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Gamma ray interactions with MoO3-doped lead phosphate glasses
The UV-Visible, Fourier transform infrared (FTIR) and Raman and electron spin resonance (ESR) spectra of undoped lead phosphate and MoO 3 -doped glassy samples have been investigated. The UV-VIS absorption spectra were re-measured after successive gamma irradiation. Before irradiation, undoped sampl...
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Published in: | Philosophical magazine (Abingdon, England) England), 2011-01, Vol.91 (3), p.341-356 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The UV-Visible, Fourier transform infrared (FTIR) and Raman and electron spin resonance (ESR) spectra of undoped lead phosphate and MoO
3
-doped glassy samples have been investigated. The UV-VIS absorption spectra were re-measured after successive gamma irradiation. Before irradiation, undoped sample exhibited strong ultraviolet absorption, which was attributed to co-absorption due to trace iron impurities (mainly Fe
3+
ions) and lead Pb
2+
ions. With the introduction of MoO
3
in progressive amounts, extra visible bands were recorded at about 400-440, 540, 750 and 870 nm. These bands are most likely correlated with the presence of Mo
3+
, Mo
4+
and Mo
5+
ions in the host glass. In the undoped specimen, gamma irradiation produced UV absorption bands that increased slightly with irradiation but no visible bands were recorded. Samples containing high MoO
3
content showed some resistance to irradiation with no bands in the visible region being observed. FTIR absorption spectra of the undoped and MoO
3
-doped samples revealed the formation of metaphosphate and pyrophosphate structural units. Highly MoO
3
-doped samples exhibited additional bands due to molybdate groups. Raman and ESR spectra were in agreement with UV-VIS and IR data, indicating the presence of molybdenum ions in lead phosphate glass, as Mo
3+
, Mo
4+
and Mo
6+
with different ratios. However, such glassy systems favor the trivalent species. |
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ISSN: | 1478-6435 1478-6443 |
DOI: | 10.1080/14786435.2010.521491 |