...
首页> 外文期刊>AIP Advances >Resonance coupling in plasmonic nanomatryoshka homo- and heterodimers
【24h】

Resonance coupling in plasmonic nanomatryoshka homo- and heterodimers

机译:等离子体纳米matryoshka同二聚体和异二聚体的共振耦合

获取原文

摘要

Here, we examine the electromagnetic (EM) energy coupling and hybridization of plasmon resonances between closely spaced concentric nanoshells known as “nanomatryoshka” (NM) units in symmetric and antisymmetric compositions using the Finite Difference Time Domain (FDTD) analysis. Utilizing plasmon hybridization model, we calculated the energy level diagrams and verified that, in the symmetric dimer (in-phase mode in a homodimer), plasmonic bonding modes are dominant and tunable within the considered bandwidth. In contrast, in the antisymmetric dimer (out-of-phase mode in a heterodimer), due to the lack of the geometrical symmetry, new antibonding modes appear in the extinction profile, and this condition gives rise to repeal of dipolar field coupling. We also studied the extinction spectra and positions of the antibonding and bonding modes excited due to the energy coupling between silver and gold NM units in a heterodimer structure. Our analysis suggest abnormal shifts in the higher energy modes. We propose a method to analyze the behavior of multilayer concentric nanoshell particles in an antisymmetric orientation employing full dielectric function calculations and the Drude model based on interband transitions in metallic components. This study provides a method to predict the behavior of the higher energy plasmon resonant modes in entirely antisymmetric structures such as compositional heterodimers.
机译:在这里,我们使用有限时域时域分析(FDTD)分析了对称和反对称成分中紧密间隔的同心纳米壳(称为“ nanomatryoshka”(NM)单元)之间的等离子共振的电磁(EM)能量耦合和杂交。利用等离激元杂交模型,我们计算了能级图,并验证了在对称二聚体(均二聚体中的同相模式)中,等离激元键合模式在考虑的带宽内是主要的且可调谐的。相反,在反对称二聚体(异二聚体中的异相模式)中,由于缺乏几何对称性,消光曲线中出现了新的反键模式,这种情况导致了偶极场耦合的废除。我们还研究了异二聚体结构中由于银和金NM单元之间的能量耦合而激发的反键和键合模式的消光光谱和位置。我们的分析表明,高能模式下的异常转变。我们提出了一种使用全介电函数计算和基于金属成分带间跃迁的Drude模型来分析多层同心纳米壳颗粒在反对称取向下行为的方法。这项研究提供了一种预测完全反对称结构(例如组成异二聚体)中高能等离子体共振模式行为的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号