Km. Murdoch et Gd. Jones, SITE SYMMETRIES, BLEACHING BEHAVIOR, AND THERMAL-STABILITY OF HYDROGENIC CENTERS IN SRF2-PR3-PR3+( AND CAF2), Physical review. B, Condensed matter, 58(18), 1998, pp. 12020-12037
Five multihydrogenic Pr3+ centers are found in both SrF2 and CaF2. All
of these centers exhibit permanent bleaching at 10 K following optica
l excitation. This bleaching is caused by the migration of vibrational
ly excited hydrogenic ions into different lattice positions. Some of t
he excited centers are reoriented to produce equivalent centers. Alter
natively, new centers with different excitation energies are created.
All bleaching effects can be reversed by warming the whole crystal abo
ve 120 K. Laser selective excitation spectroscopy was used to measure
energy levels of the D-1(2), P-3(0), P-3(1), and I-1(6) multiplets of
these multihydrogenic centers. The Pr3+ site symmetries for all five c
enters were determined from the polarization behavior of their electro
nic transitions. This required the derivation of tables of polarizatio
n ratios for the C-4 upsilon, C-2 upsilon, and C-S symmetry groups. Mo
dels are proposed for the multihydrogenic centers and their photoprodu
ct centers which are consistent with these Pr3+ Site symmetries and ac
count for the observed bleaching behavior, The D-1(2) fluorescence lif
etimes of the centers were measured and support the models presented.
The temperatures of fluorescence recovery for bleached centers and of
fluorescence depletion for photoproduct centers were measured and foun
d to be independent of the hydrogen isotope present. These temperature
s were used to determine the barrier potentials which must be surmount
ed when centers revert to their original configurations. [S0163-1829(9
8)01142-4].