work, a photothermal synergistic catalysis strategy for improving H 2 O 2 production of photocatalysts was proposed. As a proof of concept, two novel diphenoquinone‐based frameworks (COF‐JLU240 and COF‐JLU241) with donor‐acceptor character were constructed for the first time. These frameworks feature broad light harvesting, inherent photoelectric properties, and superior photothermal conversion efficiency. Under the illumination of a 660 nm laser with 100 mW cm −2 , the temperature of COF‐JLU241 drastically increased from 26.5°C to 184.6°C within 1 min. Importantly, COF‐JLU241 exhibits an impressive H 2 O 2 production rate of 4894.9 µmol h − 1 g − 1 in pure water under simulated sunlight, which is 3.86‐fold higher than that obtained at the conventional temperature (23°C). Experimental and theoretical studies revealed that increasing the reaction temperature via photothermal effect can effectively promote the separation and transport of photogenerated charges and reduce the energy barrier for surface reactions. This finding contributes a fascinating photothermal synergy strategy for increasing the conversion of solar into chemical energy and broadens the scope of COF‐based photocatalysts.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 07, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

H

Haiyang Liu

Shenzhen Key Laboratory of Biomolecular Assembling and Regulation, Department of Neuroscience, School of Life Sciences, Southern University of Science and Technology

Y

Yuxin Hou

The State Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Institute of Ecology, Peking University

X

Xianghong Niu

School of Science

S

Shanshan Zhu

L

Liuliu Yang

College of Chemistry Jilin University Changchun People's Republic of China

H

Hong Xia

S

Shuo‐Wang Yang

Institute of High Performance Computing Agency for Science, Technology and Research Singapore Singapore

X

Xiaoming Liu

Key Laboratory of Biomimetic Robots and Systems, Ministry of Education, State Key Laboratory of Intelligent Control and Decision of Complex System, and School of Mechatronics Engineering, Beijing Institute of Technology