9
Views
14
CrossRef citations to date
0
Altmetric
Original Articles

Electrical and dielectric properties of As10Ge15Te75Agx glasses

, , &
Pages 253-271 | Received 08 Jan 1979, Accepted 06 Jul 1979, Published online: 01 Dec 2006
 

Abstract

This paper analyses the effect of the addition of varying amounts of silver in concentrations from 0 to 10.0 at.% to As10Ge15Te75 glass on d.c. and a.c. conductivities, dielectric constant and various allied parameters in the temperature range 83-383 K and the frequency range from d.c. to 50 MHz. The activation energy of d.c. conductivity increases with silver content up to 1.0 at.% and shows a reversal in the trend with higher percentages (5.0 and 10.0 at.%). The a.c. conductivity and memory switching behaviour are not altered by the addition of silver. The dielectric data suggest a dipole-type relaxation mechanism. The dielectric data corroborate the observed conductivity data in suggesting a probable increase in Te-chain breakages leading to an increase in the number of charged dangling bonds with silver content up to 1.0 at.% and, at higher percentages of silver, alloy formation occurs resulting in the reversal of the trend. Most of the data can be explained by the ‘charged dangling bond’ model of Mott, Davis and Street (1975) and ‘valence-alternation pairs’ (VAPs) and ‘intimate valence-alternation pairs’ (IVAPs) suggested by Kastner, Adler and Fritzsche (1976).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.