Local structure and composition of PtRh nanoparticles produced through cathodic corrosionElectronic supplementary information (ESI) available: EXAFS functions in R-space, nanoparticle X-ray diffraction patterns, TEM-based particle sizes and 2D nanoparticle visualizations. See DOI: 10.1039/c7cp01059a

• Main Authors: Hersbach, Thomas J. P, Kortlever, Ruud, Lehtimäki, Matti, Krtil, Petr, Koper, Marc T. M
• Format: Article
• Language: English
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c7cp01059a

Alloy nanoparticles fulfill an important role in catalysis. As such, producing them in a simple and clean way is much desired. A promising alloy nanoparticle production method is cathodic corrosion, which generates particles by applying an AC voltage to an alloy electrode. However, this harsh AC potential program might affect the final elemental distribution of the nanoparticles. In this work, we address this issue by characterizing the time that is required to create 1 μmol of Rh, Pt 12 Rh 88 , Pt 55 Rh 45 and Pt nanoparticles under various applied potentials. The corrosion time measurements are complemented by structural characterization through transmission electron microscopy, X-ray diffraction and X-ray absorption spectroscopy. The corrosion times indicate that platinum and rhodium corrode at different rates and that the cathodic corrosion rates of the alloys are dominated by platinum. In addition, the structure-sensitive techniques reveal that the elemental distributions of the created alloy nanoparticles indeed exhibit small degrees of elemental segregation. These results indicate that the atomic alloy structure is not always preserved during cathodic corrosion. When preparing alloy nanoparticles through cathodic corrosion, the different corrosion behavior of the alloy components may produce both crystalline and amorphous particles.