The Method of Ion Mobility TOF Mass Spectrometry for Rapid Identification of Triphenylmethane Ball Point Pen Dyes

AbstractIn this work ion mobility time-of-flight mass spectrometry is preliminarily studied as a method for identification of the composition for triphenylmethane ball point pen dyes by their traces on paper. Components were identified as Basic violet 2, Methyl violet 6B, Methyl violet 2B, Crystal violet. All the compounds were shown to form excellent individual mass selective mobility peaks. Short time of analysis allow one to consider IMS/TOFMS as a perspective alternative for traditional methods of identification

Transmission of a Drift Tube Ion Mobility Spectrometer, Connected with a Mass Spectrometer

AbstractIn this work it is experimentally showed that transmission of atmospheric drift tube ion mobility spectrometer (DT-IMS), connected with mass spectrometer (MS), depends on ion mobility of investigated compounds, because of depletion effect of Bradbury-Nielson ion gate (IG), which previously has been approved only by standalone DT-IMS. Theoretical estimation of depletion width of IG is in good agreement with experimental data. Also it is found, that ion lost due to its pulsing work of IG are few times smaller, than its duty cycle. It's explained by difference in influence of coulomb repulsion at 100% and 1% duty cycle – in first case it's significant versus second case, when coulomb repulsion become negligibly small, that reduces lost of ions on entrance of MS interface

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

Tuning Nitrogen-Doped Carbon Electrodes via Synthesis Temperature Adjustment to Improve Sodium- and Lithium-Ion Storage

Structural imperfections, heteroatom dopants, and the interconnected pore structure of carbon materials have a huge impact on their electrochemical performance in lithium-ion and sodium-ion batteries due to the specific ion transport and the dominant storage mechanism at surface defect sites. In this work, mesopore-enriched nitrogen-doped carbon (NC) materials were produced with template-assisted chemical vapor deposition using calcium tartrate as the template precursor and acetonitrile as the carbon and nitrogen source. The chemical states of nitrogen, the volume of mesopores, and the specific surface areas of the materials were regulated by adjusting the synthesis temperature. The electrochemical testing of NC materials synthesized at 650, 750, and 850 °C revealed the best performance of the NC-650 sample, which was able to deliver 182 mA·h·g−1 in sodium-ion batteries and 1158 mA·h·g−1 in lithium-ion batteries at a current density of 0.05 A·g−1. Our study shows the role of defect sites, including carbon monovacancies and nitrogen-terminated vacancies, in the binding and accumulation of sodium. The results provide a strategy for managing the carbon structure and nitrogen states to achieve a high alkali-metal-ion storage capacity and long cycling stability, thereby facilitating the electrochemical application of NC materials

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

Laterally extended atomically precise graphene nanoribbons with improved electrical conductivity for efficient gas sensing

Narrow atomically precise graphene nanoribbons hold great promise for electronic and optoelectronic applications, but the previously demonstrated nanoribbon-based devices typically suffer from low currents and mobilities. In this study, we explored the idea of lateral extension of graphene nanoribbons for improving their electrical conductivity. We started with a conventional chevron graphene nanoribbon, and designed its laterally extended variant. We synthesized these new graphene nanoribbons in solution and found that the lateral extension results in decrease of their electronic bandgap and improvement in the electrical conductivity of nanoribbon-based thin films. These films were employed in gas sensors and an electronic nose system, which showed improved responsivities to low molecular weight alcohols compared to similar sensors based on benchmark graphitic materials, such as graphene and reduced graphene oxide, and a reliable analyte recognition. This study shows the methodology for designing new atomically precise graphene nanoribbons with improved properties, their bottom-up synthesis, characterization, processing and implementation in electronic devices