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通过光致变色分子中的光化学和电化学反复转变突破光学纳米图案化中的远场衍射极限。

Breaking the far-field diffraction limit in optical nanopatterning via repeated photochemical and electrochemical transitions in photochromic molecules.

机构信息

Department of Electrical and Computer Engineering, University of Utah, Salt Lake City, 84112, USA.

出版信息

Phys Rev Lett. 2011 Nov 11;107(20):205501. doi: 10.1103/PhysRevLett.107.205501. Epub 2011 Nov 7.

DOI:10.1103/PhysRevLett.107.205501
PMID:22181742
Abstract

By saturating a photochromic transition with a nodal illumination (wavelength, λ), one isomeric form of a small molecule is spatially localized to a region smaller than the far-field diffraction limit. A selective oxidation step effectively locks this pattern allowing repeated patterning. Using this approach and a two-beam interferometer, we demonstrate isolated lines as narrow as λ/8 (78 nm) and spacing between features as narrow as λ/4 (153 nm). This is considerably smaller than the minimum far-field diffraction limit of λ/2. Most significantly, nanopatterning is achieved via single-photon reactions and at low light levels, which in turn allow for high throughput.

摘要

通过节点照明(波长为 λ)使光致变色跃迁饱和,可以将小分子的一种异构体空间局域到小于远场衍射极限的区域。选择性氧化步骤有效地锁定了这种图案,从而可以进行重复的图案化。使用这种方法和双光束干涉仪,我们证明了线宽可以窄至 λ/8(78nm),特征之间的间距可以窄至 λ/4(153nm)。这明显小于远场衍射极限的 λ/2。最重要的是,纳米图案化是通过单光子反应和低光水平实现的,这反过来又允许高吞吐量。

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