Structure and red-ox chemistry of tin in SnO center dot NaPO3 pseudo-binary glasses

Citation
Mh. Bhat et al., Structure and red-ox chemistry of tin in SnO center dot NaPO3 pseudo-binary glasses, J NON-CRYST, 291(1-2), 2001, pp. 93-106
Citations number
44
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
JOURNAL OF NON-CRYSTALLINE SOLIDS
ISSN journal
00223093 → ACNP
Volume
291
Issue
1-2
Year of publication
2001
Pages
93 - 106
Database
ISI
SICI code
0022-3093(200110)291:1-2<93:SARCOT>2.0.ZU;2-G
Abstract
Thermal and spectroscopic investigations have been carried out on a number of binary SnO-NaPO3 glasses over a wide range of compositions; SnO : NaPO3 from 0:100 to 45:55. Structures of the glasses have been investigated using Raman, Fourier transform infrared (FTIR), P-31-HR-MAS-NMR and Sn-119 Mossb auer spectroscopies. Sn-119 Mossbauer spectra suggests that there is an equ ilibrium of Sn-II(SnO) and Sn-IV(SnO2) in the glasses in the ratio 40:60 ir respective of the composition. P-31-MAS-NMR, IR and Raman spectra confirm t he partial oxidation of SnO to SnO2. The unoxidized part of SnO in the glas s acts as a modifier up to similar to 27 mol% of nominal composition. Above this concentration, SnO acts as a glass former. SnO2 however, is always fo und to behave as a glass network former. A structural model has been propos ed, which envisages Sn-IV as playing a key role in preserving part of the m etaphosphate units in the structure so that SnO changes its role from a mod ifier to former above 27 mol% (SnO) concentration. The model is consistent with the behaviour of glass transition temperatures, molar volumes and comp ositional dependence of infrared (IR) and Raman spectroscopic features. The equilibration of Sn-II and Sn-IV in the phosphate glasses is rationalized on the basis of a kinetic approach, which visualizes the presence of a pre- equilibrium situation where the slow step is the transfer of O2- to the pho sphate matrix from the dissolved O-2(2-) species. (C) 2001 Elsevier Science B.V. All rights reserved.