Abstract
Controlled structure transformation in metal clusters is crucial for accessing novel architectures and understanding their structure-property correlations. Herein, we report a solvent-induced reverse-Ostwald ripening process between two atomically precise silver clusters, Ag56 and Ag45, which exhibit solvent-dependent structure variation: Ag56 remains stable in dichloromethane, whereas exposure to pentane induces conversion to Ag45. The compositions and structures of both clusters were determined by electrospray ionization mass spectrometry (ESI-MS) and single-crystal X-ray diffraction (SXRD). Structure analysis indicates that the Ag45 forms via fragmentation and reorganization of the Ag56 framework, distinct from the conventional Ostwald ripening observed in larger nano-systems. Although Ag45 and Ag56 share certain structural similarities, Ag45 exhibits superior stability and higher catalytic activity for the reduction of 4-nitrophenol (4-NP) than Ag56. Density functional theory (DFT) calculations further elucidate the catalytic reduction pathway on Ag45. This work demonstrates a solvent-mediated reverse-Ostwald ripening pathway in silver clusters, providing atomic-level insights into active site construction and offering a blueprint for designing robust, cluster-based catalysts. © 2026 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | e73239 |
| Number of pages | 8 |
| Journal | Small |
| Online published | 27 Mar 2026 |
| DOIs | |
| Publication status | Online published - 27 Mar 2026 |
Research Keywords
- Ag Clusters
- catalytic reduction of 4-nitrophenol
- reverse-Ostwald ripening
- solvent-induced structure conversion
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