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Mechanism of upconversion luminescence enhancement in Yb3+/Er3+ co-doped Y2O3 through Li+ incorporation
- Source :
- Physical Chemistry Chemical Physics. 22:2819-2826
- Publication Year :
- 2020
- Publisher :
- Royal Society of Chemistry (RSC), 2020.
-
Abstract
- Li+ doping is a well-known, simple, yet efficient strategy to optimize the properties of upconverting materials. Nonetheless, the position of Li+ in the lattice and the mechanism of upconversion enhancement are still controversial, especially in Yb3+/Er3+ co-doped Y2O3. This paper presents a comprehensive investigation of the above issues (i.e. the position occupied by Li+ in the lattice and the mechanism of luminescence enhancement, in terms of decreased defects) by studying (Y0.78-XYb0.20Er0.02LiX)2O3 powders. Neutron powder diffraction was employed for the first time in the literature to show that Li+ ions are accommodated in Y sites of YO6 octahedra, confirmed also by the content of oxygen defects, which was increased with the increase of Li+ concentration. FT-IR showed that there was a small change in the amount and the type of the surface-absorbed groups with the increase in the Li+ content, thus not supporting the prevailing conclusion that the quenching groups are decreased by doping Li+. Positron annihilation lifetime (PLAS) experiments showed that the total defect concentration and the large defect clusters, which are considered as quenching centers, are decreased with increasing Li+-content, resulting in the enhancement of the emission intensity in Yb3+/Er3+ co-doped Y2O3.
- Subjects :
- Materials science
Doping
Analytical chemistry
General Physics and Astronomy
chemistry.chemical_element
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Oxygen
Emission intensity
Photon upconversion
0104 chemical sciences
Ion
chemistry
Octahedron
Lattice (order)
Physical and Theoretical Chemistry
0210 nano-technology
Luminescence
Subjects
Details
- ISSN :
- 14639084 and 14639076
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Physical Chemistry Chemical Physics
- Accession number :
- edsair.doi...........cc17ef91e6e5230305046959204c9ef8