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Adapting Taylor Dispersion to Measure the Dispersion Coefficient of Electrolyte Solutions via an Accessible Microfluidic Setup
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Long-range dispersion C6 coefficient for SF6 dimer: Experimental and theoretical study.

Kira A Tatarenko1, Alexander V Lazarev1, Denis Bokhan1

  • 1Laboratory of Molecular Beams, Physical Chemistry Division, Department of Chemistry, Moscow Lomonosov State University, Moscow 119991, Russian Federation.

The Journal of Chemical Physics
|October 4, 2018
PubMed
Summary
This summary is machine-generated.

The long-range C6 dispersion coefficient for SF6 dimers was experimentally measured using supersonic jet expansion. This study confirms theoretical calculations, validating the precision of both methods for intermolecular potential analysis.

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Area of Science:

  • Chemical Physics
  • Atomic and Molecular Physics

Background:

  • Accurate determination of intermolecular forces is crucial for understanding material properties.
  • Long-range dispersion coefficients, like the C6 coefficient, govern van der Waals interactions between molecules.
  • Sulfur hexafluoride (SF6) is a molecule with significant industrial applications, making its dimer interactions of interest.

Purpose of the Study:

  • To experimentally measure the long-range dispersion C6 coefficient for the SF6 dimer.
  • To theoretically calculate the C6 coefficient using advanced computational methods.
  • To compare experimental and theoretical results for validation and to refine understanding of SF6 dimer interactions.

Main Methods:

  • Experimental measurement utilizing supersonic pulse jet expansion into a vacuum.
  • Analysis of time-of-flight spectra correlated with a dynamic jet model and intermolecular potential parameters.
  • Theoretical calculation employing the linearly approximated explicitly correlated coupled-cluster singles and doubles (CCSD(F12)) method.
  • Application of the Casimir-Polder formula for theoretical C6 coefficient determination.

Main Results:

  • The C6 dispersion coefficient for the SF6 dimer was successfully extracted from experimental data.
  • Theoretical calculations provided a C6 coefficient value for the SF6 dimer.
  • Excellent agreement was observed between the experimentally determined and theoretically calculated C6 coefficients.

Conclusions:

  • The experimental measurement and theoretical calculation of the C6 dispersion coefficient for the SF6 dimer show good agreement.
  • The study validates the reliability of the supersonic jet expansion technique for measuring intermolecular potential parameters.
  • The findings contribute to a more accurate understanding of van der Waals forces in SF6 dimers.