A high sensitivity gas sensor for formaldehyde based on CdO and In(2)O(3) doped nanocrystalline SnO(2)

The gas-sensing characteristics of In(2)O(3) and CdO doped nanocrystalline SnO(2) compounds for formaldehyde were investigated in this study. The phases of the resulting materials and the morphologies of the sensing layers were characterized by x-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. Indirect-heating sensors using SnO(2)-In(2)O(3)-CdO compounds as sensitive materials were fabricated on an alumina tube with Au electrodes and platinum wires. All measurements were performed at several operating temperatures from 100 to 180?°C. Good gas-sensing responses to formaldehyde have been found for all the prepared samples. It is shown that the sensors exhibited high sensitivity at low operating temperature (133?°C), making them promising candidates for practical detectors for formaldehyde.     

Mid-infrared chemical sensors utilizing plasma-deposited fluorocarbon membranes

In this study, plasma-polymerized films are evaluated as enrichment membranes deposited at the surface of mid-infrared transparent waveguides for liquid-phase chemical sensing utilizing evanescent field absorption spectroscopy. Fluorocarbon films were deposited onto zinc selenide (ZnSe) waveguides from plasma-polymerized pentafluoroethane (CF(3)CHF(2)) vapor. Excellent optical transmission of ZnSe waveguides after plasma deposition confirms compatibility of the infrared transparent substrate with this low-temperature, solvent-free film deposition process. The liquid-phase enrichment characteristics for plasma membranes were investigated via evanescent field absorption spectroscopy of a model analyte (tetrachloroethylene); the limits of detection were below 300 ppb (v/v) in water. Plasma-polymerized films are known for their excellent mechanical and chemical stability, while offering tunable chemical and physical characteristics during the deposition process. Future application of this coating strategy for depositing robust enrichment membranes with tunable batch production capability imparts an attractive route toward application-oriented development of next-generation mid-infrared chemical sensors applicable in harsh environments.     

Improved vapor selectivity and stability of localized surface plasmon resonance with a surfactant-coated Au nanoparticles film

Here, we report the use of tetraoctylammonium bromide (TOABr)-coated Au nanoparticles (NPs) for the optical sensing of volatile organic compounds (VOCs). We find that the film responded selectively to the presence of polar and nonpolar vapors by changes in the maximum wavelength (λ(max)) toward higher and lower wavelengths, respectively, as determined by UV-visible spectroscopy. We also observed that the organic coating reorganizes when vapors partition into the film indicated by FT-IR and the film contracts in the presence of water indicated by scanning electron microscopy (SEM). In the present sensor, the metallic Au core serves as the plasmonic signal while the organic coating acts as the receptor material providing vapor selectivity and sensor stability. Correlating changes in (λ(max)) with changes in the refractive index (RI) and nanoparticle-to-nanoparticle separation in the film is important both fundamentally and for improving selectivity in localized surface plasmon resonance (LSPR) sensors.     

Highly selective GaN-nanowire/TiO2-nanocluster hybrid sensors for detection of benzene and related environment pollutants

Nanowire-nanocluster hybrid chemical sensors were realized by functionalizing gallium nitride (GaN) nanowires (NWs) with titanium dioxide (TiO(2)) nanoclusters for selectively sensing benzene and other related aromatic compounds. Hybrid sensor devices were developed by fabricating two-terminal devices using individual GaN NWs followed by the deposition of TiO(2) nanoclusters using RF magnetron sputtering. The sensor fabrication process employed standard microfabrication techniques. X-ray diffraction and high-resolution analytical transmission electron microscopy using energy-dispersive x-ray and electron energy-loss spectroscopies confirmed the presence of the anatase phase in TiO(2) clusters after post-deposition anneal at 700?°C. A change of current was observed for these hybrid sensors when exposed to the vapors of aromatic compounds (benzene, toluene, ethylbenzene, xylene and chlorobenzene mixed with air) under UV excitation, while they had no response to non-aromatic organic compounds such as methanol, ethanol, isopropanol, chloroform, acetone and 1,3-hexadiene. The sensitivity range for the noted aromatic compounds except chlorobenzene were from 1% down to 50 parts per billion (ppb) at room temperature. By combining the enhanced catalytic properties of the TiO(2) nanoclusters with the sensitive transduction capability of the nanowires, an ultra-sensitive and selective chemical sensing architecture is demonstrated. We have proposed a mechanism that could qualitatively explain the observed sensing behavior.     

