Discovery of a Robust Single‐Atom Ruthenium Emission Control Catalyst

C Chengxiong Wang (Department of Chemistry Tsinghua University Beijing China) J Jin‐Cheng Liu (Center For Rare Earth and Inorganic Functional Materials School of Materials Science and Engineering & National Institute for Advanced Materials Nankai University Tianjin China) Z Zhi Li X Xinyu Liu X Xiao Liang (Department of Chemistry) Y Yang Li M Mengyun Wang (Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, U.K.) Y Yiming Zhao (Department of Medical Oncology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University) G Guangxin Liu (State Key Laboratory of Precious Metal Functional Materials Kunming Institute of Precious Metals Kunming China) S Shuangchao Yao (Department of Chemistry Tsinghua University Beijing China) R Rong Wang C Chen Chen D Dingsheng Wang (Department of Chemistry) Q Qing Peng (Pingyuan Laboratory, School of Chemistry and Chemical Engineering) Y Yunkun Zhao (State Key Laboratory of Precious Metal Functional Materials Kunming Institute of Precious Metals Kunming China) Y Yadong Li (Department of Chemistry)

Abstract

ABSTRACT Herein, we discover a robust emission control catalyst featuring Ru single‐atom sites even undergoing thermal oxidative aging at 850°C in a 10%H 2 O/10%O 2 /N 2 mixture gas stream, expecting to substitute the traditional Rh catalysts by cutting ∼73% of the total cost. The stability challenges in elevated‐temperature oxidizing environments were overcome via constructing the isolated Ru atoms anchored by square‐planar coordination with four lattice oxygen in ceria and suppressing Ru atom migration toward the single Ru─O x ─Ce catalytic centers by introducing the Zr‐rich materials, which are conducive to inhibiting the formation of undesirable N 2 O by‐products during catalytic NO reduction. More importantly, the challenge of low‐temperature C─H bond activation in short‐chain alkanes on the isolated single‐atom sites was broken through by constructing the CeZrO–Ru SA –CeO 2 three‐phase interfaces to promote the H‐spillover. The low‐cost Ru SA –CeO 2 /CZ single‐atom catalyst exhibited much better stability, lower selectivity of N 2 O and NH 3 by‐products, and higher activity for CO conversion under oxygen‐lean conditions compared to commercial Rh catalysts for automotive emission control applications. This work opens new avenues for developing the new generation of low‐cost, robust emission control catalysts in the future.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (16)

C

Chengxiong Wang

Department of Chemistry Tsinghua University Beijing China

J

Jin‐Cheng Liu

Center For Rare Earth and Inorganic Functional Materials School of Materials Science and Engineering & National Institute for Advanced Materials Nankai University Tianjin China

Z

Zhi Li

X

Xinyu Liu

X

Xiao Liang

Department of Chemistry

Y

Yang Li

M

Mengyun Wang

Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, U.K.

Y

Yiming Zhao

Department of Medical Oncology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University

G

Guangxin Liu

State Key Laboratory of Precious Metal Functional Materials Kunming Institute of Precious Metals Kunming China

S

Shuangchao Yao

Department of Chemistry Tsinghua University Beijing China

R

Rong Wang

C

Chen Chen

D

Dingsheng Wang

Department of Chemistry

Q

Qing Peng

Pingyuan Laboratory, School of Chemistry and Chemical Engineering

Y

Yunkun Zhao

State Key Laboratory of Precious Metal Functional Materials Kunming Institute of Precious Metals Kunming China

Y

Yadong Li

Department of Chemistry