skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Electrical conductivity of Sr{sub 2−x}VMoO{sub 6−y} (x = 0.0, 0.1, 0.2) double perovskites

Journal Article · · Journal of Applied Physics
DOI:https://doi.org/10.1063/1.4811715· OSTI ID:22277976
; ;  [1]; ;  [2]
  1. Department of Physics, EPS 264, Montana State University, Bozeman, Montana 59717 (United States)
  2. Department of Mechanical Engineering, Roberts 220, Montana State University, Bozeman, Montana 59717 (United States)

Electrical conductivity of Sr{sub 2-x}VMoO{sub 6-y} (x = 0.0, 0.1, 0.2) double perovskites has been investigated in a reducing atmosphere at temperatures up to 800 °C. This material has a key application in solid oxide fuel cell anodes as a mixed ion and electron conductor. A solid state synthesis technique was used to fabricate materials and crystal structure was verified through x-ray diffraction. Subsequent to conventional sintering in a reducing environment, elemental valence states were indentified through x-ray photoemission spectroscopy on the double perovskite material before and after annealing in a hydrogen environment. Samples exhibited metallic like conduction with electrical conductivities of 1250 S/cm (Sr{sub 2}VMoO{sub 6-y′}), 2530 S/cm (Sr{sub 1.8}VMoO{sub 6-y″}), and 3610 S/cm (Sr{sub 1.9}VMoO{sub 6-y‴}) at 800 °C in 5% H{sub 2}/95% N{sub 2}, with a substantial increase in conductivity upon cooling to room temperature. Room temperature electrical conductivity values for Sr{sub 1.9}VMoO{sub 6-y‴} make it a candidate as the highest electrically conductive oxide known. Highly insulating secondary surface phases, Sr{sub 3}V{sub 2}O{sub 8}, and SrMoO{sub 4}, begin to reduce at 400 °C in a hydrogen environment, as confirmed by X-ray photoemission and thermal gravimetric analysis. This reduction, from V{sup 5+} and Mo{sup 6+} to lower valence states, leads to a large increase in sample electrical conductivity.

OSTI ID:
22277976
Journal Information:
Journal of Applied Physics, Vol. 113, Issue 24; Other Information: (c) 2013 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-8979
Country of Publication:
United States
Language:
English