کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1489431 | 992306 | 2012 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Luminescent properties of phosphor converted LED using an orange-emitting Rb2CaP2O7:Eu2+ phosphor Luminescent properties of phosphor converted LED using an orange-emitting Rb2CaP2O7:Eu2+ phosphor](/preview/png/1489431.png)
A series of orange-emitting Rb2CaP2O7:Eu2+ phosphors were synthesized by a conventional solid-state reaction method. The as-prepared phosphors were characterized by X-ray powder diffraction (XRD), fluorescence spectroscopy, and spectroradiometry. XRD showed that all prepared samples exhibited a monoclinic Rb2CaP2O7 phase. Fluorescence spectroscopy showed that the photoluminescence efficiency of Rb2Ca1−xP2O7:Eux2+ phosphors increased with increasing Eu2+ concentration until x = 0.006, then decreased at higher concentrations, due to a concentration quenching effect. The thermal activation energy was also measured to be 0.40 eV. Furthermore, a phosphor-converted LED (pc-LED) coated with Rb2Ca0.994P2O7:Eu0.0062+ was fabricated, which exhibited bright orange emission under a forward bias, from 200 to 300 mA. The color rendering index (CRI) of pc-LED coated with Rb2Ca0.994P2O7:Eu0.0062+ was higher than the CRI of pc-LED coated with commercial red phosphor, due to the broad emission band of Rb2CaP2O7:Eu2+ phosphor. In applying with three-band pc-LEDs, moreover, white pc-LED using Rb2CaP2O7:Eu2+ phosphor had a higher CRI, than using commercial phosphor. These results indicated that Rb2CaP2O7:Eu2+ phosphor could be a good candidate for a near-UV based w-LED.
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► Phase-pure Rb2CaP2O7:Eu2+ powders were synthesized by a solid state reaction process.
► The optimum emission intensity was observed at the Eu2+ ion concentration of 0.006.
► The dipole–dipole interaction was the major concentration quenching mechanism.
► The pc-LED coated with Rb2CaP2O7:Eu2+ had higher CRI than commercial red phosphor.
Journal: Materials Research Bulletin - Volume 47, Issue 12, December 2012, Pages 4522–4526