Single-crystalline Te microtubes: Synthesis and NO2 gas sensor application

Tellurium tubular crystals were grown by direct thermal evaporation of tellurium metal in an inert atmosphere on quartz substrates at ambient pressure without employing any catalyst. Tellurium powder was evaporated by heating at 600 °C and was condensed at a substrate temperature of 300–350 °C in the downstream of argon gas at a flow rate of 100 mL/min. The structure and chemical composition of the as-synthesized samples were examined by X-ray diffraction analysis, scanning electron microscopy, energy-dispersive X-rays microanalysis and micro-Raman spectroscopy. Scanning electron microscopy images and X-ray diffraction patterns showed that the as-synthesized Te had a tubular single-crystalline morphology with a hexagonal cross-section. The Te microtubes were typically 0.5–6 mm long, 30–70 μm in external diameter, and 5–20 μm thick. NO₂ gas-sensing properties of the Te microtubes at room temperature were also investigated. They showed a promising sensitivity and response towards tested gas.     

Flexible humidity sensor in a sandwich configuration with a hydrophilic porous membrane

We constructed a wearable and flexible humidity sensor (thickness: 80 μm) in a sandwich configuration, with a hydrophilic poly-tetrafluoroethylene membrane placed between two gold deposited layers, using soft-MEMS techniques. The device was used to measure humidity level, via its electrical conductivity, using a multi-frequency LCR-meter at frequencies ranging from 100 Hz to 100 kHz. The device was calibrated at 100 Hz against moist air over the range of 30–85% RH, which includes normal humidity levels in the atmosphere and physiological air such as breath and evaporating sweat. The response sensitivity of the humidity device was extremely high, even for recovery to dry air; for example response time was less than 1 s for a conductivity shift between humid air of 80% RH and dry air of −60 °C dew point. The sensor performance was reproducible over multiple measurements, with a coefficient of variation of 1.77% (n = 5). The sensor was appropriate for physiological applications, and was successfully used in two non-invasive approaches: to monitor breath air at the mouth, and to measure sweat moisture from the nostrils.     

Development of a micrometeorological model for the estimation of methane flux from paddy fields: Validation with standard direct measurements

This work has focussed on the development of an indirect method for estimating methane fluxes from paddy fields and wetlands. A micrometeorological model, based on an analytical solution of the Eulerian advection–diffusion equation for vertical diffusion, has been used; model parameters include the location of the methane analyser and standard surface layer scaling factors. Flux chambers, which are commonly used for measuring methane fluxes from agricultural sources, are usually mechanically operated with a rated induced-draft fan and as such cannot replicate the real world atmospheric conditions. The results are not very reliable due to leakages along the piping and at fittings, especially when these chambers are used over a relatively rough surface like an agricultural field or a wetland. The results of the model have been compared with those from the direct method. The seasonal average methane flux calculated by the indirect method, for the cultivar type “Sundari”, is 7.13E+05 g/ha, while cultivar type “Shatabdi” gives a little lower value of 5.22E+05 g/ha. In case of the direct chamber method also, the seasonal average methane flux for the cultivar type “Sundari” (6.20E+05 g/ha) is more than cultivar type “Shatabdi” (4.84E+05 g/ha). When the two methods of assessment were compared, season September–December 2004 gave r² = 0.91, RMSE = 0.16 and MNB = 0.13 while we got r² = 0.94, RMSE = 1.22 and MNB = 0.06 for the season September–December 2005.In very few experiments we could cover a huge aerial plot instead of a huge number of experiments necessary for the direct chamber method.     

Pre-programmable polymer transformers as on-chip microfluidic vacuum generators

This paper develops novel polymer transformers using thermally actuated shape memory polymer (SMP) materials. This paper applies SMPs with thermally induced shape memory effect to the proposed novel polymer transformers as on-chip microfluidic vacuum generators. In this type of SMPs, the morphology of the materials changes when the temperature of materials reaches its glass transition temperature (T _g). The structure of the polymer transformer can be pre-programmed to define its functions, which the structure is reset to the temporary shape, using shape memory effects. When subjected to heat, the polymer transformer returns to its pre-memory morphology. The morphological change can produce a vacuum generation function in microfluidic channels. Vacuum pressure is generated to suck liquids into the microfluidic chip from fluidic inlets and drive liquids in the microchannel due to the morphological change of the polymer transformer. This study adopts a new smart polymer with high shape memory effects to achieve fluid movement using an on-chip vacuum generation source. Experimental measurements show that the polymer transformer, which uses SMP with a T _g of 40°C, can deform 310 μm (recover to the permanent shape from the temporary shape) within 40 s at 65°C. The polymer transformer with an effective cavity volume of 155 μl achieved negative pressures of −0.98 psi. The maximum negative up to −1.8 psi can be achieved with an effective cavity volume of 268 μl. A maximum flow rate of 24 μl/min was produced in the microfluidic chip with a 180 mm long channel using this technique. The response times of the polymer transformers presented here are within 36 s for driving liquids to the end of the detection chamber. The proposed design has the advantages of compact size, ease of fabrication and integration, ease of actuation, and on-demand negative pressure generation. Thus, this design is suitable for disposable biochips that need two liquid samples control. The polymer transformer presented in this study is applicable to numerous disposable microfluidic biochips.     

