Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10155526 | Journal of Non-Crystalline Solids | 2018 | 9 Pages |
Abstract
The atomic level structures of ternary 0.2Na2Oâ¯+â¯0.8[xBO3/2â¯+â¯(1-x)GeO2] glasses have been carefully examined for the first time using a combination of Raman, infrared (IR) and 11B magic angle spinning nuclear magnetic resonance (MAS-NMR) spectroscopies. It was found that, like in other mixed glass former (MGF) systems, there is an unequal sharing of the sodium oxide between the two glass formers, B and Ge, across this series 0â¯<â¯xâ¯<â¯1. It is found that for all xâ¯>â¯0, the Na2O preferentially reacts with boron to create a larger number of tetrahedral boron, BO4/2â1 â¡ B4, units than would be found for a binary sodium borate glass of the same mole fraction, 0.20, of Na2O. In addition to this higher than expected fraction of B4 units as determined by the 11B MAS-NMR measurements, the Raman spectra further suggest the presence of high concentrations of octahedrally coordinated GeO6/2â2, Ge6, units in the GeO2 rich end of this compositional series, xâ¯â¤â¯0.2. Across this series, it is found that there are at most five short range order (SRO) structural units present in these glasses, BO3/2 (B3), B4, GeO6/2â2 (Ge6), GeO3/2Oâ1 (Ge3), and GeO4/2 (Ge4), where the superscript gives the number of bridging oxygens (BOs) bonded to the central atom. The composition, x, dependence of all of these SRO structural units were determined by combining the results all of these spectral techniques and requiring that the total sum of all the negatively charged SRO units balance the positive (+0.4) charges from the Na+ ions and that the total amount of B balance to 0.8Ã, the total amount of Ge balance to 0.8*(1-x), and the total amount of oxygen balance to1.8-0.4à as required by the stoichiometry of this compositional series.
Keywords
Related Topics
Physical Sciences and Engineering
Materials Science
Ceramics and Composites
Authors
Brittany Curtis, David Hynek, Sydney Kaizer, Steve Feller, Steve W. Martin,