Abstract
The electrocatalytic activity of different, structurally well defined bimetallic PtRu surfaces in the oxygen reduction reaction was investigated by a combination of scanning tunnelling microscopy and electrochemical measurements performed under controlled mass transport conditions in a flow cell. We compare the effect of pseudomorphic Pt cover layers, mimicking the situation in a core–shell Pt/Ru nanoparticle, and of mixed PtxRu1−x monolayer surface alloys, reflecting the situation in an alloyed nanoparticle. The results unambiguously demonstrate that these bimetallic surfaces can reach activities well in excess of that of Pt(111), both for the film surfaces and the surface alloys, by optimizing the Pt surface content (surface alloys) or the Pt film thickness (film surfaces). The results are compared with simulated kinetic current–potential profiles based on existent density functional theory calculations (Greeley and Nørskov, J Phys Chem C 113:4932, 2009; Lischka et al., Electrochim Acta 52:2219, 2007) revealing very good agreement in trends. Potential and limits of this approach are discussed.
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Acknowledgments
This work was supported by the Deutsche Forschungsgemeinschaft via Research Group 1376 (Be 1201/18-1). A.K.E. is grateful for a fellowship from the Fonds National de la Recherche Luxembourg (PHD09-13). We would like to thank Prof. A. Groß (Ulm University) for fruitful discussions. One of the authors (RJB) wishes to thank Prof. J.K. Nørskov for stimulating and fruitful discussions over many years.
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Brimaud, S., Engstfeld, A.K., Alves, O.B. et al. Oxygen Reduction on Structurally Well Defined, Bimetallic PtRu Surfaces: Monolayer PtxRu1−x/Ru(0001) Surface Alloys Versus Pt Film Covered Ru(0001). Top Catal 57, 222–235 (2014). https://doi.org/10.1007/s11244-013-0177-0
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DOI: https://doi.org/10.1007/s11244-013-0177-0