Investigating periodic table interpolation for the rational design of nanoalloy catalysts for green hydrogen production from ammonia decomposition

Parker, Luke A., Richards, Nia, Bailey, Liam, Carter, James H., Nowicka, Ewa ORCID: https://orcid.org/0000-0001-7449-2720, Pattisson, Samuel, Dummer, Nicholas F. ORCID: https://orcid.org/0000-0002-0946-6304, He, Qian ORCID: https://orcid.org/0000-0003-4891-3581, Lu, Li, Kiely, Christopher J., Golunski, Stanislaw E. ORCID: https://orcid.org/0000-0001-7980-8624, Roldan, Alberto ORCID: https://orcid.org/0000-0003-0353-9004 and Hutchings, Graham J. ORCID: https://orcid.org/0000-0001-8885-1560 2024. Investigating periodic table interpolation for the rational design of nanoalloy catalysts for green hydrogen production from ammonia decomposition. Catalysis Letters 154 , pp. 1958-1969. 10.1007/s10562-023-04446-4

Preview

PDF - Published Version Available under License Creative Commons Attribution. Download (1MB) | Preview

Abstract

Developing highly active catalysts for the decomposition of ammonia to produce hydrogen is an important goal in the context of renewable energy. Allied with this is a need for identification strategies to efficiently design novel catalysts integral to ensuring rapid progress in this research field. We investigated the efficacy of N–binding energy and periodic table interpolation to predict active bimetallic nanoparticle catalysts. Supported iron-platinum and iron-palladium were identified and experimentally shown to be more active than their monometallic analogues. Atomic resolution electron microscopy indicated that the most active catalyst (5 wt% Fe80Pt20/γ-Al2O3) was principally formed of alloyed nanoparticles. It restructured during testing, yet no activity loss was noted at 20 h time-on-line. While these findings show that periodic table interpolation may be a viable tool for identifying active combinations of metals, the activity of the catalysts in the current work were not able to outperform the Ru/Al2O3 benchmark. Further catalyst optimization or refinement of reaction descriptors may facilitate the development of catalysts with higher intrinsic activity than the current state-of-the-art catalysts.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry Cardiff Catalysis Institute (CCI)
Publisher:	Springer
ISSN:	1011-372X
Funders:	EPSRC, ERC
Date of First Compliant Deposit:	4 October 2023
Date of Acceptance:	14 August 2023
Last Modified:	07 Nov 2024 22:20
URI:	https://orca.cardiff.ac.uk/id/eprint/162934

Actions (repository staff only)

Edit Item