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cc-by (c) Jennings, Paul C. et al., 2015
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/112264

O2 dissociation on M@Pt core-shell particles for 3d, 4d and 5d transition metals

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Density functional theory calculations are performed to investigate oxygen dissociation on 38-atom truncated octahedron platinum-based particles. This study progresses our previous work (Jennings et al. Nanoscale, 2014, 6, 1153), where it was shown that flexibility of the outer Pt shell played a crucial role in facilitating fast oxygen dissociation. In this study, the effect of forming M@Pt (M core, Pt shell) particles for a range of metal cores (M = 3d, 4d, and 5d transition metals) is considered, with respect to O2 dissociation on the Pt(111) facets. We show that forming M@Pt particles with late transition metal cores results in favorable shell flexibility for very low O2 dissociation barriers. Conversely, alloying with early transition metals results in a more rigid Pt shell because of dominant M-Pt interactions, which prevent lowering of the dissociation barriers.

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JENNINGS, Paul C., et al. O2 dissociation on M@Pt core-shell particles for 3d, 4d and 5d transition metals. Journal of Physical Chemistry C. 2015. Vol. 119, num. 20, pags. 11031-11041. ISSN 1932-7447. [consulted: 11 of August of 2026]. Available at: https://hdl.handle.net/2445/112264

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