Blocking the <i>Operando</i> Formation of Single‐Atom Spectators by Interfacial Engineering

X Xuan Tang (Key Laboratory for Advanced Materials, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering) S Shasha Ge (State Key Laboratory of Green Chemical Engineering and Industrial Catalysis Research Institute of Industrial Catalysis School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai 200237 P.R. China) Y Yao Lv G Geng Sun (Chongqing Key Laboratory of Chemical Theory and Mechanism, College of Chemistry and Chemical Engineering) Z Zhaohua Wang J Junzhong Xie (Beijing National Laboratory for Molecular Sciences, New Cornerstone Science Laboratory, College of Chemistry and Molecular Engineering) M Mi Peng Y Yao Xu (Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering) J Jie Zhang B Bingqing Yao (Department of Materials Science and Engineering) Q Qian He Y Yanglong Guo W Wangcheng Zhan L Li Wang (The Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital Zhengzhou China) L Lihui Zhou B Bingjun Xu S Sheng Dai Y Yun Guo D Ding Ma

Abstract

AbstractAside from activity and selectivity, catalyst stability is a key focus in heterogeneous catalysis research. Although sintering of metal species has been considered the primary cause for deactivation of metal catalysts, our study reveals that the loss of activity at low reaction temperatures in the CeO2‐supported Pt (Pt/CeO2) catalyst in complete propane oxidation is due to the dispersion of Pt ensemble sites (nanoclusters) and their subsequent operando conversion into Pt single atoms under reaction conditions. These Pt single‐atom species exhibit low reactivity and act as spectators in the low‐temperature reaction region. To address this issue, we engineered the surface of CeO2 by introducing NbOx, which does not directly interact with Pt. Instead, NbOx blocks the strong binding sites for Pt on CeO2, thereby preventing Pt redispersion/fragmentation and preserving reactive Pt ensembles. This strategy led to a remarkable 37‐fold increase in the reaction rate compared to the Pt/CeO2 catalyst. Our findings emphasize the importance of suppressing the formation of noble metal single‐atom spectators through innovative surface engineering strategy. These mechanistic insights not only advance the understanding of the materials science of Pt/CeO2 but also extend to critical technological fields such as energy conversion systems and environmental remediation technologies.

Article Details

Volume / Issue Vol. 64, Issue 23
Published June 02, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (19)

X

Xuan Tang

Key Laboratory for Advanced Materials, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering

S

Shasha Ge

State Key Laboratory of Green Chemical Engineering and Industrial Catalysis Research Institute of Industrial Catalysis School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai 200237 P.R. China

Y

Yao Lv

G

Geng Sun

Chongqing Key Laboratory of Chemical Theory and Mechanism, College of Chemistry and Chemical Engineering

Z

Zhaohua Wang

J

Junzhong Xie

Beijing National Laboratory for Molecular Sciences, New Cornerstone Science Laboratory, College of Chemistry and Molecular Engineering

M

Mi Peng

Y

Yao Xu

Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering

J

Jie Zhang

B

Bingqing Yao

Department of Materials Science and Engineering

Q

Qian He

Y

Yanglong Guo

W

Wangcheng Zhan

L

Li Wang

The Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital Zhengzhou China

L

Lihui Zhou

B

Bingjun Xu

S

Sheng Dai

Y

Yun Guo

D

Ding Ma