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https://dspace.iiti.ac.in/handle/123456789/9164
Title: | A free-standing platinum monolayer as an efficient and selective catalyst for the oxygen reduction reaction |
Authors: | Garg, Priyanka Rawat, Kuber Singh Bhauriyal, Preeti Pathak, Biswarup |
Keywords: | Atoms;Calculations;Catalysts;Electrolytic reduction;Monolayers;Buckling patterns;First-principles calculation;Mechanically stable;Oxygen reduction reaction;Platinum monolayers;Potential-dependent;Rate determining step;Selective catalysts;Platinum |
Issue Date: | 2017 |
Publisher: | Royal Society of Chemistry |
Citation: | Mahata, A., Garg, P., Rawat, K. S., Bhauriyal, P., & Pathak, B. (2017). A free-standing platinum monolayer as an efficient and selective catalyst for the oxygen reduction reaction. Journal of Materials Chemistry A, 5(11), 5303-5313. doi:10.1039/c7ta00685c |
Abstract: | We report a two-dimensional platinum monolayer (Pt-ML) sheet for oxygen reduction reaction (ORR) activity using first-principles calculations. Unlike previous reports of a supported hexagonal planar monolayer, the Pt-ML exhibits an orthorhombic buckled structure, where each Pt atom is coordinated with six Pt atoms. State-of-the-art calculations show that the Pt-ML is energetically, thermally, dynamically and mechanically stable and thus can be synthesized. An orbital mixing between an in-plane σ-orbital and out-of-plane π-orbital helps in stabilizing the buckling pattern. We find that the dz2 orbitals of the out-of-plane Pt atoms tilt themselves (by 30°) toward the dyz orbital of the in-plane Pt atoms to gain the maximum overlap, which in turn stabilizes the buckled structure. The potential applicability of the Pt-ML towards ORR activity has been investigated and we find that the ORR rate determining step (OH formation) is significantly improved when catalyzed by the Pt-ML compared to any other catalysts reported to date. Our potential dependent study shows that the ORR is thermodynamically favourable at 0.38 V and thus lowers the overpotential for the ORR. Besides, the Pt-ML is much more selective towards H2O formation over H2O2 formation. © The Royal Society of Chemistry. |
URI: | https://doi.org/10.1039/c7ta00685c https://dspace.iiti.ac.in/handle/123456789/9164 |
ISSN: | 2050-7488 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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