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发光粉CeO2:Eu~(3+)和SrCeO3:Eu~(3+)的合成及其发光性能研究

Synthesis and Luminescent Properties of CeO2: Eu~(3+) and SrCeO3: Eu~(3+) Powder Phosphors

【作者】 陈绍军

【导师】 刘晓华;

【作者基本信息】 汕头大学 , 材料物理与化学, 2006, 硕士

【摘要】 通过高温固相反应法制备了掺Eu3+基质为CeO2的发光粉系列样品并对其做了X射线衍射谱(XRD)和光致发光谱(PL)检测。XRD结果表明在Eu3+掺杂浓度为0.2?10at.%的范围内,Eu3+完全进入了CeO2的晶格,形成固溶体Ce1-xEuxO2;PL谱表明Eu3+的发射峰强度依赖于Eu3+的掺杂浓度,在Eu3+的含量为1at.%时最强,随后出现浓度猝灭。 采用高温固相反应法和溶胶-凝胶法(sol-gel)合成了新型发光材料SrCeO3:Eu3+。研究了材料制备的相变过程以及材料的结构性质和发光特性。对于采用sol-gel法制备了SrCeO3:Eu3+发光粉,TG-DTA和XRD分析结果表明钙钛矿结构的SrCeO3:Eu3+形成于850℃左右;1000℃焙烧的样品以SrCeO3为主晶相,伴随有少量Sr2CeO4和CeO2杂相;1250℃焙烧的样品为SrCeO3钙钛矿结构并含有极少量CeO2杂相。分析表明,在干凝胶高温焙烧过程中,SrO的过量蒸发导致了由sol-gel法制备的SrCeO3:Eu3+中残留少量的CeO2相。因而在采用sol-gel法制备SrCeO3:Eu3+发光粉时,起始反应物中SrCO3应有适当过量为宜。 采用sol-gel法制备的SrCeO3:Eu3+样品的激发光谱由峰值位于~239、~258nm激发带和270—320nm宽激发带组成。其中270—320nm激发带为Eu3+-O2-的电荷迁移带和基质Ce4+-O2-电荷迁移带的叠加。短波区的两个激发带起源于基质的能量吸收。各激发带对应的发射光谱均以5D07F1跃迁为主。 对于通过高温固相反应法制备的不同组分的SrCeO3:Eu3+发光粉。研究了EH3+离子在SrCeO3晶格中的替代规律。光谱分析表明~239nm和~258nm激发带起源于基质的紫外吸收;~273nm、~298nm的激发带为Eu3+-O2-的电荷迁移带;~285nm和~310nm激发带属于ce4+-O2-的电荷迁移带。发射峰强度随Eu3+掺杂浓度从0.5at.%到15at.%逐渐增强,在15at.%时最强,没有出现浓度猝灭。在Eu3+浓度少于5at.%的样品中,5D07F1跃迁比5D07F2跃迁强,在Eu3+浓度超过5at.%的样品中,5D07F2跃迁比5D07F1跃迁强。SrCeO3:Eu3+发光粉样品对不同激发波长表现出不同的发射强度。

【Abstract】 CeO2:Eu3+ phosphor powders with various Eu3+ concentrations have been synthesized by the solid state reaction method. X-ray diffraction (XRD) analysis showed the formation of pure solid solution Ce1-xEuxO2 up to 10at.% concentration of Eu3+. The Photoluminescence (PL) measurements indicated the dependence of PL emission intensity on the Eu3+ concentrations. The CeO-2:Eu3+ phosphor powders showed the strongest photoluminescence for 1 at.% concentration of Eu3+ and then abruptly decreased indicating the concentration quenching.SrCeO3:Eu3+ phosphor powders have been synthesized by the sol-gel method and solid state reaction method. TG-DTA and XRD were employed to analyze the synthesis process and the crystalline structure of SrCeO3:Eu3+ powders. SrCeO3:Eu3+ phosphor powders with almost pure perovskite phase were obtained at sintering temperature of 1250°C. The detailed analysis demonstrated that Eu3+ ions mainly occupy the Ce4+ sites in SrCeO3 lattice.The Photoluminescence (PL) measurements indicated the dependence of PL emission intensity on the Eu3+ concentrations. The excitation spectra of SrCeO3:Eu3+ consist of a series of excitation bands. Among these bands, the ones at 239nm and 258nm originate from ultraviolet absorption of the host; the bands at 273nm and 298nm are Eu3+-O2- charge transition band (CTB), and the bands at 285nm and 310nm are Ce4+-O2- CTB. The emission spectra of SrCeO3:Eu3+ showed Do-7F1 and 5D0-7F2 transitions of Eu3+ are the strongest emissions for the samples with Eu3+ concentration of 15at.% and no concentration quenching was observed. The sample with 5at.% Eu3+ exhibited the strongest emission band centered at 422nm. The emission intensities of SrCeO3:Eu3+ powders showed obvious dependence on the excitation wavelength. The sensitive excitation wavelengths for the emissions at 422nm, 370-470nm and 4f transitions of Eu3+ are 236nm, 241nm and 290nm, respectively.

【关键词】 srCO3CeO2Eu3+SrCeO3:Eu3+发光固相反应法溶胶-凝胶法
【Key words】 CeO2Eu3+SrCeO3:Eu3+LuminescenceSolid state reactionsol-gel method
  • 【网络出版投稿人】 汕头大学
  • 【网络出版年期】2007年 01期
  • 【分类号】TB34
  • 【被引频次】2
  • 【下载频次】182
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