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Issue 40, 2019
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Elucidating the optical spectra of [Au25(SR)18]q nanoclusters

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Ligand-protected Au nanoclusters have attracted tremendous interest due to their atomically precise structural determination and controllable optical properties. However, the origin of their optical features is not well understood. Herein, we address the effects of charge state and type of ligands on the structural, electronic, and optical properties of the Au25(SR)18 nanocluster, using first principles calculations. In particular, we analyze in detail the optical absorption spectra of phenylethanethiol-capped [Au25(SCH2CH2Ph)18]q nanocluster (q = −1, 0, and 1) and demonstrate that the nanocluster undergoes geometric changes when increasing its charge state, yielding the development of additional photoabsorption features. Moreover, by comparing the properties of the anionic [Au25(SR)18]1− nanoclusters (with SR = –SCH2CH2Ph, –SCH3 and –SH) we demonstrate that accounting for full (–SCH2CH2Ph) compared to simplified (–SCH3 and –SH) ligands leads to significant modifications in the shape of the main absorption features, such as the emergence of step-like absorption shoulders. In addition, we show that the energy of the main absorption peaks of the [Au25(SR)18]1− significantly blue-shifts when using –SH as model ligands. Overall, our computational work aids the experimental characterization of optical properties of ligand-protected nanoclusters and highlights the importance of accounting for full ligands in optical spectra calculations.

Graphical abstract: Elucidating the optical spectra of [Au25(SR)18]q nanoclusters

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Supplementary files

Article information

16 Jul 2019
29 Sep 2019
First published
30 Sep 2019

Phys. Chem. Chem. Phys., 2019,21, 22272-22282
Article type
Author version available

Elucidating the optical spectra of [Au25(SR)18]q nanoclusters

R. Juarez-Mosqueda and G. Mpourmpakis, Phys. Chem. Chem. Phys., 2019, 21, 22272
DOI: 10.1039/C9CP03982A

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