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作 者:田少华[1]
机构地区:[1]中国传媒大学理工学部理学院,北京100024
出 处:《光电子.激光》2015年第10期1942-1946,共5页Journal of Optoelectronics·Laser
基 金:中国传媒大学理科基金(132014XNG1467)资助项目
摘 要:采用固相法于550℃灼烧4h,合成了Eu3+单掺杂的NaY(MoO4)2材料,研究了材料的发光特性。X射线衍射(XRD)结果显示,掺杂少量杂质的材料仍为纯相的NaY(MoO4)2。以393nm波长近紫外光作为激发源时,NaY(MoO4)2:Eu3+可以发射主峰位于616nm波长的红色光,对应Eu3+的5D0-7F2跃迁发射。研究发现,增大Eu3+掺杂量时,对应材料的发射强度会逐渐增大,但是未发现浓度猝灭现象,通过相应的衰减曲线解释了此结果。测量不同Eu3+掺杂量下,NaY(MoO4)2:Eu3+的色坐标结果显示,色坐标基本不变,位于红色区域。上述结果表明,NaY(MoO4)2:Eu3+在白光LEDs领域有一定的应用潜力。A series of single Eua+ activated NaY(MoO4 )2 were synthesized by a solid state reaction at 550 ℃ for 4 h,and their luminescent properties are investigated. Phase formation is determined by X-ray diffraction (XRD) in a Bruker AXS I)8 advanced automatic diffractometer (Bruker Co. ,German) with Ni-filtered Cu Kal radiation (;t=0. 154 nm). Steady time resolved luminescence spectra, and excitation and emission spectra are detected by a fluorescence spectrophotometer (Hitachi F-4600). Commission International de IIEclairage (CIE) chromaticity coordinates of samples are measured by a PMS-80 spec- tra analysis system. The X-ray powder diffraction results show that there has no crystalline phase other than NaY(MoO4 )2. NaY(MoO4 )2:Eu3+ can create red emission under the 393 nm excitation, and the prominent luminescence in red (616 nm) is due to the 5 Do- 7 F2 transition of Eu3+. The emission inten- sities of Eu3+ in NaY(MoO4)2 enhance with the increase of the impurity concentration,there is no con- centration quenching effect, and the phenomena are proved by the decay curves of Eua+. Moreover, when tuning the Eu3 + doping content, the CIE chromaticity coordinates of NaY(MoO4 )2 :Eu3 + are measured, and the corresponding results present that they locate in the red region. The results indicate that the phosphors may have the potential applications in white light emitting diodes.
关 键 词:发光 Eu3+ NaY(MoO4)2
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