Tb3+→Eu3+ energy transfer and tunable photoluminescence in Ca3WO6:Tb3+, Eu3+ co-doped double perovskite

IF 3.6 3区 物理与天体物理 Q2 OPTICS
U.V.B.B. Krishna Prasad , Naresh Degda , K. Jyothi , K.V.R. Murthy
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Abstract

The energy transfer mechanism and color-tunable photoluminescence (PL) properties of Ca3WO6:0.1 Tb3+, yEu3+ phosphors were systematically investigated and discussed. The PL spectra of the co-doped phosphor predominantly highlighted the green emission centred at 545 nm, originating from the Tb3+ (5D47F5) transitions, and red emission at 616 nm, attributed to the Eu3+ (5D07F2) transitions. Upon excitation at 278 nm, a notable enhancement in Eu3+ red emission was observed, facilitated by energy transfer (ET) from Tb3+ ions acting as sensitizers to Eu3+ activators. This energy transfer process from Tb3+ → Eu3+ enabled effective modulation of the emission color, shifting from green to orange-red, depending on the Eu3+ concentration. To understand the ET dynamics, several characterization techniques were employed, including the calculation of energy transfer efficiency, calculation of critical transfer distance, and analysis of PL decay lifetimes. The highest value of the energy transfer (77.43 %) was achieved for Eu3+ doping reaches to its maximum at 0.1 %. The specific reason of the energy transfer and concentration quenching phenomena was discussed by means of the Dexter's theory. Consistency across the various approaches (intensity variation and decay lifetime) confirmed the reliability of the ET efficiency evaluation. Furthermore, a simplified energy level diagram was constructed for the Tb3+-Eu3+ co-doped system to illustrate the energy transfer pathways and the associated emission transitions, offering a clearer understanding of the primary luminescence mechanisms.
Ca3WO6:Tb3+, Eu3+共掺杂双钙钛矿中Tb3+→Eu3+的能量转移和可调光致发光
系统地研究了Ca3WO6:0.1 Tb3+, yEu3+荧光粉的能量传递机理和可调色光致发光性能。共掺杂荧光粉的PL光谱主要突出了集中在545 nm的绿色发射,来自Tb3+ (5D4→7F5)跃迁,以及616 nm的红色发射,归因于Eu3+ (5D0→7F2)跃迁。在278 nm激发时,观察到Eu3+红色发射的显著增强,这是由于Tb3+离子作为Eu3+激活剂的敏化剂的能量转移(ET)所促进的。这种从Tb3+→Eu3+的能量转移过程使发射颜色从绿色到橙红色的有效调制成为可能,这取决于Eu3+的浓度。为了了解ET动力学,采用了几种表征技术,包括能量传递效率的计算、临界传递距离的计算和PL衰变寿命的分析。Eu3+掺杂的能量转移率最高(77.43%),在0.1%时达到最大值。运用德克斯特理论探讨了能量传递和浓度猝灭现象产生的具体原因。各种方法(强度变化和衰减寿命)的一致性证实了ET效率评估的可靠性。此外,构建了Tb3+-Eu3+共掺杂体系的简化能级图,以说明能量转移途径和相关的发射跃迁,从而更清楚地了解初级发光机制。
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
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.
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