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作 者:蒋晨飞[1] 黄文娟[1] 丁明烨[1] 宋艳[1] 倪亚茹[1] 陆春华[1] 许仲梓[1]
机构地区:[1]南京工业大学材料科学与工程学院,江苏南京210009
出 处:《发光学报》2012年第7期683-687,共5页Chinese Journal of Luminescence
基 金:国家自然科学基金(20901040/B0111);江苏省高校自然科学研究重大项目(10KJA430016);江苏省普通高校研究生科研创新计划(CXLX11-0355;CXZZ11-0330);江苏高校优势学科建设工程(PADP)资助项目
摘 要:采用高温溶剂热法合成了下转换发光材料NaYF4∶Eu3+和NaYF4∶Eu3+,Tb3+,采用X射线衍射(XRD)、场发射扫描电镜(FESEM)、激发(PLE)谱和光致发光(PL)谱对材料的物相结构、形貌特征和发光性质进行了表征和研究,并分析了其发光原理。结果表明:所合成的NaYF4∶Eu3+和NaYF4∶Eu3+,Tb3+为纯六方相晶体,尺寸在100 nm左右;改变Eu3+和Tb3+的掺杂浓度后晶格结构没有发生明显变化,说明Eu3+和Tb3+取代的是Y3+的晶格位置;在394 nm光的激发下,检测到Eu3+在5D0→7F1和5D0→7F2跃迁处的特征发射光,并且可见光强度随着Eu3+离子掺杂浓度的变化而变化。另外Tb3+离子浓度对NaYF4∶Eu3+晶体结构产生了一定的影响,说明掺杂Tb3+离子改变了Eu3+离子所处的配位环境,导致红色发光带增强,而这主要源于电偶极子跃迁的贡献。Powdered samples NaYF4∶Eu^3+ and NaYF4∶Eu^3+,Tb^3+ are successfully prepared by high temperature solvothermal method.The obtained samples are characterized by X-ray power diffraction(XRD),field emission scanning electron microscopy(FESEM),and photoluminescence(PL) spectra.Experiment results revealed that as-prepared NaYF4∶Eu^3+ and NaYF4∶Eu^3+,Tb^3+ crystallized in hexagonal phase without cubic phase,and the size was about 80 nm×100 nm(side length×thickness).When the doping concentration of Eu^3+ and Tb^3+are various,the lattice structure of samples do not change,indicating that the Eu^3+ and Tb^3+ ions are completely dissolved in the NaYF4 host lattice by substitution for the Y3+.The emission from 5D0→7F1(595 nm) and 5D0→7F2(618 nm) of Eu^3+ ions was observed under excitation of 394 nm light from Xe lamp.The visible light intensity changes with the doping ions of Eu^3+ concentration and the influence to crystal structure of Tb^3+ ions concentration have been investigated.These results show that the doping ions of Tb^3+ change the coordination environment of Eu^3+,resulting to stronger red emissions,and electric dipole transition occupied the main contribution.
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