4.7 Article

Structural, electrical, and electrochemical properties of cobalt-doped NiFe2O4 as a potential cathode material for solid oxide fuel cells

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 38, Issue 33, Pages 14329-14336

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2013.08.097

Keywords

Spinel material; Solid oxide fuel cell; Electrical conductivity; Single-phase electrode; Cathode

Funding

  1. Natural Science Foundation of China [51072193]
  2. National Basic Research Program of China (973 Program) [2012CB922001]
  3. Fundamental Research Funds for the Central Universities

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In this work, Co-doped NiFe2O4 spinels (NFCO-x) are successfully fabricated and characterized as possible cathode materials for the intermediate-temperature solid oxide fuel cells (SOFC). Results of the binding energy calculations using the density functional theory suggest that the reverse spinel structure is stable when Co3+ occupies the octahedral interstitial sites. Total and ionic-only conductivities indicate that NFCO-x are a kind of mixed electronic-ionic conductors. Ionic transferring numbers are approximately 0.049 and 0.006 for NFCO-0.1 and NFCO-0.5, respectively, measured at 700 degrees C in air. Co dopant in the NFCO-x improves the electronic conductivity at the expense of the ionic conductivity. For NFCO-0.5, electronic and ionic conductivities are approximately 0.24 and 9.6 x 10(-4) S cm(-1), respectively, measured also at 700 degrees C in air. Unlike behaviour of the conductivities, the polarization resistance of symmetric cells with NFCO-x electrodes decreases when increasing the Co content (x) to a certain level, and then increases. The cell containing the NFCO-0.5 electrode exhibits the lowest polarization resistance (R-p), which is approximately 1.51 Omega cm(2) at 650 degrees C. For single cells, the maximum power density is 320 mW cm(-2) measured at 650 degrees C using a 38-mu m-thick SDC electrolyte and an NFCO-0.5 cathode. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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