Structural and spectroscopic characteristics of thermally stable Eu3+ activated barium zinc orthophosphate phosphor for white LEDs

被引:32
作者
Sahu, Mukesh K. [1 ]
Kaur, Harpreet [1 ]
Ratnam, B., V [1 ]
Kumar, J. Suresh [2 ]
Jayasimhadri, M. [1 ]
机构
[1] Delhi Technol Univ, Dept Appl Phys, Luminescent Mat Res Lab LMRL, Delhi 110042, India
[2] Univ Aveiro, Dept Phys & I3N, P-3810193 Aveiro, Portugal
关键词
Phosphor; Structural and photoluminescent properties; White LEDs; ENERGY-TRANSFER; PHOTOLUMINESCENCE PROPERTIES; LUMINESCENCE PROPERTIES; RED; EXCITATION; COLOR; SITE;
D O I
10.1016/j.ceramint.2020.07.263
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Crystalline monoclinic phase of europium (Eu3+) doped barium zinc orthophosphate [BaZn2(PO4)(2): BZP] phosphor has been synthesized via solid-state reaction technique. The phase purity, morphology and luminescent features of the as-synthesized phosphors have been examined using the results of X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL), respectively. The XRD results indicate pure phase formation of Eu3+ doped BZP (BZP:Eu3+) phosphor due to exact matching with the standard data of BZP. The SEM image specifies irregular shape of micro sized particles and non-uniform morphology. The BZP:Eu3+ phosphor exhibits intense emission at 592 nm wavelength under ultraviolet (UV), near-UV and blue light excitations. The emission spectra disclose that the emission intensity improved with increase in Eu3+ ions concentration up to 4.0 mol% and intensity decreases beyond it. The CIE coordinates (0.625, 0.363) calculated for the optimized BZP:Eu3+ phosphor, which fall in the pure red region and close to commercially available red phosphor Y2O2S:Eu3+ (0.647, 0.343). The PL intensity sustained up to 62.25% at 150 degrees C as compared to the intensity at room temperature indicating good thermal stability of BZP phosphor. All the above mentioned results signify the potential candidature of BZP:Eu3+ phosphors for white light emitting devices.
引用
收藏
页码:26410 / 26415
页数:6
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