Role of vanadium oxide on the lithium silicate glass structure and properties
authors Gaddam, A; Allu, AR; Fernandes, HR; Stan, GE; Negrila, CC; Jamale, AP; Mear, FO; Montagne, L; Ferreira, JMF
nationality International
journal JOURNAL OF THE AMERICAN CERAMIC SOCIETY
author keywords glass; ionic conductivity; lithium silicate; structure; vanadium; vanadium compounds
abstract The structural role of V in 28Li(2)O-72SiO(2) (in mol%) lithium silicate glass doped with 0.5 mol% V2O5 was assessed using Si-29 and V-51 Nuclear Magnetic Resonance (NMR), Fourier-transform infrared (FTIR), and X-ray photoelectron (XPS) spectroscopy techniques. Despite the low amount of V2O5 used, the structural information obtained or deduced from the statistical analysis of the NMR data could explain the evolution of glass properties after V2O5 addition. The XPS results indicated that all vanadium exists in 5+ oxidation state. Both the Si-29 NMR and FTIR data point toward an increase in the polymerization of the silicate network, caused by the V2O5 acting as network former, capable to form various QVn tetrahedral units (for n = 0, 1, and 2) in the glasses. These QVn units, which are similar to phosphate units, scavenge the Li+ ions and cause the silicate network to polymerize. However, in an overall balance, the entire glass network is depolymerized due to the additional nonbridging oxygens contributed by the vanadium polyhedra. The addition of vanadium causes the network to expand and increases the ionic conductivity.
publisher WILEY
issn 0002-7820
isbn 1551-2916
year published 2021
volume 104
issue 6
beginning page 2495
ending page 2505
digital object identifier (doi) 10.1111/jace.17671
web of science category 11
subject category Materials Science, Ceramics
unique article identifier WOS:000614645200001
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