Down- and upconversion luminescence in Er3+ doped CaYAl3O7

The Er<sup>3+</sup>-doped materials have been intensively studied for applications in lighting, communication technologies, luminescence thermometry, anti-counterfeiting, solid-state lasers, etc. Er<sup>3+</sup>-doped materials demonstrate multi-mode luminescence excited with UV, Vis, and NIR radiation, opening a diverse field of applications in anti-counterfeiting, luminescence thermometry, etc. The properties of melilite-type phosphor CaYAl<sub>3</sub>O<sub>7</sub> doped with Er<sup>3+</sup> ions have been studied for optical and optoelectronic applications. The samples were synthesized using the high-temperature solid-state method and analysed by X-ray diffraction and optical spectroscopy techniques in the 8.5-300 K temperature range. The down-conversion and upconversion luminescence in Er<sup>3+</sup>-doped CaYAl<sub>3</sub>O<sub>7</sub> was observed. At 8.5 K, the green emission at 552.4 nm increased 7.4 times in intensity compared to the room temperature, and the fluorescence intensity ratio (FIR) of 552.5nm/525.1 nm bands increased from 1.4 to 293.5 at 8.5 K offering applications of CYA:Er<sup>3+</sup> in luminescence thermometry. The dominating mechanism of upconversion luminescence in the studied CYA:Er<sup>3+</sup> powders is the excited-state absorption (ESA). The contribution of cross-relaxation processes in the Er<sup>3+</sup> emission in the red spectral range (at 645- 690 nm) was detected. The possibility of exciting CYA:Er<sup>3+</sup> luminescence by UV, VIS, and NIR radiation makes CYA:Er<sup>3+</sup> a promising component in technologies for anti-counterfeiting applications.

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Published
2025-04-04
DOI
https://doi.org/10.1117/12.3056494
Primary Topic
Luminescence Properties of Advanced Materials
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article
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article

Down- and upconversion luminescence in Er3+ doped CaYAl3O7

Kamila Leśniewska‐Matys, Anna Kozłowska, Meldra Ķemere, Anatolijs Šarakovskis et al.
Luminescence Properties of Advanced Materials
article

Down- and upconversion luminescence in Er3+ doped CaYAl3O7

Kamila Leśniewska‐Matys, Anna Kozłowska, Meldra Ķemere, Anatolijs Šarakovskis, Agnieszka B. Malinowska, Michał Kukielski, Aleksandra Pantoł-Boczoń
article en

Abstract

The Er<sup>3+</sup>-doped materials have been intensively studied for applications in lighting, communication technologies, luminescence thermometry, anti-counterfeiting, solid-state lasers, etc. Er<sup>3+</sup>-doped materials demonstrate multi-mode luminescence excited with UV, Vis, and NIR radiation, opening a diverse field of applications in anti-counterfeiting, luminescence thermometry, etc. The properties of melilite-type phosphor CaYAl<sub>3</sub>O<sub>7</sub> doped with Er<sup>3+</sup> ions have been studied for optical and optoelectronic applications. The samples were synthesized using the high-temperature solid-state method and analysed by X-ray diffraction and optical spectroscopy techniques in the 8.5-300 K temperature range. The down-conversion and upconversion luminescence in Er<sup>3+</sup>-doped CaYAl<sub>3</sub>O<sub>7</sub> was observed. At 8.5 K, the green emission at 552.4 nm increased 7.4 times in intensity compared to the room temperature, and the fluorescence intensity ratio (FIR) of 552.5nm/525.1 nm bands increased from 1.4 to 293.5 at 8.5 K offering applications of CYA:Er<sup>3+</sup> in luminescence thermometry. The dominating mechanism of upconversion luminescence in the studied CYA:Er<sup>3+</sup> powders is the excited-state absorption (ESA). The contribution of cross-relaxation processes in the Er<sup>3+</sup> emission in the red spectral range (at 645- 690 nm) was detected. The possibility of exciting CYA:Er<sup>3+</sup> luminescence by UV, VIS, and NIR radiation makes CYA:Er<sup>3+</sup> a promising component in technologies for anti-counterfeiting applications.

Łukasiewicz Research Network (PL), University of Latvia (LV)
Openalex Percentile: Top 96%
Luminescence Properties of Advanced Materials
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Down- and upconversion luminescence in Er3+ doped CaYAl3O7 — Kamila Leśniewska‐Matys, Anna Kozłowska, et al. · (2025) | TGRS Research Map | TGRS