Abstract
Novel nanostructures of Y3Al5O12:Tb(3+) (denoted as YAG:Tb(3+) for short) nanobelts and nanofibers were fabricated by calcination of the respective electrospun PVP/[Y(NO3)3 + Tb(NO3)3 + Al(NO3)3] composite nanobelts and nanofibers. YAG:Tb(3+) nanostructures are cubic in structure with a space group of Ia 3d. The thickness and width of the YAG:7%Tb(3+) nanobelts are respectively ca. 125 nm and 5.9 ± 0.3 m, and the diameter of YAG:7%Tb(3+) nanofibers is 166.0 ± 20 nm (95% confidence level). The YAG:Tb(3+) nanostructures emit predominantly at 544 nm from the energy levels transition of (5) D4 → (7) F5 of Tb(3+) ions under the excitation of 274-nm ultraviolet light. It was found that the optimum doping molar concentration of Tb(3+) ions for YAG:Tb(3+) nanostructures was 7%. Compared with YAG:7%Tb(3+) nanofibers, YAG:7%Tb(3+) nanobelts exhibit a stronger photoluminescence (PL) intensity under the same doping concentration. Commission International de l'Eclairage (CIE) analysis demonstrates that the emitting colors of YAG:Tb(3+) nanostructures are located in the green region and color-tuned luminescence can be obtained by changing the doping concentration of Tb(3+) and morphologies of the nanostructures, which could be applied in the field of optical telecommunication and optoelectronic devices. The possible formation mechanisms of YAG:Tb(3+) nanobelts and nanofibers are also proposed.
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