Title of article :
Enhanced UVB emission and analysis of chemical states of Ca5(PO4)3OH:Gd3+,Pr3+ phosphor prepared by co-precipitation Original Research Article
Author/Authors :
P.P. Mokoena، نويسنده , , I.M. Nagpure، نويسنده , , Vinay Kumar، نويسنده , , R.E. Kroon، نويسنده , , E.J. Olivier، نويسنده , , J.H. Neethling، نويسنده , , H.C. Swart، نويسنده , , O.M. Ntwaeaborwa، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
6
From page :
998
To page :
1003
Abstract :
Hydroxyapatite (Ca5(PO4)3OH) is a well-known bioceramic material used in medical applications because of its ability to form direct chemical bonds with living tissues. This mineral is currently used as a host for rare-earth ions (e.g. Gd3+, Pr3+, Tb3+, etc.) to prepare phosphors that can be used in light emitting devices of different types. In this study Ca5(PO4)3OH:Gd3+,Pr3+ phosphors were prepared by the co-precipitation method and were characterised by x-ray diffraction, x-ray photoelectron spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy, energy dispersive x-ray spectroscopy and photoluminescence spectroscopy. The x-ray diffraction pattern was consistent with the hexagonal phase of Ca5(PO4)3OH referenced in JCPDS card number 73-0293. The x-ray photoelectron spectroscopy data indicated that Ca2+ occupied two different lattice sites, referred to as Ca1 and Ca2. The photoluminescence data exhibited a narrowband emission located at 313 nm, which is associated with the 6P7/2→8S7/2 transition of the Gd3+ ion. This emission is classified as ultraviolet B and it is suitable for use in phototherapy lamps to treat various skin diseases. The photoluminescence intensity of the 313 nm emission was enhanced considerably by Pr3+ co-doping.
Keywords :
A. Inorganic compounds , A. Optical materials , C. Photoelectron spectroscopy , D. Crystal structure , D. Luminescence
Journal title :
Journal of Physics and Chemistry of Solids
Serial Year :
2014
Journal title :
Journal of Physics and Chemistry of Solids
Record number :
1312239
Link To Document :
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