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    South African Journal of Chemistry

    On-line version ISSN 1996-840XPrint version ISSN 0379-4350

    S.Afr.j.chem. (Online) vol.61  Durban  2008

     

    RESEARCH ARTICLE

     

    Preparation of MAl2O4: Eu2+, Sm3+ (M = Ca, Sr, Ba) phosphors by the combustion method and their luminescent properties

     

     

    Hua ZhongI,II, *; Xirui ZengI,II

    IProvincial Key Laboratory of Coordination Chemistry, Jinggangshan University, Jian, 343009, People's Republic of China
    IICollege of Chemistry and Chemical Engineering, Jinggangshan University, Jian, 343009, People's Republic of China

     

     


    ABSTRACT

    A series of MAl2O4:Eu2+,Sm3+ (M = Ca, Sr, Ba) phosphors was prepared by the combustion method, and the influence of these alkaline earth metals on the structure and luminescent performances for these phosphors was investigated. A relationship was established between their composition, crystallization capacity and luminescent properties. The results show that the CaAl2O4: Eu2+,Sm3+ and SrAl2O4:Eu2+,Sm3+ phosphors exhibit monoclinic crystal systems and that the BaAl2O4:Eu2+,Sm3+ phosphor exhibits a hexagonal structure. The alkaline earth metal has a positive effect on the crystallization process, the heat treatment procedure and the luminescent properties of the corresponding phosphors. According to the order Ca > Sr > Ba, the maximum emission wavelengths of the corresponding phosphors are found at 505 nm, 490 nm and 478 nm, and the relevant colours of emitted light are between blue and green, which indicates that there is a clear blue shift in the emission spectra, but their excitation spectra show almost no difference. The decay curve shows that the afterglow intensity and time are not only related to the activating processes and the hole transport, but also to the phase structure and the grain size, which is in the order Sr > Ca > Ba.

    Keywords: Long afterglow, alkaline earth aluminates, spectra, combustion method


     

     

    Full text available only in pdf format.

     

    Acknowledgements

    This work was supported by the Science and Technology Bureau of Jian, Jiangxi Province of China (Project No. 20052817).

     

    References

    1 T. Matsuzawa, Y. Aoki, N. Takeuchi and Y. Murayama, J. Electrochem. Soc., 1999, 143, 2670-2675.         [ Links ]

    2 T. Aitasalo, P. Deren and H. Holsa, J. Solid State Chem., 2003, 171, 114-121.         [ Links ]

    3 L. Yuanhua, T. Zilong and Z. Zhongtai, J. Eur. Ceram. Soc., 2003, 23, 175-180.         [ Links ]

    4 K. Kato, I. Tsutai, T. Kamimura, F. Kaneko, K. Shinbo, M. Ohta and T. Kawakami, J. Lumin., 1999, 82, 213-220.         [ Links ]

    5 R. Sakai, T. Katsumata, S. Komuro and T. Morikawa, J. Lumin., 1999, 85, 149-154.         [ Links ]

    6 W. Jia, H. Yuan, S. Holmstrom, H. Liu and W.M. Yen, J. Lumin, 1999, 83-84, 465-469.         [ Links ]

    7 H. Liu, Y. Wang, J. Yang and W. Su, J. Alloy Comp., 1993, 191, 1-6.         [ Links ]

    8 S.H.M. Poort and G. Blasse, J. Lumin, 1997, 72-74, 247-253.         [ Links ]

    9 F.C. Palilla, A. K. Levine and M.R. Tomkus, J. Electrochem. Soc., 1968, 115, 642-647.         [ Links ]

    10 J.R. Qiu and K. Hirao, Solid State Commun., 1998, 106, 795-801.         [ Links ]

    11 T.L. Liu, D.X. Feng and P.H. Yang, Rare Materials, 2000, 19, 297-302.         [ Links ]

    12 T. Katsumata, T. Nabae and K. Sasajima, J. Amer. Ceram. Soc., 1998, 81, 413-418.         [ Links ]

    13 Y. Murayama, Y. Aoki, N. Takeuchi and T. Matsuzawa, U.S. Patent No. 5424006 (1995).         [ Links ]

    14 H. Takasaki, S. Tanabe and T. Hanada, J. Japan. Ceram. Soc., 1996, 104, 322-327.         [ Links ]

    15 T. Katsumata, R. Sakai and S. Komuro, J. Crystal Growth., 1999, 198-199, 869-875.         [ Links ]

    16 M.D. Tang, C.K. Li and Z.W. Gao, Chin. J. Lumin, 1995, 16, 51-56.         [ Links ]

    17 K. Hayashi, S. Toyoda, H. Takebe and K. Morinaga, J. Japan. Ceram. Soc, 1991, 99, 550-556.         [ Links ]

    18 G. Blasse and A. Bril, Philips Res. Rept, 1968, 23, 201-207.         [ Links ]

    19 Y. Lin, Z. Zhang and Z. Tang, Materials Chem. Phys, 2001, 70, 156-161.         [ Links ]

    20 J. Geng and Z.P. Wu, Materials Rev., 2002, 16(5), 45-51.         [ Links ]

    21 Y.G. Chen, G.M. Qiu and Y.B. Sun, J. Rare Earths, 2002, 20, 50-55.         [ Links ]

    22 T. Katasumata, T. Nabae and K. Sasajima, J. Crystal Growth, 1998, 183, 361-367.         [ Links ]

    23 M. Ohta, M. Maruyama and T. Nishijo, J. Japan. Ceram. Soc., 2000, 108, 284-290.         [ Links ]

    24 T. Katsumata, T. Nabae and K. Sasajima, J. Electrochem. Soc., 1997, 144, L243.         [ Links ]

     

     

    Received 24 February 2006
    Revised 15 October 2007
    Accepted 24 October 2007

     

     

    * To whom correspondence should be addressed. E-mail address: hua_zh@163.com