{"title":"Tb3+→Eu3+ energy transfer and tunable photoluminescence in Ca3WO6:Tb3+, Eu3+ co-doped double perovskite","authors":"U.V.B.B. Krishna Prasad , Naresh Degda , K. Jyothi , K.V.R. Murthy","doi":"10.1016/j.jlumin.2025.121547","DOIUrl":null,"url":null,"abstract":"<div><div>The energy transfer mechanism and color-tunable photoluminescence (PL) properties of Ca<sub>3</sub>WO<sub>6</sub>:0.1 Tb<sup>3+</sup>, yEu<sup>3+</sup> 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 Tb<sup>3+</sup> (<sup>5</sup>D<sub>4</sub>→<sup>7</sup>F<sub>5</sub>) transitions, and red emission at 616 nm, attributed to the Eu<sup>3+</sup> (<sup>5</sup>D<sub>0</sub>→<sup>7</sup>F<sub>2</sub>) transitions. Upon excitation at 278 nm, a notable enhancement in Eu<sup>3+</sup> red emission was observed, facilitated by energy transfer (ET) from Tb<sup>3+</sup> ions acting as sensitizers to Eu<sup>3+</sup> activators. This energy transfer process from Tb<sup>3+</sup> → Eu<sup>3+</sup> enabled effective modulation of the emission color, shifting from green to orange-red, depending on the Eu<sup>3+</sup> 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 Eu<sup>3+</sup> 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 Tb<sup>3+</sup>-Eu<sup>3+</sup> co-doped system to illustrate the energy transfer pathways and the associated emission transitions, offering a clearer understanding of the primary luminescence mechanisms.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"288 ","pages":"Article 121547"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-16","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/S0022231325004879","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
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+ (5D4→7F5) transitions, and red emission at 616 nm, attributed to the Eu3+ (5D0→7F2) 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.
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.