| Literature DB >> 31702861 |
Tatsuya Higaki1, Chong Liu2, David J Morris3, Guiying He4, Tian-Yi Luo2, Matthew Y Sfeir4,5,6, Peng Zhang3, Nathaniel L Rosi2, Rongchao Jin1.
Abstract
The synthesis and structure of atomically precise Au130-x Agx (average x=98) alloy nanoclusters protected by 55 ligands of 4-tert-butylbenzenethiolate are reported. This large alloy structure has a decahedral M54 (M=Au/Ag) core. The Au atoms are localized in the truncated Marks decahedron. In the core, a drum of Ag-rich sites is found, which is enclosed by a Marks decahedral cage of Au-rich sites. The surface is exclusively Ag-SR; X-ray absorption fine structure analysis supports the absence of Au-S bonds. The optical absorption spectrum shows a strong peak at 523 nm, seemingly a plasmon peak, but fs spectroscopic analysis indicates its non-plasmon nature. The non-metallicity of the Au130-x Agx nanocluster has set up a benchmark to study the transition to metallic state in the size evolution of bimetallic nanoclusters. The localized Au/Ag binary architecture in such a large alloy nanocluster provides atomic-level insights into the Au-Ag bonds in bimetallic nanoclusters.Entities:
Keywords: X-ray spectroscopy; alloys; crystal structure; electron dynamics; nanoclusters
Year: 2019 PMID: 31702861 DOI: 10.1002/anie.201908694
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336