4.7 Article

Action spectroscopy of SrCl+ using an integrated ion trap time-of-flight mass spectrometer

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JOURNAL OF CHEMICAL PHYSICS
卷 141, 期 1, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.4885363

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资金

  1. U.S. Army Research Office (ARO) Undergraduate Research Apprenticeship Program (URAP)
  2. National Science Foundation (NSF)
  3. ARO [PHY-0855683, PHY-1308573, W911NF-12-1-0476, W911NF-10-1-0505]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Physics [1255526] Funding Source: National Science Foundation
  6. Division Of Physics
  7. Direct For Mathematical & Physical Scien [1308573] Funding Source: National Science Foundation

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The photodissociation cross-section of SrCl+ is measured in the spectral range of 36 000-46 000 cm(-1) using a modular time-of-flight mass spectrometer (TOF-MS). By irradiating a sample of trapped SrCl+ molecular ions with a pulsed dye laser, X-1 Sigma(+) state molecular ions are electronically excited to the repulsive wall of the A(1)Pi state, resulting in dissociation. Using the TOF-MS, the product fragments are detected and the photodissociation cross-section is determined for a broad range of photon energies. Detailed ab initio calculations of the SrCl+ molecular potentials and spectroscopic constants are also performed and are found to be in good agreement with experiment. The spectroscopic constants for SrCl+ are also compared to those of another alkaline earth halogen, BaCl+, in order to highlight structural differences between the two molecular ions. This work represents the first spectroscopy and ab initio calculations of SrCl+. (C) 2014 AIP Publishing LLC.

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