posted on 2018-10-03, 17:45authored byDavid
J. Morris, Rui Yang, Tatsuya Higaki, Matthew J. Ward, Rongchao Jin, Peng Zhang
Diversity
of core geometry for thiolate-protected gold nanoclusters
(AuSR NCs) is a fascinating phenomenon, and thus, understanding the
core geometry effect on the bonding properties of AuSR NCs is of significant
interest. Herein, we report extended X-ray absorption fine structure
(EXAFS) studies on the bonding properties of hexagonal-close-packed
(HCP) Au30(SR)18 NCs. To illustrate the core
geometry effects, Au25(SR)18 with icosahedral
core and Au36(SR)24 with face-centered-cubic
(FCC) core are selected for a comparative study. Temperature-dependent
EXAFS experiments show considerable difference in the thermally induced
core contraction/expansion behavior of the NCs. The HCP Au30(SR)18 exhibits a significant negative thermal expansion
(NTE) of 3% for the metal core, whereas the BCC Au36(SR)24 shows only a 0.5% NTE. In contrast, the icosahedral Au25(SR)18 shows a positive thermal expansion. These
experimental findings can be accounted for by considering the metal/molecule-like
behavior and the defects of metallic bonds of the NC cores, and highlight
the important role of the core structure on the bonding properties
of AuSR NCs. Comparison of solid and solution phase Au30 EXAFS results shows no change in bond distance, in contrast to the
Au25 NCs which show a decrease in size of the metal core
when it changed from solid to liquid. These results arise from the
difference in thiolate ligands present in the two NCs.