KCa4(BO3)(3):Ln(3+) (Ln = Dy, Eu, Tb) phosphors for near UV excited white-light-emitting diodes

resumo

A series of doped KCa4(BO3)(3):Ln(3+) (Ln: Dy, Eu and Tb) compositions were synthesized by solid-state reaction method and their photoluminescent properties were systematically investigated to ascertain their suitability for application in white light emitting diodes. The X-ray diffraction (XRD) and nuclear magnetic resonance (MAS-NMR) data indicates that Ln(3+)-ions are successfully occupied the non-centrosymmetric Ca2+ sites, in the orthorhombic crystalline phase of KCa4(BO3)(3) having space group Ama2, without affecting the boron chemical environment. The present phosphor systems could be efficiently excitable at the broad UV wavelength region, from 250 to 350 nm, compatible to the most commonly available UV light-emitting diode (LED) chips. Photoluminescence studies revealed optimal near white-light emission for KCa4(BO3)(3) with 5 wt.% Dy3+ doping, while warm white-light (CIE; X = 0.353, Y = 0.369) is obtained at 1wt.% Dy3+ ion concentration. The principle of energy transfer between Eu3+ and Tb3+ also demonstrates the potential white-light from KCa4(BO3)(3):Eu3+, Tb3+ phosphor. Whereas, single Tb3+ and Eu3+-doped systems showed bright green (Tb3+) and red (Eu3+) emissions, respectively. Having structural flexibility along with remarkable chemical/thermal stability and suitable quantum efficiency these phosphors can be promising candidates as white-light-emitter for near UV LEDs. Copyright 2013 Author(s). This article is distributed under a Creative Commons Attribution 3.0 Unported License. [http://dx.doi.org/10.1063/1.4794189]

palavras-chave

CA-ALPHA-SIALON; LUMINESCENCE PROPERTIES; CRYSTAL-STRUCTURE; BAMGAL10O17-EU2+ PHOSPHOR; ENERGY-TRANSFER; PHOTOLUMINESCENCE; EXCITATION; CE3+; IONS; SR

categoria

Science & Technology - Other Topics; Materials Science; Physics

autores

Reddy, AA; Das, S; Goel, A; Sen, R; Siegel, R; Mafra, L; Prakash, GV; Ferreira, JMF

nossos autores

agradecimentos

This study was financially supported by the University of Aveiro, CICECO, and FCT, Portugal (PTDC/CTM-CER/114209/2009). The support from CICECIO, University of Aveiro, is acknowledged. This work partly supported by Department of Information Technology (DIT), Govt. of India, under Photonics Development Program (ref: 12(1)/2008-PDD), NanoResearch Facility and High-Impact Research Schemes of IIT Delhi.

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