Vibrational Deactivation at Solid Surfaces.

Abstract

The loss of vibrational energy was monitored by observing the decay of infrared fluorescence following pulsed excitation with a tunable infrared laser of molecules contained within a metallic or non-metallic cylindrical cell. The probability of collisional deactivation was obtain by measuring the decay time for the infrared fluorescence and dividing by the number of collisions per unit time calculated from gas-kinetic theory. The exchange of translational and rotational energy was studied by scattering molecules from a well characterized single-crystal surface. A molecular beam was used to prepare the initial species in its lowest vibrational and rotational levels, while the scattered species were detected either in a state-selected measurement using laser-induced multiphoton ionization or in a total-flux measurement using electron impact mass spectrometry. Keywords: Surface Chemistry, Energy Transfer, Vibrations, Molecules.

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Document Details

Document Type
Technical Report
Publication Date
Mar 12, 1987
Accession Number
ADA179949

Entities

People

  • Paul Houston
  • Robert P. Merrill

Organizations

  • Cornell University

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Aluminum Oxides
  • Chemical Engineering
  • Chemistry
  • Collisions
  • Crystals
  • Desorption
  • Energy
  • Energy Transfer
  • Inelastic Scattering
  • Infrared Lasers
  • Kinetic Theory
  • Mass Spectrometry
  • Molecular Beams
  • New York
  • Single Crystals
  • Spectrometry
  • Surface Chemistry

Fields of Study

  • Physics

Readers

  • Molecular Photonics/Laser Physics

Technology Areas

  • Directed Energy
  • Directed Energy - Lasers
  • Microelectronics