Optical properties of coupled metallic nanorods for field-enhanced spectroscopy

被引:521
作者
Aizpurua, J
Bryant, GW
Richter, LJ
de Abajo, FJG
Kelley, BK
Mallouk, T
机构
[1] NIST, Gaithersburg, MD 20899 USA
[2] Donostia Int Phys Ctr, Donostia San Sebastian 20018, Spain
[3] Univ Basque Country, CSIC, Ctr Mixto, EHU, E-20080 San Sebastian, Spain
[4] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
关键词
D O I
10.1103/PhysRevB.71.235420
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The optical properties of coupled metallic nanorods are studied to investigate the use of coupled plasmonic structures in field-enhanced spectroscopies. Light scattering by coupled nanorods is calculated with the boundary element method, including retardation. The modes of coupled nanorod systems are calculated by the boundary charge method and discussed in terms of their symmetry. Similar scattering behavior for isolated nanorods and pairs of nanorods can mask the very different local responses that produce near-field enhancement. The response of isolated rods redshifts with increasing rod length because intrarod restoring forces are reduced. The near- and far-field responses increase monotonically with increasing rod length (increasing polarization along the rod). For coupled nanorods, coupling localizes charge at the gap between the rod ends and splits degenerate modes. The localized charge depolarizes the intrarod response and provides an additional redshift. Moreover, the near-field enhancement in the gap between the nanorods is dramatically increased by coupling-induced charge localization at the gap. For short nanorods, the near-field response in coupled systems is determined by the geometry of the rod ends that define the gap. For longer nanorods, the response in coupled systems is determined by the rod length. Changing the dimensions and geometry of the nanorods to modify the interrod coupling has a major effect on the local-field enhancement. The effects of the environment and the actual metallic material do not have as big an influence on the field enhancement.
引用
收藏
页数:13
相关论文
共 26 条
[1]   Nanowire-based molecular monolayer junctions: Synthesis, assembly, and electrical characterization [J].
Cai, LT ;
Skulason, H ;
Kushmerick, JG ;
Pollack, SK ;
Naciri, J ;
Shashidhar, R ;
Allara, DL ;
Mallouk, TE ;
Mayer, TS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (09) :2827-2832
[2]   LIFETIME OF AN EMITTING MOLECULE NEAR A PARTIALLY REFLECTING SURFACE [J].
CHANCE, RR ;
PROCK, A ;
SILBEY, R .
JOURNAL OF CHEMICAL PHYSICS, 1974, 60 (07) :2744-2748
[3]  
Chang R.K., 1982, Surface Enhanced Raman Scattering
[4]   Confined plasmons in metallic nanocavities [J].
Coyle, S ;
Netti, MC ;
Baumberg, JJ ;
Ghanem, MA ;
Birkin, PR ;
Bartlett, PN ;
Whittaker, DM .
PHYSICAL REVIEW LETTERS, 2001, 87 (17) :176801-176801
[5]   Gap-dependent optical coupling of single "Bowtie" nanoantennas resonant in the visible [J].
Fromm, DP ;
Sundaramurthy, A ;
Schuck, PJ ;
Kino, G ;
Moerner, WE .
NANO LETTERS, 2004, 4 (05) :957-961
[6]   Resonant field enhancements from metal nanoparticle arrays [J].
Genov, DA ;
Sarychev, AK ;
Shalaev, VM ;
Wei, A .
NANO LETTERS, 2004, 4 (01) :153-158
[7]   ELECTROMAGNETIC THEORY OF ENHANCED RAMAN-SCATTERING BY MOLECULES ADSORBED ON ROUGH SURFACES [J].
GERSTEN, J ;
NITZAN, A .
JOURNAL OF CHEMICAL PHYSICS, 1980, 73 (07) :3023-3037
[8]   High-resolution near-field Raman microscopy of single-walled carbon nanotubes -: art. no. 095503 [J].
Hartschuh, A ;
Sánchez, EJ ;
Xie, XS ;
Novotny, L .
PHYSICAL REVIEW LETTERS, 2003, 90 (09) :4
[9]   Nanosphere lithography: Surface plasmon resonance spectrum of a periodic array of silver nanoparticles by ultraviolet-visible extinction spectroscopy and electrodynamic modeling [J].
Jensen, TR ;
Schatz, GC ;
Van Duyne, RP .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (13) :2394-2401
[10]   Single molecule Raman spectroscopy at the junctions of large Ag nanocrystals [J].
Jiang, J ;
Bosnick, K ;
Maillard, M ;
Brus, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (37) :9964-9972