Abstract
Green and less intense red emissions from Er3+ (4f11)-doped sol-gel silica samples (prepared from tetraethylorthosilicate at room temperature and dried at 70°C) under 488 nm excitation were monitored as a function of sample curing temperature. These green and red emission bands, centered at 550 and 660 nm, are the 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions in Er3+ ions, respectively. The emission intensities were found to increase with increasing sample curing temperature ranging from 200 to 1000°C. Green upconversion emission from Er3+ ions in the same samples was also recorded under 647.1 nm light excitation. Its efficiency was enhanced with increased sample curing temperature. This enhancement is attributed to the Er3+-coordination environment produced by different sample curing temperatures. Increasing curing temperatures produces increasing degrees of dehydration and de-alcoholation around the Er3+ ions, thus resulting in a decrease in the non-radiative emission rate.
| Original language | English |
|---|---|
| Pages (from-to) | 235-240 |
| Number of pages | 6 |
| Journal | Journal of Non-Crystalline Solids |
| Volume | 194 |
| Issue number | 3 |
| DOIs | |
| State | Published - Feb 1996 |
Funding
Research was sponsored by the Division of Chemical Sciences, Office of Basic Energy Sciences, US Department of Energy under grant DE-FGOS-88ER13865 to the University of Tennessee, Knoxville and contract DE-AC0584GR21400 with Lockheed Martin Energy Systems, Inc.