通过雕刻DNA染料支架控制NPoM腔内单发射极强耦合

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Sara Rocchetti, Thieme Schmidt, Ulrich F. Keyser, Jeremy J. Baumberg
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引用次数: 0

摘要

光和单分子的相干耦合使下一代室温纳米光子器件的发展成为可能。等离子体可以实现小模体积光场,但在等离子体腔内放置定向发射体分子以在发射中获得一致的强耦合仍然存在挑战。利用DNA折纸技术,单发射器分子可以在金纳米粒子和金镜子之间形成的亚纳米空腔内排列。我们观察到围绕菁染料的DNA支架结构的精确设计改变了其与纳米腔的发射偶联方式,以及Au原子对光学力的响应方式,从而导致主导等离子体模式的连续调谐。通过这一点,我们展示了三种不同染料之间的强耦合和等离子体共振如何总是导致低能发光,而不依赖于失谐。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Controlling Single-Emitter Strong Coupling by Sculpting DNA Dye Scaffolds in NPoM Cavities

Controlling Single-Emitter Strong Coupling by Sculpting DNA Dye Scaffolds in NPoM Cavities
Coherent coupling of light and single molecules enables the development of next-generation room temperature-capable nanophotonic devices. Small mode-volume optical fields can be achieved with plasmonics, but challenges remain in placing oriented emitter molecules inside plasmonic cavities to access strong coupling consistently in emission. Using DNA origami, single-emitter molecules can be aligned inside subnanometric cavities created between a gold nanoparticle and a gold mirror. We observe that the exact design of DNA scaffolding architecture surrounding a cyanine dye changes how its emission couples to the nanocavity, as well as how Au atoms respond to the optical forces, leading to continuous tuning of the dominant plasmonic mode. Through this, we show how strong coupling between three different dyes and the plasmon resonance always leads to low-energy light emission, independent of detuning.
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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