Synthesis and ethanol sensing properties of Fe-doped SnO2 nanofibers

Fe-doped SnO₂ nanofibers are synthesized through an electrospinning method and characterized by scanning electron microscopy and transmission electron microscopy. The sensor fabricated from these nanofibers exhibits high sensitivity and rapid response/recovery to ethanol at 300 °C. The sensitivity is up to 15.3 when the sensor is exposed to 100 ppm ethanol, and the response and recovery time is about 1 and 3 s, respectively. The linear dependence of the sensitivity on the ethanol concentration is observed in the range of 10-300 ppm. These results demonstrate that Fe-doped SnO₂ nanofibers can be used as the sensing material for fabricating high performance ethanol sensors.     

Electrospinning route for α-Fe2O3 ceramic nanofibers and their gas sensing properties

In this paper, α-Fe₂O₃ ceramic nanofibers were prepared by electrospinning poly(vinyl alcohol)/Fe (NO₃)₃·9H₂O composite nanofibers and followed by calcination. The morphologies and structures of the as-prepared samples were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The gas sensing properties of the sensor based on the as-prepared α-Fe₂O₃ nanofibers were investigated in detail. The experimental results exhibited that our product held rapid response-recovery and high sensitivity characteristics to ethanol vapor. The response and recovery time of the sensor to C₂H₅OH vapor (from 100 to 5000 ppm) are about 3 and 5 s, respectively.     

Indium Tin Oxide thin film gas sensors for detection of ethanol vapours

Indium Tin Oxide (ITO: In₂O₃ + 17% SnO₂) thin films grown on alumina substrate at 648 K temperatures using direct evaporation method with two gold pads deposited on the top for electrical contacts were exposed to ethanol vapours (200-2500 ppm). The operating temperature of the sensor was optimized. The sensitivity variation of films having different thickness was studied. The sensitivity of the films deposited on Si substrates was studied. The response of the film with MgO catalytic layer on sensitivity and selectivity was observed. A novel approach of depositing thin stimulating layer of various metals/oxides below the ITO film was tried and tested.     

Sensing behaviour of nanosized zinc-tin composite oxide towards liquefied petroleum gas and ethanol

A chemical route has been used to synthesize composite oxides of zinc and tin. An ammonia solution was added to equal amounts of zinc and tin chloride solutions of same molarities to obtain precipitates. Three portions of these precipitates were annealed at 400, 600 and 800 °C, respectively. Results of X-ray diffraction and transmission electron microscopy clearly depicted coexistence of phases of nano-sized SnO₂, ZnO, Zn₂SnO₄ and ZnSnO₃. The effect of annealing on structure, morphology and sensing has been observed as well. It has been observed that annealing promoted growth of Zn₂SnO₄ and ZnSnO₃ at the expense of zinc. The sensing response of fabricated sensors from these materials to 250 ppm LPG and ethanol has been investigated. The sensor fabricated from powder annealed at 400 °C responded better to LPG than ethanol.     

Preparation, characterization, and gas-sensing properties of Pd-doped In2O3 nanofibers

Pure and Pd-doped In₂O₃ nanofibers are synthesized via a simple electrospinning method and characterized by scanning electron microscopy and X-ray diffraction. Comparing with pure In₂O₃ nanofibers, Pd-doped In₂O₃ nanofibers exhibit much higher sensitivity to ethanol at 200 °C. The sensor fabricated from Pd-doped In₂O₃ nanofibers can detect ethanol down to 1 ppm (the corresponding sensitivity is 4) with good selectivity, and the response and recovery times are 1 and 10 s, respectively. The sensing mechanism and the effect of Pd doping are discussed. The results indicate that the Pd-doped In₂O₃ nanofibers can be used to fabricate high performance ethanol sensors.     

Structure, properties and gas sensing behavior of Cr2 − xTixO3 films fabricated by electrostatic spray assisted vapour deposition

Single-phase eskolaite crystalline Cr_2 − xTi_xO₃ films (CTO) with a uniform porous microstructure were fabricated via an electrostatic spray assisted vapour deposition (ESAVD) method. The sensing behavior upon exposure to ammonia and ethanol was characterized in a CTO film-based sensor device in terms of response, reproducibility, humidity constraints and sensor stability. The ESAVD process has been shown to be capable of producing CTO films at low temperature (650 °C) and more importantly, it results in a more uniform titanium distribution and better microstructural control than processes based on solid-state chemical reactions. The material with a nominal composition of Cr_1.7Ti_0.3O₃ exhibited the highest sensitivity among the different Cr_2 − xTi_xO₃ compositions examined towards ammonia over the temperature range of 200-500 °C with a peak sensitivity of 2.90 at 200 °C. The CTO materials, when used as sensors, also exhibit excellent responses to ethanol concentration in air. The sensitivity was 0.64 for 10 ppm ethanol, 0.85 for 25 ppm, and 0.92 for 50 ppm, respectively.     

