Improved selective acetone sensing properties of Co-doped ZnO nanofibers by electrospinning

Pure and Co-doped (0.3 wt%, 0.5 wt%, and 1 wt%) ZnO nanofibers are synthesized by an electrospinning method and followed by calcination. The as-synthesized nanofibers are characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) spectroscopy. Comparing with pure ZnO nanofibers, Co-doped nanofibers exhibit improved acetone sensing properties at 360 °C. The response of 0.5 wt% Co-doped ZnO nanofibers to 100 ppm acetone is about 16, which is 3.5 times larger than that of pure nanofibers (about 4.4). The response and recovery times of 0.5 wt% Co-doped ZnO nanofibers to 100 ppm acetone are about 6 and 4 s, respectively. Moreover, Co-doped ZnO nanofibers can successfully distinguish acetone and ethanol/methanol, even in a complicated ambience. The high response and quick response/recovery are based on the one-dimensional nanostructure of ZnO nanofibers combining with the Co-doping effect. The selectivity is explained by the different optimized operating temperatures of Co-doped ZnO nanofibers to different gases.     

Preparation and gas-sensing performance of In2O3 porous nanoplatelets

In₂O₃ porous nanoplatelets were successfully synthesized by solvothermal treatment of indium acetylacetonate, followed by calcination in air. X-ray diffraction and Raman spectrum measurements demonstrate that the products are pure cubic phase In₂O₃. Scanning electron microscopy and transmission electron microscopy analyses reveal that the In₂O₃ nanoplatelets bounded by {1 1 0} planes with thickness less than 6 nm and length about 20-50 nm are single crystalline but with porous structure. The optical absorption property of the In₂O₃ nanoplatelets was investigated by UV-vis spectroscopy, which indicates that the In₂O₃ nanoplatelets are semiconducting with a direct band gap of 3.1 eV. The gas sensing performance of the as-prepared In₂O₃ porous nanoplatelets was investigated towards a series of typical organic solvents and fuels. It was found that the In₂O₃ porous nanoplatelets show structure-induced enhancement of gas sensing performance, and especially possess high sensitivity and rapid response towards ethanol vapor.     

Vertically aligned ZnO nanorods and graphene hybrid architectures for high-sensitive flexible gas sensors

We present the fabrication and characterization of new type of flexible gas sensors, composed mainly of a bottom ZnO conductive layer on metal foil, vertically aligned ZnO nanorod channel, and graphene-based top conductive electrode. Multiple cycling tests demonstrated the ZnO nanorods (NRs) and graphene (Gr) hybrid architectures accommodated the flexural deformation without mechanical or electrical failure for bending radius below 0.8 cm under the repeated bending and releasing up to 100 times. In addition, the hybrid architectures fabricated on glass substrate showed good optical transmittance larger than ∼70% for visible light, indicating potential application in transparent devices. Furthermore, our gas sensors demonstrated the ppm level detection of ethanol gas vapor with the sensitivity (resistance in air/resistance in target gas) as high as ∼9 for 10 ppm ethanol.     

Dispersive SnO2 nanosheets: Hydrothermal synthesis and gas-sensing properties

SnO₂ nanosheets with the thickness of 10 nm were successfully synthesized by a simple hydrothermal process at 180 °C for 12 h. The samples were characterized by X-ray power diffraction, scanning electron microscopy, transmission electron microscopy, and high-resolution transmission electron microscopy. The sensor performance of the as-prepared SnO₂ nanosheets for ethanol and carbon monoxide was measured. The results indicate that the sensor exhibited high response, quick response-recovery kinetics, and good repeatability.     

Selective acetone sensor based on dumbbell-like ZnO with rapid response and recovery

Dumbbell-like ZnO microcrystals have been obtained through a facile solution method. The structure, morphology and optical properties of the as-prepared ZnO microcrystals have been characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy and photoluminescence. The as-prepared ZnO microcrystals exhibit excellent sensing properties against acetone at an operating temperature of 300 °C. The response and recovery times are found to be 1.5 and 3 s, respectively. Moreover, the sensor holds the successful discrimination between acetone and ethanol, which makes our product a good candidate in fabricating highly selective sensors in practice.     

Synthesis and gas sensing properties of bundle-like α-Fe2O3 nanorods

Bundle-like α-Fe₂O₃ nanostructures were successfully synthesized by a simple calcination of β-FeOOH precursor derived from a hydrothermal method in the presence of poly(vinyl pyrrolidone). The as-prepared products were characterized by X-ray power diffraction, field emission scanning electron microscopy, and transmission electron microscopy. The results indicated that bundle-like nanostructures were composed of well-aligned single crystalline nanorods with the diameters of 20-30 nm and the lengths of 200-300 nm. The gas sensing properties of as-prepared products were investigated. It was found that the sensor based on α-Fe₂O₃ nanostructure exhibited high response, quick response-recovery, and good repeatability to acetone at 250 °C.     

