Medium-sized Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂ nanoclusters with distinct gold-kernel structures and spectroscopic features

Authors

• Wen Wu Xu, Shanghai Institute of Applied Physics
• Yadong Li, University of Chinese Academy of Sciences
• Yi Gao, Shanghai Institute of Applied PhysicsFollow
• Xiao Cheng Zeng, University of Nebraska-LincolnFollow

Document Type

Article

Date of this Version

2016

Citation

Nanoscale, 2016, 8, pp. 1299–1304. DOI: 10.1039/c5nr07810e

Comments

Copyright © 2016 The Royal Society of Chemistry. Used by permission.

Abstract

We have analyzed the structures of two medium-sized thiolateprotected gold nanoparticles (RS-AuNPs) Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂ and identified the distinct structural features in their Au kernels [Sci. Adv., 2015, 1, e1500425]. We find that both Au kernels of the Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂ nanoclusters can be classified as interpenetrating cuboctahedra. Simulated X-ray diffraction patterns of the RS-AuNPs with the cuboctahedral kernel are collected and then compared with the X-ray diffraction patterns of the RS-AuNPs of two other prevailing Au-kernels identified from previous experiments, namely the Ino-decahedral kernel and icosahedral kernel. The distinct X-ray diffraction patterns of RS-AuNPs with the three different types of Au-kernels can be utilized as signature features for future studies of structures of RS-AuNPs. Moreover, the simulated UV/Vis absorption spectra and Kohn–Sham orbital energy-level diagrams are obtained for the Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂, on the basis of time-dependent density functional theory computation. The extrapolated optical bandedges of Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂ are 1.1 eV and 1.25 eV, respectively. The feature peaks in the UV/Vis absorption spectra of the two clusters can be attributed to the d → sp electronic transition. Lastly, the catalytic activities of the Au₄₀(SR)₂₄ and Au₅₂(SR)₃₂ are examined using CO oxidation as a probe. Both medium-sized thiolate-protected gold clusters can serve as effective stand-alone nanocatalysts.