Wireless sensor network based wearable smart shirt for ubiquitous health and activity monitoring

Nanofibers of a composite of a silicon-containing polyelectrolyte, polyethylene oxide and polyaniline (PANI) were obtained by electrospinning and heat treatment. The morphologies of the composite nanofibers were characterized by scanning electron microscopy, which showed that the nanofibers with a diameter of 250–500 nm formed a non-woven mat with highly porous structure. It was found that the polymer composite nanofibers showed impedance change from 6.3 × 10⁶ to 2.5 × 10⁴ Ω with the increment of relative humidity (RH) from 22 to 97% at room temperature, exhibiting high sensitivity and good linearity on a semi-logarithmic scale. In addition, they exhibited fast and highly reversible response characterized by very small hysteresis of 2% RH and short response time (t_90%: 7 s and 19 s for adsorption and desorption between 33 and 97%RH, respectively). The modification of the electrode with poly(diallyldimethylammonium chloride) prior to the deposition of nanofibers improved their humidity response, which may be related to the enhanced contact between the nanofibers and underlying substrate. The effect of PANI on the humidity response of the composite nanofibers was also investigated, and it was found that PANI effectively decreased the impedance of the nanofibers. The electrospun polymer composite nanofibers may find applications in the preparation of high performance humidity sensors.     

Environmentally friendly disposable sensors with microfabricated on-chip planar bismuth electrode for in situ heavy metal ions measurement

This paper presents an environmentally friendly disposable heavy metal ion sensor for in situ and online monitoring in the nature and physiological systems. The miniaturized sensor chip consists of a non-toxic microfabricated bismuth (Bi) working electrode that replaces the conventional mercury electrodes, an integrated Ag/AgCl reference electrode, a gold counter electrode, and microfluidic channels. In this work, the electrochemical behavior of the Bi working electrode was characterized in several non-deaerated buffer solutions using cyclic voltammetry. The detection and quantification of Pb (II) and Cd (II) were statically performed using anodic stripping voltammetry inside the microchannels, in the Pb (II) concentration range of 25–400 ppb (R² = 0.991) with limit of detection of 8 ppb for 60 s deposition, and in the Cd (II) concentration range of 28–280 ppb (R² = 0.986) with limit of detection of 9.3 ppb for 90 s deposition. Particularly, the applications of this sensor chip have been reported with the examples of in situ measurement of Cd (II) concentration in soil pore and ground water and online direct measurement of Cd (II) concentration in cell culture media in its native environment.     

Estimating average daytime and daily temperature profiles within Europe

We present a methodology for estimating the average profiles of daytime and daily ambient temperature from a spatially-continuous database for any location within Europe. The primary database with 1-km grid resolution was developed by interpolation of monthly averages of 7 daily values of temperature: minimum and maximum and 5 measurements at 3-h intervals from 6:00 to 18:00 hours Greenwich Mean Time. With a little over 800 meteorological stations available, we obtained a cross-validation root mean square error of 1.0–1.2 °C, while the interpolation error is lower, at 0.5–0.7 °C.A polynomial fit was applied to estimate the daytime temperature profile (assuming only time from sunrise to sunset) from the interpolated 3-h measurements for each month. The curve fit coefficients make it possible to calculate a number of derived data, such as average daytime temperature, maximum daytime temperature and time of its occurrence within the region. An example demonstrates the coupling of the simulated daytime temperature profile with a model for assessing the relative efficiency of electricity generation by crystalline silicon photovoltaic modules.As an alternative to the polynomial fitting, a double-cosine method was applied to enable calculation of daily (24-h) temperature profiles for each month using interpolated minimum and maximum temperatures. Compared to the polynomial curve-fitting, this method does not offer lower errors, but it provides data which are more suitable for estimation of solar thermal heating or calculation of degree days for building heating/cooling.     

