Nguyen Van Hieu

DNA sensor development based on multi-wall carbon nanotubes for label-free influenza virus (type A) detection

This paper describes the DNA immobilization using carbon multi-walled nanotubes (MWCNTs) for direct and label-free detection of influenza virus (type A). The DNA probe was attached on the sensor surface by means of covalent bonding between the amine and phosphate groups of the DNA sequence. The interaction between the DNA probe and the MWCNTs were characterized by Fourier Transform Infrared (FTIR) spectrometry, Raman spectra. The hybridization of the DNA probe and the target DNA were detected by changes in the conductance on the surface of sensors leading to the change in the output signal of the system. The results show that the DNA sensor can detect as low as 0.5 nM of the target DNA samples; the response time of DNA sensor is approximately 4 min.

Effective decoration of Pd nanoparticles on the surface of SnO2 nanowires for enhancement of CO gas-sensing performance

Decoration of noble metal nanoparticles (NPs) on the surface of semiconducting metal oxide nanowires (NWs) to enhance material characteristics, functionalization, and sensing abilities has attracted increasing interests from researchers worldwide. In this study, we introduce an effective method for the decoration of Pd NPs on the surface of SnO2 NWs to enhance CO gas-sensing performance. Single-crystal SnO2 NWs were fabricated by chemical vapor deposition, whereas Pd NPs were decorated on the surface of SnO2 NWs by in situ reduction of the Pd complex at room temperature without using any linker or reduction agent excepting the copolymer P123. The materials were characterized by advanced techniques, such as high-resolution transmission electron microscopy, scanning transmission electron microscopy, and energy-dispersive X-ray spectroscopy. The Pd NPs were effectively decorated on the surface of SnO2 NWs. As an example, the CO sensing characteristics of SnO2 NWs decorated with Pd NPs were investigated at different temperatures. Results revealed that the gas sensor exhibited excellent sensing performance to CO at low concentration (1-25ppm) with ultrafast response-recovery time (in seconds), high responsivity, good stability, and reproducibility.

Selective detection of carbon dioxide using LaOCl-functionalized SnO2 nanowires for air-quality monitoring

In spite of the technical important of monitoring CO(2) gas by using a semiconductor-type gas sensor, a good sensitive and selective semiconductor CO(2) sensor has been not realized due to the rather unreactive toward CO(2) of conventional semiconductor metal oxides. In this work, a novel semiconductor CO(2) sensor was developed by functionalizing SnO(2) nanowires (NWs) with LaOCl, which was obtained by heat-treating the SnO(2) NWs coating with LaCl(3) aqueous solution at a temperature range of 500-700°C. The bare SnO(2) NWs and LaOCl-SnO(2) NWs sensors were characterized with CO(2) (250-4,000 ppm) and interference gases (100 ppm CO, 100 ppm H(2), 250 ppm LPG, 10 ppm NO(2) and 20 ppm NH(3)) at different operating temperatures for comparison. The SnO(2) NWs sensors functionalized with different concentrations of LaCl(3) solution were also examined to find optimized values. Comparative gas sensing results reveal that LaOCl-SnO(2) NWs sensors exhibit much higher response, shorter response-recovery and better selectivity in detecting CO(2) gas at 400°C operating temperature than the bare SnO(2) NWs sensors. This finding indicates that the functionalizing with LaOCl greatly improves the CO(2) response of SnO(2) NWs-based sensor, which is attributed to (i) p-n junction formation of LaOCl (p-type) and SnO(2) nanowires (n-type) that led to the extension of electron depletion and (ii) the favorable catalytic effect of LaOCl to CO(2) gas.

Chlorine Gas Sensing Performance of On-Chip Grown ZnO, WO3, and SnO2 Nanowire Sensors.

Monitoring toxic chlorine (Cl2) at the parts-per-billion (ppb) level is crucial for safe usage of this gas. Herein, ZnO, WO3, and SnO2 nanowire sensors were fabricated using an on-chip growth technique with chemical vapor deposition. The Cl2 gas-sensing characteristics of the fabricated sensors were systematically investigated. Results demonstrated that SnO2 nanowires exhibited higher sensitivity to Cl2 gas than ZnO and WO3 nanowires. The response (RCl2/Rair) of the SnO2 nanowire sensor to 50 ppb Cl2 at 50 °C was about 57. Hence, SnO2 nanowires can be an excellent sensing material for detecting Cl2 gas at the ppb level under low temperatures. Abnormal sensing characteristics were observed in the WO3 and SnO2 nanowire sensors at certain temperatures; in particular, the response level of these sensors to 5 ppm of Cl2 was lower than that to 2.5 ppm of Cl2. The sensing mechanism of the SnO2 nanowire sensor was also elucidated by determining Cl2 responses under N2 and dry air as carrier gases. We proved that the Cl2 molecule was first directly adsorbed on the metal oxide surface and was then substituted for pre-adsorbed oxygen, followed by lattice oxygen.

Outstanding gas-sensing performance of graphene/SnO2 nanowire Schottky junctions

Schottky junctions (SJ) are considered devices for sensing applications due to their unique properties. Herein, we report on the design, facile fabrication, and outstanding NO2 gas sensing properties of monolayer graphene (GP)/SnO2 nanowire (NW) SJ devices. The devices were prepared by directly growing single crystal SnO2 NWs on interdigitated Pt electrodes via thermal evaporation, followed by transferring a GP layer grown by chemical vapor deposition on top of the NW chip. The SJ-based sensor showed a reversible response to NO2 gas at concentrations of ppb levels with detection limits of about 0.024 ppb at a low operating temperature of 150 °C and bias voltage (1 V) with a response/recovery time of less than 50 s. The outstanding gas-sensing characteristics of the device were attributed to tuning the Schottky barrier height and barrier width at the tiny area of contact between GP and SnO2 NW through the adsorption/desorption of gas molecules.

