Luyan Wang (王露燕) , Jinzhe Huang (黄劲哲) , Li Chen (陈力) , Zhengye Xiong (熊正烨) , Jingyuan Guo (郭竞渊)
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引用次数: 0
Abstract
Currently, the double perovskite A2BB'O6 can be used as an ideal matrix material for the study of rare earth-doped phosphor research because of its flexible chemical composition range and stable crystal structure. In this study, Y2MgTiO6:Tm3+,Dy3+ (YMT:Tm3+,Dy3+) series phosphors were synthesized via the high-temperature solid-state method. SEM illustrated that the sample consisted of irregular micron particles with some agglomeration. XRD confirmed that the prepared Y2MgTiO6 phosphors were in a single pure phase and that Dy3+ and Tm3+ replaced the Y3+ in the crystal lattice. The photoluminescence (PL) spectra revealed three distinct emission peaks (458 nm, 484 nm and 579 nm) of the YMT:Tm3+,Dy3+ phosphors under UV excitation at 353 nm, which confirmed the existence of the energy transfer from Tm3+ to Dy3+. The thermoluminescence (TL) curves revealed that the YMT:0.05Tm3+,0.2Dy3+ sample had the strongest TL response, with four TL glow peaks at 363 K, 413 K, 463 K and 551 K. Both Tm−Tstop method and the computerized glow curve deconvolution (CGCD) method revealed that the TL curve consisted of six overlapping peaks, with trap depths ranging from 0.6 to 1.52 eV. Peak Ⅰ and Peak Ⅳ moved towards high and low temperatures, respectively, with increasing dose; and the main Peak Ⅳ (510∼640 K) of the TL curve had been saturated. The dose-response curves of each overlapping peak were further analysed via the CGCD method, and it was found that Peak 1, Peak 3 and Peak 4 tended to saturate and all other peaks increased linearly. And due to the charge hopping between the traps, it resulted that Peak 2 has not reached saturation yet. In addition, the sample has good repeatability and stability. These experimental results indicate that this rare-earth doped double perovskite phosphor has some potential for TL dosimetry applications.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.