APS March Meeting 2015
Volume 60, Number 1
Monday–Friday, March 2–6, 2015;
San Antonio, Texas
Session F27: Focus Session: Emerging Ultrafast Technologies III
8:00 AM–10:48 AM,
Tuesday, March 3, 2015
Room: 204B
Sponsoring
Unit:
DCP
Chair: Jennifer Ogilvie, University of Michigan
Abstract ID: BAPS.2015.MAR.F27.5
Abstract: F27.00005 : Ultrafast 2D Fluorescence Spectroscopy using Spectrally Entangled Photon Pairs
9:36 AM–10:12 AM
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Abstract
Author:
Michael Raymer
(University of Oregon)
We propose entangled photon-pair two-dimensional fluorescence spectroscopy
(EPP-2DFS) to probe the nonlinear electronic response of molecular systems.
[1] The method, inspired by results in [2], uses a technique from quantum
optics---a separated two-photon (Franson) interferometer, which generates
time-delayed packets of time-frequency-entangled photon pairs. This
interferometer is incorporated into the framework of a fluorescence-detected
2D optical spectroscopic experiment [3]. The continuous stream of entangled
photons are phase-modulated in the interferometer, and used to excite a
two-photon-absorbing sample, whose excited-state population is selectively
detected by simultaneously monitoring the sample fluorescence and the
transmitted exciting fields. In comparison to standard `classical' 2DFS
techniques using coherent laser pulses and standard pulse-scanning
sequences, advantages of this scheme include the suppression of uncorrelated
background signals, the suppression of diagonal 2D spectral features, the
enhancement and narrowing of off -diagonal spectral cross-peaks that contain
information about electronic coupling, and the possibility for enhancement
of simultaneous time-and-frequency resolution, including spectral
selectivity within an inhomogeneously broadened distribution. These effects
arise from the properties of parametric down-conversion light source, which
effectively creates a different interaction-scanning protocol than in
standard laser-pulse scanning. We numerically simulate the EPP-2DFS
observable for the case of an electronically coupled molecular dimer. The
EPP-2DFS spectrum is greatly simplified in comparison to its standard
classical 2D counterpart. Our results indicate that EPP-2DFS can provide
previously unattainable resolution to extract model Hamiltonian parameters
from electronically coupled molecular dimers.
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[1] M.G Raymer, A. H. Marcus, J. R. Widom, D. L. P. Vitullo, Entangled
Photon-Pair Two-Dimensional Fluorescence Spectroscopy (EPP-2DFS), J. Phys.
Chem. B, 117, 15559 (2013)
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[2] O. Roslyak, S. Mukamel, Multidimensional pump-probe spectroscopy with
entangled twin-photon states. Phys. Rev. A, 79, 063409 (2009)
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[3] P. F. Tekavec, G. A. Lott, A. H. Marcus, Fluorescence-Detected
Two-Dimensional Electronic Coherence Spectroscopy by Acousto-Optic Phase
Modulation, J. Chem. Phys. 127, 214307 (2007)
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2015.MAR.F27.5