MOSSBAUER-SPECTRA OF TIN IN BINARY SI-SN OXIDE GLASSES

Citation
Kfe. Williams et al., MOSSBAUER-SPECTRA OF TIN IN BINARY SI-SN OXIDE GLASSES, Journal of physics. Condensed matter, 7(49), 1995, pp. 9485-9497
Citations number
15
Categorie Soggetti
Physics, Condensed Matter
ISSN journal
09538984
Volume
7
Issue
49
Year of publication
1995
Pages
9485 - 9497
Database
ISI
SICI code
0953-8984(1995)7:49<9485:MOTIBS>2.0.ZU;2-D
Abstract
The Mossbauer spectra of Sn-119 in binary glasses of SnO and SiO2, in varying proportions of between 16.8 and 71.5 mol% SnO, have been obtai ned at 77 K. From these spectra the tin was found to be predominantly in the 2(+) state. The isomer shift and the quadrupole splitting were both significantly greater than those in crystalline SnO and were foun d to decrease with increasing tin content, which also corresponds to d ecreasing molar volume. A second series of spectra of two of the sampl es was taken at temperatures between 10 and 300 K. These spectra show a decrease in shift with temperature which was the same for the two sa mples and which could only partly be accounted for by the second-order Doppler shift. The remainder was ascribed to the temperature dependen ce of the isomer shift. By using these data together with the measured expansivity and increase in density with tin content, it was possible to correct the isomer shift for the effects of the change in volume, and it was found that the volume-corrected isomer shift increased with increasing tin content. This showed that there was an increase in s-e lectron density at the tin nuclei, while the accompanying decrease in quadrupole splitting showed a decrease in the p-electron character, as expected for a decrease in covalency. From the decrease in absorption area with temperature the Debye temperature of tin was estimated to b e similar to 190 K, which is slightly less than that of crystalline Sn O, and decreased with increasing tin content. All the data suggest tha t the Sn-O bonds become progressively less covalent as more tin is add ed to SnO-SiO2 glasses, and possibly indicate a change from 4-fold to 6-fold co-ordination. A third series of spectra was obtained for the g lass containing 40.9 mol% of SnO after a series of heat treatments. Th e spectra show changes in the oxidation state of the tin which depende d upon the different conditions applied.