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Autori principali: Allen, Kevin, Lane, Christopher, Morosan, Emilia, Zhu, Jian-Xin
Natura: Preprint
Pubblicazione: 2025
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Accesso online:https://arxiv.org/abs/2508.21766
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author Allen, Kevin
Lane, Christopher
Morosan, Emilia
Zhu, Jian-Xin
author_facet Allen, Kevin
Lane, Christopher
Morosan, Emilia
Zhu, Jian-Xin
contents For large-scale deployment and use of polymer electrolyte fuel cells, high-performance electrocatalysts with low platinum consumption are desirable. One promising strategy to meet this demand is to explore alternative materials that retain catalytic efficiency while introducing new mechanisms for performance enhacement. In this study, we investigate a ferromagnetic CoPt as a candidate material to accelerate oxygen reduction reactions. By using density functional theory calculations, we find the spin-polarized Co-$d$ states to enhance O$_2$ surface bonding due to local exchange splitting of Co-$d$ carriers at the Fermi level. Furthermore, O and O$_2$ adsorption and dissociation energies are found to be tuned by varying the thickness of the Pt layers. Our study gives insight into the role magnetism plays in the oxygen reduction reaction process and how magnetic ions may aid in the design of new advanced catalysts.
format Preprint
id arxiv_https___arxiv_org_abs_2508_21766
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Magnetism Enhanced Surface Bonding of O$_{2}$ on CoPt
Allen, Kevin
Lane, Christopher
Morosan, Emilia
Zhu, Jian-Xin
Materials Science
For large-scale deployment and use of polymer electrolyte fuel cells, high-performance electrocatalysts with low platinum consumption are desirable. One promising strategy to meet this demand is to explore alternative materials that retain catalytic efficiency while introducing new mechanisms for performance enhacement. In this study, we investigate a ferromagnetic CoPt as a candidate material to accelerate oxygen reduction reactions. By using density functional theory calculations, we find the spin-polarized Co-$d$ states to enhance O$_2$ surface bonding due to local exchange splitting of Co-$d$ carriers at the Fermi level. Furthermore, O and O$_2$ adsorption and dissociation energies are found to be tuned by varying the thickness of the Pt layers. Our study gives insight into the role magnetism plays in the oxygen reduction reaction process and how magnetic ions may aid in the design of new advanced catalysts.
title Magnetism Enhanced Surface Bonding of O$_{2}$ on CoPt
topic Materials Science
url https://arxiv.org/abs/2508.21766