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      Role of Yb 3+ ions on enhanced ~2.9 μm emission from Ho 3+ ions in low phonon oxide glass system

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          Abstract

          The foremost limitation of an oxide based crystal or glass host to demonstrate mid- infrared emissions is its high phonon energy. It is very difficult to obtain radiative mid-infrared emissions from these hosts which normally relax non-radiatively between closely spaced energy levels of dopant rare earth ions. In this study, an intense mid-infrared emission around 2.9 μm has been perceived from Ho 3+ ions in Yb 3+/Ho 3+ co-doped oxide based tellurite glass system. This emission intensity has increased many folds upon Yb 3+: 985 nm excitation compared to direct Ho 3+ excitations due to efficient excited state resonant energy transfer through Yb 3+: 2F 5/2 → Ho 3+: 5I 5 levels. The effective bandwidth (FWHM) and cross-section (σ em) of measured emission at 2.9 μm are assessed to be 180 nm and 9.1 × 10 −21 cm 2 respectively which are comparable to other crystal/glass hosts and even better than ZBLAN fluoride glass host. Hence, this Ho 3+/Yb 3+ co-doped oxide glass system has immense potential for the development of solid state mid-infrared laser sources operating at 2.9 μm region.

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          Deactivation effects of the lowest excited state of Ho3+ at 2.9 μm emission introduced by Pr3+ ions in LiLuF4 crystal.

          The use of Pr3+ codoping for enhancement of the Ho3+:5I6 →5I7 mid-IR emissions were investigated in the LiLuF4 crystal for the first time. It was found that Pr3+ greatly increased Ho3+ 2.9 μm emission by depopulating the Ho3+:5I7 level while having little influence on the Ho3+:5I6 level, leading to greater population inversion. The energy transfer efficiency from Ho3+:5I7 to Pr3+:3F2 is calculated to be 88%. Based on Judd-Ofelt theory, the 2.9 μm emission cross section is calculated to be 1.91×10(-20)   cm2, and the gain property of the Ho3+:5I6 →5I7 transition is discussed. We propose that the Ho, Pr:LiLuF4 crystal may be a promising material for 2.9 μm laser applications.
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            Intense 2.8 μm emission of Ho³⁺ doped PbF₂ single crystal.

            A Ho³⁺-doped PbF₂ mid-IR laser crystal was successfully grown using the vertical Bridgman method. An intense 2.8 μm emission in Ho:PbF₂ crystal was observed for the first time. By analyzing the absorption and emission measurements of the Ho:PbF₂ crystal with the Judd-Ofelt theory, the intensity parameters Ω(2,4,6), exited state lifetimes, branching ratios, and emission cross-sections were calculated. It is found that the Ho:PbF₂ crystal has high fluorescence branching ratio (20.99%), large emission cross section (1.44×10⁻²⁰ cm²), long fluorescence lifetime (5.4 ms), and high quantum efficiency (88.4%) corresponding to the stimulated emission of Ho³⁺: ⁵I₆→⁵I₇ transition. The structure of Ho:PbF₂ crystal was also analyzed by the Raman spectrum, and it was found that the Ho:PbF₂ crystal possesses low phonon energy of 257 cm⁻¹. We propose that the Ho:PbF₂ crystal may be a promising material for 2.8 μm laser applications.
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              Activation effect of Ho3+ at 2.84 μm MIR luminescence by Yb3+ ions in GGG crystal.

              The use of Yb(3+) co-doping for the enhancement of Ho(3+):(5)I(6)→(5)I(7) mid-IR (MIR) emissions was investigated in GGG crystal for the first time. It is established that Yb(3+) highly increases Ho(3+) 2.84 μm emissions by transforming pump energy from the Yb(3+):(2)F(5/2) level to the laser upper level (5)I(6) of Ho(3+). The energy-transfer efficiency from Yb(3+):(2)F(5/2) to Ho(3+):(5)I(6) is calculated to be 96.2%. The absorption cross section, emission cross section, and fluorescence quantum efficiency are estimated and discussed. It is concluded that the Yb, Ho:GGG crystal is promising material for an LD-pumped 2.84 μm laser application.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                04 July 2016
                2016
                : 6
                : 29203
                Affiliations
                [1 ]Glass Science and Technology Section, CSIR-Central Glass and Ceramic Research Institute , 196, Raja S. C. Mullick Road, Kolkata–700 032, India
                Author notes
                Article
                srep29203
                10.1038/srep29203
                4931574
                27374129
                6638343d-a160-4bd4-9c60-0dc431095d82
                Copyright © 2016, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 22 January 2016
                : 26 May 2016
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