Low-temperature wet chemical synthesis and photoluminescence properties of YVO4: Bi3+, Eu3+ nanophosphors

S Takeshita, T Isobe, S Niikura - Journal of luminescence, 2008 - Elsevier
S Takeshita, T Isobe, S Niikura
Journal of luminescence, 2008Elsevier
YVO4: Bi3+, Eu3+ nanophosphors are prepared by the citrate-assisted low-temperature wet
chemical synthesis. When the colloidal solution is aged at 60° C, the crystalline YVO4: Bi3+,
Eu3+ nanorods are formed from the amorphous gel precursors, as confirmed by
transmission electron microscopy and X-ray diffractometry (XRD). YVO4: Bi3+, Eu3+
nanophosphors emit red through energy transfer from Bi3+ to Eu3+ under near-UV-light
excitation. The emission intensity increases with increasing the fraction of the crystalline …
YVO4: Bi3+, Eu3+nanophosphors are prepared by the citrate-assisted low-temperature wet chemical synthesis. When the colloidal solution is aged at 60°C, the crystalline YVO4: Bi3+, Eu3+ nanorods are formed from the amorphous gel precursors, as confirmed by transmission electron microscopy and X-ray diffractometry (XRD). YVO4: Bi3+, Eu3+ nanophosphors emit red through energy transfer from Bi3+ to Eu3+ under near-UV-light excitation. The emission intensity increases with increasing the fraction of the crystalline phase during aging. The excitation peak corresponding to Bi3+–V5+ charge transfer relative to those of O2−–V5+ and O2−–Eu3+ charge transfers gradually becomes strong until the completion of the crystallization, although the contents of individual Bi3+ and Eu3+ ions incorporated into YVO4 keep constant. When the aging is continued after the completion of the crystallization, the content of incorporated Bi3+ gradually increases, and hence the emission intensity decreases as a result of the energy migration among Bi3+ ions. These results suggest that in addition to the fraction of the crystalline phase and the contents of incorporated Bi3+ and Eu3+ ions, the local chemical states around Bi3+ play significant roles in photoluminescence properties.
Elsevier
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