The basic spectroscopic parameters of Ho3+-doped fluoroindate glass for emission at 3.9 μm

被引:43
|
作者
Gomes, Laercio [1 ]
Fortin, Vincent [2 ]
Bernier, Martin [2 ]
Vallee, Real [2 ]
Poulain, Samuel [3 ]
Poulain, Marcel [3 ]
Jackson, Stuart D. [4 ]
机构
[1] IPEN CNEN SP, Ctr Lasers & Applicat, POB 11049, BR-05422970 Sao Paulo, SP, Brazil
[2] Univ Laval, COPL, Quebec City, PQ G1V 0A6, Canada
[3] Verre Fluore, Campus KerLann, F-35170 Bruz, Brittany, France
[4] Macquarie Univ, Fac Sci & Engn, Dept Engn, MQ Photon, N Ryde, NSW 2109, Australia
基金
澳大利亚研究理事会; 巴西圣保罗研究基金会;
关键词
Spectroscopy of laser materials; Fluoride glass; Fibre lasers; Mid-infrared; FLUORIDE FIBER LASER; ENERGY-TRANSFER;
D O I
10.1016/j.optmat.2016.08.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This report details the first study of the fundamental spectroscopic properties of a new optical material for prospective application as a gain medium for fiber laser emission at 3.9 mu m. We have investigated the decay processes that are relevant to the excited states of the I-5(5) -> I-5(6) transition in singly Ho3+-doped InF3 (fluoroindate) glass using time-resolved fluorescence spectroscopy. The HoF3 concentration in the glass was 10 mol.%. We excited the I-5(7) and I-5(6) energy levels using selective excitation at 1982 nm and 1150 nm, respectively. We have established that a strong energy-transfer upconversion process by way of the well-known dipole-dipole-interaction between two holmium ions excited to the I-5(6) level populate the I-5(5) (upper laser) level of the 3.9 mu m transition. The I-5(6) and I-5(5) energy levels emit luminescence with measured peaks located at 2.85 mu m and 3.92 mu m, respectively and the luminescence-efficiencies of these emissions are 78% and 0.2%, respectively. Results from numerical simulations show that for this high Ho3+ concentration, a population inversion for the 3.9 gm transition is reached only for a short time (t < 100 mu s) after direct upper laser level pumping at a wavelength of 889 nm. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:618 / 626
页数:9
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