Integrated Multiscale Nanoarrays With MnO <sub>2</sub> ‐Mediated Ru─O Clusters for Stable Acidic Chlorine Evolution

C Chaoyang Sun L Linjie Zhao H Hao Wang (Division of Quantitative Sciences, Department of Oncology Johns Hopkins University School of Medicine Baltimore Maryland USA) Y Yingjie Hu J Jingjie Tang (College of Chemistry and Bioengineering Hunan University of Science and Engineering Yongzhou China) D Dan Wang H Husitu Lin (State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials College of Chemical Engineering Beijing University of Chemical Technology Beijing China) B Bowen Liu (College of Chemistry and Chemical Engineering) S Sihua Xiong (State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials Beijing University of Chemical Technology Beijing China) B Baoguang Mao (State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials College of Chemical Engineering Beijing University of Chemical Technology Beijing China) C Chuangang Hu (State Key Laboratory of Organic−Inorganic Composites, College of Chemical Engineering)

Abstract

ABSTRACT The electrochemical chlorine evolution reaction (CER) is crucial for the chlor–alkali industry. While atomic Ru–O active sites hold great promise for the CER, they are severely hindered by instability and strong OH* poisoning. Herein, we report an interlayer‐engineered electrode where a MnO 2 nano‐interlayer epitaxially wraps a nanocone array to confine and modulate atomic Ru–O clusters. This interlayer induces strong electronic coupling via Ru‒O‒Mn‒O‒Ti linkages that spatially confine and anchor the clusters to suppress dissolution while triggering substantial interfacial electron redistribution. Crucially, this modulated electronic environment effectively promotes optimizes *Cl adsorption, thereby significantly enhancing intrinsic CER selectivity and kinetics. Consequently, the electrode achieves exceptional durability over 1200 h with negligible Ru dissolution. When integrated into a proton‐exchange‐membrane electrolyzer, the catalyst demonstrates superior activity and stability, benefiting from the hierarchical architecture that facilitates superaerophobic bubble release and enhanced mass transport. These findings establish a generalizable strategy unifying atomic confinement, electronic modulation, and transport engineering for designing durable CER electrocatalysts.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 28, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

C

Chaoyang Sun

L

Linjie Zhao

H

Hao Wang

Division of Quantitative Sciences, Department of Oncology Johns Hopkins University School of Medicine Baltimore Maryland USA

Y

Yingjie Hu

J

Jingjie Tang

College of Chemistry and Bioengineering Hunan University of Science and Engineering Yongzhou China

D

Dan Wang

H

Husitu Lin

State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials College of Chemical Engineering Beijing University of Chemical Technology Beijing China

B

Bowen Liu

College of Chemistry and Chemical Engineering

S

Sihua Xiong

State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials Beijing University of Chemical Technology Beijing China

B

Baoguang Mao

State Key Laboratory of Organic‐Inorganic Composites Beijing Key Laboratory of Intelligent Design and Manufacturing for Hydrogen Energy Materials College of Chemical Engineering Beijing University of Chemical Technology Beijing China

C

Chuangang Hu

State Key Laboratory of Organic−Inorganic Composites, College of Chemical Engineering