Fast response detection of H2S by CuO-doped SnO2 films prepared by electrodeposition and oxidization at low temperature

Fast response detection of H₂S by CuO-doped SnO₂ films prepared was prepared by a simple two-step process: electrodeposition from aqueous solutions of SnCl₂ and CuCl₂, and oxidization at 600 °C. The phase constitution and morphology of the CuO-doped SnO₂ films were characterized by X-ray diffraction and scanning electron microscopy. In all cases, a polycrystalline porous film of SnO₂ was the product, with the CuO deposited on the individual SnO₂ particles. Two types of CuO-doped SnO₂ films with different microstructures were obtained via control of oxidation time: nanosized CuO dotted island doped SnO₂ and ultra-uniform, porous, and thin CuO film coated SnO₂. The sensor response of the CuO doped SnO₂ films to H₂S gas at 50–300 ppm was investigated within the temperature range of 25–125 °C. Both of the CuO-doped SnO₂ films show fast response and recovery properties. The response time of the ultra-uniform, porous, and thin CuO coated SnO₂ to H₂S gas at 50 ppm was 34 s at 100 °C, and its corresponding recovery time was about 1/3 of the response time.     

The gas sensitivity of nano TiO2-SnO2 film doped with Cd(II) ion

The nanocomposite oxide (0.2TiO₂-0.8SnO₂) doped with Cd²⁺ powder have been prepared and characterized by XRD and their gas-sensing sensitivity were characterized using gas sensing measurement. Experimental results show that, bicomponent nano anatase TiO₂ and rutile SnO₂ particulate thick film doped with Cd²⁺ behaves with good sensitivity to formaldehyde gas of 200 ppm in the air, and the optimum sensing temperature was reduced from 360 °C to 320 °C compared with the undoped Cd²⁺ thick film. The gas sensing thick films doped with Cd²⁺ also show good selectivity to formaldehyde among benzene, toluene, xylene and ammonia as disturbed gas and could be effectively used as an indoor formaldehyde sensor.     

Structure and CO gas sensing properties of electrospun TiO2 nanofibers

Titanium dioxide (TiO₂) nanofibers were fabricated by electrospinning a hybrid solution, which is a mixture of the TiO₂ sol precursor, polymer, and solvent. The structure and gas sensing properties of TiO₂ nanofibers were investigated. By calcining at 600 °C, the polymeric components were decomposed and a multi-layered random network structure of TiO₂ nanofibers was obtained. Polycrystalline TiO₂ nanofibers consist of tetragonal anatase and rutile TiO₂ phases. The diameter ranged from 400 nm to 500 nm and the grain size was about 15 nm. The TiO₂ nanofibers-based sensor exhibited response to CO concentration as low as 1 ppm at 200 °C.     

Preparation and ethanol sensing properties of the superstructure SnO2/ZnO composite via alcohol-assisted hydrothermal route

Self-assembled superstructure of SnO₂/ZnO composite was synthesized by using alcohol-assisted hydrothermal method gas sensing properties of the material were investigated by using a static test system. The structure and morphology of the products were characterized by X-ray diffraction (XRD) and field-emission scanning electron microscope (FE-SEM). The diameter of the SnO₂ nanorods was about 40 nm with a length of about 300 nm, SnO₂ nanorods and ZnO nanosheets interconnect each other to form a superstructure. The gas sensing properties of superstructure SnO₂/ZnO composite with different content of ZnO were investigated. Furthermore, the superstructure SnO₂/ZnO composite sensor is characterized at different operating temperatures and its long-term stability in response to ethanol vapor is tested over a period of 3 months.     

HCHO sensing properties of Ag-doped In2O3 nanofibers synthesized by electrospinning

Ag-doped In₂O₃ nanofibers with diameters ranging from 60 to 130 nm and lengths of several tens of micrometers were synthesized by an electrospinning method. The XRD results indicated that the dopant in the nanofibers was metal Ag. The sensor fabricated from these fibers exhibited excellent HCHO sensing properties at 115 °C. The sensitivity was up to 3 when the sensor was exposed to 5 ppm HCHO, and the response and recovery time were about 5 and 10 s, respectively. Good selectivity was also observed in our investigations. These results indicated that the Ag-doped In₂O₃ nanofibers could be used to fabricate high performance HCHO sensors in practice.     

