Complete Phase Transformation of Ir Nanowire Network into Defect‐Rich Oxide Catalyst for High‐Performance PEM Water Electrolysis

H Heting Pu Y Yuxiao He (Department of Materials Science and Engineering) Y Yi Chen S Shaohua Xie (Department of Chemical and Environmental Engineering, Bourns College of Engineering, Center for Environmental Research and Technology (CE-CERT), Materials Science and Engineering (MSE) Program, UCR Center for Catalysis) A Ao Zhang K Kai‐Yuan Hsiao (Materials Sciences Division Lawrence Berkeley National Laboratory Berkeley California USA) C Chengzhang Wan (Department of Chemistry and Biochemistry) Y Yu‐Han Joseph Tsai (Department of Materials Science and Engineering University of California, Los Angeles Los Angeles California USA) Y Yibo Wang Y Yang Liu N Ning Su J Joshua Wright (Department of Physics Illinois Institute of Technology Chicago Illinois USA) Q Qingying Jia (Department of Chemistry and Chemical Biology) D Deborah J. Myers (Chemical Sciences and Engineering Division) C Carlo U. Segre (Department of Physics and CSRRI) F Fudong Liu (Department of Chemical and Environmental Engineering, Bourns College of Engineering, Center for Environmental Research and Technology (CE-CERT), Materials Science and Engineering (MSE) Program, UCR Center for Catalysis) H Haimei Zheng X Xiangfeng Duan Y Yu Huang

Abstract

ABSTRACT Iridium‐based catalysts remain the most reliable option for the oxygen evolution reaction (OER) in proton exchange membrane water electrolyzers (PEMWEs). However, their high cost and limited performance represent critical barriers to the commercialization of this green hydrogen production technology. Herein, we report the creation of a metallic Ir nanowire network (IrNWN), which exhibits superior OER performance through its in situ transition into an oxide structure with high intrinsic activity. At a low loading of 0.25 mg Ir /cm 2 in PEMWEs, IrNWN achieved a current density of 3.13 A/cm 2 at a cell voltage of 1.8 V, outperforming the commercial Ir‐based catalyst and surpassing the Department of Energy (DOE) 2026 technical target. Moreover, the high activity of IrNWN was maintained for 900 h in a durability test at 2 A/cm 2 , showing a low degradation rate of 0.042 mV/hour. Structural analysis of the electrochemically oxidized IrNWN revealed the presence of mixed Ir oxidation states and a high density of surface terminal oxygen groups (µ1‐O), which contributed to a reduced energy barrier for the rate‐determining O‐O coupling step.

Article Details

Volume / Issue Vol. 1, Issue 1
Published May 22, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (19)

H

Heting Pu

Y

Yuxiao He

Department of Materials Science and Engineering

Y

Yi Chen

S

Shaohua Xie

Department of Chemical and Environmental Engineering, Bourns College of Engineering, Center for Environmental Research and Technology (CE-CERT), Materials Science and Engineering (MSE) Program, UCR Center for Catalysis

A

Ao Zhang

K

Kai‐Yuan Hsiao

Materials Sciences Division Lawrence Berkeley National Laboratory Berkeley California USA

C

Chengzhang Wan

Department of Chemistry and Biochemistry

Y

Yu‐Han Joseph Tsai

Department of Materials Science and Engineering University of California, Los Angeles Los Angeles California USA

Y

Yibo Wang

Y

Yang Liu

N

Ning Su

J

Joshua Wright

Department of Physics Illinois Institute of Technology Chicago Illinois USA

Q

Qingying Jia

Department of Chemistry and Chemical Biology

D

Deborah J. Myers

Chemical Sciences and Engineering Division

C

Carlo U. Segre

Department of Physics and CSRRI

F

Fudong Liu

Department of Chemical and Environmental Engineering, Bourns College of Engineering, Center for Environmental Research and Technology (CE-CERT), Materials Science and Engineering (MSE) Program, UCR Center for Catalysis

H

Haimei Zheng

X

Xiangfeng Duan

Y

Yu Huang