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基于纳米粒子的光学物质阵列中的电动力学干涉和诱导极化

Electrodynamic Interference and Induced Polarization in Nanoparticle-Based Optical Matter Arrays.

作者信息

Peterson Curtis, Parker John, Valenton Emmanuel, Yifat Yuval, Chen Shiqi, Rice Stuart A, Scherer Norbert F

机构信息

Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, United States.

James Franck Institute, The University of Chicago, Chicago, Illinois 60637, United States.

出版信息

J Phys Chem C Nanomater Interfaces. 2024 Apr 26;128(18):7560-7571. doi: 10.1021/acs.jpcc.3c08459. eCollection 2024 May 9.

Abstract

Optical matter (OM) arrays are self-organizing, ordered arrangements of nanometer- to micrometer-size particles, where interparticle forces are mediated by incident and scattered coherent light. The structures that form and their dynamics depend on the properties (e.g., material, size) of the constituent particles, as well as the incident and scattered light. While significant progress has been made toward understanding how the OM arrays are affected by the phase, polarization, and intensity profile of the incident light, the polarization induced in the particles and the light scattered by OM arrays have received less attention. In this paper, we establish the roles of electrodynamic interference, many-body coupling, and induced-polarization concomitant with the coherent light scattered by OM arrays. Experiments and simulations together demonstrate that the spatial profile and directionality of coherent light scattered by OM arrays in the far field are primarily influenced by interference, while electrodynamic coupling (interactions) and the associated polarization induced in the nanoparticle constituents have a quantitative wavelength-dependent effect on the total amount of light scattered by the arrays. Furthermore, the electrodynamic coupling in silver nanoparticle OM arrays is significantly enhanced by constructive interference and increases superextensively with the number of particles in the array. Particle size, and hence polarizability, also has a significant effect on the strength of the coupling. Finally, we simulate larger hexagonal OM arrays of Ag nanoparticles to demonstrate that the electrodynamic coupling and scattering enhancement observed in small OM arrays develop into surface lattice resonances observed in the infinite array limit. Our work provides insights for designing OM arrays to tune many-body forces and the coherent light that they scatter.

摘要

光学物质(OM)阵列是纳米级至微米级粒子的自组织有序排列,其中粒子间力由入射和散射的相干光介导。形成的结构及其动力学取决于组成粒子的性质(例如材料、尺寸),以及入射光和散射光。虽然在理解入射光的相位、偏振和强度分布如何影响OM阵列方面已经取得了重大进展,但粒子中诱导的偏振以及OM阵列散射的光受到的关注较少。在本文中,我们确定了与OM阵列散射的相干光相关的电动力学干涉、多体耦合和诱导偏振的作用。实验和模拟共同表明,远场中OM阵列散射的相干光的空间分布和方向性主要受干涉影响,而电动力学耦合(相互作用)以及纳米粒子成分中相关的诱导偏振对阵列散射的总光量有定量的波长依赖性影响。此外,银纳米粒子OM阵列中的电动力学耦合通过相长干涉得到显著增强,并随着阵列中粒子数量的增加而超广泛增加。粒径以及由此产生的极化率,也对耦合强度有显著影响。最后,我们模拟了更大的银纳米粒子六边形OM阵列,以证明在小OM阵列中观察到的电动力学耦合和散射增强在无限阵列极限下发展为表面晶格共振。我们的工作为设计OM阵列以调节多体力和它们散射的相干光提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59f/11089571/3559a644da90/jp3c08459_0001.jpg

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