Studies of ionic transport and oxygen exchange on oxide materials for electrochemical gas sensors

Wiemhofer H, Bremes H, Nigge U, Zipprich W

Research article (journal)

Abstract

Theory and examples for the application of electron blocking microelectrodes to the study of ion transport and electrode processes in mixed electronic and ionic conductors are given for a couple of mixed conducting oxidic perovskites. Emphasis was laid on the analysis of steady state current-voltage and cyclic voltammetric curves. Yttria-stabilized zirconia (YSZ) was used as the oxygen ion conducting microcontact material. The measurements were performed in the temperature range between 500 and 750 degreesC both on encapsulated and non-encapsulated oxide surfaces in order to detect the relative importance of surface oxygen exchange as compared to bulk oxygen ion transport and changes of stoichiometry. Gd0.8Sr0.2CoO3-delta and La0.8Sr0.2FeO3-delta proved to be typical mixed conductors with medium oxygen ion conductivities. Both show increasing ion conductivities for decreasing oxygen activities indicating a typical vacancy transport mechanism of oxygen ions. At 700 C in air, we obtained for the oxygen ion conductivity of Gd0.8Sr0.2CoO3-delta a value of 2x10(-4) S cm(-1) with very weak dependence on the oxygen partial pressure and for La0.8Sr0.2FeO3-delta, a value of 1.2 x 10(-5) S cm-1. The oxygen ion conductivity of La0.8Sr0.2FeO3-delta was proportional to p(O2)(-0.22) in the investigated range of temperatures and oxygen partial pressures between 10 and 10(-4) bar. In addition to that, a series of manganites was investigated with the composition A(0.7)E(0.3)MnO(3) (A=Gd, Y, Pr and E=Ca, Sr). The presence of slow diffusion coupled redox processes could be detected in all manganites at low and high oxygen activities versus air. The oxygen ion conductivity was considerably lower than 10-5 S cm-1 in all investigated manganites. Nevertheless, the comparison of results for glass encapsulated and non-encapsulated microcontacts showed that Pr0.7Ca0.3MnO3 and in particular Pr0.7Sr0.3MnO3 are quite active catalysts for the oxygen electrode reaction at the three-phase boundary air/zirconia/manganite, whereas Y0.7Sr0.3MnO3 does not catalyze the oxygen electrode reaction significantly at the surface. (C) 2002 Elsevier Science B.V All rights reserved.

Details about the publication

JournalSolid State Ionics
Volume150
Issue1-2
Page range63-77
StatusPublished
Release year2002
Language in which the publication is writtenEnglish
Keywordsoxide ion conductivity; electrode kinetics; microelectrode; perovskites; oxides

Authors from the University of Münster

Bremes, Hans-Gerhard
Institute of Physical Chemistry
Wiemhöfer, Hans-Dieter
Professorship of Inorganic Chemistry (Prof. Wiemhöfer)