Influence of Pt Alloying on the Fluorescence of Fully Inorganic, Colloidal Gold Nanoclusters

Noble metal alloy nanoclusters (NCs) are interesting systems as the properties of two or more elements can be combined in one particle, leading to interesting fluorescence phenomena. However, previous studies have been exclusively performed on ligand‐capped NCs from wet chemical synthesis. This make...

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Published inChemphyschem Vol. 23; no. 10; pp. e202200033 - n/a
Main Authors Ziefuss, Anna R., Willeke, Michael, Miertz, Matthias, Heinemann, Alexander, Rehbock, Christoph, Barcikowski, Stephan
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 18.05.2022
John Wiley and Sons Inc
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Summary:Noble metal alloy nanoclusters (NCs) are interesting systems as the properties of two or more elements can be combined in one particle, leading to interesting fluorescence phenomena. However, previous studies have been exclusively performed on ligand‐capped NCs from wet chemical synthesis. This makes it difficult to differentiate to which extent the fluorescence is affected by ligand‐induced effects or the elemental composition of the metal core. In this work, we used laser fragmentation in liquids (LFL) to fabricate colloidal gold‐rich bi‐metallic AuPt NCs in the absence of organic ligands and demonstrate the suitability of this technique to produce molar fraction series of 1nm alloy NC. We found that photoluminescence of ligand‐free NCs is not a phenomenon limited to Au. However, even minute amounts of Pt atoms in the AuPt NCs lead to quenching and red‐shift of the fluorescence, which may be attributed to the altered surface charge density. Laser‐generated, colloidal, and fully inorganic gold nanoclusters show a pronounced fluorescence. This study is a proof of concept on the former and reveals that the observed photoluminescence of these particles is not a phenomenon limited to Au. Herein, it is shown that colloidal, fully inorganic Pt and Au rich AuPt NCs are also fluorescent but behave differently in terms of emission energy and intensity.
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ISSN:1439-4235
1439-7641
DOI:10.1002/cphc.202200033