Characterization of Pt⁴⁺ in Alumino-Metaphosphate Laser Glasses
Abstract
The Pt4+ optical spectra (16 600-50 000 cm−1) in a series of alkali/alkaline alumino-metaphosphate glasses are reported. The four observed spectral bands are assigned to the d-d transitions from the 1A1g ground state to the 3T1g (23 500 cm−1), 3T2g (28 000 cm−1), 1T1g (33 300 cm−1) and 1T2g (40 000 cm−1) excited states assuming Pt4+ resides in a distorted octahedral site. The absorption band intensities are found to exist in two groups, with the low compositionally averaged modifier field strength (<3.5 Å−2) having the greater absorption intensities. The ligand splitting energy and Racah parameter B vary between 38 000 and 40 000 cm−1 and between 435 and 650 cm−1, respectively, depending on the choice of modifier. The Pt4+ absorption coefficient, α, at 25 000 cm−1 is correlated with the platinum concentration (ppmw) in a potassium magnesium-alumino-metaphosphate glass by the equation: [Pt] ppmw=526α (cm−1). A comparison of relative Pt uptake during melting shows that the rare-earth doped potassium magnesium alumino-phosphate melt has the greatest uptake and is approximately 25 times greater than the concentration reported for the commercial silicate laser glass, ED-2. The effect of Pt4+ (0-860 ppmw) on fluorescence quenching rate from the Nd3+ 4F3/2 state is small (kA≈0.3 Hz/ppmw) in agreement with predictions based on the Förster-Dexter theory for dipolar energy transfer.
Recommended Citation
C. A. Click et al., "Characterization of Pt⁴⁺ in Alumino-Metaphosphate Laser Glasses," Journal of Non-Crystalline Solids, Elsevier, May 2003.
The definitive version is available at https://doi.org/10.1016/S0022-3093(02)01962-2
Department(s)
Materials Science and Engineering
Sponsor(s)
Lawrence Livermore National Laboratory
Keywords and Phrases
I130; L100; P150
International Standard Serial Number (ISSN)
0022-3093; 1873-4812
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2003 Elsevier, All rights reserved.
Publication Date
01 May 2003