Continuous Surface Strain Regulation in Trimetallic PtPbRu/Pt Nanoplates for Promoted Formic Acid Oxidation Catalysis

P Peidie Fang (State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China) C Changhong Zhan (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) Y Yongle Kang (College of Energy Xiamen University Xiamen P. R. China) S Shize Geng M Mingzi Sun (Department of Chemistry) B Bolong Huang (Department of Chemistry) J Jing Xia (Chinese Academy of Sciences , , ,) T Tingjie Mao (Wenzhou Key Lab of Advanced Energy Storage and Conversion, Zhejiang Province Key Lab of Leather Engineering, College of Chemistry and Materials Engineering) J Juan Wang (Department of Chemical and Biomolecular Engineering) W Weizhong Liao (State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China) Z Zhou Chen (Australian Institute for Bioengineering and Nanotechnology) T Ting‐Shan Chan (National Synchrotron Radiation Research Centre Hsinchu Taiwan) Y Yu‐Cheng Huang (National Synchrotron Radiation Research Center Hsinchu 300092 Taiwan) Z Zhiwei Hu (Max Planck Institute for Chemical Physics of Solids, Nothnitzer Strasse 40, Dresden 01187, Germany) X Xiaoqing Huang (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) L Lingzheng Bu

Abstract

ABSTRACT Regulating surface strain of platinum (Pt)‐based nanomaterials to achieve efficient formic acid oxidation reaction (FAOR) catalysis for direct formic acid fuel cell (DFAFC) is crucial yet challenging. Herein, we adopt a continuous surface tensile strain modulation strategy to realize the superior activity, excellent stability, strong CO resistance, and high direct pathway selectivity for DFAFC. Atomic‐level analysis reveals that controlling the partial substitution of Pb with Ru atoms modulates the lattice constant of the intermetallic core, thereby enabling precise control of biaxial strain in the Pt shell. The optimized 2.4%‐PtPbRu/Pt nanoplates/C exhibits a mass activity of 10.0 A mg Pt+Ru −1 for FAOR, 100.0 times higher than that of commercial Pt/C. Furthermore, its membrane electrode assembly achieves a high power density of 465.4 W g Pt+Ru −1 , 3.2 times greater than that of commercial Pt/C, along with an unprecedented lifetime at 0.4 V for 469.1 h with only 7.4% power density decay, representing the best FAOR catalysts reported to date. The introduced Ru increases tensile strain and downshifts Pt‐5 d orbitals, enhancing d ‐ d orbital coupling, weakening CO * adsorption, and promoting the HCOO * adsorption to facilitate the direct formate pathway. It breaks through the strain‐performance relationship bottleneck of traditional Pt‐based catalysts, providing an atomic‐scale design blueprint of efficient anodic catalysts for DFAFC.

Article Details

Volume / Issue Vol. 38, Issue 13
Published March 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

P

Peidie Fang

State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China

C

Changhong Zhan

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

Y

Yongle Kang

College of Energy Xiamen University Xiamen P. R. China

S

Shize Geng

M

Mingzi Sun

Department of Chemistry

B

Bolong Huang

Department of Chemistry

J

Jing Xia

Chinese Academy of Sciences , , ,

T

Tingjie Mao

Wenzhou Key Lab of Advanced Energy Storage and Conversion, Zhejiang Province Key Lab of Leather Engineering, College of Chemistry and Materials Engineering

J

Juan Wang

Department of Chemical and Biomolecular Engineering

W

Weizhong Liao

State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen P. R. China

Z

Zhou Chen

Australian Institute for Bioengineering and Nanotechnology

T

Ting‐Shan Chan

National Synchrotron Radiation Research Centre Hsinchu Taiwan

Y

Yu‐Cheng Huang

National Synchrotron Radiation Research Center Hsinchu 300092 Taiwan

Z

Zhiwei Hu

Max Planck Institute for Chemical Physics of Solids, Nothnitzer Strasse 40, Dresden 01187, Germany

X

Xiaoqing Huang

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

L

Lingzheng Bu