Plasmon Polaritons in Disordered Nanoparticle Assemblies

IF 6.7 1区 物理与天体物理 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Tanay Paul, , , Allison M. Green, , , Delia J. Milliron*, , and , Thomas M. Truskett*, 
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Abstract

Multilayer assemblies of metal nanoparticles can act as photonic structures, where collective plasmon resonances hybridize with cavity modes to create plasmon-polariton states. For sufficiently strong coupling, plasmon polaritons qualitatively alter the optical properties of light-matter systems, with applications ranging from sensing to solar energy. However, results from experimental studies have raised questions about the role of nanoparticle structural disorder in plasmon-polariton formation and the strength of light-matter coupling in plasmonic assemblies. Understanding how disorder affects optical properties has practical implications since methods for assembling low-defect nanoparticle superlattices are slow and scale poorly. Modeling realistic disorder requires large system sizes, which is challenging using conventional electromagnetic simulations. We employ Brownian dynamics simulations to construct large-scale nanoparticle multilayers with controlled structural order. We investigate their far- and near-field optical response using a superposition T-matrix method with two-dimensional periodic boundary conditions. We find that while structural disorder broadens the polaritonic stop band and the near-field hot-spot distribution, the polariton dispersion and coupling strength remain unaltered. To understand the effects of nanoparticle composition, we consider assemblies with Drude model particles mimicking gold or tin-doped indium oxide (ITO) nanocrystals. Assemblies of ITO nanocrystals, which have lower carrier concentrations, exhibit ultrastrong coupling, in contrast to Au nanoparticle multilayers that display deep strong coupling. Finally, we demonstrate that while computationally efficient mutual polarization method calculations employing the quasistatic approximation modestly overestimate the strength of collective plasmon coupling in these assemblies, they reproduce the polariton dispersion relations determined by electrodynamic simulations.

Abstract Image

无序纳米粒子组合中的等离子激元极化子
多层金属纳米粒子组件可以作为光子结构,其中集体等离子体共振与腔模式杂交产生等离子体偏振态。对于足够强的耦合,等离子激元极化子定性地改变光-物质系统的光学性质,应用范围从传感到太阳能。然而,实验研究的结果提出了关于纳米粒子结构无序在等离子体-极化子形成中的作用以及等离子体组装中光-物质耦合强度的问题。了解无序如何影响光学性质具有实际意义,因为组装低缺陷纳米粒子超晶格的方法速度慢且规模小。模拟真实的混乱需要大的系统尺寸,这是传统电磁模拟的挑战。我们采用布朗动力学模拟来构建具有可控结构顺序的大尺度纳米颗粒多层膜。我们用二维周期边界条件下的叠加t矩阵方法研究了它们的远场和近场光学响应。我们发现,虽然结构失序拓宽了极化子的禁带和近场热点分布,但极化子色散和耦合强度保持不变。为了理解纳米颗粒组成的影响,我们考虑了模拟金或锡掺杂氧化铟(ITO)纳米晶体的德鲁德模型颗粒的组装。ITO纳米晶体具有较低的载流子浓度,表现出超强耦合,而Au纳米颗粒多层则表现出深度强耦合。最后,我们证明,虽然采用准静态近似的计算效率互极化方法计算适度高估了这些组件中集体等离子体耦合的强度,但它们再现了由电动力学模拟确定的极化色散关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Photonics
ACS Photonics NANOSCIENCE & NANOTECHNOLOGY-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
11.90
自引率
5.70%
发文量
438
审稿时长
2.3 months
期刊介绍: Published as soon as accepted and summarized in monthly issues, ACS Photonics will publish Research Articles, Letters, Perspectives, and Reviews, to encompass the full scope of published research in this field.
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