| Literature DB >> 26276184 |
Jakub Szlachetko1,2, Jacinto Sá1,3, Maarten Nachtegaal1, Urs Hartfelder1,4, Jean-Claude Dousse5, Joanna Hoszowska5, Daniel Luis Abreu Fernandes6, Hongqing Shi7, Catherine Stampfl7.
Abstract
Chemical reactions are always associated with electronic structure changes of the involved chemical species. Determining the electronic configuration of an atom allows probing its chemical state and gives understanding of the reaction pathways. However, often the reactions are too complex and too fast to be measured at in situ conditions due to slow and/or insensitive experimental techniques. A short-lived Au2O compound has been detected for the first time under in situ conditions during the temperature-programmed reduction of Au2O3. A time-resolved resonant inelastic X-ray scattering experiment (RIXS) allowed the determination of changes in the Au electronic structure, enabling a better understanding of the reaction mechanism of Au(III) reduction. On the basis of time-resolved RIXS data analysis combined with genetic algorithm methodology, we determined the electronic structure of the metastable Au2O intermediate species. The data analysis showed a notably larger value for the lattice constant of the intermediate Au as compared to the theoretical predictions. With support of DFT calculations, we found that such a structure may indeed be formed and that the expanded lattice constant is due to the termination of Au2O on the Au2O3 structure.Entities:
Keywords: DFT calculations; X-ray spectroscopy; short-lived Au2O intermediate; time-resolved RIXS
Year: 2013 PMID: 26276184 DOI: 10.1021/jz402309s
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475