Issue 29, 2015

Electronic coupling between ligand and core energy states in dithiolate-monothiolate stabilized Au clusters

Abstract

Electron transfer activities of metal clusters are fundamentally significant and have promising potential in catalysis, charge or energy storage, sensing, biomedicine and other applications. Strong resonance coupling between the metal core energy states and the ligand molecular orbitals has not been established experimentally, albeit exciting progress has been achieved in the composition and structure determination of these types of nanomaterials recently. In this report, the coupling between core and ligand energy states is demonstrated by the rich electron transfer activities of Au130 clusters. Quantized electron transfers to the core and multi-electron transfers involving the durene-dithiolate ligands were observed at lower and higher potentials, respectively, in voltammetric studies. After a facile multi-electron oxidation from +1.34 to +1.40 V, several reversal reduction processes at more negative potentials, i.e. +0.91 V, +0.18 V and −0.34 V, were observed in an electrochemically irreversible fashion or with sluggish kinetics. The number of electrons and the shifts of the respective reduction potentials in the reversal process were attributed to the electronic coupling or energy relaxation processes. The electron transfer activities and subsequent relaxation processes are drastically reduced at lower temperatures. The time- and temperature-dependent relaxation, involving multiple energy states in the reversal reduction processes upon the oxidation of ligands, reveals the coupling between core and ligand energy states.

Graphical abstract: Electronic coupling between ligand and core energy states in dithiolate-monothiolate stabilized Au clusters

Supplementary files

Article information

Article type
Paper
Submitted
08 May 2015
Accepted
17 Jun 2015
First published
17 Jun 2015

Phys. Chem. Chem. Phys., 2015,17, 19342-19349

Electronic coupling between ligand and core energy states in dithiolate-monothiolate stabilized Au clusters

T. Ahuja, D. Wang, Z. Tang, D. A. Robinson, J. W. Padelford and G. Wang, Phys. Chem. Chem. Phys., 2015, 17, 19342 DOI: 10.1039/C5CP02685G

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