Loading…
Sol-gel synthesis and up-conversion luminescence of GdPO4–Gd3PO7:Yb3+, Ln3+ (Ln = Er, Ho, Tm) phosphor
•GdPO4–Gd3PO7:Yb3+, (Ln3+ = Er, Ho, Tm) by Pechini sol-gel promotes a mixed crystalline phase.•Morphology differences due to the influence of Yb3+ mol% and synthesis route.•Up conversion spectra change significantly as a function of morphology and Yb3 + mol% content.•Yb3+ mol% influences morphology,...
Saved in:
Published in: | Materials letters 2018-09, Vol.226, p.34-37 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •GdPO4–Gd3PO7:Yb3+, (Ln3+ = Er, Ho, Tm) by Pechini sol-gel promotes a mixed crystalline phase.•Morphology differences due to the influence of Yb3+ mol% and synthesis route.•Up conversion spectra change significantly as a function of morphology and Yb3 + mol% content.•Yb3+ mol% influences morphology, emission and chromaticity coordinates of the samples.
This work reports the structural, morphological and luminescent properties of GdPO4–Gd3PO7:Yb3+, Ln3+ (Ln = Er, Ho, Tm) phosphors which have been synthesized by Pechini sol-gel process. The XRD patterns indicated that all the samples are crystalline and have a mixture of monoclinic monazite and monoclinic phases. Some samples were synthesized with ammonium hydroxide (NH4OH) and had better crystallinity than these synthesized without NH4OH. The up-conversion emissions were obtained under excitation at 967 nm. According to our results, the color emission was tuned from red to green by increasing the Yb3+ concentration from 5 mol% to 20 mol%. Moreover, the use of NH4OH to synthesize the samples doped with 20 mol% of Yb3+ enhanced their green emission band ≈3 times. The results reveal that doping the GdPO4–Gd3PO7 particles with rare earths produce an up-conversion emission which can be useful for the fabrication of luminescent coatings or lighting devices. |
---|---|
ISSN: | 0167-577X 1873-4979 |
DOI: | 10.1016/j.matlet.2018.04.117 |