Disorder and cluster formation during ion irradiation of Au nanoparticles in SiO2

被引:48
作者
Kluth, P.
Johannessen, B.
Foran, G. J.
Cookson, D. J.
Kluth, S. M. [1 ]
Ridgway, M. C.
机构
[1] Australian Natl Univ, Dept Elect Mat Engn, Canberra, ACT 0200, Australia
[2] Australian Nucl Sci & Technol Org, Menai, NSW, Australia
[3] Australian Synchrotron Res Program, Argonne, IL 60439 USA
关键词
X-RAY-ABSORPTION; FINE-STRUCTURE; THIN SIO2; NANOCRYSTALS; IMPLANTATION; EXAFS; GOLD; NANOSTRUCTURES; AMORPHIZATION; GROWTH;
D O I
10.1103/PhysRevB.74.014202
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Au nanoparticles (NPs) have been formed by ion beam synthesis in 600 nm thin SiO2. Subsequently the NPs were irradiated with 2.3 MeV Sn ions at liquid nitrogen temperature. Samples were analyzed using extended x-ray absorption fine structure (EXAFS) spectroscopy and small angle x-ray scattering (SAXS) as a function of Sn irradiation dose. Transmission electron microscopy shows that the NPs largely retain their spherical shape upon irradiation. However, we observe a reduction in average NP size and a concomitant significant narrowing of the size distribution with increasing irradiation dose as consistent with inverse Ostwald ripening. At lower irradiation doses, significant structural disorder is apparent with an effective bond length expansion as consistent with amorphous material. At higher irradiation doses, EXAFS measurements indicate dissolution of a significant fraction of Au from the NPs into the SiO2 matrix (as monomers) and the formation of small Au clusters (dimers, trimers, etc.). We estimate the volume fraction of such monomers/clusters. Ion irradiation thus yields disordering then dissolution of Au NPs. (c) 2006 American Institute of Physics.
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页数:9
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