{"title":"Ultraviolet afterglow of undoped MgAl2O4 derived via solution combustion","authors":"Yungao Cai , Yinghong Dong , Yuan Ming Huang","doi":"10.1016/j.jlumin.2025.121212","DOIUrl":null,"url":null,"abstract":"<div><div>Combining experiments to density functional calculations, photoluminescence (PL) and afterglow properties of solution-combustion derived MgAl<sub>2</sub>O<sub>4</sub> were investigated. Under the 255 nm photoexcitation, the PL spectrum of undoped MgAl<sub>2</sub>O<sub>4</sub> exhibits two ultraviolet subbands peaking at 3.41 eV (363.6 nm) and 3.18 eV (389.9 nm), respectively. After the irradiation of a high-pressure mercury lamp is terminated, undoped MgAl<sub>2</sub>O<sub>4</sub> exhibits ultraviolet afterglow that lasts for about 20.5 min. The afterglow spectrum of undoped MgAl<sub>2</sub>O<sub>4</sub> consists of dual ultraviolet subbands peaking at about 360 and 390 nm, correspondingly. Within the scheme of meta generalized gradient approximation, defect energy levels of oxygen vacancies (F<sup>0</sup>, F<sup>+</sup>, F<sup>2+</sup>), aluminum vacancy and magnesium vacancy are determined numerically via density functional calculations. In terms of the defect energy levels of oxygen and aluminum vacancies, optical transitions arising from these defects are constructed for undoped MgAl<sub>2</sub>O<sub>4</sub>, both the dual-subband PL and the dual-subband afterglow can be interpreted. The ultraviolet afterglow with dual subbands validates our hypothesis of the oxygen and cation vacancies in host acting as the origins of the afterglow of undoped MgAl<sub>2</sub>O<sub>4</sub>. Apart from opening a window for exploring the afterglow mechanisms of rare-earth doped MgAl<sub>2</sub>O<sub>4</sub>, the validity of the hypothesis unlocks the power of harnessing intrinsic defects as luminescence center of afterglow to develop novel afterglow materials.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"281 ","pages":"Article 121212"},"PeriodicalIF":3.3000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325001528","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Combining experiments to density functional calculations, photoluminescence (PL) and afterglow properties of solution-combustion derived MgAl2O4 were investigated. Under the 255 nm photoexcitation, the PL spectrum of undoped MgAl2O4 exhibits two ultraviolet subbands peaking at 3.41 eV (363.6 nm) and 3.18 eV (389.9 nm), respectively. After the irradiation of a high-pressure mercury lamp is terminated, undoped MgAl2O4 exhibits ultraviolet afterglow that lasts for about 20.5 min. The afterglow spectrum of undoped MgAl2O4 consists of dual ultraviolet subbands peaking at about 360 and 390 nm, correspondingly. Within the scheme of meta generalized gradient approximation, defect energy levels of oxygen vacancies (F0, F+, F2+), aluminum vacancy and magnesium vacancy are determined numerically via density functional calculations. In terms of the defect energy levels of oxygen and aluminum vacancies, optical transitions arising from these defects are constructed for undoped MgAl2O4, both the dual-subband PL and the dual-subband afterglow can be interpreted. The ultraviolet afterglow with dual subbands validates our hypothesis of the oxygen and cation vacancies in host acting as the origins of the afterglow of undoped MgAl2O4. Apart from opening a window for exploring the afterglow mechanisms of rare-earth doped MgAl2O4, the validity of the hypothesis unlocks the power of harnessing intrinsic defects as luminescence center of afterglow to develop novel afterglow materials.
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.