Abstract

Thin film metal oxide materials exhibit a bell-shaped variation of the gas sensitivity with sensor operation temperature. With respect to the temperature T M at which a sensitivity maximum occurs, the distribution of the gas sensitivity is asymmetric exhibiting a relatively steep increase below T M and a more moderate drop-off above T M. In this paper a rate equation approach is described, which successfully reproduces temperature- and gas-concentration dependent sensitivity distributions S( T, c gas) experimentally determined for a number of reducing analyte gas molecules. We show that such distributions are determined by two energetic parameters, which are specific for the special adsorbate/adsorbent system involved. These are (i) the strength of adsorption of neutral analyte gas molecules E ads and (ii) the kinetic barrier E a that needs to be overcome to induce a surface combustion event involving an adsorbed analyte gas molecule and a surface oxygen ion.

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