| Autor: |
Eshun A; Department of Chemistry, University of Michigan, 930 N University Ave., Ann Arbor, Michigan 48109, United States., Gu B; Department of Chemistry & Department of Physics and Astronomy, University of California, Irvine, Irvine, California 92697, United States., Varnavski O; Department of Chemistry, University of Michigan, 930 N University Ave., Ann Arbor, Michigan 48109, United States., Asban S; Department of Chemistry & Department of Physics and Astronomy, University of California, Irvine, Irvine, California 92697, United States., Dorfman KE; State Key Laboratory of Precision Spectroscopy, East China Normal University, Shanghai 200062, China., Mukamel S; Department of Chemistry & Department of Physics and Astronomy, University of California, Irvine, Irvine, California 92697, United States., Goodson T 3rd; Department of Chemistry, University of Michigan, 930 N University Ave., Ann Arbor, Michigan 48109, United States. |
| Abstrakt: |
Entangled photon pairs have been used for molecular spectroscopy in the form of entangled two-photon absorption and in quantum interferometry for precise measurements of light source properties and time delays. We present an experiment that combines molecular spectroscopy and quantum interferometry by utilizing the correlations of entangled photons in a Hong-Ou-Mandel (HOM) interferometer to study molecular properties. We find that the HOM signal is sensitive to the presence of a resonant organic sample placed in one arm of the interferometer, and the resulting signal contains information pertaining to the light-matter interaction. We can extract the dephasing time of the coherent response induced by the excitation on a femtosecond time scale. A dephasing time of 102 fs is obtained, which is relatively short compared to times found with similar methods and considering line width broadening and the instrument entanglement time As the measurement is done with coincidence counts as opposed to simply intensity, it is unaffected by even-order dispersion effects, and because interactions with the molecular state affect the photon correlation, the observed measurement contains only these effects and no other classical losses. The experiments are accompanied by theory that predicts the observed temporal shift and captures the entangled photon joint spectral amplitude and the molecule's transmission in the coincidence counting rate. Thus, we present a proof-of-concept experimental method based of entangled photon interferometry that can be used to characterize optical properties in organic molecules and can in the future be expanded on for more complex spectroscopic studies of nonlinear optical properties. |
