Luminescence Dynamics of BaAl2O4:Eu2+ Phosphor.

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Journal of Fluorescence Pub Date : 2025-05-01 Epub Date: 2024-05-11 DOI:10.1007/s10895-024-03759-w
Manash Kalita, J M Kalita
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Abstract

We studied steady-state and time-resolved photoluminescence of Eu doped BaAl2O4 phosphor. The undoped BaAl2O4 sample shows a dominant blue emission band at ~ 428 nm and two secondary maxima at ~ 405 and 456 nm due to F-centre and aggregate defects such as F2 -centre. The samples after doping of Eu at 1-5% show additional emission bands at ~ 485 and 518 nm due to Eu2+ centre and a red emission band at ~ 657 nm is attributed to Eu3+ centre. The sample doped with 2% of Eu shows anomalous emission having the dominant peak at ~ 494 nm. The average luminescence lifetime of the emission band at ~ 428 nm in the undoped sample was estimated to be (3.29 ± 0.91) ns. The average luminescence lifetime of this emission band after doping of Eu was found to increase by 102 orders of magnitude. The intensity of the 428 nm blue emission band was found to quench after doping of Eu beyond 3%. The concentration quenching effect was attributed to dipole-quadrupole interaction. Further, a non-radiative fluorescence energy transfer mechanism from an extrinsic Eu2+ centre to an intrinsic F-centre is proposed to describe the luminescence dynamics of the samples.

Abstract Image

BaAl2O4:Eu2+ 磷光体的发光动力学。
我们研究了掺 Eu 的 BaAl2O4 荧光粉的稳态和时间分辨光致发光。未掺杂的 BaAl2O4 样品在 ~ 428 纳米波长处显示出一个主要的蓝色发射带,在 ~ 405 和 456 纳米波长处显示出两个次级最大值,这是由于 F 中心和 F2 中心等聚集缺陷造成的。掺杂 1-5% Eu 的样品在 ~ 485 和 518 纳米波长处显示出额外的发射带,这是由于 Eu2+ 中心造成的,而 ~ 657 纳米波长处的红色发射带则是由于 Eu3+ 中心造成的。掺杂 2% Eu 的样品显示出异常发射,其主峰位于 ~ 494 纳米。据估计,未掺杂样品中 ~ 428 nm 处发射带的平均发光寿命为 (3.29 ± 0.91) ns。发现掺入 Eu 后,该发射带的平均发光寿命增加了 102 个数量级。发现掺杂 Eu 超过 3% 后,428 nm 蓝色发射带的强度会淬灭。浓度淬灭效应归因于偶极-四极相互作用。此外,还提出了一种从外在 Eu2+ 中心到内在 F 中心的非辐射荧光能量转移机制来描述样品的发光动力学。
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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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