Site-selective spectroscopy ofHo3+ions inCsCdBr3crystals

Abstract
With the use of laser-selective excitation, an extensive set of energy levels has been established for the principal Ho3+ dimer center in CsCdBr3:Ho3+ crystals. The observed splittings of around 2 cm1 of the transitions to or from energy levels assigned as having γ3 symmetry under C3v symmetry is indicative of deviations of the Ho3+ ion-site symmetry from exact C3v symmetry. As for the previously studied Er3+ pair center in CsCdBr3, the Ho3+ pair center exhibits strong upconversion fluorescence with up to one-third the intensity of the direct fluorescence under cw laser excitation of the 5 I8 5 S2 transition in the green and up to one-fifteenth the intensity for comparable cw laser excitation of the 5 I8 5 F5 transition in the red. Additional small splittings of up to 0.5 cm1 appear for the sharper transitions and are attributed to the ion-pair interaction. Energy levels are also reported for three varieties of minority centers with one of these centers being present in both 0.3% and 0.1% Ho3+ crystals, another in 0.01% Ho3+ crystals and the third in Na+ codoped crystals. Crystal-field analyses are reported for the principal dimer center and two of the minority centers. Fluorescence lifetimes were determined for several transitions of the dimer center and used to infer energy-transfer rates. Preliminary high-resolution results are reported for the excitation profiles of the two lowest-energy 5 I8 5