Loading…
Luminescence and structural analysis of Ce 3+ and Er 3+ doped and Ce 3+ –Er 3+ codoped Ca 3 Sc 2 Si 3 O 12 garnets: influence of the doping concentration in the energy transfer processes
We present research on Ca 3 Sc 2 Si 3 O 12 garnets doped with Ce 3+ and Er 3+ ions that were synthesized by the freeze-drying precursor method. The structural characterization was performed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Scanning electron microscopy (SEM) imag...
Saved in:
Published in: | RSC advances 2016, Vol.6 (18), p.15054-15061 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | We present research on Ca
3
Sc
2
Si
3
O
12
garnets doped with Ce
3+
and Er
3+
ions that were synthesized by the freeze-drying precursor method. The structural characterization was performed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Scanning electron microscopy (SEM) images of the calcined material were studied. Nanocrystals of Ca
3
Sc
2
Si
3
O
12
were obtained by calcining the precursor at 1200 °C for 4 h with a mean size of about 100 nm. The luminescence features of Ce
3+
and Er
3+
doped samples indicated that these ions are effectively incorporated into the crystalline phase. In addition, codoping with Ce
3+
–Er
3+
ions results in energy transfer processes from Ce
3+
to Er
3+
ions which led to the enhancement of near-infrared luminescence at 1.5 μm. The efficiency of this non-radiative energy transfer process has been studied by means of excited state dynamics as a function of the doping concentration. From these results we have found that near-infrared Er
3+
luminescence efficiency under VIS Ce
3+
excitation is at maximal for 1Ce
3+
–1Er
3+
codoped Ca
3
Sc
2
Si
3
O
12
garnets (in mol%). Luminescence quenching at higher Er
3+
ion concentrations is observed. |
---|---|
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C5RA22630A |