UV-Light-Tunable p-/n-Type Chemiresistive Gas Sensors Based on Quasi-1D TiS\u3csub\u3e3\u3c/sub\u3e Nanoribbons: Detection of Isopropanol at ppm Concentrations

The growing demand of society for gas sensors for energy-efficient environmental sensing stimulates studies of new electronic materials. Here, we investigated quasi-one-dimensional titanium trisulfide (TiS3) crystals for possible applications in chemiresistors and on-chip multisensor arrays. TiS3 nanoribbons were placed as a mat over a multielectrode chip to form an array of chemiresistive gas sensors. These sensors were exposed to isopropanol as a model analyte, which was mixed with air at low concentrations of 1–100 ppm that are below the Occupational Safety and Health Administration (OSHA) permissible exposure limit. The tests were performed at room temperature (RT), as well as with heating up to 110 oC, and under an ultraviolet (UV) radiation at λ = 345 nm. We found that the RT/UV conditions result in a n-type chemiresistive response to isopropanol, which seems to be governed by its redox reactions with chemisorbed oxygen species. In contrast, the RT conditions without a UV exposure produced a p-type response that is possibly caused by the enhancement of the electron transport scattering due to the analyte adsorption. By analyzing the vector signal from the entire on-chip multisensor array, we could distinguish isopropanol from benzene, both of which produced similar responses on individual sensors. We found that the heating up to 110 oC reduces both the sensitivity and selectivity of the sensor array

UV-Light-Tunable p-/n-Type Chemiresistive Gas Sensors Based on Quasi-1D TiS3 Nanoribbons: Detection of Isopropanol at ppm Concentrations

The growing demand of society for gas sensors for energy-efficient environmental sensing stimulates studies of new electronic materials. Here, we investigated quasi-one-dimensional titanium trisulfide (TiS(3)) crystals for possible applications in chemiresistors and on-chip multisensor arrays. TiS(3) nanoribbons were placed as a mat over a multielectrode chip to form an array of chemiresistive gas sensors. These sensors were exposed to isopropanol as a model analyte, which was mixed with air at low concentrations of 1–100 ppm that are below the Occupational Safety and Health Administration (OSHA) permissible exposure limit. The tests were performed at room temperature (RT), as well as with heating up to 110 °C, and under an ultraviolet (UV) radiation at λ = 345 nm. We found that the RT/UV conditions result in a n-type chemiresistive response to isopropanol, which seems to be governed by its redox reactions with chemisorbed oxygen species. In contrast, the RT conditions without a UV exposure produced a p-type response that is possibly caused by the enhancement of the electron transport scattering due to the analyte adsorption. By analyzing the vector signal from the entire on-chip multisensor array, we could distinguish isopropanol from benzene, both of which produced similar responses on individual sensors. We found that the heating up to 110 °C reduces both the sensitivity and selectivity of the sensor array

Energy-Efficient Chemiresistive Sensor Array Based on SWCNT Networks, WO3 Nanochannels and SWCNT-Pt Heterojunctions for NH3 Detection against the Background Humidity

Recently, promising results have been achieved in improving the sensitivity to ammonia in gas sensors through the use of structures composed of heterojunctions or nanochannels. However, their sensitivity is highly dependent on the background humidity under air conditions. The sensor structures which could ensure selective ammonia detection with a low detection limit, despite interference from changing background humidity, remain highly demanded. In this work, we consider sensing units containing (i) nanochannels formed by a continuous tungsten oxide nanolayer to appear in contact between single-walled carbon nanotubes (SWCNTs) and a Pt sublayer and (ii) SWCNT-Pt junctions in frames of mass-scale microelectronic technologies. SWCNTs were deposited by spray-coating on a thin WO3/Pt/W sublayer formed by a photolithographic pattern to be accompanied by satellite samples with just SWCNTs for reference purposes. We elucidate the specific differences that appeared in the response of sensors based on SWCNT-Pt junctions and WO3 nanochannels relative to satellite SWCNT samples with a similar SWCNT network density. Particularly, while a similar response to NH3 vapors mixed with dry air is observed for each sensor type, the response to NH3 is reduced significantly in the presence of background humidity, of 45 rel.%, especially in the case of WO3 nanochannel structures even at room temperature. A multisensor array based on the four various sensing structures involving SWCNT-Pt junctions, WO3 nanochannels, and their satellite-only-SWCNT ones allowed us to determine a correct ammonia concentration via utilizing the linear discriminant analysis despite the presence of background air humidity. Thus, such an energy-efficient multisensor system can be used for environmental monitoring of ammonia content, health monitoring, and other applications

Energy-Efficient Chemiresistive Sensor Array Based on SWCNT Networks, WO₃ Nanochannels and SWCNT-Pt Heterojunctions for NH₃ Detection against the Background Humidity

