Selective detection of oxidising or reducing species is achieved via selecting operating temperatures and metal loading of single crystalline In2O3 octahedra.

An innovative concept for an electronic nose (eNose) system based on a unique combination of analog and digital sensors for online monitoring is presented. The developed system consists of small sensing arrays of commercially available semiconducting metal oxide (MOX) gas sensors in a compact, modular, low sample volume, temperature-controlled sensing chamber. The sensing chamber comprises three compartments, each of which may contain several analog and/or digital MOX sensors. Additional sensors within the digital compartment allow for pressure, humidity, and temperature measurements. The presented prototype eNose system comprises one compartment with 8 analog MOX sensors and two compartments with 10 digital sensors each and was explicitly tested here for the discrimination between midrange (3–18 ppm) concentrations of ethanol and acetone at dry and moderately humid conditions.

No abstract

No abstract

In this work, a new generation of eNose systems particularly suited for exhaled breath gas analysis is presented. The developed analyzer system comprises a compact modular, low volume, temperature controlled sensing chamber explicitly tested for the detection of acetone, isoprene, pentane and isopropanol. The eNose system sensing chamber consists of three compartments, each of which can contain 8 analog Metal Oxide (MOX) sensors or 10 digital MOX sensors. Additional sensors within the digital compartment allow for pressure, humidity and temperature measurements. The presented eNose system contains a sensor array with up to 30 physical sensors and provides the ability to discriminate between low VOC concentrations under dry and humid conditions. The MOX sensor signals were analyzed by pattern recognition methods.

No abstract

We report on the use of combined heating and pulsed UV light activation of indium oxide gas sensors for enhancing their performance in the detection of nitrogen dioxide in air. Indium oxide nano-octahedra were synthesized at high temperature (900 °C) via vapour-phase transport and screen-printed onto alumina transducers that comprised interdigitated electrodes and a heating resistor. Compared to the standard, constant temperature operation of the sensor, mild heating (e.g., 100 °C) together with pulsed UV light irradiation employing a commercially available, 325 nm UV diode (square, 1 min period, 15 mA drive current signal), results in an up to 80-fold enhancement in sensitivity to nitrogen dioxide. Furthermore, this combined operation method allows for making savings in power consumption that range from 35% to over 80%. These results are achieved by exploiting the dynamics of sensor response under pulsed UV light, which convey important information for the quantitative analysis of nitrogen dioxide.

Here we report on the use of pulsed UV light for activating the gas sensing response of metal oxides. Under pulsed UV light, the resistance of metal oxides presents a ripple due to light-induced transient adsorption and desorption phenomena. This methodology has been applied to tungsten oxide nanoneedle gas sensors operated either at room temperature or under mild heating (50 °C or 100 °C). It has been found that by analyzing the rate of resistance change caused by pulsed UV light, a fast determination of gas concentration is achieved (ten-fold improvement in response time). The technique is useful for detecting both oxidizing (NO2) and reducing (NH3) gases, even in the presence of different levels of ambient humidity. Room temperature operated sensors under pulsed UV light show good response towards ammonia and nitrogen dioxide at low power consumption levels. Increasing their operating temperature to 50 °C or 100 °C has the effect of further increasing sensitivity.