Amplifying Intermetal Bias of Pt‐Rh Alloy Nanolayers for Facilitated Hydrogen Inter‐Diffusion and Evolution

S Shi‐Nan Zhang (State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China) Q Qian‐Yu Liu (State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China) B Bing‐Liang Leng (State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China) Z Zhong‐Qi Wang (Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China) Z Zi‐Hao Zhang (Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China) Z Zhao‐Zhe Zhong (Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China) X Xi Liu (School of Chemistry and Chemical Engineering) J Jie‐Sheng Chen (Frontiers Science Center for Transformative Molecules State Key Laboratory of Polyolefins and Catalysis School of Chemistry and Chemical Engineering Zhangjiang Institute for Advanced Study Shanghai Jiao Tong University Shanghai 200240 China) X Xin‐Hao Li (State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China)

Abstract

Abstract Proton exchange membrane water electrolyzer driven by renewable electricity has been regarded as a sustainable energy production technology, but is greatly limited by the high cost and unsatisfactory durability of noble metal catalysts. Here, we present the proof‐of‐concept application of the amplified intermetal bias in PtRh alloy nanolayer to promote the intrinsic catalytic activity of hydrogen evolution reaction and the lifespan of the proton exchange membrane water electrolyzer. Both experimental and theoretical results revealed the key role of the intermetal bias between Pt and Rh amplified by the rectifying contact with nitrogen‐doped carbons support in accelerating the pre‐enrichment of protons on Rh sites, diffusion of H species from Rh to Pt sites, and final H dissociation from Pt sites. Consequently, the optimized Pt 3 Rh 2 /NC cathode with the most pronounced intermetal bias gives a record‐high mass activity of 282 A mg Pt+Rh −1 at a cell voltage of 1.8 V in proton exchange membrane water electrolyzer. Moreover, the Pt 3 Rh 2 /NC cathode can reduce the proton diffusion resistance from 0.95 Ω of Pt/C to 0.69 Ω at a cell voltage of 1.5 V due to the promoted hydrogen species diffusion on catalyst surface, largely decreasing the cell voltage and extending the lifespan by 3.2 times.

Article Details

Volume / Issue Vol. 64, Issue 39
Published September 22, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

S

Shi‐Nan Zhang

State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China

Q

Qian‐Yu Liu

State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China

B

Bing‐Liang Leng

State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China

Z

Zhong‐Qi Wang

Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China

Z

Zi‐Hao Zhang

Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China

Z

Zhao‐Zhe Zhong

Toyota Motor Technical Research and Service (Shanghai) Co., Ltd. Shanghai 200240 P.R. China

X

Xi Liu

School of Chemistry and Chemical Engineering

J

Jie‐Sheng Chen

Frontiers Science Center for Transformative Molecules State Key Laboratory of Polyolefins and Catalysis School of Chemistry and Chemical Engineering Zhangjiang Institute for Advanced Study Shanghai Jiao Tong University Shanghai 200240 China

X

Xin‐Hao Li

State Key Laboratory of Synergistic Chem‐Bio Synthesis, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P.R. China