Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Heliyon ; 9(8): e19063, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-37654452

RESUMO

In recent years, double perovskite has become a research hotspot of luminescent matrix materials due to its flexible structure, easy doping and good thermal stability. By using a high temperature solid-state technique, Bi3+ and Eu3+ co-doped Y2-x-yBixEuyMgTiO6 (0 ≤ x ≤ 0.1, 0 ≤ y ≤ 0.5) phosphors were made. X-ray diffraction (XRD) analysis shows that the crystal structure of all samples is monoclinic system, P21/n; Bi3+ and Eu3+ can be doped into the position of Y3+ in the substitution system of Y2MgTiO6. Both photoluminescence spectroscopy (PL) and X-ray excitation luminescence spectroscopy (XEL) were used to investigate the link between Bi3+ and Eu3+ doping concentrations and luminescence intensity. PL shows that: When 375 nm is used as the excitation wavelength, by varying the doping concentration of Eu3+ in the Y1.995-yBi0.005EuyMgTiO6 phosphor, it is possible to create the color-tunable emission from blue to red; The introduction of an appropriate amount of Bi3+ will increase the typical Eu3+ emission; The way that the system's Bi3+ and Eu3+ exchange energy can be observed by combining the fluorescence decay curve and photoluminescence. Fitting by concentration quenching model shows that the resonant dipole-dipole transition is the mechanism of energy transfer between Bi3+→Eu3+; X-rays may successfully stimulate the phosphor, and the spectral distribution of XEL and PL is basically the same; The introduction of an appropriate amount of Bi3+ is also beneficial to improving the sensitivity of XEL; Changes in temperature affect the sample's emission intensity; In addition, the samples remain stable for an extended period while being continuously exposed to X-rays at various environmental temperatures. The a forementioned findings suggest that the phosphor has potential use value in the lighting industry, X-ray imaging and temperature sensor.

2.
RSC Adv ; 13(8): 4949-4957, 2023 Feb 06.
Artigo em Inglês | MEDLINE | ID: mdl-36762087

RESUMO

Olivine-type phosphate LiMgPO4 doped with rare earth elements is considered a novel dosimetric material with excellent performance that is suitable for thermoluminescence (TL) and optically stimulated luminescence (OSL) measurements. Novel LiMgPO4:Tm,Er samples were synthesized by a high-temperature solid-state reaction method. A detailed study of the TL and OSL of the samples was performed using ß-ray irradiation and X-ray-excited optical luminescence (XEOL) spectroscopy. Density functional theory (DFT) calculations were performed to predict the preferential positions of thulium and erbium, and photoluminescence (PL) spectra and TL 3D spectra were analyzed. The DFT calculation results show that Mg is preferentially replaced by Tm/Er in the LiMgPO4 system. The PL/TL3D/XEOL spectra of the samples are dominated by the characteristic luminescence of Tm3+, and the OSL decay curve of photoluminescence has fast and slow decay components with decay constants of 5 s and 42 s, respectively. The TL and XEOL results show that LiMgPO4:Tm,Er has strong emission signals under different types of radiation rays. The PL/TL3D/XEOL spectral results show that Er3+ has no radiative excitation, but Tm3+ has strong luminescence, such that the sample still emits strong TL and PL signals. Two TL emission peaks occur at approximately 120 °C and 300 °C, where the high-temperature peak is significantly more intense than the low-temperature peak, promoting the stability of the TL and OSL signals of the samples. The TL curve consists of 6 general TL dynamic peaks. The nonlinear parameters of the TL dose response are R = 0.08 and D 0 = 479 Gy, and the OSL dose response is linear in the range of 0.2-1000 Gy. The TL and OSL signals of the LiMgPO4:Tm,Er phosphor have good repeatability. Therefore, the LiMgPO4:Tm,Er phosphor can be used for radiation dose measurement.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...