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作 者:姜桂铖[1] 韦先涛[1] 王林香[1,2] 王晓纯[1] 陈永虎[1] 尹民[1]
机构地区:[1]中国科学技术大学物理系,安徽合肥230026 [2]新疆师范大学物理系,新疆乌鲁木齐830054
出 处:《光谱学与光谱分析》2011年第2期331-334,共4页Spectroscopy and Spectral Analysis
基 金:国家自然科学基金项目(10774140;10904139);国家自然科学基金国际(地区)合作与交流项目(50711120504);中国科学院知识创新工程重要方向项目(KJCX2-YW-M11);高等学校博士学科点专项科研基金项目(20060358054);安徽省人才开发基金项目(2007Z021)资助
摘 要:利用水热法合成了粉末发光材NaYF4∶Tb3+,Yb3+。分别用X射线衍射(XRD),光致发光谱(PL)和激发谱(PLE)测试了合成材料的物相结构和发光性质。研究结果表明:合成的NaYF4∶Tb3+,Yb3+材料为六方相的晶体,无立方相的。改变Tb3+和Yb3+的掺杂浓度后晶格结构没有变化,说明离子Tb3+和Yb3+取代的是Y3+离子的晶格位置。在355nm脉冲激光激发下,检测到了Tb3+的5 D3→7 FJ(J=5-0)和5 D4→7 FJ(J=6,5,4,3)可见波段特征发射光和Yb3+950~1 050nm(2 F5/2→2 F7/2)的近红外发光,研究了可见和近红外的发射强度随Yb3+掺杂浓度的变化,表明Tb3+和Yb3+之间存在能量传递,其可能的能量传递方式是共合作能量传递过程。当Tb3+和Yb3+的掺杂摩尔浓度分别是1mol%和6mol%时具有最强的近红外发射。NaYF4∶Tb3+,Yb3+ down-conversion(DC) phosphors were synthesized by hydrothermal method.X-ray diffraction(XRD),photoluminescence(PL) and photoluminescence excitation(PLE) spectra were used to characterize the samples.Experiment results revealed that samples of NaYF4∶Tb3+,Yb3+ crystallized in hexagonal shape without cubic shape.When the doping concentration of Tb3+and Yb3+ was altered,the lattice structure of samples did not change,indicating that the Tb3+ and Yb3+ ions are completely dissolved in the NaYF4 host lattice by substitution for the Y3+.The emission from 5D4→7F6(489 nm),5D4→7F5(542 nm),5D4→7F4(584 nm),and 5D4→7F3(619 nm) of Tb3+ ions was observed,in which the dominant emission was at 542 nm.With single Tb3+ doping,no near-infrared(NIR) emission was observed under excitation of 355 nm pulsed laser.However,while with Tb3+ and Yb3+ codoping,the NIR emission at around 950~1 100 nm from Yb3+(2F5/2→2F7/2) was observed under the same excitation.The dependence of the visible and NIR-emissions on Yb3+ doping concentration has been investigated.These results show that there is energy transfer process between Tb3+and Yb3+.Furthermore,it is a possible DC process through cooperative energy transfer from Tb3+ to Yb3+.When the doping concentration is 1% mol Tb3+ and 6% mol Yb3+ respectively,the intensity of NIR emission reaches its strongest.
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