Isotopically labeled oxygen studies of the NOx exchange behavior of La2CuO4 to determine potentiometric sensor response mechanism

• Published in: Solid state ionics 2008-12, Vol.179 (39), p.2225-2233
• Main Authors: VANASSCHEIV, F, WACHSMAN, E
• Format: Article
• Language: English
• ISSN: 0167-2738
• DOI: 10.1016/j.ssi.2008.08.014

The harmful nature of nitrogen oxides (NOx) to environmental systems necessitates sensors to detect their presence. One effective means is the use of solid state sensors. These sensors are compact, rugged, and can be inexpensively fashioned, making them a viable option for measuring gas concentration. A non-Nernstian potentiometric sensor can be used to detect low concentrations of NOx gas in multiple regions of oxygen concentration. Understanding the mechanism for this behavior can assist in optimizing the sensor couple for a given application. Previous studies using Temperature Programmed Reaction and Desorption (TPR/TPD), along with IR and XPS analysis, have identified the formation of charge-building compounds that establish voltage on the sensing electrode when exposed to NOx gas. To further elucidate the mechanism, TPR and TPD were performed using isotopically labeled oxygen with simultaneous exposure to NOx. The material was examined under multiple gas conditions of NOx and 16O2/18O2 atmospheres, as well as varied levels of 18O enrichment in the lattice itself. Through these studies, it was determined that the formation of charged surface complexes occurs solely through the use of lattice oxygen (vs. gas phase O2) with adsorbed NOx.