Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Electro-chemo-mechanical studies of perovskite-structured mixed ionic-electronic conducting SrSn[subscript 1-x]Fe[subscript x]O[subscript 3-x/2+δ] part I: Defect chemistry

Electro-chemo-mechanical studies of perovskite-structured mixed ionic-electronic conducting SrSn[subscript 1-x]Fe[subscript x]O[subscript 3-x/2+δ] part I: Defect chemistry

Thumbnail Image
Download
Name

10832_2017_64_ReferencePDF.pdf

Size

847.06 KB

Format

Adobe PDF

Checksum (MD5)

66c6558977ea96ac70cdbdb2d0287008

Download all files submitted through automated deposit
art_5507551709185277604.zip (763.49 KB)
Author(s)
Kim, Chang Sub
•
Bishop, Sean
•
Perry, Nicola
•
Tuller, Harry L
Alternative Title
Electro-chemo-mechanical studies of perovskite-structured mixed ionic-electronic conducting SrSn1-xFexO3-x/2+δpart I: Defect chemistry
Date Issued
January 2017
Journal
Journal of Electroceramics
Publisher
Springer US
Citation
Kim, Chang Sub, Sean R. Bishop, Nicola H. Perry, and Harry L. Tuller. “Electro-Chemo-Mechanical Studies of Perovskite-Structured Mixed Ionic-Electronic Conducting SrSn1-xFexO3-X/2+δ part I: Defect Chemistry.” Journal of Electroceramics 38, no. 1 (January 11, 2017): 74–80.
Version
Author's final manuscript
Abstract
Oxygen nonstoichiometry and the defect chemistry of the SrSn[subscript 1-x]Fe[subscript x]O[subscript 3-x/2+δ] (SSF) system were examined by means of thermogravimetry as a function of oxygen partial pressure in the temperature range of 700–1000 °C and compared against the corresponding mixed ionic-electronic conducting titanate, SrTi[subscript 1-x]Fe[subscript x]O[subscript 3-x/2+δ] (STF) system. The alternate B site host cation, Sn, was selected to replicate and extend the STF studies, given its distinct band structure and higher electron mobility associated with its 5s derived conduction band as compared to the 3d nature of the conduction band in the titanate. Though shifted slightly by the larger size of Sn, the defect equilibria – including the oxygen vacancy concentration – were found to be largely dominated by Fe oxidation state, and thus differed only in a limited way from those in STF. Key thermodynamic parameters for SrSn[subscript 0.65]Fe[subscript 0.35]O[subscript 2.825+δ] (SSF35) were derived including the reduction enthalpy (4.137 ± 0.175 eV), the high temperature electronic band gap (1.755 ± 0.015 eV) and the anion Frenkel enthalpy (0.350 ± 0.350 eV). The implications these observations have for cathode behavior in solid oxide fuel cells are briefly discussed.
MIT Department
MIT Materials Research Laboratory
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Terms of Use
Creative Commons Attribution-Noncommercial-Share Alike
http://creativecommons.org/licenses/by-nc-sa/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/107976
DOI of Published Version
https://doi.org/10.1007/s10832-017-0064-3
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.