State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, PR China.
J Colloid Interface Sci. 2010 Sep 1;349(1):166-72. doi: 10.1016/j.jcis.2010.05.053. Epub 2010 May 20.
One-dimensional Lu(2)O(3):Eu(3+) nanofibers have been prepared by a combination method of sol-gel process and electrospinning technology. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), energy-dispersive X-ray spectrum (EDS), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), photoluminescence (PL), and cathodoluminescence (CL) spectra were used to characterize the samples. The XRD, FT-IR and TG-DTA results show that Lu(2)O(3):Eu(3+) samples crystallize at 900 degrees C. SEM images indicate that as prepared precursor samples and those annealed at 900 degrees C present uniform fiberlike morphology. After being heated at 900 degrees C, the diameters of fibers decrease greatly, ranging from 90 to 180nm. TEM image further manifests that the as-formed Lu(2)O(3):Eu(3+) nanofibers consist of nanoparticles (the crystallite size is about 16.5nm). Under the short wavelength ultraviolet irradiation and the low-voltage electron beam excitation, Lu(2)O(3):Eu(3+) nanofibers all exhibit typical red ((5)D(0)-(7)F(J)) emission. The optimum doping concentration of Eu(3+) in the Lu(2)O(3) nanofibers also has been investigated.
一维 Lu(2)O(3):Eu(3+) 纳米纤维通过溶胶-凝胶工艺和静电纺丝技术的组合方法制备。采用 X 射线衍射 (XRD)、傅里叶变换红外光谱 (FT-IR)、热重分析和差热分析 (TG-DTA)、扫描电子显微镜 (SEM)、能谱 (EDS)、透射电子显微镜 (TEM)、高分辨率透射电子显微镜 (HRTEM)、光致发光 (PL) 和阴极发光 (CL) 光谱对样品进行了表征。XRD、FT-IR 和 TG-DTA 结果表明,Lu(2)O(3):Eu(3+) 样品在 900°C 下结晶。SEM 图像表明,制备的前驱体样品和在 900°C 下退火的样品呈现均匀的纤维状形态。在 900°C 加热后,纤维的直径大大减小,范围从 90nm 到 180nm。TEM 图像进一步表明,形成的 Lu(2)O(3):Eu(3+) 纳米纤维由纳米颗粒组成(晶粒尺寸约为 16.5nm)。在短波长紫外光和低电压电子束激发下,Lu(2)O(3):Eu(3+) 纳米纤维均表现出典型的红色发射((5)D(0)-(7)F(J))。还研究了 Lu(2)O(3)纳米纤维中 Eu(3+)的最佳掺杂浓度。