994.
The kinetics of oxygen exchange are of primary importance for the application of titanates as fast resistive oxygen sensors.
The sensor’s conductivity is correlated with the oxygen partial pressure pO
2 of the surrounding atmosphere: Due to oxygen surface transfer and subsequent diffusion of oxygen vacancies V
O
··
, a pO
2 change gives rise to a conductivity change of the sample. While bulk diffusion usually occurs very fast, the surface transfer
reaction becomes the rate determining step for thin samples and for low temperatures. We have shown that in the case of acceptor
doped SrTiO
3 the kinetics of the surface transfer reaction can be strongly influenced through stoichiometric changes brought about by
thin coatings of alkaline earth metal oxides (e.g. SrO). In contrast to the commonly used jump method (conductivity response
to a sudden pO
2 change in the time domain), a model is presented which is based on the frequency-domain analysis of amplitude and phase shift
of the response signal obtained from a pO
2 modulation in a fast kinetic measurement set-up. This method allows not only for measuring response times in the sub-millisecond
range but also for distinguishing between behaviour either controlled by volume diffusion or by surface transfer reaction.
Paper presented at the 9th EuroConference on Ionics, Ixia, Rhodes, Greece, Sept. 15 – 21, 2002.
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