Detection of amines with chromium-doped WO3 mesoporous material

Chromium-doped mesoporous tungsten trioxide – with KIT-6 structure – was prepared through a chemical route. The resulting material was deposited on a micromechanically fabricated hot-plate and tested as a sensor for ammonia and trimethylamine in the temperature range of 200–500 °C. Maximum response was reached at 350 and 450 °C for ammonia and TMA, respectively. It was also found that the sensor shows a non-linear cross-sensitivity to the gases.     

Application of sulfuric acid doped poly (m-aminophenol) as aliphatic alcohol vapor sensor material

Chemically synthesized processable poly (m-aminophenol) (PmAP) film was cast from dimethyl sulfoxide solution and doped with sulfuric acid by solution doping technique. This sulfuric acid doped PmAP film shows a good electrical conductivity. The response of doped film under continuous flow of various aliphatic alcohols vapor and air mixture was examined at room temperature (30 °C) and humidity (65% RH). The doped polymer only showed good result for methanol and ethanol vapor and some week response for the isopropanol vapor. A decrease in resistivity of the doped PmAP film was separately observed in air–alcohol vapor at different concentrations. The response of the film increases as the concentration of the alcohol vapor increases in air–alcohols vapor mixture. The kinetics of the response with respect to the alcohol concentration was studied for methanol and ethanol. Sulfuric acid doped and methanol vapor absorbed doped films were characterized by ultraviolet–visible spectroscopic, attenuated total reflectance Fourier transformed infrared spectroscopic and X-ray diffraction analyses. The mechanism of alcohol vapor sensing by sulfuric acid doped PmAP film has been explained on the basis of the above characterizations. All the above facts are trying to explain from the proposed mechanistic point of view.     

Influence of Cs doping in spray deposited SnO2 thin films for LPG sensors

Detection of low concentrations of petroleum gas was achieved using transparent conducting SnO₂ thin films doped with 0–4 wt.% caesium (Cs), deposited by spray pyrolysis technique. The electrical resistance change of the films was evaluated in the presence of LPG upon doping with different concentrations of Cs at different working temperatures in the range 250–400 °C. The investigations showed that the tin oxide thin film doped with 2% Cs with a mean grain size of 18 nm at a deposition temperature of 325 °C showed the maximum sensor response (93.4%). At a deposition temperature of 285 °C, the film doped with 3% Cs with a mean grain size of 20 nm showed a high response of 90.0% consistently. The structural properties of Cs-doped SnO₂ were studied by means of X-ray diffraction (XRD); the preferential orientation of the thin films was found to be along the (3 0 1) directions. The crystallite sizes of the films determined from XRD are found to vary between 15 and 60 nm. The electrical investigations revealed that Cs-doped SnO₂ thin film conductivity in a petroleum gas ambience and subsequently the sensor response depended on the dopant concentration and the deposition temperature of the film. The sensors showed a rapid response at an operating temperature of 345 °C. The long-term stability of the sensors is also reported.     

Piezoresistive biochemical sensors based on hydrogels

Already 8 years ago, the usage of piezoresistive sensors for chemical measurands was proposed at the Solid State Electronics Laboratory of the Dresden University of Technology. Adding functionalised polymer coating which shows swelling due to chemical or biological values leads to a similar deflection of the thin silicon bending plate like for pressure sensors. The application of “stimuli-responsive” or “smart” cross-linked gels in chemical sensors is based on their ability to a phase transition under the influence of external excitations (pH, concentration of additives in water, temperature). Combining a “smart” hydrogel and a micro fabricated pressure sensor chip allows to continuously monitor the analyte-dependent swelling of a hydrogel and hence the analyte concentration in ambient aqueous solutions. The sensitivity of hydrogels with regard to the concentration of such additives as H⁺-ions (pH sensor), transition-metal ions, salts, organic solvents and proteins in water was investigated.     

Impedance spectroscopy on immobilized streptavidin horseradish peroxidase layer for biosensing

In this work, a mixed self-assembled monolayer (SAM) formed by 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl) (biotinyl-PE) and 16-mercaptohexadecanoic acid was grafted on gold electrode. Horseradish peroxidase conjugated streptavidin was attached on the SAM through biotin–streptavidin interaction. Cyclic voltammetry and impedance spectroscopy were applied to characterize the electric properties of the self-assembled monolayer and to monitor biosensor building-up process. During impedance measurements, the charge transfer resistance decreased significantly after enzymatic reaction with hydrogen peroxide. The response was very sensitive in the range of 10–100 mM and the detection limit attained 10 μM. The constructed biosensor was successfully tested in milk samples and was able to detect as low as 50 μM of hydrogen peroxide.     

