Du Hai-yan, Yang Zhi-ping, Sun Jia-yue
School of Chemical Engineering, Beijing Technology and Business University, Beijing 100037, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2009 Sep;29(9):2317-20.
The sample of NaYF4:Eu,Tm,Yb was synthesized by coprecipitation method. The emission of NaYF4:Eu,Tm,Yb excited by 360 nm is blue light with the peak at 452 nm from the transition of (1)D2-->(3)F4 of Tm3+. After being excited by 395 nm, NaYF4:Eu,Tm,Yb emits orange light with the peak at 591 nm originating from the transition of (5)D0-->(7)F1 of Eu3+. When excited by 409 nm, NaYF4:Eu,Tm,Yb emits red light with the peak at 613 nm from the transition of (5)D0-->(7)F2 of Eu3+. The color of upconversion luminescence of NaYF4:Eu,Tm,Yb excited by 980 nm was blue and red. The upconversion spectrum exhibits distinct emission peaks at 459, 478 and 641 nm. The blue light comes from the transition of (1)G4--(3)H6 and (1)D2-->(3)F4 of Tm3+. The absorption spectrum was also researched. The red light results from the transition of (1)G4--(3)F4 of Tm3+. The slope of the emission of 474 and 646 nm is 2.1 and 2.4 respectively. The emission of 478 and 641 nm is all due to three photon process. The structural properties of sample were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results show that NaYF4:Tm3+,Yb3+ prepared by coprecipitation method exhibits a hexagonal crystal.
采用共沉淀法合成了NaYF4:Eu,Tm,Yb样品。NaYF4:Eu,Tm,Yb在360 nm光激发下发射蓝光,其峰值位于452 nm,源于Tm3+的(1)D2-->(3)F4跃迁。在395 nm光激发下,NaYF4:Eu,Tm,Yb发射橙色光,峰值位于591 nm,源于Eu3+的(5)D0-->(7)F1跃迁。当被409 nm光激发时,NaYF4:Eu,Tm,Yb发射红光,峰值位于613 nm,源于Eu3+的(5)D0-->(7)F2跃迁。980 nm光激发下NaYF4:Eu,Tm,Yb的上转换发光颜色为蓝色和红色。上转换光谱在459、478和641 nm处呈现出明显的发射峰。蓝光来自Tm3+的(1)G4--(3)H6和(1)D2-->(3)F4跃迁。还研究了吸收光谱。红光来自Tm3+的(1)G4--(3)F4跃迁。474和646 nm发射的斜率分别为2.1和2.4。478和641 nm的发射均归因于三光子过程。通过X射线衍射(XRD)和扫描电子显微镜(SEM)对样品的结构性质进行了表征。结果表明,采用共沉淀法制备的NaYF4:Tm3+,Yb3+呈现六方晶体结构。