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Cobalt-doped Ca12Al14O33 mayenite oxide ion conductors: phases, defects, and electrical properties

Cobalt-doped Ca12Al14O33 mayenite oxide ion conductors: phases, defects, and electrical properties Mayenite Ca12Al14O33, as a good oxygen ion conductor with conductivity slightly lower than stabilized ZrO2, has been investigated through doping strategy over the last few decades, but with little success in further improving its oxide ionic conductivity. Here, cobalt-doped Ca12Al14-x Co x O33+δ (0 ≤ x ≤ 1.6) materials were prepared by traditional solid-state reaction method, and then studied by complementary techniques, including X-ray diffraction (XRD), scanning electron microscope coupled with energy dispersion spectrum (EDS) analysis, X-ray photoelectron spectroscopy, and static lattice atomistic simulations. The results showed that these doped materials had much lower Co contents in the crystal structure than their nominal compositions, which was consistent with the high calculated defect formation energy (~ 6.25 eV). The minor divalent Co ions in the crystal structure would reduce the amount of mobile oxide ions and accordingly slightly decreased the bulk conductivities, while most of the Co ions existed in the form of Co2O3 and segregated along grain boundaries in the ceramic samples, which could apparently increase the grain boundary conductions of Ca12Al14O33. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Ionics Springer Journals

Cobalt-doped Ca12Al14O33 mayenite oxide ion conductors: phases, defects, and electrical properties

Ionics , Volume 25 (11) – Jun 18, 2019

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References (43)

Publisher
Springer Journals
Copyright
Copyright © 2019 by Springer-Verlag GmbH Germany, part of Springer Nature
Subject
Chemistry; Electrochemistry; Renewable and Green Energy; Optical and Electronic Materials; Condensed Matter Physics; Energy Storage
ISSN
0947-7047
eISSN
1862-0760
DOI
10.1007/s11581-019-03088-0
Publisher site
See Article on Publisher Site

Abstract

Mayenite Ca12Al14O33, as a good oxygen ion conductor with conductivity slightly lower than stabilized ZrO2, has been investigated through doping strategy over the last few decades, but with little success in further improving its oxide ionic conductivity. Here, cobalt-doped Ca12Al14-x Co x O33+δ (0 ≤ x ≤ 1.6) materials were prepared by traditional solid-state reaction method, and then studied by complementary techniques, including X-ray diffraction (XRD), scanning electron microscope coupled with energy dispersion spectrum (EDS) analysis, X-ray photoelectron spectroscopy, and static lattice atomistic simulations. The results showed that these doped materials had much lower Co contents in the crystal structure than their nominal compositions, which was consistent with the high calculated defect formation energy (~ 6.25 eV). The minor divalent Co ions in the crystal structure would reduce the amount of mobile oxide ions and accordingly slightly decreased the bulk conductivities, while most of the Co ions existed in the form of Co2O3 and segregated along grain boundaries in the ceramic samples, which could apparently increase the grain boundary conductions of Ca12Al14O33.

Journal

IonicsSpringer Journals

Published: Jun 18, 2019

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