1985
DOI: 10.1016/0009-2614(85)85216-7
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Spectroscopy of praseodymium(III) in zirconium fluoride glass

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Cited by 105 publications
(21 citation statements)
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“…For glasses doped with different concentrations of Pr 3+ ion, the gain properties of 3 P 0 -3 H 4 level are higher than 1 D 2 -3 H 4 level. The magnitude of (s e  t m ) obtained for 1 D 2 -3 H 4 level for 0.1 mol% Pr 3+ -doped glass is exactly one third to the value obtained for ZBLA glass, whereas for 3 P 0 -3 H 4 level in 0.5 mol% Pr 3+ glass, the value is nearly equal to the ZBLA glass [41]. Based on the measured radiative parameters it is suggested that PbO-H 3 BO 3 -TiO 2 -AlF 3 glasses activated with 0.5 mol% Pr 3+ ions can be used for blue laser emission at 461 nm corresponding to 3 P 0 -3 H 4 transition.…”
Section: Radiative Transition Parametersmentioning
confidence: 43%
“…For glasses doped with different concentrations of Pr 3+ ion, the gain properties of 3 P 0 -3 H 4 level are higher than 1 D 2 -3 H 4 level. The magnitude of (s e  t m ) obtained for 1 D 2 -3 H 4 level for 0.1 mol% Pr 3+ -doped glass is exactly one third to the value obtained for ZBLA glass, whereas for 3 P 0 -3 H 4 level in 0.5 mol% Pr 3+ glass, the value is nearly equal to the ZBLA glass [41]. Based on the measured radiative parameters it is suggested that PbO-H 3 BO 3 -TiO 2 -AlF 3 glasses activated with 0.5 mol% Pr 3+ ions can be used for blue laser emission at 461 nm corresponding to 3 P 0 -3 H 4 transition.…”
Section: Radiative Transition Parametersmentioning
confidence: 43%
“…Because of this small energy separation, a negative value for the parameter˝2 has been reported [27] and there is usually a poor agreement between the theoretically estimated and experimentally measured results for various optical parameters [27]. Many authors [28][29][30] have therefore excluded the 3 H 4 → 3 P 2 transition in applying the Judd-Ofelt theory to the observed spectrum of Pr 3+ ions. The Judd-Ofelt parameters have been recalculated after excluding this transition but it was noted that neither the calculated oscillator strength nor the ı RMS deviation showed any significant improvement.…”
Section: Absorption Spectra and Oscillator Strengthmentioning
confidence: 90%
“…This can be explained as due to the hyperfine nature of the transition. The larger difference between the calculated and observed oscillator strengths arises because of the strong 4f-5d mixing [12] which is known to bring about contribution to intensities through the odd matrix elements which are usually neglected in the J-O model.…”
Section: Absorption Spectramentioning
confidence: 96%