Reduced-temperature ethanol sensing characteristics of flower-like ZnO nanorods synthesized by a sonochemical method

Flower-like ZnO nanorods with diameters less than 15?nm were synthesized by a sonochemical method. The sensors fabricated from the nanorods exhibited excellent ethanol sensing properties. At the working temperature of 300?°C, their sensitivity was 176.8-100?ppm ethanol vapour. While the working temperature was reduced to 140?°C, they were still able to detect ethanol vapour at the ppm level. The reduced working temperature may be attributed to the small sizes of the nanorods.     

Rapid and ultrahigh ethanol sensing based on Au-coated ZnO nanorods

Rapid and ultrahigh sensing is realized from Au-coated ZnO rods with diameters down to 15?nm. Both the small diameters and the Au coating make the surface-depletion effect more pronounced for gas sensing. Such enhanced surface depletion increases the sensitivity, lowers the operation temperature and decreases the response time. A sensitivity of 89.5-100?ppm ethanol is obtained with response time shorter than 2?s at 300?°C, and the operation temperature can be as low as 150?°C. It is found that the Au coating improves the sensitivity by three times; this is much higher than that of noble metal-doped metal oxide sensors controlled by a grain-boundary barrier. Our results imply that the surface-depletion model is very helpful in fabricating high performance gas sensors.     

Nanostructured SnO(2) films prepared from evaporated Sn and their application as gas sensors

This paper describes the morphology, stoichiometry, microstructure and gas sensing properties of nanoclustered SnO(x) thin films prepared by Sn evaporation followed by a rheotaxial growth and thermal oxidation process. Electron microscopy was used to investigate, in detail, the evolution of the films as the oxidation temperature was increased. The results showed that the contact angle, perpendicular height, volume and microstructure of the clusters all changed significantly as a result of the thermal oxidation processes. Electron diffraction and x-ray photoelectron spectroscopy measurements revealed that after oxidation at a temperature of 600?°C, the Sn clusters were fully transformed into porous three-dimensional polycrystalline SnO(2) clusters. On the basis of these results, a prototype SnO(2) sensor was fabricated and sensing measurements were performed with H(2) and NO(2) gases. At operating temperatures of 150-200?°C the film produced measurable responses to concentrations of H(2) as low as 600?ppm and NO(2) as low as 500?ppb.     

Novel fabrication of an SnO(2) nanowire gas sensor with high sensitivity

We fabricated a nanowire-based gas sensor using a simple method of growing SnO(2) nanowires bridging the gap between two pre-patterned Au catalysts, in which the electrical contacts to the nanowires are self-assembled during the synthesis of the nanowires. The gas sensing capability of this network-structured gas sensor was demonstrated using a diluted NO(2). The sensitivity, as a function of temperature, was highest at 200?°C and was determined to be 18 and 180 when the NO(2) concentration was 0.5 and 5?ppm, respectively. Our sensor showed higher sensitivity compared to different types of sensors including SnO(2) powder-based thin films, SnO(2) coating on carbon nanotubes or single/multiple SnO(2) nanobelts. The enhanced sensitivity was attributed to the additional modulation of the sensor resistance due to the potential barrier at nanowire/nanowire junctions as well as the surface depletion region of each nanowire.     

Enhanced acetone detection using Au doped ZnO thin film sensor

Zinc oxide (ZnO) thin films are prepared using sol–gel method for acetone vapor sensing. Zinc acetate dihydrate (Zn(CH₃COO)₂·2H₂O) was taken as starting material and a stable and homogeneous solution was prepared in ethanol by deliquescing the zinc acetate and distinct amount of monoethanolamine as a stabilizing agent. The prepared solution was then coated on silicon substrates by spin coating method and then annealed at 650 °C for preparing ZnO thin films. The thickness of the film was maintained at 410 nm. The structural, morphological and optical studies were done for the synthesized ZnO thin films. The operating temperature and sensor response is considered to be an important parameter for the gas sensing behavior of any material. Therefore, the present study examined the effect of sensing behavior of 3% v/v gold (Au) doped ZnO thin films as a sensor. The response characteristics of 410 nm ZnO thin film for temperature ranging from 180 to 360 °C were determined for the acetone vapors. The reported study provides a significant development towards acetone sensors, where a very high sensitivity with rapid response and recovery times are reported with lowered optimal operating temperature as compared to bare ZnO nano-chains like structured thin films. In comparison to the bare ZnO thin films giving a response of 63 at an operating temperature of 320 °C, a much better response of 132.3 was observed for the Au doped ZnO thin films at an optimised operating temperature of 280 °C for a concentration of 500 ppm of acetone vapors.     

