Citation

BibTex format

@article{Téllez:2017:10.1080/14686996.2017.1402661,
author = {Téllez, Lozano H and Druce, J and Cooper, SJ and Kilner, JA},
doi = {10.1080/14686996.2017.1402661},
journal = {Science and Technology of Advanced Materials},
pages = {977--986},
title = {Double perovskite cathodes for proton-conducting ceramic fuel cells: are they triple mixed ionic electronic conductors?},
url = {http://dx.doi.org/10.1080/14686996.2017.1402661},
volume = {18},
year = {2017}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Published by National Institute for Materials Science in partnership with Taylor & Francis. 18 O and 2 H diffusion has been investigated at a temperature of 300 °C in the double perovskite material PrBaCo 2 O 5+δ (PBCO) in flowing air containing 200 mbar of 2 H 2 16 O. Secondary ion mass spectrometry (SIMS) depth profiling of exchanged ceramics has shown PBCO still retains significant oxygen diffusivity (~1.3 × 10 −11 cm 2 s −1 ) at this temperature and that the presence of water ( 2 H 2 16 O), gives rise to an enhancement of the surface exchange rate over that in pure oxygen by a factor of ~3. The 2 H distribution, as inferred from the 2 H 2 16 O − SIMS signal, shows an apparent depth profile which could be interpreted as 2 H diffusion. However, examination of the 3-D distribution of the signal shows it to be nonhomogeneous and probably related to the presence of hydrated layers in the interior walls of pores and is not due to proton diffusion. This suggests that PBCO acts mainly as an oxygen ion mixed conductor when used in PCFC devices, although the presence of a small amount of protonic conductivity cannot be discounted in these materials.
AU - Téllez,Lozano H
AU - Druce,J
AU - Cooper,SJ
AU - Kilner,JA
DO - 10.1080/14686996.2017.1402661
EP - 986
PY - 2017///
SN - 1468-6996
SP - 977
TI - Double perovskite cathodes for proton-conducting ceramic fuel cells: are they triple mixed ionic electronic conductors?
T2 - Science and Technology of Advanced Materials
UR - http://dx.doi.org/10.1080/14686996.2017.1402661
UR - http://hdl.handle.net/10044/1/55736
VL - 18
ER -