Selective gas sensing response from different loading of Ag in sol-gel mesoporous titania powders

Bare and Ag loaded TiO₂ (0.05, 0.5, and 5.0 mol% Ag) powders prepared by sol-gel process have been used for the detection of ethanol, LPG, acetone and toluene gases. These materials were well characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) specific surface area analysis techniques. Specific surface area increased with increasing Ag loading in these mesoporous materials. A thorough TEM/HRTEM investigation with X-ray maps of the modified particles shows the extent of TiO₂ surface coverage by Ag nanoparticles. From the comparative study of the sensor response of Ag-TiO₂ powders for various gases, it is observed that each Ag loading resulted in the highest response towards a particular gas or in other words, every gas responded best towards a particular Ag loading of the sensor material, i.e. 0.05 mol% Ag-TiO₂ sensor showed highest response towards ethanol, 0.5 mol% Ag-TiO₂ sensor showed best response towards toluene, whereas, bare TiO₂ proved to be the best sensor for both acetone and LPG gases. This establishes that Ag loading is not required for detection of acetone and LPG gases. On the basis of detailed materials characterization, a mechanism for the gas sensing response of each analyte has been discussed.     

LPG sensing properties of Pd-sensitized vertically aligned ZnO nanorods

One-dimensional (1-D) vertically aligned ZnO nanorods are synthesized on glass substrate through a simple chemical route and their liquefied petroleum gas (LPG) sensing properties are studied. The morphology and structure of vertically aligned ZnO nanorods has been characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The LPG sensing properties of the vertically aligned ZnO nanorods are improved significantly after palladium (Pd) sensitization. The unsensitized vertically aligned ZnO nanorods exhibited the maximum response of 37% at 573 K upon exposure to 2600 ppm LPG, which improved to 60% at operating temperature of 498 K after the Pd sensitization. The Pd-sensitized vertically aligned ZnO nanorods showed more selectivity towards LPG as compared to CO₂. Our results demonstrate that the chemically grown vertically aligned ZnO nanorods along with Pd sensitization are promising material for the fabrication of cost effective and high performance gas sensors.     

Electrospun Cu-doped ZnO nanofibers for H2S sensing

Pure and Cu-doped ZnO nanofibers were synthesized via electrospinning technology. The morphology and structure of the as-synthesized nanofibers were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and Raman spectroscopy. The effects of Cu doping on H₂S sensing properties at low concentration (1-10 ppm) were investigated at 230 °C. The results show that the H₂S sensing properties of ZnO nanofibers are effectively improved by Cu doping: 6 at% Cu-doped ZnO nanofibers show a maximum sensitivity to H₂S gas, and the response to 10 ppm H₂S is one order of magnitude higher than the one of pure ZnO nanofibers.     

Co-precipitation synthesis and gas-sensing properties of ZnO hollow sphere with porous shell

ZnO hollow sphere with porous shell has been prepared by co-precipitation method using Zn(NO₃)₂·6H₂O and (CH₂)₆N₄ as reactants, sodium citrate as surfactant. The BET surface area of as-prepared ZnO hollow sphere sample is 41.84 m²/g. The response of gas sensor made from the obtained ZnO hollow sphere reaches 7.4 to 10 ppm ammonia, with a response time of 10 s, implying the potential for practical applications.     

Highly sensitive NO2 sensor based on square-like tungsten oxide prepared with hydrothermal treatment

The square-like WO₃ nanosheets were synthesized by hydrothermal treatment of irregular WO₃ nanosheets prepared through acidification of Na₂WO₄·2H₂O. The obtained square-like and irregular WO₃ nanosheets were characterized with field emission scanning electron microscopy, X-ray powder diffraction and transmission electron microscopy. The gas sensing properties of sensors based on as-prepared samples were investigated. The results indicated that both samples exhibited high response to NO₂. The sensor based on square-like WO₃ nanosheets exhibited remarkably enhanced response and faster response/recovery time for NO₂ compared with that based on irregular nanosheets. Especially, the sensor based on square-like WO₃ nanosheets could detect NO₂ down to 40 ppb, which covered environmental standard. A possible reason for the influence of unique structure on the sensing properties of sensors based on square-like WO₃ was proposed.     

