Hydrothermal synthesis and photoluminescence of SrWO4:Tb3+ novel green phosphor
Introduction
Luminescent materials containing rare-earth ions have become popular in the progress of the optical material of significant importance [1], [2], [3], [4]. Commercial powder phosphors are usually based on the host matrices of tungstates [5], phosphates [6], borates [7], silicates [8] and aluminates [9] etc. Among them, tungstates have two types of structure: wolframite and scheelite. Strontium tungstate has the scheelite structure which is tetragonal with space group I41/a () [10]. The luminescent properties of strontium tungstate have been extensively investigated because it is a widely used in a variety of fields, such as laser materials [11], microwave ceramics [12], and photoluminescence [13].
At present, the traditional synthesis for commercial green fluorescent lamp phosphors (LaPO4:Ce,Tb) is usually solid-state reaction over 1100 °C, including a long processing time and reducing atmosphere [6]. Moreover, the LaPO4:Ce,Tb phosphor particles prepared by the conventional solid-state reaction method had large size and irregular morphology. Therefore, it is important to develop new processing material method with low costs, environmentally friendly and with possibility of formation of materials on macro- and nanoscale with well-defined morphologies, such as sol–gel process [14] and hydrothermal method [15]. There have been some reports about the hydrothermal synthesis and properties of the alkaline-earth tungstate materials, all of them were concentrated on pure SrWO4 [16] and Eu3+-doped CaWO4 [15], [17]. But to the best of our knowledge, hydrothermal synthesis and photoluminescence properties of SrWO4:Tb3+ phosphors have not yet been reported till now.
In this paper, we report the preparation of SrWO4:Tb3+ spherical phosphors with different Tb3+-doped concentration by a mild hydrothermal method. The luminescence properties of SrWO4:Tb3+ phosphors were investigated by changing doping concentration of Tb3+ ions in the host. Our results show that SrWO4:Tb3+ has good properties as a green phosphor for fluorescence lamps application.
Section snippets
Sample preparation
The starting materials were Na2WO4·2H2O (AR), Sr(NO3)2·2H2O (AR),Tb4O7 (99.99%) and citric acid (AR), and all of them were of analytical grade without any further purification. SrWO4:Tb3+ phosphors were typically synthesized as follows: 0.1459 g Tb4O7 was first dissolved in dilute nitric acid under heating. After the Tb4O7 was completely dissolved, the extra nitrite acid was removed by evaporation. Then deionized water was added to obtain Tb(NO3)3 solution. Meanwhile 1.2234 g of Sr(NO3)2·2H2O and
Results and discussion
Fig. 1 shows the XRD patterns of SrWO4:Tb3+ phosphors with different Tb3+-doped concentration. From Fig. 1, it can be seen that all samples agree well with the reported data of scheelite phase SrWO4 (JCPDS Card No. 08-0490) and no trace of characteristic peaks are observed for other impurity phases, showing that the simple hydrothermal method is a feasible route to prepare pure phase SrWO4:Tb3+ phosphors. It could be found that SrWO4:Tb3+ phosphors with different Tb3+ concentration are sheelite
Conclusions
The spherical SWO4:Tb3+ phosphors with different Tb3+ concentration can be prepared by a mild hydrothermal method at 180 °C for 12 h. The excitation spectra show the strong energy transfer from WO42− group of the host material to the Tb3+ ions. The optimum concentration for Tb3+ was determined to be about 12 at.% of Tb3+ ions in SWO4:Tb3+ phosphors. Furthermore, the reaction temperature for SWO4:Tb3+ phosphors is much lower than that for LaPO4:Ce,Tb. Therefore, this material seems to be promising
Acknowledgements
This work has been financially supported by the startup foundation from talent introduction of Jiangxi University of Science and Technology, and Ganzhou City public services platform for technical innovation of nonferrous metal (Grant No. PT08006).
References (22)
- et al.
Mater. Res. Bull.
(2006) - et al.
Mater. Chem. Phys.
(2008) - et al.
Chem. Phys. Lett.
(2004) - et al.
J. Lumin.
(1991) - et al.
J. Lumin.
(2007) - et al.
Opt. Mater.
(2003) - et al.
J. Eur. Ceram. Soc.
(2006) - et al.
J. Colloid Interface Sci.
(2009) - et al.
J. Solid State Chem.
(2008) - et al.
J. Solid State Chem.
(2003)