Simulation, fabrication and characterization of a 3D piezoresistive force sensor

In this contribution we report on a miniaturized bulk micro-machined three-axes piezoresistive force sensor. The force sensor consists of a full membrane with 16 conventional two terminal p-type diffused piezoresistors on the surface of the membrane. The die size of the chip is 6.5 mm × 6.5 mm. Piezoresistors with four different designs were placed on the membrane. Sensitivities were found to be in the range of 0.37–0.79 mV/(V mN) and 1.68–2.92 mV/(V mN) in Z-direction and X- or Y-direction, respectively. The stiffness of the measured microprobes in the range of 5–8 mN/μm and 0.27–0.48 mN/μm were obtained in vertical and lateral direction, respectively. Various single and twin membranes designs were simulated to calculate stiffness of the microprobe. The measurement results show a cross-axis sensitivity of <2.5% at full scale of 25 mN.     

A novel biosensor using entangled carbon nanotubes layer grown on an alumina substrate by CCVD of methane on FeOx–MgO

Glucose oxidase (GOx) was immobilized on entangled and high surface area carbon nanotubes (CNTs) grown on an alumina substrate, and direct electron transfer reaction between GOx and the electrode was revealed. Fe/MgO catalyst layer was spin-coated on the insulating alumina substrate and the CNT layer was grown on the catalyst by chemical vapor deposition of methane at 950 °C for 15 min. About 20–30 nm bundles of about 1 nm single-wall as well as 10 nm multiwall CNTs are formed. The redox process was surface-controlled and electron transfer coefficient and the rate constant were estimated to be 0.35 and 0.64 s⁻¹, respectively. In addition GOx immobilized on CNT layer showed a linear response range between 12 and 62 μM of glucose concentration. A detection limit and sensitivity of 0.1 μM and 635 μA mM⁻¹ cm⁻², respectively, were obtained for the biosensor.     

Characterization of electrospun ZnO–SnO2 nanofibers for ethanol sensor

ZnO–SnO₂ nanofibers have been developed through in situ electrospinning technique and calcination. Poly(vinyl pyrrolidone) (PVP) is selected as fiber template. The composition of products can be controlled concisely by adjusting the compositions in their precursors. Under the optimized experimental conditions, the prepared product shows the desirable sensing characteristics towards ethanol gas at 300 °C, such as high response, excellent linearity in the range of 1–300 ppm, quick response time (5 s) and recovery time (6 s), good reproducibility, stability and selectivity.     

Conductimetric immunosensor for atrazine detection based on antibodies labelled with gold nanoparticles

A novel conductimetric immunosensor for atrazine detection has been designed and developed. This immunosensor is mainly based on antibodies labelled with gold nanoparticles. Additionally, the immunosensor consists of an array of two coplanar non-passivated interdigitated metallic μ-electrodes (IDμE) and immunoreagents specifically developed to detect this pesticide. The chemical recognition layer was covalent immobilized on the interdigital space. Immunochemical detection of the concentration of atrazine is achieved by a competitive reaction that occurs before the inclusion of the labelled antibodies. It is shown that the gold nanoparticles provide an amplification of the conductive signal and hence makes possible to detect atrazine by means of simple DC measurements.The conductimetric immunosensor and its biofunctionalization steps have been characterized by chemical affinity methods and impedance spectroscopy.This work describes the immunosensor structure, fabrication, physico-chemical and analytical characterization, and the immunosensor response using conductivity measurements. The immunosensor developed detects atrazine with limits of detection in the order of 0.1–1 μg L⁻¹, far below the maximum residue level (MRL) (100 μg L⁻¹) established by European Union (EU) for residues of this herbicide in the wine.Although in this paper the competitive reaction occurs in buffer, an initial study of the wine matrix effect is also described.     

Research on forming and application of U-form glass micro-nanofluidic chip with long nanochannels

The forming process of U-form glass micro-nanofluidic chip with long nanochannels is presented in this paper, in which the fabrication of channels and the assembly of plates are included. The micro-nanofluidic chip is composed of two glass plates in which there are microchannels and nanochannels, respectively. This chip can be used for trace sample enrichment, molecule filtration, and sample separation, etc. In fabrication process, the two-step photolithograph on one wafer is often required in early papers, as nano and micro structure designed in one plate have different depths. In this paper, the channels in micro-nanofluidic chip are designed in two glass plates instead of in one wafer. The nanochannels and microchannels are, respectively, formed on plates using wet etching and two-step photolithograph on one wafer is not required. Since the channels are formed, the upper plate and the bottom plate are assembled together by alignment, preconnection and thermal bonding orderly. Firstly these plates are aligned with the cross-marks on an inverted microscope. The aqueous film between plates is controlled to decrease the static friction force for accurate adjustment. Then the adhesion strength of connection is enhanced with semi-dry status for limiting movement from slight inclining and shaking. At last, the bottom plate and the upper one are irreversibly linked together with thermal bonding. The heating period and max temperature of thermal bonding are optimized to eliminate thermal stress gradient and the size shrinking. With the micro-nanofluidic chip, the 1 μM fluorescein isothiocyanate in 10 mM PBS buffer is concentrated successfully. The sample concentrating factor of light intensity varies from 2.2 to 8.4 with applied voltages between 300 and 2,000 V. The switch effect and the instability effect in concentrating process are described and analyzed too.     

