Abstract
Engineering surface architectures in multimetallic nanoparticles is crucial for controlling their properties. This work investigates Ru-decorated CoNi nanoparticles prepared by an organometallic approach, yielding Ru as nanoparticles, subnanometric clusters, or isolated atoms. High-resolution electron microscopy (EM) and X-ray absorption spectroscopy (XAS) unambiguously establish these distinct Ru configurations, while X-ray photoelectron spectroscopy (XPS) reveals that Ru binding energies are influenced by coordination environment. Hydrogen–deuterium isotopic exchange further shows that subnanometric Ru maximizes activity, providing superior per-site reactivity. Together, these results demonstrate how the organometallic approach enables the controlled decoration of a platinum-group metal (i.e., Ru) on base metal (i.e., CoNi) nanoparticles, establishing direct correlations between surface architecture, electronic signatures, and potential catalytic functions.
| Original language | English |
|---|---|
| Pages (from-to) | 17918-17926 |
| Number of pages | 9 |
| Journal | Nano Letters |
| Volume | 25 |
| Issue number | 51 |
| Early online date | 16 Dec 2025 |
| DOIs | |
| Publication status | Published - 24 Dec 2025 |
Keywords
- Hydrogen activation
- Multimetallic nanoparticles
- Organometallic approach
- Ru decoration
ASJC Scopus subject areas
- Bioengineering
- General Chemistry
- General Materials Science
- Condensed Matter Physics
- Mechanical Engineering
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