Stretchable Electronic Sensors of Nanocomposite Network Films for Ultrasensitive Chemical Vapor Sensing

A stretchable, transparent, and body‐attachable chemical sensor is assembled from the stretchable nanocomposite network film for ultrasensitive chemical vapor sensing. The stretchable nanocomposite network film is fabricated by in situ preparation of polyaniline/MoS₂ (PANI/MoS₂) nanocomposite in MoS₂ suspension and simultaneously nanocomposite deposition onto prestrain elastomeric polydimethylsiloxane substrate. The assembled stretchable electronic sensor demonstrates ultrasensitive sensing performance as low as 50 ppb, robust sensing stability, and reliable stretchability for high‐performance chemical vapor sensing. The ultrasensitive sensing performance of the stretchable electronic sensors could be ascribed to the synergistic sensing advantages of MoS₂ and PANI, higher specific surface area, the reliable sensing channels of interconnected network, and the effectively exposed sensing materials. It is expected to hold great promise for assembling various flexible stretchable chemical vapor sensors with ultrasensitive sensing performance, superior sensing stability, reliable stretchability, and robust portability to be potentially integrated into wearable electronics for real‐time monitoring of environment safety and human healthcare.     

MWCNT-polymer composites as highly sensitive and selective room temperature gas sensors

Multi-walled carbon nanotubes (MWCNTs)-polymer composite-based hybrid sensors were fabricated and integrated into a resistive sensor design for gas sensing applications. Thin films of MWCNTs were grown onto Si/SiO(2) substrates via xylene pyrolysis using the chemical vapor deposition technique. Polymers like PEDOT:PSS and polyaniline (PANI) mixed with various solvents like DMSO, DMF, 2-propanol and ethylene glycol were used to synthesize the composite films. These sensors exhibited excellent response and selectivity at room temperature when exposed to low concentrations (100 ppm) of analyte gases like NH(3) and NO(2). The effect of various solvents on the sensor response imparting selectivity to CNT-polymer nanocomposites was investigated extensively. Sensitivities as high as 28% were observed for an MWCNT-PEDOT:PSS composite sensor when exposed to 100 ppm of NH(3) and - 29.8% sensitivity for an MWCNT-PANI composite sensor to 100 ppm of NO(2) when DMSO was used as a solvent. Additionally, the sensors exhibited good reversibility.     

Detection of mercury(II) by quantum dot/DNA/gold nanoparticle ensemble based nanosensor via nanometal surface energy transfer

An ultrasensitive fluorescent sensor based on the quantum dot/DNA/gold nanoparticle ensemble has been developed for detection of mercury(II). DNA hybridization occurs when Hg(II) ions are present in the aqueous solution containing the DNA-conjugated quantum dots (QDs) and Au nanoparticles. As a result, the QDs and the Au nanoparticles are brought into the close proximity, which enables the nanometal surface energy transfer (NSET) from the QDs to the Au nanoparticles, quenching the fluorescence emission of the QDs. This nanosensor exhibits a limit of detection of 0.4 and 1.2 ppb toward Hg(II) in the buffer solution and in the river water, respectively. The sensor also shows high selectivity toward the Hg(II) ions.     

Mercuric ion sensing by a film bulk acoustic resonator

This paper describes a film bulk acoustic resonator (FBAR) mass sensor for detecting Hg2+ ion in water with excellent sensitivity and selectivity. When a thin Au film was deposited on the surface of an FBAR, the resonant frequency shifted to a lower value when the film was exposed to Hg2+ in aqueous solution. The FBAR sensor detected as low as 10(-9) M Hg2+ (0.2 ppb Hg2+) in water. Other ions such as K+, Ca2+, Mg2+, Zn2+, and Ni2+ had little or no effect on the resonant frequency of the FBAR. Coating of the FBAR Au surface with a self-assembled monolayer (SAM) of 4-mercaptobenzoic acid decreased the Hg2+ response.     

