Lowest 4f5d Transition of Trivalent Rare-Earth Ions in CaF2 Crystals

Eugene Loh
Phys. Rev. 147, 332 – Published 8 July 1966
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Abstract

The lowest 4f5d ultraviolet absorption band of eleven (Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, and Yb) of the fourteen trivalent rare-earth (RE) ions in host CaF2 crystals has been measured. The room temperature absorption cross section [cm2] and half-width [cm1] of these bands for the first-half series of RE3+ are larger than that of the second-half series (from Tb3+ on), possibly because of some spin-forbiddenness in the transition of the latter. Typically, they are ∼5×1018 cm2 and ∼1700 cm1, respectively, for the former and ∼3×1018 cm2 and ∼1300 cm1, respectively, for the latter at typical concentration of ∼104. The oscillator strength is estimated to be ∼102 for the first half-series and ∼4×103 for the second half-series RE3+. At liquid nitrogen temperature the band sharpens and shifts ∼200 cm1 toward lower wave number, probably because of increasing crystal field in the contracted lattice; a zero-phonon line and some vibrational structure are also developed in Ce3+-and Pr3+-doped CaF2. The location of the band ranges from ∼33 000 cm1 (Ce3+) to ∼71 000 cm1 (Yb3+), with that of Gd3+ and Lu3+ outside (≳80 000 cm1) of the transparent region of CaF2 crystal. Compared with the data available for the free ions Ce3+, Pr3+, and Yb3+, the location of the lowest 4f5d transition of (RE)3+ ions in CaF2 is found to be lowered ∼18 000 cm1 in the crystal environment. The energy of the lowest 4f5d transition is described satisfactorily by a formula due to Jørgensen for 4fn4fn1 5d transitions in the free ion, decreased by 18 000 cm1.

  • Received 20 January 1966

DOI:https://doi.org/10.1103/PhysRev.147.332

©1966 American Physical Society

Authors & Affiliations

Eugene Loh*

  • Hughes Research Laboratories, Malibu, California

  • *Presently with Douglas Aircraft Company, Inc., Physical Science Department, Research and Development.

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Issue

Vol. 147, Iss. 1 — July 1966

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