The solid-electrolyte cell in which AgsSI was used as electrolyte shows a fairly large polarization; a theoretical equation is derived to explain it. The polarization of the cell with a silver plate anode can be explained by reaction polarization, the reaction between interstitial silver ions and s
The Ag/Ag3SI/I2 solid-electrolyte cell
β Scribed by T. Takahashi; O. Yamamoto
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- English
- Weight
- 651 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0013-4686
No coin nor oath required. For personal study only.
β¦ Synopsis
A new solid electrolyte, Ag,SI, was used for the solidelectrolyte cell. A@1 was synthesized by the solid-state reaction of the equivalent moles of silver iodide and silver sulphide. The electrical conduction of AgaS was almost entirely ionic; 10-l hz-l cm-l at room temperature.
the ionic conductivity was about 1 x
The anodic and cathodu: polarizations of a solid-electrolyte cell, Ag/Ag$I/I,, were studied at room temperature with the help of a silver wire reference electrode. When a silver plate was used as the anode, anode polarization was dominant, whereas when a silver amalgam anode was used, the polarization was greatly decreased. A cell with iodine and acetylene black mixture as cathode material had the lowest polarization at the cathode.
In the cell, silver amalgam/Ag$I/I~-acetylene black, the voltage dropped by only 100 mV after 3 h at steady current discharge of 1000 PA/cm*. The internal resistance of the cell did not change during the discharge, probably because the cell reaction product, AgI, dissolves in Ag$I.
Rh&Emploi
d'un nouvel &ctrolyte, Ag,SI, dans les cellties B Clectrolyte solide. On le syn-th&ise. par r&action en proportions $ est excltivement ionique (1 X lO-*
π SIMILAR VOLUMES
Electrochemical investigation of the solid electrolyte Ag,I,W04 (0.8 A,@ + 0.2 Ag,WO, mixture) was performed. By means of cyclic volmmmetry, normal pulse polarography and ac polarography methods the electrode processes and the capacity of electric double layer on electrode/electrolyte interface were