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作 者:王孝东[1] 刘晓华[1] 陈绍军[1] 黎明[1] 刘敏[1]
出 处:《光谱学与光谱分析》2007年第11期2182-2185,共4页Spectroscopy and Spectral Analysis
基 金:广东省自然科学基金项目(04010998);人事部留学人员科技活动项目择优资助经费;教育部回国留学人员基金资助
摘 要:采用溶胶-凝胶法制备了不同浓度Eu3+掺杂的CeO2发光粉,样品粉末在紫外光激发下发出明亮的橙红色光。利用X射线衍射(XRD)、热重-差热分析(TG-DTA)和光致发光光谱(PL)对样品的结晶过程和发光性质进行了表征。XRD分析表明在0.2at.%~10at.%的Eu3+掺杂范围内,用溶胶-凝胶法合成的样品在500℃就结晶成纯相的CeO2∶Eu3+多晶粉末。由于Ce4+和Eu3+离子半径十分接近,因而Eu3+在CeO2中具有较高的固溶度。PL激发谱中出现在300~390nm的宽带激发峰起源于基质CeO2的吸收,电子吸收能量后,发生O2-—Ce4+的电荷迁移,再将能量传递给Eu3+。PL发射谱显示Eu3+含量为6at.%的样品发光强度最强,随后出现浓度猝灭。导致发光出现浓度猝灭的机制是电偶极-电四极相互作用。样品烧结温度的升高,促使晶粒长大和结晶完整性提高,从而显著提高了CeO2∶Eu3+粉末的发光强度。CeO2 : Eu^3+ phosphor powders with various Eu^3+ concentrations have been prepared by the sol-gel method. Upon excitation with UV light, the CeO2 : Eu^3+ powders showed bright orange red emissions due to the 4f-4f transitions of Eu^3+ ions. X-ray diffraction (XRD), TG-DTA and Photoluminescence (PL) measurements were used to characterize the samples. XRD analysis showed that the powders with pure cubic fluorite-type CeO2 phase at an up to 10at. % concentration of Eu^3+ was obtained at the sintering temperatures from 500 to 1 250 ℃. The large solubility for doping Eu3+ ions in CeO2 is due to the nearness of ionic radius between Ce^4+ and Eu^3+. It was also found that an increase in sintering temperature promotes the grain growth of CeO2 and improves its crystallinity. The excitation spectra of the CeO2 : Eu^3+ powders were dominated by a broad band at 300- 390 nm, suggesting the efficient energy transfer from the O^2--Ce^4+ charge-transfer state to the doping Eu^3+ in the CeCh : Eu^3+ powders. The CeO2 : Eu^3+phosphor powders with a 6at. % concentration of Eu^3+ sintered at 1 250 ℃ revealed the stron- gest photoluminescence and then in abruptly decreased with increasing the doping concentration indicating the concentration quenching. The mechanism of concentration quenching could be explained as the result of the dipole-quadrupole interaction of neighboring Eu^3+.
关 键 词:CeO2:Eu^3+ 发光 溶胶-凝胶法
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