Giant enhancement of H2S gas response by decorating n-type SnO2 nanowires with p-type NiO nanoparticles

Metal oxide nanowires (NWs) are widely considered as promising materials for gas sensor applications. Here, we demonstrate that by decorating NiO nanoparticles on SnO2 NWs, the gas response to 10 ppm H2S increased up to ∼351-fold. The response of the NiO-decorated SnO2 NWs sensor to 10 ppm H2S at 300 °C reached ∼1372, whereas the cross-gas responses to 5 ppm NH3, 200 ppm C2H5OH, and 1 ppm NO2 were negligible (1.8 to 2.9). The enhanced H2S sensing performance was attributed by the catalytic effect of NiO and the formation of a continuous chain of n-p-n-p junctions.

Fabrication of highly sensitive and selective H2 gas sensor based on SnO2 thin film sensitized with microsized Pd islands

Ultrasensitive and selective hydrogen gas sensor is vital component in safe use of hydrogen that requires a detection and alarm of leakage. Herein, we fabricated a H2 sensing devices by adopting a simple design of planar-type structure sensor in which the heater, electrode, and sensing layer were patterned on the front side of a silicon wafer. The SnO2 thin film-based sensors that were sensitized with microsized Pd islands were fabricated at a wafer-scale by using a sputtering system combined with micro-electronic techniques. The thicknesses of SnO2 thin film and microsized Pd islands were optimized to maximize the sensing performance of the devices. The optimized sensor could be used for monitoring hydrogen gas at low concentrations of 25-250 ppm, with a linear dependence to H2 concentration and a fast response and recovery time. The sensor also showed excellent selectivity for monitoring H2 among other gases, such as CO, NH3, and LPG, and satisfactory characteristics for ensuring safety in handling hydrogen. The hydrogen sensing characteristics of the sensors sensitized with Pt and Au islands were also studied to clarify the sensing mechanisms.

Meso-/Nanoporous semiconducting metal oxides for gas sensor applications

Development and/or design of new materials and/or structures for effective gas sensor applications with fast response and high sensitivity, selectivity, and stability are very important issues in the gas sensor technology. This critical review introduces our recent progress in the development of meso-/nanoporous semiconducting metal oxides and their applications to gas sensors. First, the basic concepts of resistive gas sensors and the recent synthesis of meso-/nanoporous metal oxides for gas sensor applications are introduced. The advantages of meso-/nanoporous metal oxides are also presented, taking into account the crystallinity and ordered/disordered porous structures. Second, the synthesis methods of meso-/nanoporous metal oxides including the soft-template, hard-template, and temple-free methods are introduced, in which the advantages and disadvantages of each synthetic method are figured out. Third, the applications of meso-/nanoporous metal oxides as gas sensors are presented. The gas nanosensors are designed based on meso-/nanoporous metal oxides for effective detection of toxic gases. The sensitivity, selectivity, and stability of the meso-/nanoporous gas nanosensors are also discussed. Finally, some conclusions and an outlook are presented.

Modified interdigitated arrays by novel poly(1,8-diaminonaphthalene)/carbon nanotubes composite for selective detection of mercury(II)

This study describes a novel type of interdigitated arrays (IDA), microfabricated by electropolymerizing structured Poly(1,8-diaminonaphthalene)/functionalized multi-walled carbon nanotubes (PDAN/CNT) thin film onto a silicon chip for square wave voltammetry (SWV) multi-element heavy metal ion detection. The structure of PDAN/CNT was characterized by Raman, FE-SEM and AFM techniques. Analysed experiments reveal that the uptake of Hg(2+) by PDAN/CNT is quite specific and it can be used advantageously for electrochemical sensing of Hg(2+) thanks to original feature of (Hg(2+)/Hg(2)(2+)) redox potential with the respect to that of PDAN/CNT. As-developed IDA type electrode can extend its utility in other sensing applications.

Novel silver nanoparticles: synthesis, properties and applications

In this paper, we present versatile and effective techniques to synthesise silver nanoparticles (Ag-NPs)-based compounds such as colloidal silver nanoparticles (CSNPs) and silver nanoparticles powders (SNPPs). The CSNPs stabilised by a surfactant oleic acid were produced for the first time through the reduction of [Ag(NH3)2]+(aq) complex by glucose with UV irradiation treatment, while the SNPPs were formed by thermal decomposition of silver-oleate complex at 330°C for 1 h. The CNPPs and CSNPs with average diameters (~9–10 nm) and highly stableaqueous dispersions were obtained. Noticeably, these synthesised Ag-NPs exhibited an excellent antibacterial activity against gram-negative Escherichia coli (ATCC 43888-O157:k-:H7) and methicillin-resistant gram-positive Staphylococcus aureus (ATCC 43300) bacteria. The electron microscopic technique provided deeper insights on the interaction and bactericidal mechanism of the Ag-NPs. Potential applications of the synthesised CSNPs and SNPPs for antibacterial – masterbatchs, acrylic emulsion paint as well as coating layer on cotton textiles were demonstrated.