Hydrogen‐Bonded Perovskite Heterojunction Photocatalytic Membrane with Efficient Proton Supply for Boosting CO <sub>2</sub> Methanation

Q Qiao Chen (Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science) M Mingzheng Gu (Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science) Y Yixin Hao L Ling Jiang (Optogenetics & Synthetic Biology Interdisciplinary Research Center, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China) G Guangfeng Wang (Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science) X Xiaojun Zhang (Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science) F Feng Hu (Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)) L Linlin Li (College of Materials Science and Technology) Y Yuping Wu (Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center) S Shengjie Peng (Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center)

Abstract

Abstract Efficient proton supply and enhanced *CO intermediate adsorption are crucial strategies for boosting CO 2 methanation. Herein, we construct a hydrogen‐bonded (H‐bonded) photocatalytic membrane by integrating a MAPbBr 3 /cyano‐g‐C 3 N 4 (MPB/CN‐g‐CN) heterojunction with ethyl cellulose (ECE) binder through a simple sol–gel process, achieving significantly enhanced CO 2 methanation efficiency. ECE functions as a novel proton source, with hydroxyl (‐OH) groups that are readily oxidized by photogenerated holes, resulting in efficient proton supply compared to H 2 O. Moreover, ECE facilitates membrane assembly via interfacial H‐bonding between the ‐OH moieties of ECE and the modified nitrogen sites of MPB/CN‐g‐CN, generating proton‐rich interfaces and local H‐bond microenvironments that synergistically enhance proton supply and CO adsorption, thus steering the reaction toward CH 4 production. As a result, the MPB/CN‐g‐CN membrane achieves a remarkable increase in CH 4 yield from 0.01 to 35.85 µmol g −1 h −1 and selectivity from 0.4% to 82% compared to the pristine heterojunction. Furthermore, the MPB/CN‐g‐CN/ECE membrane demonstrates exceptional recyclability through a re‐crosslinking membrane formation process, effectively reactivating proton‐supply sites while maintaining superior CH 4 selectivity across multiple operational cycles.

Article Details

Volume / Issue Vol. 64, Issue 38
Published September 15, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

Q

Qiao Chen

Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science

M

Mingzheng Gu

Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science

Y

Yixin Hao

L

Ling Jiang

Optogenetics & Synthetic Biology Interdisciplinary Research Center, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China

G

Guangfeng Wang

Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science

X

Xiaojun Zhang

Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science

F

Feng Hu

Department of Chemistry, Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education)

L

Linlin Li

College of Materials Science and Technology

Y

Yuping Wu

Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center

S

Shengjie Peng

Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center