Broadband near-IR photoluminescence in Ni2+ doped gallium silicate glass–ceramics
Broadband and tunable near-infrared (NIR) emission of Ni 2+ doped glass–ceramics (GCs) is highly attractive due to their potential to address the challenge of broadband optical amplification in the optical communication band. However, optical activity of Ni 2+ in different glass matrix as well as nu...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2019-10, Vol.30 (19), p.17715-17724 |
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Sprache: | eng |
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Zusammenfassung: | Broadband and tunable near-infrared (NIR) emission of Ni
2+
doped glass–ceramics (GCs) is highly attractive due to their potential to address the challenge of broadband optical amplification in the optical communication band. However, optical activity of Ni
2+
in different glass matrix as well as nucleation and crystallization processes in relevant glasses have not been understood fully. Here, broadband NIR photoluminescence was realized through precipitation of LiGa
5
O
8
:Ni
2+
nanocrystals (NCs) within an alkali gallium-silicate glass matrix by melt-quenching and successive heat treatment. Upon exciting by a 980 nm laser diode, we observed NIR photoluminescence band centered at ~ 1310 nm with full width at half maximum of wider than 300 nm, which was originated from
3
T
2g
(
3
F) →
3
A
2g
(
3
F) electronic transition of octahedral coordinated Ni
2+
in LiGa
5
O
8
NCs embedded in the GCs. Controlled precipitation of NCs, LiGa
5
O
8
:Ni
2+
and Ga
2
O
3
:Ni
2+
were achieved by tailoring the composition of alkali gallium-silicate glass matrix. ab initio molecular dynamics simulation was carried out to clarify the formation of nanophases in the glass system. We confirmed that optical properties of transparent GCs containing Ni
2+
NCs can be realized by changing molar percentages of Ga
2
O
3
. Our results offer a new insight into the precipitation of NCs in oxide glasses and Ni
2+
doped GCs, which may be applicable in the photonic fields, such as optical amplifier and laser. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-019-02121-2 |