Alkanethiolate Gold Cluster Molecules with Core Diameters from 1.5 to 5.2 nm:  Core and Monolayer Properties as a Function of Core Size

Michael J. Hostetler(Iowa State University), Julia E. Wingate(Iowa State University), Chuan‐Jian Zhong(Iowa State University), Jay E. Harris(Oak Ridge National Laboratory), Richard W. Vachet(Oak Ridge National Laboratory), Michael R. Clark(Oak Ridge Institute for Science and Education), J. D. Londono(Iowa State University), Stephen J. Green(Oak Ridge Institute for Science and Education), Jennifer J. Stokes(Oak Ridge National Laboratory), G. D. Wígnall(Oak Ridge Institute for Science and Education), Gary L. Glish(Oak Ridge Institute for Science and Education), Marc D. Porter(Oak Ridge Institute for Science and Education), Neal D. Evans(Iowa State University), Royce W. Murray(Oak Ridge National Laboratory)
Langmuir
January 1, 1998
Cited by 1,819

Abstract

The mean size of the gold (Au) core in the synthesis of dodecanethiolate-stabilized Au cluster compounds can be finely adjusted by choice of the Au:dodecanethiolate ratio and the temperature and rate at which the reduction is conducted. The Au clusters have been examined with a large number of independent analytical tools, producing a remarkably consistent picture of these materials. Average cluster and core dimensions, as ascertained by 1H NMR line broadening, high-resolution transmission electron microscopy, small-angle X-ray scattering, and thermogravimetric analysis, vary between diameters of 1.5 and 5.2 nm (∼110−4800 Au atoms/core). The electronic properties of the Au core were examined by UV/vis and X-ray photoelectron spectroscopy; the core appears to remain largely metallic in nature even at the smallest core sizes examined. The alkanethiolate monolayer stabilizing the Au core ranges with core size from ∼53 to nearly 520 ligands/core, and was probed by Fourier transform infrared spectroscopy, differential scanning calorimetry, contact-angle measurements, and thermal desorption mass spectrometry. The dodecanethiolate monolayer on small and large core clusters exhibits discernable differences; the line dividing “3-dimensional” monolayers and those resembling self-assembled monolayers on flat Au (2-dimensional monolayers) occurs at clusters with ∼4.4 nm core diameters.


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