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Time-resolved Fourier-transform infrared emission spectroscopy of Ag in the (1300-3600)-cm(-1) region: Transitions involving f and g states and oscillator strengths

  1. 1.
    SYSNO ASEP0347583
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTime-resolved Fourier-transform infrared emission spectroscopy of Ag in the (1300-3600)-cm(-1) region: Transitions involving f and g states and oscillator strengths
    Author(s) Civiš, Svatopluk (UFCH-W) RID, ORCID, SAI
    Matulková, Irena (UFCH-W)
    Cihelka, Jaroslav (UFCH-W)
    Kubelík, Petr (UFCH-W) RID, ORCID
    Source TitlePhysical Review. A. - : American Physical Society - ISSN 1050-2947
    Roč. 82, č. 2 (2010), 022502
    Number of pages16 s.
    Languageeng - English
    CountryUS - United States
    Keywordsspectroscopy ; transitions ; oscillator strengths
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsIAA400400705 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    KAN100500652 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000280549300003
    DOI10.1103/PhysRevA.82.022502
    AnnotationWe report on a study of the emission spectra of Ag vapor in a vacuum (10(-2) Torr) formed in ablation of an Ag metal target by a high-repetition rate (1.0 kHz) pulsed nanosecond ArF laser (lambda = 193 nm, output energy of 15 mJ). The time-resolved infrared emission spectrum of Ag was recorded in the 1300- to 3600-cm(-1) spectral region using the Fourier transform infrared spectroscopy technique with a resolution of 0.02 cm(-1). The time profiles of the measured lines have maxima at 5-6 mu s after a laser shot and display nonexponential decay with a decay time of 3-7 mu s. The lines reported here are given with an uncertainty of 0.0005-0.016 cm(-1). The line classification is performed using relative line strengths expressed in terms of transition dipole matrix elements calculated with the help of the Fues model potential; these calculations show agreement with the large experimental and calculated data sets available in the literature.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2011
Number of the records: 1  

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