Elastic properties of fast ion conducting lithium based borate glasses

Elastic properties of $Li_{2}O-PbO-B_{2}O_{3}$ glasses have been investigated using sound velocity measurements at 10 MHz. Four series of glasses have been investigated with different concentrations of $Li_{2}O$, PbO and $B_{2}O_{3}$. The variations of molar volume have been examined for the influences of $Li_{2}O$ and PbO. The elastic moduli reveal trends in their compositional dependence. The bulk and shear modulus increases monotonically with increase in the concentration of tetrahedral boron which increases network dimensionality. The variation of bulk moduli has also been correlated to the variation in energy densities. The Poisson's ratio found to be insensitive to the concentration of tetrahedral boron in the structure. The experimental Debye temperatures are in good agreement with the expected theoretical values. Experimental observations have been examined in view, the presence of borate network and the possibility of non-negligible participation of lead in network formation

Ion conductivity and dielectric relaxation behavior in FIC silver based phospho-molybdate glasses

Electrical conductivity and dielectric relaxation studies of silver ion-conducting glasses have been prepared using xAg(2)SO(4)-15Ag(2)O-(90-X)(90P(2)O(5)-10MoO(3)) glass system over a temperature range of 298-353 K and frequencies of 10 Hz to 10 MHz. DC conductivities exhibit Arrhenius behavior over the entire temperature range with a single activation barrier. The ac conductivity behavior of these glasses has been analyzed using single power law; conductivity increases linearly in logarithmic scale with Ag2SO4 concentration. The power law exponent (s) decreases, while stretched exponent (beta) is insensitive to increase of temperature. Scaling behavior has also been carried out using the reduced plots of conductivity and frequency, which suggest that ion transport mechanism remains unaffected at all temperatures and compositions

A new approach for understanding ion transport in glasses; example of complex alkali diborate glasses containing lead, bismuth and tellurium oxides

Mechanism of ion transport in glasses continues to be incompletely understood. Several of the theoretical models in vogue fail to rationalize conductivity behaviour when d.c. and a.c. measurements are considered together. While they seem to involve the presence of at least two components in d.c. activation energy, experiments fail to reveal that feature. Further, only minor importance is given to the influence of structure of the glass on the ionic conductivity behaviour. In this paper, we have examined several general aspects of ion transport taking the example of ionically conducting glasses in pseudo binary, yNa(2)B(4)O(7)center dot(1-y) M (a) O (b) (with y = 0 center dot 25-0 center dot 79 and M (a) O (b) = PbO, TeO2 and Bi2O3) system of glasses which have also been recently characterized. Ion transport in them has been studied in detail. We have proposed that non-bridging oxygen (NBO) participation is crucial to the understanding of the observed conductivity behaviour. NBO-BO switching is projected as the first important step in ion transport and alkali ion jump is a subsequent event with a characteristically lower barrier which is, therefore, not observed in any study. All important observations in d.c. and a.c. transport in glasses are found consistent with this model

Ion transport studies in lithium phospho-molybdate glasses containing Cl- ion

Ion conducting glasses in xLiCl-20Li(2)O-(80-x) 0.80P(2)O(5)-0.20MoO(3)] glass system have been prepared over a wide range of composition (X = 5, 10, 15, 20 and 25 mol%). The electrical conductivity and dielectric relaxation of these glasses were analyzed using impedance spectroscopy in the frequency range of 10 Hz-10 MHz and in the temperature range of 313-353 K. D.c. activation energies extracted from Arrhenius plots using regression analysis, decreases with increasing LiCl mol%. A.c. conductivity data has been fitted to both single and double power law equation with both fixed and variable parameters. The increased conductivity in the present glass system has been correlated with the volume increasing effect and the coordination changes that occur due to structural modification resulting in the creation of non-bridging oxygens (NBO's) of the type O-Mo-O- bonds in the glass network. Dielectric relaxation mechanism in these glasses is analyzed using Kohlrausch-Williams-Watts (KWW) stretched exponential function and stretched exponent (beta) is found to be insensitive to temperature

Fragility correlates thermodynamic and kinetic properties of glass forming liquids

In our earlier communication we proposed a simple fragility determining function, (NBO]/(VmTg)-T-3), which we have now used to analyze several glass systems using available thermal data. A comparison with similar fragility determining function, Delta C-p/C-p(1), introduced by Chryssikos et al. in their investigation of lithium borate glasses has also been performed and found to be more convenient quantity for discussing fragilities. We now propose a new function which uses both Delta C-p and Delta T and which gives a numerical fragility parameter, F whose value lies between 0 and 1 for glass forming liquids. F can be calculated through the use of measured thermal parameters Delta C-p, C-p(1), T-g and T-m. Use of the new fragility values in reduced viscosity equation reproduces the whole range of viscosity curves of the Angell plot. The reduced viscosity equation can be directly compared with the Adam-Gibbs viscosity equation and a heat capacity function can be formulated which reproduces satisfactorily the Delta C-p versus In(T-r) curves and hence the configurational entropy. (C) 2014 Elsevier Ltd. All rights reserved

Structural investigations of sodium diborate glasses containing PbO, Bi2O3Bi_2O_3 and TeO2TeO_2: Elastic property measurements and spectroscopic studies

Pseudo-binary sodium borate glasses containing (1 − y)Na2B4O7–yMaOb (where MaOb = PbO, Bi2O3 and TeO2) (y = 0.25, 0.5, 0.67 and 0.79) have been investigated. Sound velocities (longitudinal and shear) have been measured at 10 MHz frequency using quartz transducers. Density increases with increase of y and the molar volume decreases. Sound velocities also decrease with increasing y till y ≈ 0.66 above which it increases slightly. Steeper decrease in velocities has been observed in TeO2 containing glasses. Elastic moduli, Poisson’s ratio and Debye temperature have been calculated. Glass transition temperatures have also been determined and it decreases with increase of y. Tg also exhibits a dependence on the cationic charge in MaOb. Infrared spectra of the glasses reveal that the strong network consisting of diborate units is affected only by PbO and only very marginally by Bi2O3 and TeO2. Only glasses with high concentrations of Bi2O3 and TeO2 reveal the presence of mixed bridges such as Bi–O–B and Te–O–B. Consistent with the IR spectral observations, the N4 values of 11B MAS-NMR remain close to the ideal value of 0.5 of the diborate composition in most of the glasses. A structural model based on the observation that the diborate network is unaffected by Bi2O3 and TeO2 where as PbO opens up and breaks the diborate units is shown to be consistent with all of the experimental observations including mechanical properties