Lattice Coupling Enables Gradient Strain Tuning Toward Platinum Skin at Intermetallic Nanocatalysts for Boosting Hydrogen Electrocatalysis

T Tao Zhang W Wanqing Song (School of Materials Science and Engineering, Tianjin University, Tianjin, China.) X Xin Wang P Panzhe Qiao (Shanghai Synchrotron Radiation Facility) J Jiahui Feng (School of Materials Science and Engineering, Tianjin University, Tianjin, China.) H Huachen Shi (School of Materials Science and Engineering Tianjin Key Laboratory of Composite and Functional Materials Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education) Tianjin University Tianjin China) H Haozhi Wang (State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study and National Center for Translational Medicine) X Xinyi Yang (School of Materials Science and Engineering, Tianjin University, Tianjin, China.) J Jinfeng Zhang J Jia Ding (School of Materials Science and Engineering, Tianjin University, Tianjin, China.) W Wenbin Hu

Abstract

Abstract Strain engineering in core–shell nanocatalysts is crucial for optimizing the activity of surficial sites. However, due to the significant difficulty in precise strain control, achieving optimal strain effect and insightful strain‐activity correlations is challenging. In this context, a novel strategy is proposed of precisely tuning the surface strain by leveraging the lattice coupling between Pt shell and the superlattice ordering Pt‐based intermetallic compound core. Two‐atom‐layer Pt‐skinned PtCo‐IMC nanocrystals are synthesized and subjected to heteroatom substitution in IMC core, yielding Pt@Pt 2 CoM (M═Co, Cu, Fe, Cr) nanocatalysts. Gradient strains in ultra‐thin Pt skin are constructed by continuously modulating the lattice parameters of Pt 2 CoM‐IMC cores. Based on this nanocatalyst platform, the influences of gradient strain on both the surface H‐adsorption/desorption and interfacial mass transportation are revealed, which synergistically regulate the hydrogen electrocatalysis kinetics. Pt@Pt 2 CoFe with optimal 5.8% compressive surface strain demonstrates impressive bifunctional hydrogen electrocatalytic activities for hydrogen oxidation (1.33 A/mg Pt ) and evolution (4.58 A/mg Pt ) reactions that are respectively 22.2 and 6.0 times over the strain‐free Pt. Additionally, Pt@Pt 2 CoFe exhibits robust CO tolerance and high stability for long‐term hydrogen electrocatalysis. This work provides a promising route of ingenious surface strain design for developing high‐performance nanocatalysts.

Article Details

Volume / Issue Vol. 38, Issue 6
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

T

Tao Zhang

W

Wanqing Song

School of Materials Science and Engineering, Tianjin University, Tianjin, China.

X

Xin Wang

P

Panzhe Qiao

Shanghai Synchrotron Radiation Facility

J

Jiahui Feng

School of Materials Science and Engineering, Tianjin University, Tianjin, China.

H

Huachen Shi

School of Materials Science and Engineering Tianjin Key Laboratory of Composite and Functional Materials Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education) Tianjin University Tianjin China

H

Haozhi Wang

State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study and National Center for Translational Medicine

X

Xinyi Yang

School of Materials Science and Engineering, Tianjin University, Tianjin, China.

J

Jinfeng Zhang

J

Jia Ding

School of Materials Science and Engineering, Tianjin University, Tianjin, China.

W

Wenbin Hu