Home > Publications database > Spectro-Microscopy of Individual Pt–Rh Core–Shell Nanoparticles during Competing Oxidation and Alloying |
Journal Article | PUBDB-2025-00003 |
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2025
Soc.
Washington, DC
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Please use a persistent id in citations: doi:10.1021/acsnano.5c07668 doi:10.3204/PUBDB-2025-00003
Abstract: The surface chemical composition of supported single Pt-Rh core-shell nanoparticles was studied to understand the Rh behavior in oxidizing and reducing gas environments using spectro-microscopy with high spatial resolution. We combined in situ X-ray photoemission electron microscopy with ex situ scanning electron-, atomic force- and scanning Auger-microscopy to distinguish Rh oxidation-reduction, dewetting-sintering and alloying-segregation during the course of the experiment. A more than 20% higher Rh 3d$_{5/2}$ oxide to metal photoemission intensity ratio for the Rh layer on top of the Pt-core was found as compared to the bare strontium titanate (STO) oxide catalyst support in close vicinity, where Rh/RhO$_x$ nanoparticles are forming. At elevated temperatures, Rh diffuses into the Pt particle, and this alloying at the Pt metal surface competes with the Rh oxidation, whereas the Rh/RhO$_x$ nanoparticles on the STO support are observed to sinter under identical oxidizing and temperature environments. A nanoparticle facet dependent analysis of selected Pt-core nanoparticles suggests that Rh oxidation is most advanced on a small nanoparticle with a low coordination top facet that we indexed by electron back scatter diffraction, demonstrating the strength of our correlative approach.
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