PNNL

Abstract

The Au-O and Au-S interactions are essential in nanogold catalysis and nanotechnology, for which mono-gold oxide and sulfide clusters serve as the simplest molecular models. We report a combined photoelectron spectroscopy and ab initio study on AuO- and AuO2- and their valent isoelectronic AuS- and AuS2- species to probe their electronic structure and to elucidate the Au-O and Au-S chemical bonding. Vibrationally-resolved spectra were obtained at different photon energies, providing a wealth of electronic structure information for each species. Similar spectra were observed for AuO- and AuS- and for the linear OAuO- and SAuS- species. A bent isomer was also observed as Au(S2)- in the AuS2- spectra, whereas a similar Au(O2)- complex was not observed in the case of AuO2-. High-level ab initio calculations were conducted to aid spectral assignments and provide insight into the chemical bonding in the AuX- and AuX2- molecules. Excellent agreement is achieved between the calculated electronic excitations and the observed spectra. Configuration interactions and spin-orbit couplings were shown to be important and were necessary to achieve good agreement between theory and experiment. Strong covalent bonding was found in both the AuX- and the XAuX- species with multiple bonding characters. While Au(S2)- was found to be a low-lying isomer with a significant binding energy, Au(O2)- was shown to be unbound consistent with the experimental observation. The latter is understood in the context of the size-dependent reactivity of Aun- clusters with O2.