Rational Assembly of Optoplasmonic Hetero-nanoparticle Arrays with Tunable Photonic-Plasmonic Resonances

被引:38
作者
Hong, Yan [1 ,2 ]
Qiu, Yue [1 ,2 ]
Chen, Tianhong [1 ,2 ]
Reinhard, Bjoern M. [1 ,2 ]
机构
[1] Boston Univ, Dept Chem, Boston, MA 02215 USA
[2] Boston Univ, Photon Ctr, Boston, MA 02215 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
nanoparticle arrays; hybrid materials; metamaterials; photonic crystals; gold; titanium dioxide; plasmonics; ENHANCED RAMAN-SPECTROSCOPY; METAL NANOPARTICLE; CLUSTER ARRAYS; BAND-GAPS; GOLD; SCATTERING; CRYSTALS; SERS; NANOSTRUCTURES; INTEGRATION;
D O I
10.1002/adfm.201301837
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metallic and dielectric nanoparticles (NPs) have synergistic electromagnetic properties but their positioning into morphologically defined hybrid arrays with novel optical properties still poses significant challenges. A template-guided self-assembly strategy is introduced for the positioning of metallic and dielectric NPs at pre-defined lattice sites. The chemical assembly approach facilitates the fabrication of clusters of metallic NPs with interparticle separations of only a few nanometers in a landscape of dielectric NPs positioned hundreds of nanometers apart. This approach is used to generate two-dimensional interdigitated arrays of 250 nm diameter TiO2 NPs and clusters of electromagnetically strongly coupled 60 nm Au NPs. The morphology-dependent near- and far-field responses of the resulting multiscale optoplasmonic arrays are analyzed in detail. Elastic and inelastic scattering spectroscopy in combination with electromagnetic simulations reveal that optoplasmonic arrays sustain delocalized photonic-plasmonic modes that achieve a cascaded E-field enhancement in the gap junctions of the Au NP clusters and simultaneously increase the E-field intensity throughout the entire array.
引用
收藏
页码:739 / 746
页数:8
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