[Zn-Ge] co-substitutes [Ga-Ga] to coordinately broaden the near-infrared emission of Cr in GaO phosphors
Here, a "chemical unit co-substitution" method is used to improve the near-infrared (NIR) emission of phosphors, using [Zn 2+ -Ge 4+ ] to co-substitute [Ga 3+ -Ga 3+ ] sites to reduce crystal field splitting to affect the structure of gallium oxide. A series of broadband NIR phosphors are...
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Published in | Physical chemistry chemical physics : PCCP Vol. 25; no. 3; pp. 29 - 297 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Published |
18.01.2023
|
Online Access | Get full text |
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Summary: | Here, a "chemical unit co-substitution" method is used to improve the near-infrared (NIR) emission of phosphors, using [Zn
2+
-Ge
4+
] to co-substitute [Ga
3+
-Ga
3+
] sites to reduce crystal field splitting to affect the structure of gallium oxide. A series of broadband NIR phosphors are synthesized by a high-temperature solid-phase method, and their phase structures, crystal structures, morphologies, diffuse reflectance spectra, and luminescence lifetimes are investigated. The Ga
1.68
(Zn-Ge)
0.3
O
3
:0.02Cr
3+
(GZGOC) phosphor exhibits NIR wide-band emission, with a peak wavelength of 766 nm and a half-width of 138 nm. Meanwhile, the quantum yield of photoluminescence can reach 81.2%. The phosphor has good thermal stability. When the temperature reaches 373 K, its emission intensity still remains at 73.4% of that at room temperature. A 460 nm LED chip and this phosphor are used to fabricate a phosphor-converted light emitting diode (pc-LED) device which can be used as a NIR light source. All these results show the application potential of the as-prepared phosphor in NIR imaging.
This paper focuses on the use of [Zn
2+
-Ge
4+
] to co-replace [Ga
3+
-Ga
3+
], which redshifts the near-infrared emission of Cr
3+
in Ga
2
O
3
, and broadens the full width at half maximum. |
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Bibliography: | https://doi.org/10.1039/d2cp04737c Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/d2cp04737c |