Electrical Conductivity and Structural Properties of Cesium Iron Phosphate Glasses: A Potential Host for Vitrifying Nuclear Waste
Abstract
The thermally stimulated current (TSC) and dc conductivity for iron phosphate glasses containing up to 28 mol% Cs2O have been measured in a temperature range from 120 to 400 K. The dc conductivity and activation energy were constant and independent of Cs2O content. With increasing cesium concentration in cesium iron phosphate glasses the slowly moving cesium ions are more tightly bound to the non-bridging oxygen ions and make no measurable contribution to dc conductivity. The dc conduction in these glasses is totally electronic, controlled by electron hopping between iron ions. The ionic conduction is immeasurably small because of the low mobility of the cesium ions. This agreement is reinforced by the excellent chemical durability of the glasses, where the dissolution rate at 90°C changes little with increasing Cs2O content. Raman spectroscopy indicated that the structure of these glasses was composed of predominantly pyrophosphate (P2O7) groups, but the metaphosphate chains (PO3) also existed.
Recommended Citation
A. Mogus-Milankovic et al., "Electrical Conductivity and Structural Properties of Cesium Iron Phosphate Glasses: A Potential Host for Vitrifying Nuclear Waste," Materials Research Society Symposium - Proceedings, vol. 663, pp. 153 - 160, Materials Research Society (MRS), Jan 2001.
The definitive version is available at https://doi.org/10.1557/PROC-663-153
Meeting Name
Scientific Basis for Nuclear Waste Management XXIV (2000: Aug. 27-31, Sydney, Australia)
Department(s)
Materials Science and Engineering
Keywords and Phrases
Activation energy; Carrier mobility; Cesium; Electric conductivity; Electric currents; Ionic conduction; Radioactive wastes; Raman spectroscopy; Thermal effects; Phosphate glasses
International Standard Serial Number (ISSN)
0272-9172
Document Type
Article - Conference proceedings
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2001 Materials Research Society (MRS), All rights reserved.
Publication Date
01 Jan 2001