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纳米结中电子的局域调控。

Stark control of electrons along nanojunctions.

机构信息

Department of Chemistry, University of Rochester, Rochester, NY, 14627, USA.

Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.

出版信息

Nat Commun. 2018 May 25;9(1):2070. doi: 10.1038/s41467-018-04393-4.

Abstract

Ultrafast control of currents on the nanoscale is essential for future innovations in nanoelectronics. Recently it was experimentally demonstrated that strong non-resonant few-cycle 4 fs laser pulses can be used to induce phase-controllable currents along gold-silica-gold nanojunctions in the absence of a bias voltage. However, since the effect depends on a highly non-equilibrium state of matter, its microscopic origin is unclear and the subject of recent controversy. Here we present atomistically detailed (time-dependent non-equilibrium Green's function) electronic transport simulations that recover the main experimental observations and offer a simple intuitive picture of the effect. The photoinduced currents are seen to arise due to a difference in effective silica-metal coupling for negative and positive field amplitudes induced by lasers with low temporal symmetry. These insights can be employed to interpret related experiments, and advance our ability to control electrons in matter using lasers.

摘要

在纳米电子学的未来创新中,对纳米尺度上电流的超快控制至关重要。最近的实验证明,强非共振的少周期 4fs 激光脉冲可用于在没有偏置电压的情况下诱导沿金-二氧化硅-金纳米结的相控电流。然而,由于该效应取决于物质的高度非平衡状态,其微观起源尚不清楚,这也是最近争议的主题。在这里,我们提出了原子细节的(时间相关非平衡格林函数)电子输运模拟,该模拟恢复了主要的实验观察结果,并提供了该效应的简单直观图像。可以看出,光致电流是由于具有低时间对称性的激光产生的负场和正场幅度引起的有效二氧化硅-金属耦合的差异而产生的。这些见解可用于解释相关实验,并提高我们使用激光控制物质中电子的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68db/5970263/9b8227ee419d/41467_2018_4393_Fig1_HTML.jpg

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