APS March Meeting 2013
Volume 58, Number 1
Monday–Friday, March 18–22, 2013;
Baltimore, Maryland
Session G20: Focus Session: Metamaterials - Nanoparticles and Nanoparticle Arrays
11:15 AM–2:15 PM,
Tuesday, March 19, 2013
Room: 322
Sponsoring
Unit:
DMP
Chair: Shun Shang Lo, University of Notre Dame
Abstract ID: BAPS.2013.MAR.G20.4
Abstract: G20.00004 : Optical Spectroscopy of Single Gold Nanoparticles
11:51 AM–12:27 PM
Preview Abstract
Abstract
Author:
Michel Orrit
(Leiden University)
Compared to electron microscopy or to scanning probe microscopy, the optical
selection of individual nanoparticles in a far-field microscope provides
non-invasive probing of deep layers and commands a wide range of
time-resolved and frequency-resolved techniques. Optical signals provide
unique insights into the dynamics of nano-objects and of their surroundings
[1]. I shall illustrate applications of single-nanoparticle optics with
recent topics from our group.
i) We study single gold nanoparticles by photothermal and pump-probe
microscopy [2]. These experiments can be done in an optical trap, where a
single nanorod orients along the trapping polarization, and studied the
acoustic damping of gold nanoparticles.
ii) Photothermal microscopy opens the study of non-fluorescent absorbers,
down to single-molecule sensitivity [3]. Combining photothermal contrast
with photoluminescence, we can measure the luminescence quantum yield on a
single-particle basis. Moreover, the high signal-to-noise ratio opens up
uses of individual gold nanoparticles for local plasmonic and chemical
probing, down to single-protein level [4].
iii) Gold nanorods generate strong field enhancements near their tips. By
matching the rod's aspect ratio to a dye's fluorescence and excitation
spectra, we could observe thousand-fold enhancements for the fluorescence of
single Crystal Violet molecules [5]. Gold nanorods can produce local fields
as high as those of bow-tie antennas, thanks to their narrow plasmon
resonance, but they are much easier to synthesize, functionalize and
disperse in solution than lithographically made nanostructures.
Acknowledgement : The work presented was done over the last 7 years by F.
Kulzer, M. Lippitz, A. Tchebotareva, A. Gaiduk, P. Zijlstra, S. Khatua, M.
A. van Dijk, P. V. Ruijgrok, M. Yorulmaz, HF. Yuan, and N. Verhart in the
author's group.\\[4pt]
[1] F. Kulzer et al., Angew. Chem. \textbf{49} (2010) 854.\\[0pt]
[2] A. L. Tchebotareva et al., Laser Photon. Rev. \textbf{4} (2010) 581-597.\\[0pt]
[3] A. Gaiduk et al. Science \textbf{330} (2010) 353\\[0pt]
[4] P. Zijlstra et al., Nature Nanotech. \textbf{7} (2012) 379.\\[0pt]
[5] HF. Yuan et al., Angew. Chem., in press (2013).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2013.MAR.G20.4