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各向异性对纳米颗粒二聚体等离子体响应的影响。

Anisotropy Effects on the Plasmonic Response of Nanoparticle Dimers.

作者信息

Varas Alejandro, García-González Pablo, García-Vidal F J, Rubio Angel

机构信息

†Nano-Bio Spectroscopy group, Universidad del País Vasco UPV/EHU, CFM CSIC-UPV/EHU-MPC and DIPC, Avenida de Tolosa 72, E-20018 Donostia/San Sebastián, Spain.

‡ETSF Scientific Development Centre, Avenida de Tolosa 72, E-20018 Donostia/San Sebastián, Spain.

出版信息

J Phys Chem Lett. 2015 May 21;6(10):1891-8. doi: 10.1021/acs.jpclett.5b00573. Epub 2015 May 6.

Abstract

We present an ab initio study of the anisotropy and atomic relaxation effects on the optical properties of nanoparticle dimers. Special emphasis is placed on the hybridization process of localized surface plasmons, plasmon-mediated photoinduced currents, and electric-field enhancement in the dimer junction. We show that there is a critical range of separations between the clusters (0.1-0.5 nm) in which the detailed atomic structure in the junction and the relative orientation of the nanoparticles have to be considered to obtain quantitative predictions for realistic nanoplasmonic devices. It is worth noting that this regime is characterized by the emergence of electron tunneling as a response to the driven electromagnetic field. The orientation of the particles not only modifies the attainable electric field enhancement but can lead to qualitative changes in the optical absorption spectrum of the system.

摘要

我们对纳米粒子二聚体光学性质的各向异性和原子弛豫效应进行了从头算研究。特别强调了局域表面等离子体的杂化过程、等离子体介导的光致电流以及二聚体结中的电场增强。我们表明,团簇之间存在一个临界间距范围(0.1 - 0.5纳米),在这个范围内,为了对实际的纳米等离子体器件获得定量预测,必须考虑结中的详细原子结构和纳米粒子的相对取向。值得注意的是,这一区域的特征是作为对驱动电磁场的响应出现了电子隧穿。粒子的取向不仅会改变可实现的电场增强,还可能导致系统光学吸收光谱的定性变化。

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