Recently, promising results have been achieved in improving the sensitivity to ammonia in gas sensors through the use of structures composed of heterojunctions or nanochannels. However, their sensitivity is highly dependent on the background humidity under air conditions. The sensor structures which could ensure selective ammonia detection with a low detection limit, despite interference from changing background humidity, remain highly demanded. In this work, we consider sensing units containing (i) nanochannels formed by a continuous tungsten oxide nanolayer to appear in contact between single-walled carbon nanotubes (SWCNTs) and a Pt sublayer and (ii) SWCNT-Pt junctions in frames of mass-scale microelectronic technologies. SWCNTs were deposited by spray-coating on a thin WO3/Pt/W sublayer formed by a photolithographic pattern to be accompanied by satellite samples with just SWCNTs for reference purposes. We elucidate the specific differences that appeared in the response of sensors based on SWCNT-Pt junctions and WO3 nanochannels relative to satellite SWCNT samples with a similar SWCNT network density. Particularly, while a similar response to NH3 vapors mixed with dry air is observed for each sensor type, the response to NH3 is reduced significantly in the presence of background humidity, of 45 rel.%, especially in the case of WO3 nanochannel structures even at room temperature. A multisensor array based on the four various sensing structures involving SWCNT-Pt junctions, WO3 nanochannels, and their satellite-only-SWCNT ones allowed us to determine a correct ammonia concentration via utilizing the linear discriminant analysis despite the presence of background air humidity. Thus, such an energy-efficient multisensor system can be used for environmental monitoring of ammonia content, health monitoring, and other applications

UV-Light-Tunable p-/n-Type Chemiresistive Gas Sensors Based on Quasi-1D TiS3 Nanoribbons: Detection of Isopropanol at ppm Concentrations

The growing demand of society for gas sensors for energy-efficient environmental sensing stimulates studies of new electronic materials. Here, we investigated quasi-one-dimensional titanium trisulfide (TiS3) crystals for possible applications in chemiresistors and on-chip multisensor arrays. TiS3 nanoribbons were placed as a mat over a multielectrode chip to form an array of chemiresistive gas sensors. These sensors were exposed to isopropanol as a model analyte, which was mixed with air at low concentrations of 1–100 ppm that are below the Occupational Safety and Health Administration (OSHA) permissible exposure limit. The tests were performed at room temperature (RT), as well as with heating up to 110 °C, and under an ultraviolet (UV) radiation at λ = 345 nm. We found that the RT/UV conditions result in a n-type chemiresistive response to isopropanol, which seems to be governed by its redox reactions with chemisorbed oxygen species. In contrast, the RT conditions without a UV exposure produced a p-type response that is possibly caused by the enhancement of the electron transport scattering due to the analyte adsorption. By analyzing the vector signal from the entire on-chip multisensor array, we could distinguish isopropanol from benzene, both of which produced similar responses on individual sensors. We found that the heating up to 110 °C reduces both the sensitivity and selectivity of the sensor array

Expression, purification, crystallization and preliminary X-ray structure analysis of Vibrio cholerae uridine phosphorylase in complex with thymidine

A high-resolution structure of the complex of Vibrio cholerae uridine phosphorylase (VchUPh) with its physiological ligand thymidine is important in order to determine the mechanism of the substrate specificity of the enzyme and for the rational design of pharmacological modulators. Here, the expression and purification of VchUPh and the crystallization of its complex with thymidine are reported. Conditions for crystallization were determined with an automated Cartesian Dispensing System using The Classics, MbClass and MbClass II Suites crystallization kits. Crystals of the VchUPh–thymidine complex (of dimensions ∼200–350 µm) were grown by the sitting-drop vapour-diffusion method in ∼7 d at 291 K. The crystallization solution consisted of 1.5 µl VchUPh (15 mg ml(−1)), 1 µl 0.1 M thymidine and 1.5 µl reservoir solution [15%(w/v) PEG 4000, 0.2 M MgCl(2).6H(2)O in 0.1 M Tris–HCl pH 8.5]. The crystals diffracted to 2.12 Å resolution and belonged to space group P2(1) (No. 4), with unit-cell parameters a = 91.80, b = 95.91, c = 91.89 Å, β = 119.96°. The Matthews coefficient was calculated as 2.18 Å(3) Da(−1); the corresponding solvent content was 43.74%

The room-temperature chemiresistive properties of potassium titanate whiskers versus organic vapors

The development of portable gas-sensing units implies a special care of their power efficiency, which is often approached by operation at room temperature. This issue primarily appeals to a choice of suitable materials whose functional properties are sensitive toward gas vapors at these conditions. While the gas sensitivity is nowadays advanced by employing the materials at nano-dimensional domain, the room temperature operation might be targeted via the application of layered solid-state electrolytes, like titanates. Here, we report gas-sensitive properties of potassium titanate whiskers, which are placed over a multielectrode chip by drop casting from suspension to yield a matrix mono-layer of varied density. The material synthesis conditions are straightforward both to get stable single-crystalline quasi-one-dimensional whiskers with a great extent of potassium replacement and to favor the increase of specific surface area of the structures. The whisker layer is found to be sensitive towards volatile organic compounds (ethanol, isopropanol, acetone) in the mixture with air at room temperature. The vapor identification is obtained via processing the vector signal generated by sensor array of the multielectrode chip with the help of pattern recognition algorithms.Peer reviewe

The Ti wire functionalized with inherent TiO2 nanotubes by anodization as one-electrode gas sensor

We propose a Ti wire functionalized with inherent anatase TiO2 nanotubes by an anodization process to serve as a one-electrode gas sensor. The design is similar to other known one-electrode gas sensors when the wire is employed both as a heater and measuring resistive element. We discuss the low-cost fabrication protocol, the structure of the sensor characterized by Raman spectroscopy and electron microscopy, and show the proof-of-concept sensor responses to a few organic vapors, acetone and alcohols, in mixture with air. We have found the response-to-concentration curves to follow a linear fit with a detection limit below 1000 ppm. These findings enlarge the range of possible gas sensor architectures based on nanostructured material for research and practical applications.Peer reviewe