Ab initio insights into support-induced sulfur resistance of Ni-based reforming catalysts

Chaudhari, Amit, Stishenko, Pavel, Hiregange, Akash, Hawkins, Christopher R., Sarwar, Misbah, Poulston, Stephen and Logsdail, Andrew J. ORCID: https://orcid.org/0000-0002-2277-415X 2026. Ab initio insights into support-induced sulfur resistance of Ni-based reforming catalysts. Catalysis Science & Technology 10.1039/d5cy01279a

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Abstract

Ni-based catalysts are well established for industrial H2 production via methane steam reforming; however, their susceptibility to sulfur poisoning necessitates expensive desulfurisation and limits the development of low temperature processes using renewable feedstocks. Designing next-generation catalysts requires an atomic-level understanding of the factors that affect the catalyst sulfur tolerance, but this is difficult to obtain due to complex interactions between the Ni catalyst and non-inert metal oxide supports. In this work, we investigate the atomic-level mechanisms driving the support-induced sulfur resistance of Ni catalysts, emphasising the role of disorder in Ni-bound sulfur–oxygen adsorption complexes and support defect chemistry in promoting catalyst regeneration. The thermodynamic driving force for oxygen-mediated sulfur removal from a Ni(111) surface, which is indicative of the regenerative effects of support oxygen buffering, is investigated using grand canonical Monte Carlo (GCMC) sampling of a lattice model that is parameterised using density functional theory (DFT). The outcome is predictions of the equilibrium surface coverage and composition of co-adsorbed S and O atoms on Ni(111) at length scales that are inaccessible to DFT simulations. The GCMC predictions are validated using a fine-tuned machine learned interatomic potential to reveal entropic contributions for catalyst regeneration at experimentally relevant surface coverages, demonstrating an integrated approach for efficiently exploring the complex combinatorial space of adsorption complexes with near ab initio accuracy. Simulations of the surface chemistry of Ni(111) are complemented by predictions of the energetics of bulk defect formation in prototypical metal oxide support materials to provide insights into the proclivity for oxygen release and phase transformation during catalytic reactions. The computational modelling is correlated with experimental characterisation and methane steam reforming activity tests for H2S-poisoned Ni nanoparticle catalysts, allowing us to rationalise the experimentally observed differences in the catalyst sulfur tolerance and establish strategies for future catalyst optimisation. The work demonstrates the integration of ab initio computational modelling, statistical sampling and machine learning, in a combined framework that complements experimental characterisation, to inform the rational design of catalyst support materials for sustainable H2 production.

Item Type:	Article
Date Type:	Published Online
Status:	In Press
Schools:	Schools > Chemistry Research Institutes & Centres > Cardiff Catalysis Institute (CCI)
Additional Information:	License information from Publisher: LICENSE 1: URL: https://creativecommons.org/licenses/by/3.0/, Start Date: 2026-01-20
Publisher:	Royal Society of Chemistry
ISSN:	2044-4753
Date of First Compliant Deposit:	3 February 2026
Date of Acceptance:	19 January 2026
Last Modified:	03 Feb 2026 11:45
URI:	https://orca.cardiff.ac.uk/id/eprint/184366

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