Facile sonochemical synthesis and photoluminescent properties of lanthanide orthophosphate nanoparticles
Uniform lanthanide orthophosphate LnPO 4 ( Ln=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho) nanoparticles have been systematically synthesized via a facile, fast, efficient ultrasonic irradiation of inorganic salt aqueous solution under ambient conditions without any surfactant or template. X-ray diffract...
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Veröffentlicht in: | Journal of solid state chemistry 2009-02, Vol.182 (2), p.339-347 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Uniform lanthanide orthophosphate
LnPO
4 (
Ln=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho) nanoparticles have been systematically synthesized via a facile, fast, efficient ultrasonic irradiation of inorganic salt aqueous solution under ambient conditions without any surfactant or template. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), photoluminescence (PL) spectra as well as kinetic decays were employed to characterize the samples. The SEM and the TEM images show that the hexagonal structured lanthanide orthophosphate
LnPO
4 (
Ln=La, Ce, Pr, Nd, Sm, Eu, Gd) products have nanorod bundles morphology, while the tetragonal
LnPO
4 (
Ln=Tb, Dy, Ho) samples prepared under the same experimental conditions are composed of nanoparticles. HRTEM micrographs and SAED results prove that these nanostructures are polycrystalline in nature. The possible formation mechanism for
LnPO
4 (
Ln=La–Gd) nanorod bundles is proposed. Eu
3+-doped LaPO
4 and Tb
3+-doped CePO
4 samples were also prepared by using the same synthetic process, which exhibit an orange–red (Eu
3+:
5D
0–
7F
1, 2, 3, 4) and green (Tb
3+,
5D
4–
7F
3, 4, 5, 6) emission, respectively.
Hexagonal
LnPO
4 (
Ln=La, Ce, Pr, Nd, Sm, Eu, Gd) and tetragonal
LnPO
4 (
Ln=Tb, Dy, Ho) nanoparticles have been synthesized by a simple and facile sonochemical method |
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ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2008.10.023 |