Ion beam surface nanostructuring of noble metal films with localized surface plasmon excitation

被引:6
|
作者
Meng, Xuan [1 ,2 ]
Shibayama, Tamaki [1 ]
Yu, Ruixuan [1 ]
Ishioka, Junya [1 ]
Watanabe, Seiichi [1 ]
机构
[1] Hokkaido Univ, Fac Engn, Ctr Adv Res Energy & Mat, Sapporo, Hokkaido 0608628, Japan
[2] Lanzhou Univ, Sch Nucl Sci & Technol, Lanzhou 730000, Gansu, Peoples R China
来源
基金
日本学术振兴会;
关键词
Ion induced dewetting; Ion induced surface nanostructuring; Thermal spike model; Viscous flow; Surface enhanced Raman Scattering (SERS); Localized surface plasmon (LSP) excitation; FIELD ENHANCEMENT; FABRICATION; SCATTERING; DAMAGE; LIGHT; SIO2; FLOW;
D O I
10.1016/j.cossms.2017.01.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Noble metal nanoparticles strongly adhered to dielectric matrices have been extensively studied because of their potential applications in plasmonic devices based on tunable localized surface plasmon (LSP) excitation. Compared with conventional synthesis methods, the noble metal nanoparticles formed by ion-beam irradiation draw significant interest in recent years because a single layer dispersion of nanoparticles strongly bonded on the dielectric substrate can be obtained. In this paper, important phenomena related to ion-beam surface nanostructuring including ion-induced reshaping of metal nanoparticles, ion-induced core-satellite structure formation, and ion-induced burrowing of these nanoparticles are discussed, with their individual effects on LSP excitation. Consequently, ion-induced surface nanostructuring of Ag-Au bimetallic films on amorphous silica glass and sapphire with tunable LSP excitation are presented. In addition, theoretical studies of far-field and near-field optical properties of these nanoparticles under ion irradiation are introduced, and the enhanced localized electric field (hot spot) is interpreted. Finally, the futures and challenges of the emerging plasmonic applications based on tunable LSP excitations in bio-sensing and surface enhanced Raman spectroscopy (SERS) are presented. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:177 / 188
页数:12
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