Effect of doping and substrate temperature on the structural and optical properties of reactive pulsed laser ablated tin oxide doped tantalum oxide thin films

5% SnO₂ doped tantalum oxide (Ta₂O₅) films are deposited on quartz substrates at different substrate temperatures of 300 K, 773 K, 873 K and 973 K using pulsed laser deposition in an oxygen ambient of 0.002 mbar. Undoped Ta₂O₅ films are also deposited on quartz substrates kept at substrate temperature 973 K under the same oxygen ambient using PLD. The films are characterized using GIXRD, AFM, FTIR, micro-Raman and UV-visible spectroscopy. Undoped films show an amorphous nature even at a substrate temperature of 973 K, whereas, SnO₂ doped films show crystalline nature even for deposition at 300 K. As far as our knowledge goes, this is the first report of crystalline Ta₂O₅ films deposited at room temperature. The average size of the crystallites calculated using the Debye-Scherrer formula, shows that the size of the crystallite decreases with increase in substrate temperature. FTIR and micro-Raman spectroscopic analysis reveals the presence of Ta-O-Ta, O-Ta and O-Ta-O vibrational bands in the films. Raman analysis indicates that the addition of SnO₂ suppresses the bond formation and changes the magnitude of bonds in Ta₂O₅. AFM patterns reveal the formation of Ta₂O₅ nanorods of diameter about 100 nm for the doped film deposited at 973 K. Optical transmittance of the films is found to be sensitive to substrate temperature as well as to the presence of SnO₂. A blue shift in the band-gap of the doped films is observed. The decrease of band-gap with decrease of particle size observed for SnO₂ doped films can be due to a band-bending effect. The transmittance of the films is found to depend on SnO₂ doping and substrate temperature.     

Gas-sensing properties of nanostructured SnO2-based sensor synthesized with different methods

Herein we report the preparation of SnO₂ nanomatierials by chemical precipitation, sol-gel and dissolution-pyrolysis. Furthermore, we studied their sensing properties. The composition, crystal structure and ceramic microstructure of the powders obtained are characterized by X-ray diffractometer (XRD) and scanning electron microscopy (SEM). The results show SnO₂ fabricated through the three methods has rutile structure and the sizes of spherical particles are below 30 nm. From the result, we can also know that the thick films deposited onto alumina substrates show different morphology, and which are fabricated by dissolution-pyrolysis has fibrous structure. We investigate the sensitivities, response and recovery times of the three sensors. The results of gas sensing measurement show that SnO₂-based sensor prepared by dissolution-pyrolysis method has high sensitivity, quick response and recovery behavior to the gases we studied. It also has wider range of working temperature that is from 25 to 400 °C compared with SnO₂-based sensor fabricated by the other two methods.     

Synthesis and gas sensing characteristics of SnO2 “dandelions”

SnO₂ dandelions-like architectures that composed of numerous one-dimensional tetragonal prism nanorods were synthesized by a simple hydrothermal method with the help of the surfactant poly(vinyl pyrrolidone) (PVP). The structure and morphology of resulting samples were characterized by means of X-ray powder diffraction (XRD) and field-emission scanning electron microscopy (FESEM). The results show that diameter of as-synthesized nanorods are less than 50 nm. The sensors fabricated from the SnO₂ nanorods exhibited good sensitivity, high selectivity and rapid response and recovery times to ethanol vapors at 280 °C.     

Enhanced H2S gas sensing properties of multiple-networked Pd-doped SnO2-core/ZnO-shell nanorod sensors

Pd-doped SnO₂-core/ZnO-shell nanorods were synthesized by using a three-step process: thermal evaporation of Sn powders in an oxygen atmosphere, atomic layer deposition of ZnO, and Pd diffusion followed by annealing. The sensitivity of the multiple networked SnO₂-core/ZnO-shell nanorod sensor to H₂S gas was found to be improved further significantly by Pd doping. The Pd-doped SnO₂-core/ZnO-shell nanorod sensor showed sensitivities of 6.4, 15.4, and 36.2% at H₂S concentrations of 20, 50, and 100 ppm at room temperature. The sensitivity of the nanorods was improved by more than 10 times at a H₂S concentration of 100 ppm. The sensitivity enhancement of the SnO₂-core/ZnO-shell nanorods by Pd doping may be attributed to the spillover effect, active reaction site generation, and the enhancement of chemisorption and dissociation of gas.     