Potassium ion sensing using a self-assembled calix[4]crown monolayer by surface plasmon resonance

The precise detection of K⁺ ion is crucial because K⁺ ion plays a leading role in membrane transport. Current K⁺ ion detection methods suffered low resolution and detection limit. Calix[4]crown-5 derivatives are well known as K⁺ ionophores. We described here a K⁺ ion-sensing system using a self-assembled monolayer of calix[4]crown-5 derivative (calix[4]crown) modified gold chip based on surface plasmon resonance (SPR). The calix[4]crown sensing layer was characterized by atomic-force microscopy (AFM), SPR, Fourier transform infrared reflection absorption spectroscopy (FTIR-RAS) and cyclic voltammetry (CV). It was found calix[4]crown was assembled as a monolayer on Au surface. The SPR angle was found to be modulated by various concentrations of K⁺ ion due to the interaction between the calix[4]crown and K⁺ ion. This calix[4]crown monolayer showed a more sensitive and selective binding toward potassium ion over other alkali and alkaline earth metal ions. From the simple SPR spectroscopic analysis, we were able to monitor K⁺ ion concentration with a wide range of 1.0 × 10⁻¹² to 1.0 × 10⁻² M in an aqueous solution with a pH 6–8. These experimental results showed a useful method for the design of simple and precise potassium ion biosensors.     

Bean sprout peroxidase biosensor based on l-cysteine self-assembled monolayer for the determination of dopamine

A new bean sprout peroxidase was immobilized on a gold electrode modified with self-assembled monolayers (SAM) of l-cysteine for the determination of dopamine in pharmaceutical samples using square wave voltammetry. In the bean sprout–(SAM)–Au electrode, the peroxidase, in the presence of hydrogen peroxide, catalyzes the oxidation of dopamine to the corresponding quinone, which is electrochemically reduced back to dopamine at +0.15 V vs. Ag/AgCl. The performance and the factors influencing the response of this biosensor were studied in detail. The best performance was obtained using 0.1 mol L⁻¹ phosphate buffer solution (pH 6.0), 6.0 × 10⁻⁵ mol L⁻¹ hydrogen peroxide, frequency of 100 Hz, pulse amplitude of 80 mV and scan increment of 4.0 mV. The analytical curve was linear for dopamine concentrations from 9.91 × 10⁻⁶ to 2.21 × 10⁻⁴ mol L⁻¹ and the detection limit was 4.78 × 10⁻⁷ mol L⁻¹. The recovery of dopamine ranged from 98.0 to 111.8% and the relative standard deviation was 3.1% for a solution containing 1.30 × 10⁻⁵ mol L⁻¹ dopamine (n = 6). The lifetime of this biosensor was 15 days (at least 300 determinations). The results obtained for dopamine determination in pharmaceutical formulations using the proposed bean sprout–SAM–Au electrode were in agreement with those obtained with the standard method at the 95% confidence level.     

Fabrication of micro sensors on a flexible substrate

Flexible micro temperature and humidity sensors on parylene thin films were designed and fabricated using a micro-electro-mechanical-systems (MEMS) process. Based on the principles of the thermistor and the ability of a polymer to absorb moisture, the sensing device comprised gold wire and polyimide film. The flexible micro sensors were patterned between two pieces of parylene thin film that had been etched using O₂ plasma to open the contact pads. The sacrificial Cr spacer layer was removed from the Cr etchant to release the flexible temperature and humidity sensors from the silicon substrate. Au was used to form the sensing electrode of the sensors while Ti formed the adhesion layer between the parylene and Au. The thickness of the device was 7 ± 1 μm, so the sensors attached easily to highly curved surfaces. The sensitivities of the temperature and humidity sensor were 4.81 × 10⁻³ °C⁻¹ and 0.03 pF/%RH, respectively. This work demonstrates the feasibility and compatibility of thin film sensor applications based on flexible parylene. The sensor can be applied to fuel cells or components that must be compressed.