Gas sensing properties of a clad modified fiber optic sensor with Ce, Li and Al doped nanocrystalline zinc oxides

Spectral characteristics of a clad modified fiber optic gas sensor are studied for various concentrations (0-500 ppm) of ammonia, methanol and ethanol at room temperature. Cerium, aluminum and lithium doped (6 at.%) nanocrystalline zinc oxides are replaced with a clad and used as gas sensing materials. The study shows that the spectral intensity increases linearly with concentration for ammonia whereas it decreases for methanol and ethanol. The Ce doped ZnO exhibits higher gas sensitivity compared to Al and Li doped zinc oxides. The time response of the sensor is presented for a Ce doped ZnO with ammonia gas. A model is proposed for understanding the spectral intensity variations.     

Improving the ethanol sensing of ZnO nano-particle thin films—The correlation between the grain size and the sensing mechanism

ZnO and Sn doped ZnO (ZnO:Sn) thin films at various doping concentrations from 1 to 10 at.% were prepared by the sol-gel method for an ethanol sensing application. The Sn doping significantly influenced the film growth, grain size and response of the films. The XRD patterns showed that the hexagonal wurtzite structure of the ZnO film was retained even after the Sn doping. The crystallite grain sizes of the ZnO:Sn thin films at 0, 2 and 4 at.% were estimated by using the typical Scherrer's equation. The crystalline quality of the films at 6, 8 and 10 at.% of Sn was degenerated. Typical FESEM images demonstrated the different morphologies for the ZnO:Sn thin films at various Sn concentrations; many pores of various dimensions were observed depending on the doping level. A TEM analysis of the ZnO:Sn thin films at 0, 2 and 4 at.% was performed to verify the grain size. The optimum Sn doping level of ZnO:Sn thin film for ethanol sensing was estimated to be 4 at.%. The 4 at.% sample obtained the highest response to ethanol vapor in the 10-400 ppm level range at a low operating temperature of 250 °C. The sensing mechanism was explained by a variation in the sensitivity model from a neck-grain-boundary controlled sensitivity to a neck-controlled sensitivity. Our work demonstrates the ability to reduce the working temperature as well as to increase the response of ZnO thin film based gas sensors to detect ethanol, which would be of great merit for commercialized applications.     

SnO2 thin film sensor with enhanced response for NO2 gas at lower temperatures

Semiconducting SnO₂ thin films having higher value of electrical conductivity have been deposited using RF sputtering technique in the reactive gas environment (30% O₂ + 70% Ar) using a metallic tin (Sn) target for detection of oxidizing NO₂ gas. The effect of growth pressure (12-18 mTorr) on the surface morphology and structural property of SnO₂ film was studied using Atomic force microscopy (AFM), Scanning electron microscopy (SEM) and X-ray Diffraction (XRD) respectively. Film deposited at 16 mTorr sputtering pressure was porous with rough microstructure and exhibits high sensor response (∼2.9 × 10⁴) towards 50 ppm NO₂ gas at a comparatively low operating temperature (∼100 °C). The sensor response was found to increase linearly from 1.31 × 10² to 2.9 × 10⁴ while the response time decrease from 12.4 to 1.6 min with increase in the concentration of NO₂ gas from 1 to 50 ppm. The reaction kinetics of target NO₂ gas on the surface of SnO₂ thin film at the Sn sites play important role in enhancing the response characteristics at lower operating temperature (∼100 °C). The results obtained in the present study are encouraging for realization of SnO₂ thin film based sensor for efficient detection of NO₂ gas with low power consumption.     

Gas sensing properties at room temperature of a quartz crystal microbalance coated with ZnO nanorods

Gas sensors based on a quartz crystal microbalance (QCM) coated with ZnO nanorods were developed for detection of NH₃ at room temperature. Vertically well-aligned ZnO nanorods were synthesized by a novel wet chemical route at a low temperature of 90 °C, which was used to grow the ZnO nanorods directly on the QCM for the gas sensor application. The morphology of the ZnO nanorods was examined by field-emission scanning electron microscopy (FE-SEM). The diameter and length of the nanorods were 100 nm and 3 μm, respectively. The QCM coated with the ZnO nanorods gas sensor showed excellent performance to NH₃ gas. The frequency shift (Δf) to 50 ppm NH₃ at room temperature was about 9.1 Hz. It was found that the response and recovery times were varied with the ammonia concentration. The fabricated gas sensors showed good reproducibility and high stability. Moreover, the sensor showed a high selectivity to ammoniac gas over liquefied petroleum gas (LPG), nitrous oxide (N₂O), carbon monoxide (CO), nitrogen dioxide (NO₂), and carbon dioxide (CO₂).     

