Structural electronic study via XPS and TEM of subnanometric gold particles protected by calixarenes for silicon surface anchoring

被引:9
作者
Boccia, Alice [1 ]
Zanoni, Robertino [1 ]
Arduini, Arturo [2 ,3 ]
Pescatori, Luca [2 ,3 ]
Secchi, Andrea [2 ,3 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
[2] Univ Parma, Dipartimento Chim Organ & Ind, I-43124 Parma, Italy
[3] Univ Parma, Unita INSTM Sez 4 UdR Parma, I-43124 Parma, Italy
关键词
gold nanoparticles; subnanometric; calixarenes; XPS; ENHANCED RAMAN-SCATTERING; ADSORPTION CHARACTERISTICS; SUPRAMOLECULAR CHEMISTRY; LIGAND-EXCHANGE; SILVER SURFACES; NANOPARTICLES; THIOL; MONOLAYERS; MOLECULES; SI(100);
D O I
10.1002/sia.4842
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of differently sized gold nanoparticles stabilized by bidentate calixarene ligands, prepared by the BrustSchiffrin two-phase synthesis, were characterized by XPS, in combination with TEM. The experimental data show that the particular conditions in the synthesis reaction allow to obtain subnanometric gold nanoparticles. Such nanoparticles with controlled and reduced size are the best candidate for anchoring on a Si surface, through specific and reversible supramolecular interactions, in view of the development of new hybrid nanomaterials. XPS measurements allow to separate the Au atoms in two subsets, on the basis of their clearly distinct Au 4f binding energy: central and surface atoms bound to S. The S 2p spectra present a main component due to thiolateAu bond, compatible with the structural staple motif reported in the literature. Because very small nanoparticles have a larger percentage of surface atoms, the experimental S/Au and AuS/Aucentral ratios are an indirect evaluation of the cluster nuclearity, likely to be assigned to Au11 or Au13, both compatible with the observed diameters. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:1086 / 1090
页数:5
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