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Improvement of 4 I 11/2 → 4 I 13/2 Transition Rate and Thermal Stabilities in Er 3+ ‐Doped TeO 2 ‐B 2 O 3 (GeO 2 )‐ZnO‐K 2 O Glasses
Author(s) -
Cho Doo Hee,
Choi Yong Gyu,
Kim Kyong Hon
Publication year - 2001
Publication title -
etri journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.295
H-Index - 46
eISSN - 2233-7326
pISSN - 1225-6463
DOI - 10.4218/etrij.01.0101.0401
Subject(s) - materials science , doping , quantum efficiency , fiber amplifier , analytical chemistry (journal) , glass transition , optical amplifier , relaxation (psychology) , atomic physics , amplifier , optics , chemistry , optoelectronics , laser , physics , polymer , psychology , social psychology , cmos , chromatography , composite material
Spectroscopic and thermal analysis indicates that tellurite glasses doped with B 2 O 3 and GeO 2 are promising candidate host materials for wide‐band erbium doped fiber amplifier (EDFA) with a high 980 nm pump efficiency. In this study, we measured the thermal stabilities and the emission cross‐sections for Er 3+ : 4 I 13/2 → 4 I 15/2 transition in this tellurite glass system. We also determined the Judd‐Ofelt parameters and calculated the radiative transition rates and the multiphonon relaxation rates in this glass system. The 15 mol% substitution of B 2 O 3 for TeO 2 in the Er 3+ ‐doped 75TeO 2 ‐20ZnO‐5K 2 O glass raised the multiphonon relaxation rate for 4 I 11/2 → 4 I 13/2 transition from 4960 s −1 to 24700 s −1 , but shortened the lifetime of the 4 I 13/2 level by 14 % and reduced the emission cross‐section for the 4 I 13/2 → 4 I 15/2 transition by 11%. The 15 mol% GeO 2 substitution in the same glass system also reduced the emission cross‐section but increased the lifetime by 7%. However, the multiphonon relaxation rate for 4 I 11/2 → 4 I 13/2 transition was raised merely by 1000 s −1 . Therefore, a mixed substitution of B 2 O 3 and GeO 2 for TeO 2 was concluded to be suitable for the 980 nm pump efficiency and the fluorescence efficiency of 4 I 13/2 → 4 I 15/2 transition in Er 3+ ‐doped tellurite glasses.

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