Study on the Enhanced Luminescence of GdTaO4∶Eu3+ Phosphors by Li+ Codopant
FU Shang-yi, GU Mu*, LIU Xiao-lin, NI Chen, LIU Bo, HUANG Shi-ming
Shanghai Key Laboratory of Special Artificial Microstructure Materials and Technology, Department of Bohr Solid Physics, Tongji University, Shanghai 200092, China
Abstract:The XRD, emission and IR transmission spectra of Li-doped GdTaO4∶Eu3+ phosphors were measured. Judd-Ofelt theory was applied, and the intensity parameters Ω2 of Eu3+ for optical transition were calculated. The results show that Li+ codoping can enhance the luminescence intensity of GdTaO4∶Eu3+. The intensity can be improved up to 1.7 and 1.5 times, respectively, when x=0.06 and 0.10. The phenomenon results not from the assumption that Li+ codopant can reduce the crystal symmetry of GdTaO4∶Eu3+ so as to relax the parity forbidden transition, but from the flux effect of Li+ codopant which can improve the crystallinity of GdTaO4∶Eu3+ and suppress the Gd2O3 and Ta2O5 hetero phases. Gd0.92-xLixTaO4∶Eu3+0.08 has not only quite a good crystallinity but also less Gd2O3 and Ta2O5 hetero phases when x=0.06 or 0.10. Therefore, their luminescence intensities can be improved evidently.
傅尚怡,顾 牡*,刘小林,倪 晨,刘 波,黄世明 . Li+共掺杂GdTaO4∶Eu3+发光增强效应的研究 [J]. 光谱学与光谱分析, 2010, 30(09): 2317-2320.
FU Shang-yi, GU Mu*, LIU Xiao-lin, NI Chen, LIU Bo, HUANG Shi-ming . Study on the Enhanced Luminescence of GdTaO4∶Eu3+ Phosphors by Li+ Codopant . SPECTROSCOPY AND SPECTRAL ANALYSIS, 2010, 30(09): 2317-2320.
[1] Brixner L H. J. Electrochem. Soc.: Solid-State Sci. Technol., 1964, 111: 690. [2] Blasse G, Bril A. J. Lumin., 1970, 3: 109. [3] Blasse G. Chem. Phys. Lett., 1990, 173: 409. [4] Li B, Gu Z N, Lin J H, et al. J. Mater. Sci., 2000, 35: 1139. [5] Issler S L, Torardi C C. J. Alloys Compd., 1995, 229: 54. [6] Li B, Gu Z N, Lin J H, et al. Mater. Res. Bull., 2000, 35: 1921. [7] Liu B, Han K, Liu X L, et al. Solid State Commun., 2007, 144: 484. [8] Liu L X, Kun H, Mu G, et al. Solid State Commun., 2007, 142: 680. [9] Takeda T, Koshiba D, Kikkawa S J. J. Alloys Compd., 2006, 408: 879. [10] Park J C, Moon H K, Kim D K. Appl. Phys. Lett., 2000, 77: 2162. [11] Su Q, Lin J, Li B. J. Alloys Compd., 1995, 225: 120. [12] Judd B R. Phys. Rev., 1962, 127: 750. [13] Ofelt G S. J. Chem. Phys., 1962, 37: 511. [14] CHEN Bao-jiu, WANG Hai-yu, E Shu-hua, et al(陈宝玖,王海宇,鄂书华,等). Chinese J. Lumin.(发光学报), 2001, 22: 139. [15] WANG Ji-wei, SONG Hong-wei, XIA Hai-ping, et al(王绩伟,宋宏伟,夏海平,等). Journal of the Chinese Rare Earth Society(中国稀土学报), 2003, 21(2): 322. [16] Mandarino J A. Can. Mineral., 1976, 14: 498. [17] Boyer J C, Vetrone F, Capobianco J A, et al. J. Phys. Chem. B, 2004, 108: 20137. [18] Oomen E W J L, van Dongen A M A. J. Non-Cryst. Solids, 1989, 111: 205. [19] Blasse G. J. Solid State Chem.,1973,7: 169. [20] Xu L L, Wei B, An W W, et al. J. Alloys Compd., 2008, 460: 525. [21] Huang A P, Xu S L, Zhu M K, et al. Appl. Phys. Lett., 2003, 83: 3278.