CdO activated Sn-doped ZnO for highly sensitive, selective and stable formaldehyde sensor

Sn-, Ni-, Fe- and Al-doped ZnO and pure ZnO are prepared by coprecipitation method, and characterized by scanning electron microscope (SEM), energy diffraction spectra (EDS) and X-ray diffraction (XRD). Their formaldehyde gas sensing properties are evaluated and the results show that 2.2 mol% Sn dopant can increase the response of ZnO by more than 2 folds, while other dopants increase little response or even decrease response. Further, CdO is used to activate ZnO based formaldehyde sensing material. It is demonstrated that 10 mol% CdO activated 2.2 mol% Sn-doped ZnO has the highest formaldehyde gas response, with a linear sensitivity of ∼10/ppm at lowered work temperature of 200 °C than 400 °C of pure ZnO, and high selectivity over toluene, CO and NH₃, as well as good stability tested in 1 month.     

C-doped WO3 microtubes assembled by nanoparticles with ultrahigh sensitivity to toluene at low operating temperature

Novel C-doped WO₃ microtubes (MTs) were successfully synthesized by a facile infiltration and calcination process using the cotton fibers as templates. The prepared MTs were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), N₂ adsorption and desorption measurements and ultraviolet-visible spectroscopy. XPS spectra show the carbon was doped into the lattice of the WO₃ phase, resulting in a decrease of the band gap of the C-doped WO₃ MTs from 2.45 eV to 2.12 eV. Moreover, the WO₃ MTs were assembled by nanoparticles in size of ca. 40 nm and had larger specific surface area (21.3 m²/g) due to existence of meso/macro-pores inside them. At low operating temperature of 90 °C, the gas sensor based on the C-doped WO₃ MTs had a detected limit of 50 ppb to the toluene gas (response of 2.0). The enhancement of toluene sensing performance of C-doped WO₃ MTs was attributed to a larger surface area and higher porosity, which arises from its unique MTs. Furthermore, the band gap reduction and a new intragap band formation for C-doped WO₃ MTs were proposed as the reason for the decrease in optimal operating temperature.     

Tin-copper mixed metal oxide nanowires: Synthesis and sensor response to chemical vapors

Tin-copper mixed metal oxide nanowires were successfully prepared by thermally oxidizing electrodeposited metallic nanowires (Sn-8 at.% Cu, Sn-43 at.% Cu and Sn-86 at.% Cu). The structure and composition of these nanowires before and after thermal oxidation were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), and X-ray diffraction (XRD). Dielectrophoresis was utilized to align the nanowires in contact with pre-fabricated interdigitated electrodes to form a chemiresistive gas sensor circuit. The sensitivity variation of the nanowires with different compositions was tested with acetone, ethanol and ethyl acetate vapors at different concentration levels, and the temperature effect was studied at five operating temperatures, ranging from 200 °C to 440 °C. All the three mixed metal oxide nanowire sensors exhibited higher sensitivity than that of pure tin oxide nanowire sensor. The sensor performance was also investigated in terms of response/recovery time and repeatability. An interesting positive/negative response was observed by varying the element composition of the mixed oxide nanowires.     

Facile synthesis of hierarchical SnO2 semiconductor microspheres for gas sensor application

Hierarchical SnO₂ microspheres were synthesized by a hydrothermal method at 140 °C using stannic chloride hydrate and sodium hydroxide as starting materials. The individual hierarchical SnO₂ microsphere ranged from 700 to 900 nm in diameter. After these microspheres were heated at 600 °C for 2 h, the spheres were cross-linked into clusters by short SnO₂ nanorods as revealed by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Most importantly, SnO₂ hierarchical microsphere sensor exhibits excellent selectivity and fast response to ethanol. Response and recovery times were 0.6 s and 11 s when the sensor was exposed to 50 ppm ethanol at an operating temperature of 300 °C. Thus, hierarchical structures play a significant role in the field of gas sensing.     

Synthesis of quantum size ZnO crystals and their gas sensing properties for NO2

Quantum size ZnO crystals have been synthesized successfully by a room temperature sol-gel process. Oleic acid (OA) has been used as capping agent to control the particle size of ZnO. The crystal structure and size of the ZnO are characterized by the X-ray diffraction (XRD) and transmission electron microscope (TEM). The XRD results show the as-synthesized ZnO has hexagonal wurtzite structure and the average crystallite size is 5.7 nm which is little less than TEM result. It is testified by photoluminescence (PL) and Raman spectra that the quantum size ZnO keeps the crystal structure of the bulk ZnO and possesses more surface defects. The quantum size ZnO has the highest response of 280 to NO₂ and the highest selectivity of 31 and 49 corresponding to CO and CH₄ at operating temperature of 290 °C. The effect of calcination temperatures on sensing property and transient response of the ZnO sensor are also investigated.