Atomic‐Mesoscale Synergy in Amorphous Iridium Oxide Catalysts for Proton Exchange Membrane Water Electrolysis

H Hui Chen J Jiale Li K Ke Sun K Kun Qi (State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics) X Xinyue Ni (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun China) X Xiyang Wang (Department of Applied Physics) H Haidong Xu (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun 130012, P. R. China) M Muhan Na (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun China) X Xiao Zhao Z Zizhun Wang (Electron Microscopy Center Jilin University Changchun China) Y Yongcun Zou (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China) X Xiaoxin Zou (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry)

Abstract

ABSTRACT Amorphous iridium oxide (IrO x ) is among the most active Ir‐based catalysts for the acidic oxygen evolution reaction (OER), yet its stability is severely limited because lattice‐oxygen participation often triggers irreversible oxygen loss that leads to iridium dissolution and structural degradation. Here, we present a surfactant‐directed synthesis of mesoporous IrO x electrocatalysts featuring a hollandite‐type local structure. This unique structure creates an atomic‐mesoscale synergy that enhances OER activity without sacrificing stability and improves high‐current‐density performance. At the atomic level, the hollandite‐type local structure promotes high OER activity and corrosion resistance. In situ spectroscopic and isotopic labeling experiments reveal a reversible cycle of lattice oxygen loss and reformation during OER. This process enables the flexible iridium local structure to transition between an initial six‐coordinate state and a low‐coordinated active state. At the mesoscale, an interconnected porous network ensures efficient mass transport and maximizes active‐site accessibility. As a result, this mesoporous electrocatalyst achieves a low cell voltage (1.75 V @ 2 A cm −2 ) and excellent stability for more than 2000 h (@ 2 A cm −2 ) in proton exchange membrane water electrolysis (PEMWE).

Article Details

Volume / Issue Vol. 65, Issue 14
Published March 27, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

H

Hui Chen

J

Jiale Li

K

Ke Sun

K

Kun Qi

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics

X

Xinyue Ni

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun China

X

Xiyang Wang

Department of Applied Physics

H

Haidong Xu

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Qianjin Street 2699, Changchun 130012, P. R. China

M

Muhan Na

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun China

X

Xiao Zhao

Z

Zizhun Wang

Electron Microscopy Center Jilin University Changchun China

Y

Yongcun Zou

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China

X

Xiaoxin Zou

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry