Synthesis and gas sensing properties of inorganic semiconducting, p-n heterojunction nanomaterials

En aquesta tesis utilitzant principalment Aerosol Assited Chemical Vapor Deposition, AACVD, com a metodologia de síntesis d'òxid de tungstè nanoestructurat s'han fabricat diferents sensors de gasos. Per tal d'estudiar la millora en la selectivitat i la sensibilitat dels sensors de gasos basats en òxid de tungstè aquest s'han decorat, via AACVD, amb nanopartícules d'altres òxids metàl·lics per a crear heterojuncions per tal d'obtenir un increment en la sensibilitat electrònica, les propietats químiques del material o bé ambdues. En particular, s'han treballat en diferents sensors de nanofils d'òxid de tungstè decorats amb nanopartícules d'òxid de níquel, òxid de cobalt i òxid d'iridi resultant en sensors amb un gran increment de resposta i selectivitat cap al sulfur d'hidrogen, per a l'amoníac i per a l'òxid de nitrogen respectivament a concentracions traça. A més a més, s'han estudiat els mecanismes de reacció que tenen lloc entre les espècies d'oxigen adsorbides a la superfície del sensor quan interactua amb un gas. I també s'ha treballat en intentar controlar el potencial de superfície de les capes nanoestructurades per tal de controlar la deriva en la senyal al llarg del temps, quan el sensor està operant, a través d'un control de temperatura.En esta tesis utilizando principalmente Aerosol Assited Chemical Vapor Deposition, AACVD, como metodología de síntesis de óxido de tungsteno nanoestructurado se han fabricado diferentes sensores de gases. Para estudiar la mejora en la selectividad y la sensibilidad de los sensores de gases basados en óxido de tungsteno estos se han decorado, vía AACVD, con nanopartículas de otros óxidos metálicos para crear heterouniones para obtener un incremento en la sensibilidad electrónica, las propiedades químicas del material o bien ambas. En particular, se han trabajado en diferentes sensores de nanohilos de óxido de tungsteno decorados con nanopartículas de óxido de níquel, óxido de cobalto y óxido de iridio resultante en sensores con un gran incremento de respuesta y selectividad hacia el sulfuro de hidrógeno, para el amoníaco y para el óxido de nitrógeno respectivamente a concentraciones traza. Además, se han estudiado los mecanismos de reacción que tienen lugar entre las especies de oxígeno adsorbidas en la superficie del sensor cuando interactúa con un gas. Y también se ha trabajado en intentar controlar el potencial de superficie de las capas nanoestructuradas para controlar la deriva en la señal a lo largo del tiempo, cuando el sensor está trabajando, a través de un control de temperatura.In this thesis, using mainly Aerosol Assited Chemical Vapor Deposition, AACVD, as a synthesis methodology for nanostructured tungsten oxide, different gas sensors have been manufactured. To study the improvement in the selectivity and sensitivity of gas sensors based on tungsten oxide, they have been decorated, via AACVD, with nanoparticles of other metal oxides to create heterojunctions to obtain an increase in electronic sensitivity, in the chemical properties of the material or at the same time in both. Particularly, we have worked on different tungsten oxide nanowire sensors decorated with nanoparticles of nickel oxide, cobalt oxide and iridium oxide resulting in sensors with a large increase in response and selectivity towards hydrogen sulfide, for ammonia. and for nitrogen oxide respectively at trace concentrations. In addition, the reaction mechanisms that take place between oxygen species adsorbed on the sensor surface when it interacts with a gas have been also studied. Furthermore, efforts have been put on trying to control the surface potential of the nanostructured layers to control the drift in the signal over time, when operating the sensors, through temperature control

Chemical vapour deposited ZnO nanowires for detecting Ethanol and NO2

Randomly oriented ZnO nanowires were grown directly onto alumina substrates having platinum interdigitated screen-printed electrodes via the chemical vapor deposition method using Au as catalyst. Three different Au film thicknesses (i.e., 3, 6 or 12 nm) were used in the growth of nanowires, and their gas sensing properties were studied for ethanol and NO2 as reducing and oxidizing species, respectively. ZnO nanowires grown employing the 6 nm thick layers were the less defective and showed the most stable, repeatable gas sensing properties. Despite ZnO nanowires grown employing the thickest Au layers reached the highest responses under dry conditions, ZnO nanowires grown using the thinnest Au film were more resilient at detecting NO2 in the presence of ambient moisture. The gas sensing results are discussed in light of the defects and the presence of Au impurities in the ZnO nanowires, as revealed by the characterization techniques used, such as X-ray diffraction, field-emission scanning electron microscopy, X-ray photoelectron spectroscopy and photoluminescence spectroscopy. Promising results were obtained by the implementation of ZnO NWs directly grown over alumina substrates for the detection of ethanol and NO2, substantially ameliorating our previously reported results

Facile synthesis of Pd@ZnO core@shell nanoparticles for selective ethanol detection

In this work, we reported a high-performance ethanol gas sensor based on novel Pd@ZnO core@shell nanoparticles (CSNPs). The Pd@ZnO CSNPs were synthesized by chemical method and characterized by XRD, TEM and EDS techniques. Gas sensing results demonstrated that Pd@ZnO CSNPs show high sensitivity and remarkable selectivity towards ethanol at 250 °C. The response value of Pd@ZnO CSNPs is 152, which is almost six times higher than the response value (27) of ZnO NPs at 250 °C. The mechanism of enhancement in sensing properties can be ascribed to the chemical and electronic sensitization effect of Pd NPs and also due to the unique core@shell structure. These characteristics may shed light on the development of a selective ethanol sensor based on Pd@ZnO CSNPs

Understanding noise-shaping in sigma-delta controls of surface potential for MOX gas sensors

The objective of this paper is to explain how quantization noise-shaping can be achieved for the output bitstream of sigma-delta controls of surface potential (SP) in MOX gas sensors. These controllers use temperature modulation to keep constant the surface potential of the nanostructures. The rate equations describing the time evolution of the state variables in the sensing layer (concentration of ionized species on the surface of the nanostructures) are nonlinear. It will be shown that under the condition of constant surface potential, the sensor using the proposed temperature modulations can be seen as an example of affine switching and that quantization noise shaping may be achieved.Peer ReviewedPostprint (author's final draft

Acceleration and drift reduction of MOX gas sensors using active sigma-delta controls based on dielectric excitation

The objective of this paper is to apply a closed-loop control based on dielectric excitation to MOX gas sensors in order to improve their response time. The control implements a feedback loop in which temperature modulations keep constant the sensor reactance, measured at constant temperature. The required fast temperature switching has been implemented on MEMS microhotplates. The mean temperature generated by the control is the new output signal. This technique is applied to an in-house sensor made of WO3 nanowires decorated with gold nanoparticles to detect NH3 and to a commercial MEMS MOX sensor (CCS801).Postprint (author's final draft