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Lookup NU author(s): Professor Ian Metcalfe
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
© 2023 The Authors. Published by American Chemical Society. The reforming reactions of greenhouse gases require catalysts with high reactivity, coking resistance, and structural stability for efficient and durable use. Among the possible strategies, exsolution has been shown to demonstrate the requirements needed to produce appropriate catalysts for the dry reforming of methane, the conversion of which strongly depends on the choice of active species, its interaction with the support, and the catalyst size and dispersion properties. Here, we exploit the exsolution approach, known to produce stable and highly active nanoparticle-supported catalysts, to develop iridium-nanoparticle-decorated perovskites and apply them as catalysts for the dry reforming of methane. By studying the effect of several parameters, we tune the degree of exsolution, and consequently the catalytic activity, thereby identifying the most efficient sample, 0.5 atomic % Ir-BaTiO3, which showed 82% and 86% conversion of CO2 and CH4, respectively. By comparison with standard impregnated catalysts (e.g., Ir/Al2O3), we benchmark the activity and stability of our exsolved systems. We find almost identical conversion and syngas rates of formation but observe no carbon deposition for the exsolved samples after catalytic testing; such deposition was significant for the traditionally prepared impregnated Ir/Al2O3, with almost 30 mgC/gsample measured, compared to 0 mgC/gsample detected for the exsolved system. These findings highlight the possibility of achieving in a single step the mutual interaction of the parameters enhancing the catalytic efficiency, leading to a promising pathway for the design of catalysts for reforming reactions.
Author(s): Cali E, Saini S, Kerherve G, Skinner WS, Metcalfe IS, Payne DJ, Kousi K
Publication type: Review
Publication status: Published
Journal: ACS Applied Nano Materials
Year: 2024
Volume: 7
Issue: 16
Pages: 18398-18409
Print publication date: 23/08/2024
Online publication date: 01/12/2023
Acceptance date: 06/11/2023
ISSN (electronic): 2574-0970
Publisher: American Chemical Society
URL: https://doi.org/10.1021/acsanm.3c04126
DOI: 10.1021/acsanm.3c04126
Data Access Statement: Supporting research data for this article may be accessed at 10.15126/surreydata.900802
