Cheng Xiaoyu, Anthony Taryn P, West Claire A, Hu Zhongwei, Sundaresan Vignesh, McLeod Aaron J, Masiello David J, Willets Katherine A
Department of Chemistry , Temple University , Philadelphia , Pennsylvania 19122 , United States.
Department of Chemistry , University of Washington , Seattle , Washington 98195 , United States.
J Phys Chem Lett. 2019 Mar 21;10(6):1394-1401. doi: 10.1021/acs.jpclett.9b00079. Epub 2019 Mar 12.
Single-molecule fluorescence microscopy is used to follow dynamic ligand reorganization on the surface of single plasmonic gold nanorods. Fluorescently labeled DNA is attached to gold nanorods via a gold-thiol bond using a low-pH loading method. No fluorescence activity is initially observed from the fluorescent labels on the nanorod surface, which we attribute to a collapsed geometry of DNA on the metal. Upon several minutes of laser illumination, a marked increase in fluorescence activity is observed, suggesting that the ligand shell reorganizes from a collapsed, quenched geometry to an upright, ordered geometry. The ligand reorganization is facilitated by plasmon-mediated photothermal heating, as verified by controls using an external heat source and simulated by coupled optical and heat diffusion modeling. Using super-resolution image reconstruction, we observe spatial variations in which ligand reorganization occurs at the single-particle level. The results suggest the possibility of nonuniform plasmonic heating, which would be hidden with traditional ensemble-averaged measurements.
单分子荧光显微镜用于追踪单个等离子体金纳米棒表面的动态配体重组。使用低pH加载方法通过金硫醇键将荧光标记的DNA连接到金纳米棒上。最初在纳米棒表面未观察到荧光标记的荧光活性,我们将其归因于金属上DNA的折叠几何结构。经过几分钟的激光照射后,观察到荧光活性显著增加,这表明配体壳从折叠、猝灭的几何结构重组为直立、有序的几何结构。通过使用外部热源的对照验证并通过耦合光学和热扩散建模模拟,等离子体介导的光热加热促进了配体重组。使用超分辨率图像重建,我们观察到在单粒子水平上发生配体重组的空间变化。结果表明存在非均匀等离子体加热的可能性,这在传统的总体平均测量中会被掩盖。