等离子体子
激子
材料科学
联轴节(管道)
散射
光电子学
表面等离子共振
纳米颗粒
纳米结构
纳米技术
光学
凝聚态物理
物理
冶金
作者
Eva-Maria Roller,Christos Argyropoulos,Alexander Högele,Tim Liedl,Mauricio Pilo‐Pais
出处
期刊:Nano Letters
[American Chemical Society]
日期:2016-08-17
卷期号:16 (9): 5962-5966
被引量:100
标识
DOI:10.1021/acs.nanolett.6b03015
摘要
Coherent energy exchange between plasmons and excitons is a phenomenon that arises in the strong coupling regime resulting in distinct hybrid states. The DNA-origami technique provides an ideal framework to custom-tune plasmon-exciton nanostructures. By employing this well controlled self-assembly process, we realized hybrid states by precisely positioning metallic nanoparticles in a defined spatial arrangement with fixed nanometer-sized interparticle spacing. Varying the nanoparticle diameter between 30 nm and 60 nm while keeping their separation distance constant allowed us to precisely adjust the plasmon resonance of the structure to accurately match the energy frequency of a J-aggregate exciton. With this system we obtained strong plasmon-exciton coupling and studied far-field scattering at the single-structure level. The individual structures displayed normal mode splitting up to 170 meV. The plasmon tunability and the strong field confinement attained with nanodimers on DNA-origami renders an ideal tool to bottom-up assembly plasmon-exciton systems operating at room temperature.
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