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Title: Luminescence spectroscopy of matrix-isolated atomic manganese: Excitation of the 'forbidden' a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions

Abstract

Laser-induced excitation spectra recorded for the electric-quadrupole 3d{sup 6}4s a{sup 6}D{sub J}<-3d{sup 5}4s{sup 2}a{sup 6}S{sub 5/2} transitions of atomic Mn, allow assignment of the red emission features, previously observed in Mn/RG (RG=Ar, Kr and Xe) matrices with resonance 3d{sup 5}4s4pz{sup 6}P{sub 5/2}<-3d{sup 5}4s{sup 2} a{sup 6}S{sub 5/2} excitation, to the metastable a{sup 6}D{sub 9/2} state. Narrow excitation bands recorded for the red site in the Mn/Kr system allow identification of all five spin-orbit levels (J=1/2, 3/2, 5/2, 7/2 and 9/2) in the a{sup 6}D state. The coincidence of the lowest energy excitation band and the observed 585.75 nm (17 072 cm{sup -1}) emission band of atomic Mn in Kr matrices, yielded a definitive assignment of this emission to a transition from the J=9/2 spin-orbit level. Temperature dependent emission scans lead to the identification of the zero phonon line for the a{sup 6}D{sub 9/2}{yields}a{sup 6}S{sub 5/2} transition at 585.75 nm. The identified matrix-shift of +20 cm{sup -1} allows an assessment of the extent of the ground state stabilization in the red (2 deg.) site of atomic Mn isolation in solid Kr. Emission produced with direct a{sup 6}D state excitation yielded both the 585.75 and 626 nm features. The former band arisesmore » for Mn atoms occupying the red site--the latter from blue site occupancy in solid Kr. The excitation linewidths recorded for these two sites differ greatly, with the blue site yielding a broad featureless profile, in contrast to the narrow, structured features of the red site. The corresponding red site a{sup 6}D{sub J}{r_reversible}a{sup 6}S{sub 5/2} transitions in Ar and Xe matrices are broader than in Kr--a difference considered to originate from the site sizes available in these hosts and the interatomic Mn{center_dot}RG potentials. The millisecond decay times recorded for the red emission bands in the Mn/RG systems are all much shorter than the 3 s value predicted for the gas phase a{sup 6}D{sub 9/2}{yields}a{sup 6}S{sub 5/2} transition. This enhancement allows optical pumping of the forbidden a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions with low laser powers when atomic manganese is isolated in the solid state. However all the emission decays are complex, exhibiting triple exponential decays. This behavior may be related to the dependence of the excitation linewidths on the J value, indicating removal of the J degeneracy due to weak matrix-induced, crystal field splitting.« less

Authors:
; ;  [1]
  1. Department of Chemistry, National University of Ireland--Maynooth, Maynooth, County Kildare (Ireland)
Publication Date:
OSTI Identifier:
20722999
Resource Type:
Journal Article
Journal Name:
Journal of Chemical Physics
Additional Journal Information:
Journal Volume: 123; Journal Issue: 4; Other Information: DOI: 10.1063/1.1961531; (c) 2005 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); Journal ID: ISSN 0021-9606
Country of Publication:
United States
Language:
English
Subject:
74 ATOMIC AND MOLECULAR PHYSICS; EXCITATION; GROUND STATES; L-S COUPLING; MANGANESE; METASTABLE STATES; PHOTOLUMINESCENCE; PHOTON-ATOM COLLISIONS; SPECTROSCOPY

Citation Formats

Collier, Martin A, Ryan, Maryanne C, and McCaffrey, John G. Luminescence spectroscopy of matrix-isolated atomic manganese: Excitation of the 'forbidden' a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions. United States: N. p., 2005. Web. doi:10.1063/1.1961531.
Collier, Martin A, Ryan, Maryanne C, & McCaffrey, John G. Luminescence spectroscopy of matrix-isolated atomic manganese: Excitation of the 'forbidden' a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions. United States. doi:10.1063/1.1961531.
Collier, Martin A, Ryan, Maryanne C, and McCaffrey, John G. Fri . "Luminescence spectroscopy of matrix-isolated atomic manganese: Excitation of the 'forbidden' a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions". United States. doi:10.1063/1.1961531.
@article{osti_20722999,
title = {Luminescence spectroscopy of matrix-isolated atomic manganese: Excitation of the 'forbidden' a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions},
author = {Collier, Martin A and Ryan, Maryanne C and McCaffrey, John G},
abstractNote = {Laser-induced excitation spectra recorded for the electric-quadrupole 3d{sup 6}4s a{sup 6}D{sub J}<-3d{sup 5}4s{sup 2}a{sup 6}S{sub 5/2} transitions of atomic Mn, allow assignment of the red emission features, previously observed in Mn/RG (RG=Ar, Kr and Xe) matrices with resonance 3d{sup 5}4s4pz{sup 6}P{sub 5/2}<-3d{sup 5}4s{sup 2} a{sup 6}S{sub 5/2} excitation, to the metastable a{sup 6}D{sub 9/2} state. Narrow excitation bands recorded for the red site in the Mn/Kr system allow identification of all five spin-orbit levels (J=1/2, 3/2, 5/2, 7/2 and 9/2) in the a{sup 6}D state. The coincidence of the lowest energy excitation band and the observed 585.75 nm (17 072 cm{sup -1}) emission band of atomic Mn in Kr matrices, yielded a definitive assignment of this emission to a transition from the J=9/2 spin-orbit level. Temperature dependent emission scans lead to the identification of the zero phonon line for the a{sup 6}D{sub 9/2}{yields}a{sup 6}S{sub 5/2} transition at 585.75 nm. The identified matrix-shift of +20 cm{sup -1} allows an assessment of the extent of the ground state stabilization in the red (2 deg.) site of atomic Mn isolation in solid Kr. Emission produced with direct a{sup 6}D state excitation yielded both the 585.75 and 626 nm features. The former band arises for Mn atoms occupying the red site--the latter from blue site occupancy in solid Kr. The excitation linewidths recorded for these two sites differ greatly, with the blue site yielding a broad featureless profile, in contrast to the narrow, structured features of the red site. The corresponding red site a{sup 6}D{sub J}{r_reversible}a{sup 6}S{sub 5/2} transitions in Ar and Xe matrices are broader than in Kr--a difference considered to originate from the site sizes available in these hosts and the interatomic Mn{center_dot}RG potentials. The millisecond decay times recorded for the red emission bands in the Mn/RG systems are all much shorter than the 3 s value predicted for the gas phase a{sup 6}D{sub 9/2}{yields}a{sup 6}S{sub 5/2} transition. This enhancement allows optical pumping of the forbidden a{sup 6}D{sub J}{r_reversible}a{sup 6}S transitions with low laser powers when atomic manganese is isolated in the solid state. However all the emission decays are complex, exhibiting triple exponential decays. This behavior may be related to the dependence of the excitation linewidths on the J value, indicating removal of the J degeneracy due to weak matrix-induced, crystal field splitting.},
doi = {10.1063/1.1961531},
journal = {Journal of Chemical Physics},
issn = {0021-9606},
number = 4,
volume = 123,
place = {United States},
year = {2005},
month = {7}
}