Dizygotic Atomic Platinum and Palladium on Carbon for High‐Performance Ethanol and Methanol Electro‐Oxidation

Z Zhiqi Zhang (CAS Key Lab of Bio-Medical Diagnostics) J Jiapeng Liu (School of Advanced Energy) S Shangqian Zhu Y Yuhao Wang (Key Laboratory of Biomedical Polymers-Ministry of Education, College of Chemistry and Molecular Sciences) J Jian Wang M Minhong Xu (Department of Chemical and Biological Engineering The Hong Kong University of Science and Technology Hong Kong P.R. China) J Jie Zhao Z Zheng Wang D Dewang Zeng (Key Laboratory of Energy Thermal Conversion and Control (Ministry of Education) School of Energy and Environment Southeast University Nanjing P.R. China) J Jianrong Zeng (Shanghai Synchrotron Radiation Facility) Y Yufei Song C Chih‐Wen Pao (National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan) Z Zhiwei Hu (Max Planck Institute for Chemical Physics of Solids, Nothnitzer Strasse 40, Dresden 01187, Germany) J Jongwoo Lim (Department of Chemistry) R Rui Xiao M Minhua Shao (The Hong Kong University of Science and Technology , , ,) F Francesco Ciucci (Chair of Electrode Design for Electrochemical Energy Systems)

Abstract

Abstract Dizygotic‐atom‐site catalysts (DASCs), consisting of multi‐atomic dispersed catalytic centers, perform well in several reactions but have poor electrocatalytic activity toward alcohol electro‐oxidation. In this study, DASCs of atomically dispersed platinum and palladium on nitrogen‐doped carbon nanocages (Pt 1 Pd 1 /NCNC) are successfully synthesized using an impregnation–adsorption method. The Pt 1 Pd 1 /NCNC catalyst has higher mass activity toward ethanol and methanol oxidation than commercial Pt/C and Pd/C. In contrast, Pt or Pd single‐atom catalysts on nitrogen‐doped carbon nanocages are virtually inert. Ethanol and methanol on Pt 1 Pd 1 /NCNC are electro‐oxidized to acetate ion and CO 2 as the final product, respectively. Pt 1 Pd 1 /NCNC exhibits long‐term stability toward ethanol and methanol oxidation due to the absence of the CO intermediate. Ab initio simulations show that Pt 1 Pd 1 /NCNC optimizes the ethanol oxidation pathway thanks to a lower energy barrier and onset potential than individual single Pt or Pd atom catalysts on NCNC. This study opens a new path to developing advanced DASCs for alcohol oxidation.

Article Details

Volume / Issue Vol. 64, Issue 37
Published September 08, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (17)

Z

Zhiqi Zhang

CAS Key Lab of Bio-Medical Diagnostics

J

Jiapeng Liu

School of Advanced Energy

S

Shangqian Zhu

Y

Yuhao Wang

Key Laboratory of Biomedical Polymers-Ministry of Education, College of Chemistry and Molecular Sciences

J

Jian Wang

M

Minhong Xu

Department of Chemical and Biological Engineering The Hong Kong University of Science and Technology Hong Kong P.R. China

J

Jie Zhao

Z

Zheng Wang

D

Dewang Zeng

Key Laboratory of Energy Thermal Conversion and Control (Ministry of Education) School of Energy and Environment Southeast University Nanjing P.R. China

J

Jianrong Zeng

Shanghai Synchrotron Radiation Facility

Y

Yufei Song

C

Chih‐Wen Pao

National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan

Z

Zhiwei Hu

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

J

Jongwoo Lim

Department of Chemistry

R

Rui Xiao

M

Minhua Shao

The Hong Kong University of Science and Technology , , ,

F

Francesco Ciucci

Chair of Electrode Design for Electrochemical Energy Systems