Fluorescent Au nanoclusters stabilized by silane: facile synthesis, color-tunability and photocatalytic propertiesElectronic supplementary information (ESI) available: Fig. S1-S13 and Table S1. See DOI: 10.1039/c7nr01052d

Synthesis of tunable, luminescent metal nanoclusters remains challenging due to their tendency to aggregate. Herein, we report a simple photoreduction method to synthesize fluorescent silane-stabilized Au nanoclusters. By altering the molar ratio of stabilizer and Au precursor, emissions of the as-p...

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Hauptverfasser: Zhou, Shaochen, Duan, Yanyan, Wang, Fu, Wang, Chuanyi
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Sprache:eng
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Zusammenfassung:Synthesis of tunable, luminescent metal nanoclusters remains challenging due to their tendency to aggregate. Herein, we report a simple photoreduction method to synthesize fluorescent silane-stabilized Au nanoclusters. By altering the molar ratio of stabilizer and Au precursor, emissions of the as-prepared Au nanoclusters can be tuned in the wavelength range of 538-580 nm. High resolution transmission electron microscopy results showed that the variation in the size of the as-formed nanoclusters (1.2-2.0 nm) might be responsible for this emission shift. The as-synthesized gold nanoclusters have a relatively long fluorescence lifetime, from 34.04 to 46.83 ns, and luminescence quantum yields of 0.26-3.16%, depending on the fluorescence at the specific emission wavelength. Compared with bulk gold, these silane-stabilized Au nanoclusters possess special electronic structures and exhibit semiconductor-like features such as an absorption edge in the visible region, which gives rise to their visible excitation at 400-450 nm. As demonstrated by the degradation of methylene blue under visible irradiation, the synthesized Au nanoclusters can also function as a promising cluster photocatalyst, just like many other semiconductor counterparts. An easy photoreduction strategy was developed to synthesize silane-stabilized Au nanoclusters with tunable sizes and fluorescence, exhibiting semiconductor-like features such as photocatalytic properties.
ISSN:2040-3364
2040-3372
DOI:10.1039/c7nr01052d