Issue 18, 2009

One-dimensional CaWO4 and CaWO4:Tb3+nanowires and nanotubes: electrospinning preparation and luminescent properties

Abstract

One-dimensional CaWO4 and CaWO4:Tb3+ nanowires and nanotubes have been prepared by a combination method of sol-gel process and electrospinning. X-Ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), photoluminescence (PL), low voltage cathodoluminescence (CL) and time-resolved emission spectra, as well as kinetic decays were used to characterize the resulting samples. The results of XRD, FT-IR, TG-DTA indicate that the CaWO4 and CaWO4:Tb3+ samples begin to crystallize at 500 °C with the scheelite structure. Under ultraviolet excitation and low-voltage electron beams excitation, the CaWO4 samples exhibit a blue emission band with a maximum at 416 nm originating from the WO42−groups, while the CaWO4:Tb3+ samples show the characteristic emission of Tb3+ corresponding to 5D47F6,5,4,3 transitions due to an efficient energy transfer from WO42− to Tb3+. The energy transfer process was further studied by the time-resolved emission spectra as well as kinetic decay curves of Tb3+ upon excitation into the WO42−groups. Furthermore, the PL emission colour of CaWO4: x mol %Tb3+ can be tuned from blue to green by changing the concentrations (x) of the Tb3+ ion, making the materials have potential applications as fluorescent lamps and field emission displays (FEDs).

Graphical abstract: One-dimensional CaWO4 and CaWO4:Tb3+ nanowires and nanotubes: electrospinning preparation and luminescent properties

Supplementary files

Article information

Article type
Paper
Submitted
23 Oct 2008
Accepted
29 Jan 2009
First published
03 Mar 2009

J. Mater. Chem., 2009,19, 2737-2746

One-dimensional CaWO4 and CaWO4:Tb3+ nanowires and nanotubes: electrospinning preparation and luminescent properties

Z. Hou, C. Li, J. Yang, H. Lian, P. Yang, R. Chai, Z. Cheng and J. Lin, J. Mater. Chem., 2009, 19, 2737 DOI: 10.1039/B818810F

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