4.8 Article

Investigations of Molecular Optical Properties Using Quantum Light and Hong-Ou-Mandel Interferometry

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 24, 页码 9070-9081

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c02514

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资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0020168]
  2. U.S. Air Force Office of Scientific Research in the Biophysics Program [FA9550-20-10380]
  3. NSF [CHE-1953045]
  4. National Science Foundation of China [11934011]
  5. Zijiang Endowed Young Scholar Fund
  6. Overseas Expertise Introduction Project for Discipline Innovation (111 Project) [B12024]
  7. East China Normal University
  8. U.S. Department of Energy (DOE) [DE-SC0020168] Funding Source: U.S. Department of Energy (DOE)

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Entangled photon pairs are utilized for molecular spectroscopy and quantum interferometry, with the experiment showcasing a combination of both techniques to study molecular properties. By utilizing the correlations of entangled photons in an HOM interferometer, the experiment successfully extracts the dephasing time of the coherent response induced by excitation. The measurement method using coincidence counts is unaffected by even-order dispersion effects, providing a more accurate representation of the light-matter interaction.
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.

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