Harmonizing Nanoparticle Exsolution From Ce–Sm Oxide Matrix for Stable Methane Dry Reforming

Y Yongjie Ye H Haofan Lei Y Yuanbin Qin Z Zhen Wang S Sunpei Hu (Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics) T Tao Zhou (College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.) L Lijun Zhang (Key Laboratory of Functionalized Molecular Solids of Ministry of Education, Anhui Laboratory of Molecule-Based Materials, College of Chemistry and Materials Science) R Ruyang Wang Z Zizhen Xiao X Xinhua Gao Q Qingxiang Ma (State Key Laboratory of High‐efficiency Utilization of Coal and Green Chemical Engineering College of Chemistry and Chemical Engineering Ningxia University Yinchuan 750021 P.R. China) S Shucheng Shi (School of Physical Science and Technology; Center for Transformative Science) H Hui Zhang (The Fourth Hospital of Hebei Medical University Shijiazhuang China) H Han Yan S Shiming Zhou (Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, National Synchrotron Radiation Laboratory, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics) C Chao Ma Z Zhi Liu (Laboratory of Atmospheric Environment and Pollution Control) J Jing Tao J Jie Zeng (School of Chemistry & Chemical Engineering)

Abstract

Abstract Catalyst deactivation hinders the application of high‐temperature catalysis such as methane dry reforming, where nanoparticle exsolution will likely clear the path. However, the harsh reaction conditions often easily unbalance the exsolution degree, leading to either sintering or insufficient exsolution of metal nanoparticles. Here, we achieve the fabrication of highly dispersed yet exposed Rh nanoparticles exsolved from the Ce–Sm oxide matrix. Starting from examining the metal‐support interaction of Rh–CeO 2 and Rh–Sm 2 O 3 , the exsolution dynamics of Rh nanoparticles are studied via multiple in situ techniques. Rapid exsolution from CeO 2 induces Rh sintering and catalytic deactivation, whereas sluggish exsolution from Sm 2 O 3 results in Rh encapsulation with poor activity. The balanced metal‐support interaction harmonizes the exsolution of Rh nanoparticles from the Ce–Sm oxide matrix, fabricating an antisintering and coke‐resistant catalyst for methane dry reforming. This work provides insights into the development of catalysts with structural robustness, where the essence lies in the engineering of nanoparticle exsolution.

Article Details

Volume / Issue Vol. 64, Issue 31
Published July 28, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (19)

Y

Yongjie Ye

H

Haofan Lei

Y

Yuanbin Qin

Z

Zhen Wang

S

Sunpei Hu

Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics

T

Tao Zhou

College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.

L

Lijun Zhang

Key Laboratory of Functionalized Molecular Solids of Ministry of Education, Anhui Laboratory of Molecule-Based Materials, College of Chemistry and Materials Science

R

Ruyang Wang

Z

Zizhen Xiao

X

Xinhua Gao

Q

Qingxiang Ma

State Key Laboratory of High‐efficiency Utilization of Coal and Green Chemical Engineering College of Chemistry and Chemical Engineering Ningxia University Yinchuan 750021 P.R. China

S

Shucheng Shi

School of Physical Science and Technology; Center for Transformative Science

H

Hui Zhang

The Fourth Hospital of Hebei Medical University Shijiazhuang China

H

Han Yan

S

Shiming Zhou

Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Strongly-Coupled Quantum Matter Physics of Chinese Academy of Sciences, National Synchrotron Radiation Laboratory, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes, Department of Chemical Physics

C

Chao Ma

Z

Zhi Liu

Laboratory of Atmospheric Environment and Pollution Control

J

Jing Tao

J

Jie Zeng

School of Chemistry & Chemical Engineering