Alcohol sensing of tin oxide thin film prepared by sol-gel process

The present paper describes the alcohol sensing characteristics of spin coated SnO₂ thin film deposited by using sol-gel process. The sensitivity of the film was measured at different temperatures and different concentrations of alcohol at ppm level. Alcohol detection result shows peak sensitivity at 623 K. The variation of sensitivity and ethanol concentration has shown a linear relationship up to 1150 ppm and after that it saturates. The response time measurement of the sensor was also observed and it was found that the response time is 30 sec. The results obtained favour the sol-gel process as a low cost method for the preparation of thin films with a high sensing characteristic.     

X-ray absorption near-edge spectroscopy investigation of the oxidation state of Pd species in nanoporous SnO2 gas sensors for methane detection

We report the correlation of the aging of Pd-doped SnO₂ methane sensors with the change of the oxidation state of Pd. Mesoporous SnO₂ doped with palladium species was prepared and exposed to different gas mixtures at high temperature (600 °C) to simulate long term usage. After each exposure step a fraction of the sample was cooled down to “freeze” the current oxidation state of Pd which was then analyzed by X-ray Absorption Near-Edge Spectroscopy (XANES) using the 'white line' (i.e. the absorption peak corresponding to the transition from the 2p_3/2 core level to unoccupied 4 d states) intensity of the L(III) edge as a probe for the oxidation state. The Pd oxidation state correlates with the response of the resistive SnO₂ sensor to methane gas, as determined by measuring the gas response to different concentrations of methane. Samples treated with 5000 ppm methane in air show a significant reduction of Pd(II) to Pd(0), depending clearly on the carrier gas (synthetic air, pure nitrogen) and on the temperature (600 °C vs. 300 °C).     

Nature of V ions in SnO2: EPR and photoluminescence studies

SnO₂ and 5 at.% V doped SnO₂ samples were prepared by citrate-gel method. From Raman study on vanadium doped SnO₂, the existence of phase separated V₂O₅ clusters has been established. EPR study on the V doped sample clearly revealed the existence of V⁴⁺ ions, which are incorporated in SnO₂ lattice and the existence of conduction electrons with g = 1.993. For vanadium doped SnO₂ sample, there is a decrease in luminescence at 400 nm and an increase in activation energy of electrical conduction compared to undoped SnO₂, and this has been attributed to the decrease in oxygen vacancies brought about by the incorporation of V⁵⁺ in the SnO₂ lattice.     

Synthesis and selective gas-sensing properties of hierarchically porous intestine-like SnO2 hollow nanostructures

Hierarchically porous intestine-like SnO₂ hollow nanostructures of different dimension were successfully synthesized via a facile, organic template free, H₂O₂-assisted method at room temperature. The morphology as well as texture (congregated solid sphere, intestine-like solid nanostructure, hollow core–shell one, and intestine-like hollow one) of SnO₂ materials can be controlled by varying H₂O₂ concentration and the size of intestine-like hollow SnO₂ can be tuned in the range of 20–120 nm by changing SnSO₄ concentration. The hierarchically porous intestine-like SnO₂ has high specific surface area (142 m² g⁻¹). The gas-sensing behaviors of the intestine-like SnO₂ material to different gas probes such as ethanol, H₂, CO, methane, and butane have been investigated; among them a high selectivity to ethanol was achieved.     

Fabrication of novel SnO2 nanofibers bundle and their optical properties

Here we report on the synthesis of novel SnO₂ nanofibers bundle (NFB) by using ball milled Fe powders via chemical vapor deposition (CVD). The reaction was carried out in a horizontal tube furnace (HTF) at 1100 °C under Ar flow. The as prepared product was characterized by X-ray diffraction (XRD), scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, high resolution transmission electron microscopy and selected area electron diffraction (SAED). The microscopy analysis reveals the existence of tubular structure that might be formed by the accumulation of nanofibers. The Raman spectrum reveals that the product is rutile SnO₂ with additional peaks ascribed to defects or oxygen vacancies. Room temperature Photoluminescence (PL) spectrum exhibits three emission bands at 369, 450 and 466.6 nm. Using optical absorbance data, a direct optical bandgap of 3.68 eV was calculated.