Published October 2015 | Version v1
Journal article

Synthesis and luminescence properties of highly uniform SiO2@LaPO4:Eu3+ core–shell phosphors

  • 1. College of Materials Science and Technology, Qingdao University of Science & Technology, Qingdao 266042 (China)

Description

Highlights: • SiO2@LaPO4:Eu3+ phosphors were synthesized by a wet-chemical method. • The pH value plays an important role in the formation of core shell-structured particles. • The SiO2@LaPO4:Eu3+ phosphors show strong orange–red luminescence. • This synthesis route can lower the cost of precious phosphors. - Abstract: SiO2@LaPO4:Eu3+ core–shell phosphors have been successfully synthesized by a one-step and economical wet-chemical route at low temperature. The as-obtained products were characterized by means of photoluminescence spectroscopy (PL), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive spectrometer (EDS) and X-ray photoelectron spectroscopy (XPS). The SEM, EDS and XPS analysis indicate that SiO2@LaPO4:Eu3+ core–shell phosphors can only be synthesized in a pH range of 8–11 and the possible mechanism has been proposed. The XRD results demonstrate that the structure of LaPO4:Eu3+ layers is transferred into monoclinic phase from hexagonal phase after annealing at 800 °C for 2 h. The SiO2@LaPO4:Eu3+ phosphors show strong orange–red luminescence under ultraviolet excitation. The relative emission intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles, and the optimum concentration for Eu3+ was determined to be 5 mol% of La3+ in SiO2@LaPO4 phosphors.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matdes.2015.06.060

Additional details

Identifiers

DOI
10.1016/j.matdes.2015.06.060;
PII
S0264127515004104;

Publishing Information

Journal Title
Materials and Design
Journal Volume
83
Journal Page Range
p. 795-800
ISSN
0264-1275

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.