Structure and ionic transport in disordered silicates

2000 ◽  
Vol 64 (3) ◽  
pp. 441-446 ◽  
Author(s):  
G. N. Greaves

AbstractA brief review is given of the ways in which the local structure in glass can influence the microstructure that supports ionic transport. This in turn contributes to the co-operative nature of ion dynamics and ways in which this underpins the ‘mixed alkali effect’ are discussed. Glass microstructure too is expected to affect glass fracture as well as the chemistry of glass surfaces. In melts, though, these restrictions appear to vanish as the rigidity of intermediate range order is lost.

1989 ◽  
Vol 32-33 ◽  
pp. 954-958 ◽  
Author(s):  
H IYETOMI ◽  
P VASHISHTA ◽  
R KALIA

1995 ◽  
Vol 29 (7) ◽  
pp. 549-553 ◽  
Author(s):  
P Armand ◽  
M Beno ◽  
A. J. G Ellison ◽  
G. S Knapp ◽  
D. L Price ◽  
...  

1991 ◽  
Vol 43 (1) ◽  
pp. 1194-1197 ◽  
Author(s):  
S. Susman ◽  
K. J. Volin ◽  
D. L. Price ◽  
M. Grimsditch ◽  
J. P. Rino ◽  
...  

2002 ◽  
Vol 754 ◽  
Author(s):  
Jürgen Horbach ◽  
Anke Winkler ◽  
Walter Kob ◽  
Kurt Binder

ABSTRACTWe present the results of large scale computer simulations to discuss the structural and dynamic properties of silicate melts with the compositions (Na2O)(2·SiO2), (Na2O)(20·SiO2) and (Al2O3)(2·SiO2). We show that these systems exhibit additional intermediate range order as compared to silica (SiO2) where the characteristic intermediate length scales stem from the tetrahedral network structure. Furthermore we show that the sodium dynamics in the sodium silicate systems exhibits a very peculiar feature: the long–time decay of the incoherent intermediate scattering function can be described by a Kohlrausch law with a constant exponent β for q > qth whereby qth is smaller than the location of the main peak in the static structure factor for the Na–Na correlations.


Author(s):  
M. G. Proietti ◽  
S. Mobilio ◽  
A. Gargano ◽  
L. Incoccia ◽  
F. Evangelisti

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