Abstract

Solid-state NO 2 sensors based on yttria stabilized zirconia (YSZ), an O 2- conductor, combined either with an n- (WO 3), or a p-type semiconducting oxide (LaFeO 3), or a mixed electronic and ionic conductor (La 0.8Sr 0.2FeO 3) were investigated. Platinum parallel finger electrodes were applied on the surface of tape-casted YSZ layers and attached with gold wires for current collection. Nanocrystalline perovskite powders were prepared using different chemical methods: LaFeO 3 by the thermal decomposition of the LaFe–hexacyanide complex, and La 0.8Sr 0.2FeO 3 by a sol-gel route. A sub-micrometric commercial WO 3 powder was used. The oxide powders were mixed with a screen-printing oil and deposited on one Pt finger electrode. The presence of the oxide powder makes one of the electrodes different from the other in terms of catalytic activity, specific surface area, gas adsorption and reaction kinetics. Both electrodes were wholly exposed to the same gas atmosphere, without using reference air. The sensors were investigated at fixed temperature (450–700 °C) by measuring the electromotive force (EMF) at different concentrations of NO 2 and CO in air in the range 20–1000 ppm. A fast and stable response was measured for all the tested sensors. An EMF of opposite sign was measured for p- and n-type semiconducting based sensors upon exposure to the same gas. After increasing the grain size of the nano-structured La 0.8Sr 0.2FeO 3 powder by a heat treatment at 900 °C for 4 h, the response to NO x became small, slow and unstable.

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