A high sensitive and low detection limit of formaldehyde gas sensor based on hierarchical flower-like CuO nanostructure fabricated by sol–gel method

The hierarchical flower-like CuO nanostructure was synthesized by a facile sol–gel method without template. Indirectly-heated sensors are fabricated by coating the sol–gel on ceramic tubes with signal electrodes and subsequent annealing. The obtained nanostructures are analyzed by X-ray diffraction and scanning electron microscopy. Their gas sensing performances were investigated. The results indicated that the sensor based on hierarchical flower-like CuO exhibited excellent sensing properties towards ethanol, formaldehyde, acetone and dimethylbenzene. The sensor based on the CuO exhibited the optimal gas sensing performance, giving a ppb-level detection limit and a high response (R_g/R_a) of 1.378 to 50 ppb formaldehyde at 250 °C. The response and recovery time of the flower-like CuO nanostructure sensor are 11.9 and 8.4 s, respectively. The significantly enhanced sensing properties to formaldehyde could be attributed to the changes in crystallite size and specific surface area. The results indicate that the hierarchical flower-like CuO nanostructure gas sensor can be a simple and useful platform for formaldehyde and other volatile organic compounds sensing application.     

A universal sensor for mercury (Hg, Hg(I), Hg(II)) based on silver nanoparticle-embedded polymer thin film

Detection of mercury at concentration levels down to parts-per-billion is a problem of fundamental and practical interest due to the high toxicity of the metal and its role in environmental pollution. The extensive research in this area has been focused primarily on specific sensing of mercuric (Hg(2+)) ion. As mercury exists in the oxidation states, +2, +1 and 0 all of which are highly toxic, a universal sensor covering all the three while ensuring high sensitivity, selectivity, and linearity of response, and facilitating in situ as well as ex situ deployment, would be very valuable. Silver nanoparticle-embedded poly(vinyl alcohol) (Ag-PVA) thin film fabricated through a facile protocol is shown to be a fast, efficient and selective sensor for Hg(2+), Hg(2)(2+) and Hg in aqueous medium with a detection limit of 1 ppb. The sensor response is linear in the 10 ppb to 1 ppm concentration regime. A unique characteristic of the thin film based sensor is the blue shift occurring concomitantly with the decrease in the surface plasmon resonance absorption upon interaction with mercury, making the sensing highly selective. Unlike the majority of known sensors that work only in situ, the thin film sensor can be used ex situ as well. Examination of the thin film using microscopy and spectroscopy through the sensing process provides detailed insight into the sensing event.     

Hydrogen sensing in titanate nanotubes associated with modulation in protonic conduction

Hydrogen/sodium titanate nanotubes (TNTs) were investigated as hydrogen (H(2)) sensors. TNT films exhibit good sensing properties and a large response, in particular at room temperature. Electrical conductivity measurements performed under different atmospheres from 25 to 300?°C indicate that, for T > 100?°C, conduction is thermally activated and can be attributed to electronic transport, whereas for T < 100?°C conduction is dominated by protonic transport. The T dependence of the H(2) sensitivity was determined and related to this variation in the dominant transport mechanism. For low T, H(2) sensing originates from the modulation in protonic conduction. Such modulation was attributed to the creation/destruction of surface hydroxyl groups.     

