Probing Complex Photophysics in Gold Nanoclusters

Authors

  • Luis E. Llanes-Montesino Department of Physical Chemistry, Faculty of Sciences (II), University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Genève 4, Switzerland
  • Gonzalo Angulo Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland
  • Jiangtao Zhao Department of Physical Chemistry, Faculty of Sciences (II), University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Genève 4, Switzerland
  • Thomas Bürgi Department of Physical Chemistry, Faculty of Sciences (II), University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Genève 4, Switzerland
  • Arnulf Rosspeintner Department of Physical Chemistry, Faculty of Sciences (II), University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Genève 4, Switzerland

DOI:

https://doi.org/10.2533/chimia.2026.215

Keywords:

Excitation dynamics, Gold nanocluster, Luminescence, Photophysics

Abstract

We report striking photophysical behaviour of Au25(PET)18 (PET = 2-phenylethanethiol) nanoclusters in both anionic and neutral forms. Using broad spectral coverage and tuneable excitation, steady-state, and time-resolved measurements reveal low-energy absorption and emission features, weak photoluminescence, and multiexponential decay dynamics. Notably, the neutral species shows excitation-wavelength-dependent emissions and a pronounced mismatch between excitation and absorption spectra, violating Kasha’s and Vavilov’s rules. These results point towards complex excited-state behaviour of these systems and the crucial role of instrumentation design in their accurate characterisation.

Funding data

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Published

2026-04-29

How to Cite

[1]
L. E. Llanes-Montesino, G. Angulo, J. Zhao, T. Bürgi, A. . Rosspeintner, Chimia 2026, 80, 215, DOI: 10.2533/chimia.2026.215.