Metal‐Mediated Nitrogen Doping of Carbon Supports Boosts Hydrogen Production from Ammonia

T Thomas J. Liddy (School of Chemistry University of Nottingham Nottingham NG7 2RD UK) B Benjamin J. Young E Emerson C. Kohlrausch (School of Chemistry University of Nottingham Nottingham NG7 2RD UK) A Andreas Weilhard (School of Chemistry University of Nottingham Nottingham NG7 2RD UK) G Gazi N. Aliev (School of Physics and Astronomy University of Birmingham Edgbaston B15 2TT UK) Y Yifan Chen M Manfred E. Schuster (Johnson Matthey Technology Centre Blounts Court Sonning Common RG4 9NH UK) M Mohsen Danaie (Electron Physical Science Imaging Centre (ePSIC) Harwell Science & Innovation Campus Didcot OX11 0DE UK) L Luke L. Keenan D Donato Decarolis (Diamond Light Source) D Diego Gianolio (Diamond Light Source Ltd., Harwell Science & Innovation Campus, Didcot OX11 0DE, U.K.) S Siqi Wang (State Key Laboratory of Special Materials Surface Engineering, School of Materials Science and Engineering) M Mingming Zhu G Graham J. Hutchings D David M. Grant W Wolfgang Theis (School of Physics and Astronomy University of Birmingham Edgbaston B15 2TT UK) T Tien‐Lin Lee (Diamond Light Source Ltd. Harwell Science & Innovation Campus Didcot OX11 0DE UK) D David A. Duncan A Alberto Roldan A Andrei N. Khlobystov (School of Chemistry) J Jesum Alves Fernandes (School of Chemistry University of Nottingham Nottingham NG7 2RD UK)

Abstract

Abstract Ammonia is an attractive hydrogen carrier, yet its practical use is limited by the need for efficient catalytic decomposition. We demonstrate that in‐situ N‐doping of Ru nanoparticles and graphitized carbon nanofiber supports during reaction produces a sharp increase in hydrogen production during the first 40 h, followed by stable activity. Spectroscopic and microscopic analyses, together with density functional theory simulations, reveal that Ru nitridation is rapid and support‐independent, resulting in a mechanistic shift from the traditional Langmuir–Hinshelwood to a Mars–van Krevelen pathway, further confirmed by isotopic labelling experiments. In contrast, the progressive nitridation of the carbon support, observed via X‐ray photoelectron spectroscopy, modulates the electronic environment of Ru and functions as a dynamic nitrogen reservoir that enables reversible N atoms exchange with the Ru particles, facilitating N desorption from the Ru surface and thereby governing the catalytic activity enhancement. These new findings provide new mechanistic insight into ammonia decomposition and establish progressive nitrogen doping of carbon supports as a strategy for designing efficient metal‐based catalysts for hydrogen production.

Article Details

Volume / Issue Vol. 65, Issue 8
Published February 16, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (21)

T

Thomas J. Liddy

School of Chemistry University of Nottingham Nottingham NG7 2RD UK

B

Benjamin J. Young

E

Emerson C. Kohlrausch

School of Chemistry University of Nottingham Nottingham NG7 2RD UK

A

Andreas Weilhard

School of Chemistry University of Nottingham Nottingham NG7 2RD UK

G

Gazi N. Aliev

School of Physics and Astronomy University of Birmingham Edgbaston B15 2TT UK

Y

Yifan Chen

M

Manfred E. Schuster

Johnson Matthey Technology Centre Blounts Court Sonning Common RG4 9NH UK

M

Mohsen Danaie

Electron Physical Science Imaging Centre (ePSIC) Harwell Science & Innovation Campus Didcot OX11 0DE UK

L

Luke L. Keenan

D

Donato Decarolis

Diamond Light Source

D

Diego Gianolio

Diamond Light Source Ltd., Harwell Science & Innovation Campus, Didcot OX11 0DE, U.K.

S

Siqi Wang

State Key Laboratory of Special Materials Surface Engineering, School of Materials Science and Engineering

M

Mingming Zhu

G

Graham J. Hutchings

D

David M. Grant

W

Wolfgang Theis

School of Physics and Astronomy University of Birmingham Edgbaston B15 2TT UK

T

Tien‐Lin Lee

Diamond Light Source Ltd. Harwell Science & Innovation Campus Didcot OX11 0DE UK

D

David A. Duncan

A

Alberto Roldan

A

Andrei N. Khlobystov

School of Chemistry

J

Jesum Alves Fernandes

School of Chemistry University of Nottingham Nottingham NG7 2RD UK