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利用方位角和径向偏振对单分子进行取向成像。

Orientational imaging of single molecules by using azimuthal and radial polarizations.

机构信息

Nanophotonics Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.

出版信息

J Phys Chem B. 2010 Mar 4;114(8):2565-71. doi: 10.1021/jp905719b.

Abstract

Three-dimensional molecular orientations of single fluorescence molecules in polymeric thin films were measured by focused azimuthally and radially polarized light, in which we found that the fluorescence intensity was dependent on the depth position of the molecule with respect to the film surface. We found that the fluorescence intensity for a molecule which is 80 nm deep in the film excited by radial polarization is appreciably larger when compared with the fluorescence intensity for a molecule which is also excited by radial polarization but which is closer to the polymer/air interface, a feature which leads to different fluorescence intensities, under excitation by radial polarization, for molecules with the same polar orientation but with different depths inside the film. We also found that the variation of fluorescence intensity from a molecule inside an 80 nm film in radial polarization is appreciably larger compared with one in azimuthal polarization. These findings were confirmed by comparing experiments using different thickness films with theoretically calculated electric field distributions.

摘要

采用聚焦的角向和径向偏振光测量了聚合物薄膜中单荧光分子的三维分子取向,我们发现荧光强度取决于分子相对于薄膜表面的深度位置。我们发现,与靠近聚合物/空气界面的分子相比,当薄膜中 80nm 深的分子受到径向偏振激发时,其荧光强度明显更大,这一特性导致了具有相同极向但在薄膜内部不同深度的分子在受到径向偏振激发时具有不同的荧光强度。我们还发现,与角向偏振相比,在径向偏振激发下,80nm 薄膜内分子的荧光强度变化明显更大。这些发现通过比较使用不同厚度薄膜的实验和理论计算的电场分布得到了证实。

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