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通过分子跨键隧穿双势垒隧道结实现表面等离激元极化激元的定向激发

Directional Excitation of Surface Plasmon Polaritons via Molecular Through-Bond Tunneling across Double-Barrier Tunnel Junctions.

作者信息

Du Wei, Han Yingmei, Hu Hongting, Chu Hong-Son, Annadata Harshini V, Wang Tao, Tomczak Nikodem, Nijhuis Christian A

机构信息

Department of Chemistry , National University of Singapore , 3 Science Drive 3 , 117543 Singapore.

Department of Electronics and Photonics, Institute of High Performance Computing , A*STAR (Agency for Science, Technology and Research) , 1 Fusionopolis Way, #16-16 Connexis , 138632 Singapore.

出版信息

Nano Lett. 2019 Jul 10;19(7):4634-4640. doi: 10.1021/acs.nanolett.9b01665. Epub 2019 Jun 17.

DOI:10.1021/acs.nanolett.9b01665
PMID:31184489
Abstract

Directional excitation of surface plasmon polaritons (SPPs) by electrical means is important for the integration of plasmonics with molecular electronics or steering signals toward other components. We report electrically driven SPP sources based on quantum mechanical tunneling across molecular double-barrier junctions, where the tunneling pathway is defined by the molecules' chemical structure as well as by their tilt angle with respect to the surface normal. Self-assembled monolayers of S(CH)BPh (BPh = biphenyl, = 1-7) on Au, where the alkyl chain and the BPh units define two distinct tunnel barriers in series, were used to demonstrate and control the geometrical effects. The tilt angle of the BPh unit with respect to the surface normal depends on the value of and is 45° when is even and 23° when is odd. The tilt angle of the alkyl chain is fixed at 30° and independent of . For values of = 1-3, SPPs are directionally launched via directional tunneling through the BPh units. For values of > 3, tunneling along the alkyl chain dominates the SPP excitation. Molecular level control of directionally launching SPPs is achieved without requiring additional on-chip optical elements, such as antennas, or external elements, such as light sources. Using the molecular tunneling junctions, we provide the first direct experimental demonstration of molecular double-barrier tunneling junctions.

摘要

通过电学手段对表面等离激元极化激元(SPPs)进行定向激发,对于等离激元学与分子电子学的集成或向其他组件引导信号而言至关重要。我们报道了基于量子力学隧穿穿过分子双势垒结的电驱动SPP源,其中隧穿路径由分子的化学结构及其相对于表面法线的倾斜角确定。在金上自组装的S(CH)BPh(BPh = 联苯, = 1 - 7)单分子层,其中烷基链和BPh单元串联定义了两个不同的隧道势垒,用于演示和控制几何效应。BPh单元相对于表面法线的倾斜角取决于 的值,当 为偶数时为45°,当 为奇数时为23°。烷基链的倾斜角固定为30°且与 无关。对于 = 1 - 3的值,SPPs通过定向隧穿穿过BPh单元而被定向发射。对于 > 3的值,沿烷基链的隧穿主导了SPP激发。无需额外的片上光学元件(如天线)或外部元件(如光源),即可实现对SPPs定向发射的分子水平控制。利用分子隧穿结,我们首次对分子双势垒隧穿结进行了直接实验演示。

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