Electrolyte‐Free Electrosynthesis of Pure H <sub>2</sub> O <sub>2</sub> via Triple‐Phase Interface Engineering

X Xinxin Li (College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China) C Cheng Tang (Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering) L Linchuan Cong (Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering) K Kaijie Wu (Tsinghua Center for Green Chemical Engineering Electrification Department of Chemical Engineering Tsinghua University Beijing 100084 P.R. China) J Jinhui Liu C Changli Wang (Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering) E Eugenia Angelica (Tsinghua Center for Green Chemical Engineering Electrification Department of Chemical Engineering Tsinghua University Beijing 100084 P.R. China) S Sheng Chen (Beijing Frontier Research Center for Biological Structures, State Key Laboratory of Membrane Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.) Q Qiang Zhang

Abstract

Abstract Electrosynthesis of pure H 2 O 2 through proton exchange membrane electrolyzers offers a promising route for decentralized, on‐demand production. However, conventional approaches face critical challenges in balancing O 2 supply and H 2 O 2 removal at the gas–liquid–solid interface. In this study, we propose a triple‐phase interface engineering strategy by integrating a three‐dimensional (3D) hydrophobic grid gas diffusion electrode (GDE) with gas–liquid two‐phase flow. This design achieves a peak Faradic efficiency (FE) of 84.6% at −10.0 mA cm −2 using deionized water as the catholyte. Simulations reveal that bubble wake‐induced toroidal vortices enhance O 2 transport, while shear‐driven convection accelerates directional H 2 O 2 transport. Integrated with a T‐junction microfluidic unit, it achieves real‐time organic pollutant degradation while maintaining an FE above 60% over 50 h. The system demonstrates high flexibility, scalability (25 cm 2 electrode), and tunable H 2 O 2 concentrations (153.6–2443.7 mg L −1 ), rendering a robust platform for sustainable, on‐demand chemical electrosynthesis.

Article Details

Volume / Issue Vol. 65, Issue 4
Published January 22, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

X

Xinxin Li

College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China

C

Cheng Tang

Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering

L

Linchuan Cong

Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering

K

Kaijie Wu

Tsinghua Center for Green Chemical Engineering Electrification Department of Chemical Engineering Tsinghua University Beijing 100084 P.R. China

J

Jinhui Liu

C

Changli Wang

Tsinghua Center for Green Chemical Engineering Electrification, Department of Chemical Engineering

E

Eugenia Angelica

Tsinghua Center for Green Chemical Engineering Electrification Department of Chemical Engineering Tsinghua University Beijing 100084 P.R. China

S

Sheng Chen

Beijing Frontier Research Center for Biological Structures, State Key Laboratory of Membrane Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.

Q

Qiang Zhang