Ultrahigh-sensitive tin-oxide microsensors for H/sub 2/S detection

Ultrahigh-sensitivity SnO/sub 2/-CuO sensors were fabricated on Si(100) substrates for detection of low concentrations of hydrogen sulfide. The sensing material was spin coated over platinum electrodes with a thickness of 300 nm applying a sol-gel process. The SnO/sub 2/-based sensors doped with copper oxide were prepared by adding various amounts of Cu(NO/sub 3/)/sub 2/.3H/sub 2/O to a sol suspension. Conductivity measurements of the sensors annealed at different temperatures have been carried out in dry air and in the presence of 100 ppb to 10-ppm H/sub 2/S. The nanocrystalline SnO/sub 2/-CuO thin films showed excellent sensing characteristics upon exposure to low concentrations of H/sub 2/S below 1 ppm. The 5% CuO-doped sensor having an average grain size of 20 nm exhibits a high sensitivity of 2.15/spl times/10/sup 6/ (R/sub a//R/sub g/) for 10-ppm H/sub 2/S at a temperature of 85/spl deg/C. By raising the operating temperature to 170/spl deg/C, a high sensitivity of /spl sim/10/sup 5/ is measured and response and recovery times drop to less than 2 min and 15 s, respectively. Selectivity of the sensing material was studied toward various concentrations of CO, CH/sub 4/, H/sub 2/, and ethanol. SEM, XRD, and TEM analyses were used to investigate surface morphology and crystallinity of SnO/sub 2/ films.     

Synthesis of mesoporous tin oxide and its application as a LNG sensor

The nanostructured SnO2 gas sensor with Au electrodes and Pt heater has been fabricated as one unit via screen printing process. The gas sensor was tested for CH4 sensing behavior at 350 degrees C in the concentration range of 500-10,000 ppm. Those mesoporous SnO2 sensors exhibited the similar sensoring properties in CH4 and CO detection. The fast speed of response and high sensitivity were obtained for mesoporous tin oxide sensor as compared to non-porous one.     

Ultralow-Power Alcohol Vapor Sensors Using Chemically Functionalized Multiwalled Carbon Nanotubes

Alcohol sensors, batch fabricated by forming bundles of chemically functionalized multiwalled carbon nanotubes (f-CNTs) across Au electrodes on SiO₂/Si substrates using an AC electrophoretic technique, were developed for alcohol vapor detection using an ultralow input power of ~ 0.01 - 1 muW, which is lower than the power required for most commercially available alcohol sensors by more than four orders of magnitude. The multiwalled carbon nanotubes (MWCNTs) have been chemically functionalized with the COOH groups by oxidation. We found that the sensors are selective with respect to flow from air, water vapor, and alcohol vapor. The sensor response is linear for alcohol vapor concentrations from 1 to 21 ppm with a detection limit of 0.9 ppm. The transient response of these sensors is experimentally shown to be ~1 s and the variation of the responses at each concentration is within 10% for all of the tested sensors. The sensors could also easily be reset to their initial states by annealing the f-CNTs sensing elements at a current of 100-200 muA within ~ 100-200 s. We demonstrated that the response of the sensors can be increased by one order of magnitude after adding the functional group COOH onto the nanotubes, i.e., from ~0.9% of a bare MWCNTs sensor to ~9.6% of an f-CNTs sensor with a dose of 21 ppm alcohol vapor.     

Gas sensitivity comparison of polymer coated SAW and STW resonators operating at the same acoustic wave length

Results from systematic gas sensing experiments on polymer coated surface-transverse-wave (STW) and surface-acoustic-wave (SAW) based two-port resonators on rotated Y-cut quartz, operating at the same acoustic wavelength of 7.22 /spl mu/m, are presented. The acoustic devices are coated with chemosensitive films of different viscoelastic properties and thicknesses, such as solid hexamethyldisiloxane (HMDSO), semisolid styrene (ST), and soft allyl alcohol (AA). The sensor sensitivities to vapors of different chemical analytes are automatically measured in a sensor head, evaluated, and compared. It is shown that thin HMDSO- and ST-coated STW sensors are up to 3.8 times more sensitive than their SAW counterparts, while SAW devices coated with thick soft AA-films are up to 3.6 times more sensitive than the STW ones. This implies that SAWs are more suitable for operation with soft coatings while STWs perform better with solid and semisolid films. A close-to-carrier phase noise evaluation shows that the vapor flow homogeneity, the analyte concentration, its sorption dynamics, and the sensor oscillator design are the major limiting factors for the sensor noise and its resolution. A well designed ST-coated 700 MHz STW sensor provides a 178 kHz sensor signal at a 630 ppm concentration of tetra-chloroethylene and demonstrates short-term stability of 3/spl times/10/sup -9//s which results in a sensor resolution of about 7 parts per billion (ppb).