Carbon and Oxygen Double Defects‐Enhanced Ru‐Based Catalyst for Ammonia Decomposition

L Likang Lv (State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering) P Peiqi Chu (State Key Laboratory of Materials Low‐Carbon Recycling College of Materials Science and Engineering Beijing University of Technology Beijing China) T Tong Han (State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering) Y Yunpeng Jiang (State Key Laboratory of Materials Low‐Carbon Recycling College of Materials Science and Engineering Beijing University of Technology Beijing China) Z Zhiwei Wang (International Joint Research Laboratory of Nano-Micro Architecture Chemistry, Institute of Theoretical Chemistry and College of Chemistry) Y Yuxi Liu (State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering) H Hongxing Dai (State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering) L Lu Wei J Jiguang Deng (State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering)

Abstract

AbstractAlthough ammonia is widely recognized as one of the most promising candidates for hydrogen storage and transformation, the catalytic mechanisms involved in ammonia decomposition remain insufficiently understood, and the stability of catalysts continues to present significant challenges. In this study, Ru/CeO2‐CNTs catalysts with double defect sites were synthesized by a straightforward method, achieving an outstanding hydrogen production rate of 2230 mmol−1 gRu−1 min−1 at 500 °C, outperforming most Ru‐based catalysts. Experimental characterization and theoretical calculations revealed that the CeO2‐CNTs interface promotes the formation of oxygen vacancies (Ov) and carbon defects (Cd) through carbon–oxygen interactions. These defects enhance electron transfer from the support to Ru nanoparticles (NPs), modulate NH3 adsorption and activation and modulate the recombination and desorption of adsorbed N species (N*). Moreover, the coating of CeO2 significantly improved the stability of CNTs, which weakens undesired reactions under high‐temperature and hydrogen‐rich conditions. The study introduced a rational design strategy that enhances the multiple elementary stages of the NH3 decomposition by constructing double defect sites and offering new insights into the design of efficient and durable catalysts under harsh environments.

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 (9)

L

Likang Lv

State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering

P

Peiqi Chu

State Key Laboratory of Materials Low‐Carbon Recycling College of Materials Science and Engineering Beijing University of Technology Beijing China

T

Tong Han

State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering

Y

Yunpeng Jiang

State Key Laboratory of Materials Low‐Carbon Recycling College of Materials Science and Engineering Beijing University of Technology Beijing China

Z

Zhiwei Wang

International Joint Research Laboratory of Nano-Micro Architecture Chemistry, Institute of Theoretical Chemistry and College of Chemistry

Y

Yuxi Liu

State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering

H

Hongxing Dai

State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering

L

Lu Wei

J

Jiguang Deng

State Key Laboratory of Materials Low-Carbon Recycling, College of Materials Science and Engineering