4.8 Article

Optical Kerr Effect of Liquid Acetonitrile Probed by Femtosecond Time-Resolved X-ray Liquidography

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 35, Pages 14261-14273

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c06088

Keywords

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Funding

  1. Institute for Basic Science [IBS-R004]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT, and Future Planning [2016R1E1A1A01941978, 2020K1A3A7A09080401]
  3. Ministry of Science and the ICT of Korea
  4. National Research Foundation of Korea [2020K1A3A7A09080401] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this study, an alternative method, femtosecond time-resolved X-ray liquidography (fs-TRXL), was used to monitor microscopic structural motions related to the Optical Kerr effect response in molecular liquids using X-ray solution scattering. Different types of molecular motions were successfully resolved selectively without the need for theoretical modeling, based on anisotropy and extra structural information in the scattering data.
Optical Kerr effect (OKE) spectroscopy is a method that measures the time-dependent change of the birefringence induced by an optical laser pulse using another optical laser pulse and has been used often to study the ultrafast dynamics of molecular liquids. Here we demonstrate an alternative method, femtosecond time-resolved X-ray liquidography (fs-TRXL), where the microscopic structural motions related to the OKE response can be monitored using a different type of probe, i.e., X-ray solution scattering. By applying fs-TRXL to acetonitrile and a dye solution in acetonitrile, we demonstrate that different types of molecular motions around photoaligned molecules can be resolved selectively, even without any theoretical modeling, based on the anisotropy of two-dimensional scattering patterns and extra structural information contained in the q-space scattering data. Specifically, the dynamics of reorientational (libration and orientational diffusion) and translational (interaction-induced motion) motions are captured separately by anisotropic and isotropic scattering signals, respectively. Furthermore, the two different types of reorientational motions are distinguished from each other by their own characteristic scattering patterns and time scales. The measured time-resolved scattering signals are in excellent agreement with the simulated scattering signals based on a molecular dynamics simulation for plausible molecular configurations, providing the detailed structural description of the OKE response in liquid acetonitrile.

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