Sub‐Nano Ir‐Based Alloy Clusters by Hierarchical Confinement Effect for Water Splitting

X Xuemin Cao H Han Cheng (State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science) R Renjie Gui (State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science) H Huijuan Zhang (Department of Oncology The Affiliated Yantai Yuhuangding Hospital of Qingdao University Medical College Yantai China) C Caijie Su (Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science University of Science and Technology of China Hefei Anhui P. R. China) C Chen Chen Y Yifan Yin Y Yi Tan (State Key Laboratory of Bioactive Molecules and Druggability Assessment, and School of Pharmacy, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China) H Huijuan Wang W Wangsheng Chu (National Synchrotron Radiation Laboratory) Y Yue Lin G Gongming Wang (State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science) Y Yi Xie C Changzheng Wu (State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science)

Abstract

Abstract The synthesis of sub‐nanoscale noble metal catalysts is pivotal for enhancing electrocatalytic performance, yet achieving precise control over particle size at this scale remains a critical challenge. In this work, we propose a hierarchical confinement strategy which combines spatial confinement at nanoscale and anchoring confinement at atomic scale, to overcome the size limitations imposed by high‐temperature sintering. Using this strategy, a series of uniformly sized (∼1 nm) Ir‐based alloy clusters, including IrMn, IrFe, IrCo and IrNi, are successfully fabricated. The synthesized sub‐nanoscale IrCo alloy clusters (denoted as sub‐IrCo cluster) demonstrate exceptional oxygen evolution reaction (OER) catalytic performance, with an ultralow overpotential of 210 mV at 10 mA cm ‐ 2 and a remarkable mass activity 87.5 times greater than that of commercial IrO 2 . Density functional theory (DFT) and molecular dynamics (MD) simulations reveal that the incorporation of N enhances the interaction between Ir atoms and the support. This work provides an effective strategy for preventing particle sintering via a hierarchical confinement effect and achieves precise size control at sub‐nanoscale, opening a new avenue for the development of efficient noble metal catalysts with high atomic utilization.

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 (14)

X

Xuemin Cao

H

Han Cheng

State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science

R

Renjie Gui

State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science

H

Huijuan Zhang

Department of Oncology The Affiliated Yantai Yuhuangding Hospital of Qingdao University Medical College Yantai China

C

Caijie Su

Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science University of Science and Technology of China Hefei Anhui P. R. China

C

Chen Chen

Y

Yifan Yin

Y

Yi Tan

State Key Laboratory of Bioactive Molecules and Druggability Assessment, and School of Pharmacy, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China

H

Huijuan Wang

W

Wangsheng Chu

National Synchrotron Radiation Laboratory

Y

Yue Lin

G

Gongming Wang

State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science

Y

Yi Xie

C

Changzheng Wu

State Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science