4.7 Article

Alloying bulk-immiscible metals at the nanoscale: An XPS/STM study of bimetallic Ag-Pt/HOPG nanoparticles

Journal

APPLIED SURFACE SCIENCE
Volume 636, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2023.157872

Keywords

Bimetallic nanoparticles; Ag-Pt nanoparticles; Alloy design; Heterogeneous supported catalysts; Scanning tunneling microscopy; X-ray photoelectron spectroscopy

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The intentional tailoring of surface structure in bimetallic nanoparticles, especially those containing bulk-immiscible metals like Pt and Ag, has attracted great interest in academic research and industry. However, our investigation on the Ag-Pt/HOPG bimetallic system reveals that while partial alloying of Ag and Pt occurs at the preparation stage, thermal annealing does not further enhance the alloying degree due to surface segregation of silver. Increasing the annealing temperatures leads to structure ruins and even partial phase separation. These findings highlight the limited alloying capability of Pt and Ag at the nanoscale, which should be considered for the design and functioning of bimetallic catalysts.
The intentional tailoring of surface structure in bimetallic nanoparticles is of high interest for academic research and industry, and many attempts have been made to improve the control over the distribution mode of the constituent elements which ranges from homogeneously mixed nanoalloys to core-shell nanostructures. However, some metal combinations exhibit a wide miscibility gap in the bulk, which nonetheless could be overcome under definite conditions at the nanoscale due to size effects. Here we present the detailed XPS/STM investigation of alloying capability of bulk-immiscible metals on the example of the Ag-Pt/HOPG bimetallic system prepared by thermal vacuum deposition. We found out that partial alloying of Ag and Pt occurs already at the preparation stage, and the following thermal annealing of the Ag-Pt/HOPG samples at 300-400 degrees C does not help to enhance the alloying degree owing to thermodynamically driven surface segregation of silver. Increasing the annealing temperature ruins the structure of Ag-Pt bimetallic nanoparticles due to silver sublimation, while even longer annealing time leads to partial phase separation. Our results demonstrate a limited alloying capability of Pt and Ag at the nanoscale which will be relevant for further research on the design and functioning of bimetallic catalysts containing bulk-immiscible metals.

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