Single-molecule localization to imaging the LDOS modification by an array of plasmonic hollow conical nanopillars

R. M. Córdova-Castro, D. Jonker, C. Cabriel, B. V. Dam, Y. D. Wilde, I. Izeddin, A. S. Arce, V. Krachmalnicoff
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Abstract

We study the modification of fluorescence emission and decay rate of single fluorescent molecules in the near field of a periodic plasmonic nanostructure formed by a square lattice of Au hollow conical pillars with a periodicity of 250 nm. We perform nanometer-resolved imaging of the LDOS by simultaneously mapping the position and the decay rate of photoactivatable single-molecules with a novel super-resolved microscopy approach which enables multiplexed and super-resolved fluorescence lifetime imaging at the single-molecule level (smFLIM) with a field of view of ~10 µm2. We observe the LDOS modification of such optically rich material at different illumination conditions and we measure a large Purcell factor enhancement which increases for oblique illumination of the nanostructure.
等离子体空心锥形纳米柱阵列对LDOS修饰的单分子定位成像
本文研究了周期为250nm的金空心锥柱方形晶格形成的周期等离子体纳米结构近场中单个荧光分子荧光发射和衰减率的变化。我们通过同时绘制光激活单分子的位置和衰减率,使用一种新颖的超分辨显微镜方法对LDOS进行纳米分辨率成像,该方法可以在单分子水平(smFLIM)上进行多路复用和超分辨荧光寿命成像,视野为~10µm2。我们在不同的光照条件下观察了这种富光学材料的LDOS修饰,并测量了纳米结构在倾斜光照下的Purcell因子增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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