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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Plasmon coupling in nanorod assemblies: Optical absorption, discrete dipole approximation simulation, and exciton-coupling model
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Plasmon coupling in nanorod assemblies: Optical absorption, discrete dipole approximation simulation, and exciton-coupling model

机译:纳米棒组件中的等离激元耦合:光吸收,离散偶极近似仿真和激子耦合模型

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摘要

The shape anisotropy of nanorods gives rise to two distinct orientational modes by which nanorods can be assembled, i.e., end-to-end and side-by-side, analogous to the well-known H and J aggregation in organic chromophores. Optical absorption spectra of gold nanorods have earlier been observed to show a red-shift of the longitudinal plasmon band for the end-to-end linkage of nanorods, resulting from the plasmon coupling between neighboring nanoparticles, similar to the assembly of gold nanospheres. We observe, however, that side-by-side linkage of nanorods in solution shows a blue-shift of the longitudinal plasmon band and a red-shift of the transverse plasmon band. Optical spectra calculated using the discrete dipole approximation method were used to simulate plasmon coupling in assembled nanorod dimers. The longitudinal plasmon band is found to shift to lower energies for end-to-end assembly, but a shift to higher energies is found for the side-by-side orientation, in agreement with the optical absorption experiments. The strength of plasmon coupling was seen to increase with decreasing internanorod distance and an increase in the number of interacting nanorods. For both side-by-side and end-to-end assemblies, the strength of the longitudinal plasmon coupling increases with increasing nanorod aspect ratio as a result of the increasing dipole moment of the longitudinal plasmon. For both the side-by-side and end-to-end orientation, the simulation of a dimer of nanorods having dissimilar aspect ratios showed a longitudinal plasmon resonance with both a blue-shifted and a red-shifted component, as a result of symmetry breaking. A similar result is observed for a pair of similar aspect ratio nanorods assembled in a nonparallel orientation. The internanorod plasmon coupling scheme concluded from the experimental results and simulations is found to be qualitatively consistent with the molecular exciton coupling theory, which has been used to describe the optical spectra of H and J aggregates of organic molecules. The coupled nanorod plasmons are also suggested to be electromagnetic analogues of molecular orbitals. Investigation of the plasmon coupling in assembled nanorods is important for the characterization of optical excitations and plasmon propagation in these nanostructures. The surface plasmon resonance shift resulting from nanorod assembly also offers a promising alternative for analyte-sensing assays.
机译:纳米棒的形状各向异性产生了可以组装纳米棒的两种不同的取向模式,即端对端和并排地组装,类似于有机发色团中众所周知的H和J聚集。较早前已观察到金纳米棒的光吸收光谱显示纳米棒的端对端连接的纵向等离激元带发生红移,这是由相邻纳米颗粒之间的等离激元耦合引起的,类似于金纳米球的组装。但是,我们观察到溶液中纳米棒的并排连接显示了纵向等离激元带的蓝移和横向等离激元带的红移。使用离散偶极近似法计算的光谱用于模拟组装的纳米棒二聚体中的等离激元耦合。发现纵向等离激元带对于端到端组装转移到较低的能量,但是对于并排取向,发现转移到较高的能量,这与光吸收实验一致。等离子体激元耦合的强度被认为是随着纳米节距的减少和相互作用的纳米棒数量的增加而增加。对于并排和端对端组件,由于纵向等离激元的偶极矩增加,纵向等离激元耦合的强度随着纳米棒长宽比的增加而增加。对于并列和端对端方向,具有对称长宽比的纳米棒的二聚体的模拟显示,由于对称性,纵向等离子体激元共振同时具有蓝移和红移分量打破。对于以非平行取向组装的一对相似的长宽比纳米棒,观察到相似的结果。从实验结果和模拟得出的纳米粒子间等离子体激元耦合方案与分子激子耦合理论在质量上是一致的,分子激子耦合理论已被用于描述有机分子的H和J聚集体的光谱。还建议偶合的纳米棒等离子体激元是分子轨道的电磁类似物。研究组装纳米棒中的等离激元耦合对于表征这些纳米结构中的光激发和等离激元传播非常重要。由纳米棒组装产生的表面等离振子共振位移也为分析物传感测定提供了有希望的替代方法。

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