Radiation dose dependence of the Bi3+ luminescence in YPO4

The UV persistent phosphors YPO 4 :Bi were synthesized using both solid-state reaction and hydrothermal methods . XRD and SEM analyses confirmed the formation of single-phase powders. The solid-state synthesis resulted in ‘large’ particle sizes (1–4 μm), while the hydrothermal synthesis produced ‘small’ particle sizes (30–45 nm). The emission centers providing UV-C and UV-A luminescence under X-ray excitation are single Bi 3+ ion and Bi 3+ – Bi 3+ pairs. The highest emission yield was observed for samples with a Bi 3+ concentration of 0.6 mol.%. An analysis of thermoluminescence glow curves using the general order kinetics model, revealed hole traps with an activation energy of 0.93–1.05 eV and electron traps with an activation energy of 0.75–0.85 eV. The dominant mechanisms for UV-C and UV-A emission involve hole recombination at Bi 2+ ions and electron recombination at Bi3+– Bi 4+ pairs, respectively. The optimal X-ray irradiation dose is 10–12 Gy. The UV-C and UV-A afterglow curves at room temperature follow the sum of exponential and first-order hyperbola functions, corresponding to electron recombination through the conduction band and hole recombination via tunneling, respectively. The afterglow durations for the solid-state prepared powder are 40 min for UV-A and 10 min for UV-C. The powder synthesized by hydrothermal method shows a significant reduction in intensity of afterglow due to the surface energy losses . Notably, despite the decreased intensity, there is a significant increase in the duration of the tunneling component responsible for UV-C emission, attributed to the reduced average distance between the emission center and the hole trap. Methods for improving the afterglow characteristics of YPO 4 :Bi nanoparticles are proposed. • We synthesized YPO 4 :Bi phosphors using solid-state and hydrothermal methods . • We found that isolated Bi 3+ -ions and Bi 3+ –Bi 3+ pairs are responsible for UV-afterglow. • We identified electron and hole processes in YPO 4 :Bi. • We found the optimal X-ray radiation dose to be 10–12 Gy. • We revealed the influence of size-factor on afterglow parameters.

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Publication Details

Journal
Journal of Luminescence
Published
2025-04-05
DOI
https://doi.org/10.1016/j.jlumin.2025.121222
Citations
4
Primary Topic
Luminescence Properties of Advanced Materials
Type
article
Field-Weighted Citation Impact
2.07

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article

Radiation dose dependence of the Bi3+ luminescence in YPO4

S.A. Kiselev, D.V. Raikov, М. А. Машковцев, А. В. Чукин et al.
4 citations
Journal of Luminescence
Luminescence Properties of Advanced Materials
2.07
article

Radiation dose dependence of the Bi3+ luminescence in YPO4

S.A. Kiselev, D.V. Raikov, М. А. Машковцев, А. В. Чукин, И. Н. Огородников, V.S. Voynov, Yu. A. Kuznetsova, Denis Khionin, Evgeny Gorodnichiy
article en
4 citations

Abstract

The UV persistent phosphors YPO 4 :Bi were synthesized using both solid-state reaction and hydrothermal methods . XRD and SEM analyses confirmed the formation of single-phase powders. The solid-state synthesis resulted in ‘large’ particle sizes (1–4 μm), while the hydrothermal synthesis produced ‘small’ particle sizes (30–45 nm). The emission centers providing UV-C and UV-A luminescence under X-ray excitation are single Bi 3+ ion and Bi 3+ – Bi 3+ pairs. The highest emission yield was observed for samples with a Bi 3+ concentration of 0.6 mol.%. An analysis of thermoluminescence glow curves using the general order kinetics model, revealed hole traps with an activation energy of 0.93–1.05 eV and electron traps with an activation energy of 0.75–0.85 eV. The dominant mechanisms for UV-C and UV-A emission involve hole recombination at Bi 2+ ions and electron recombination at Bi3+– Bi 4+ pairs, respectively. The optimal X-ray irradiation dose is 10–12 Gy. The UV-C and UV-A afterglow curves at room temperature follow the sum of exponential and first-order hyperbola functions, corresponding to electron recombination through the conduction band and hole recombination via tunneling, respectively. The afterglow durations for the solid-state prepared powder are 40 min for UV-A and 10 min for UV-C. The powder synthesized by hydrothermal method shows a significant reduction in intensity of afterglow due to the surface energy losses . Notably, despite the decreased intensity, there is a significant increase in the duration of the tunneling component responsible for UV-C emission, attributed to the reduced average distance between the emission center and the hole trap. Methods for improving the afterglow characteristics of YPO 4 :Bi nanoparticles are proposed. • We synthesized YPO 4 :Bi phosphors using solid-state and hydrothermal methods . • We found that isolated Bi 3+ -ions and Bi 3+ –Bi 3+ pairs are responsible for UV-afterglow. • We identified electron and hole processes in YPO 4 :Bi. • We found the optimal X-ray radiation dose to be 10–12 Gy. • We revealed the influence of size-factor on afterglow parameters.

Journal of LuminescenceVol. 282
Ural Federal University (RU), Institute of Physics and Technology (RU), Institute of High Temperature Electrochemistry (RU)
Russian Science Foundation
Openalex Percentile: Top 14%
Luminescence Properties of Advanced Materials
2.07
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