Structural order enhances charge carrier transport in self-assembled Au-nanoclusters

Florian Fetzer, Andre Maier, Martin Hodas, Olympia Geladari, Kai Braun, Alfred J. Meixner, Frank Schreiber, Andreas Schnepf () and Marcus Scheele ()
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Florian Fetzer: Institut für Anorganische Chemie Universität Tübingen
Andre Maier: Universität Tübingen
Martin Hodas: Universität Tübingen
Olympia Geladari: Universität Tübingen
Kai Braun: Universität Tübingen
Alfred J. Meixner: Universität Tübingen
Frank Schreiber: Universität Tübingen
Andreas Schnepf: Institut für Anorganische Chemie Universität Tübingen
Marcus Scheele: Universität Tübingen

Nature Communications, 2020, vol. 11, issue 1, 1-8

Abstract: Abstract The collective properties of self-assembled nanoparticles with long-range order bear immense potential for customized electronic materials by design. However, to mitigate the shortcoming of the finite-size distribution of nanoparticles and thus, the inherent energetic disorder within assemblies, atomically precise nanoclusters are the most promising building blocks. We report an easy and broadly applicable method for the controlled self-assembly of atomically precise Au32(nBu3P)12Cl8 nanoclusters into micro-crystals. This enables the determination of emergent optoelectronic properties which resulted from long-range order in such assemblies. Compared to the same nanoclusters in glassy, polycrystalline ensembles, we find a 100-fold increase in the electric conductivity and charge carrier mobility as well as additional optical transitions. We show that these effects are due to a vanishing energetic disorder and a drastically reduced activation energy to charge transport in the highly ordered assemblies. This first correlation of structure and electronic properties by comparing glassy and crystalline self-assembled superstructures of atomically precise gold nanoclusters paves the way towards functional materials with novel collective optoelectronic properties.

Date: 2020
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DOI: 10.1038/s41467-020-19461-x

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