ZnO-CuO Core-Hollow Cube Nanostructures for Highly Sensitive Acetone Gas Sensors at the ppb Level.

This paper presents a ZnO-CuO p-n heterojunction chemiresistive sensor that comprises CuO hollow nanocubes attached to ZnO spherical cores as active materials. These ZnO-CuO core-hollow cube nanostructures exhibit a remarkable response of 11.14 at 1 ppm acetone and 200 °C, which is a superior result to those reported by other metal-oxide-based sensors. The response can be measured up to 40 ppb, and the limit of detection is estimated as 9 ppb. ZnO-CuO core-hollow cube nanostructures also present high selectivity toward acetone against other volatile organic compounds and demonstrate excellent stability for up to 40 days. The outstanding gas-sensing performance of the developed nanocubes is attributed to their uniform and unique morphology. Their core-shell-like structures allow the main charge transfer pathways to pass the interparticle p-p junctions, and the p-n junctions in each particle increase the sensitivity of the reactions to gas molecules. The small grain size and high surface area of each domain also enhance the surface gas adsorption.

High-Performance Field-Effect Transistor and Logic Gates Based on GaS-MoS2 van der Waals Heterostructure.

This work demonstrates a high-performance and hysteresis-free field-effect transistor based on two-dimensional (2D) semiconductors featuring a van der Waals heterostructure, MoS2 channel, and GaS gate insulator. The transistor exhibits a subthreshold swing of 63 mV/dec, an on/off ratio over 106 within a gate voltage of 0.4 V, and peak mobility of 83 cm2/(V s) at room temperature. The low-frequency noise characteristics were investigated and described by the Hooge mobility fluctuation model. The results suggest that the van der Waals heterostructure of 2D semiconductors can produce a high-performing interface without dangling bonds and defects caused by lattice mismatch. Furthermore, a logic inverter and a NAND gate are demonstrated, with an inverter voltage gain of 14.5, which is higher than previously reported by MoS2-based transistors with oxide dielectrics. Therefore, this transistor based on van der Waals heterostructure exhibits considerable potential in digital logic applications with low-power integrated circuits.

Flexible and transparent gas molecule sensor integrated with sensing and heating graphene layers.

Graphene leading to high surface-to-volume ratio and outstanding conductivity is applied for gas molecule sensing with fully utilizing its unique transparent and flexible functionalities which cannot be expected from solid-state gas sensors. In order to attain a fast response and rapid recovering time, the flexible sensors also require integrated flexible and transparent heaters. Here, large-scale flexible and transparent gas molecule sensor devices, integrated with a graphene sensing channel and a graphene transparent heater for fast recovering operation, are demonstrated. This combined all-graphene device structure enables an overall device optical transmittance that exceeds 90% and reliable sensing performance with a bending strain of less than 1.4%. In particular, it is possible to classify the fast (≈14 s) and slow (≈95 s) response due to sp(2) -carbon bonding and disorders on graphene and the self-integrated graphene heater leads to the rapid recovery (≈11 s) of a 2 cm × 2 cm sized sensor with reproducible sensing cycles, including full recovery steps without significant signal degradation under exposure to NO2 gas.

An electrochemically reduced graphene oxide-based electrochemical immunosensing platform for ultrasensitive antigen detection.

We present an electrochemically reduced graphene oxide (ERGO)-based electrochemical immunosensing platform for the ultrasensitive detection of an antigen by the sandwich enzyme-linked immunosorbent assay (ELISA) protocol. Graphene oxide (GO) sheets were initially deposited on the amine-terminated benzenediazonium-modified indiun tin oxide (ITO) surfaces through both electrostatic and π-π interactions between the modified surfaces and GO. This deposition was followed by the electrochemical reduction of graphene oxide (GO) for preparing ERGO-modified ITO surfaces. These surfaces were then coated with an N-acryloxysuccinimide-activated amphiphilic polymer, poly(BMA-r-PEGMA-r-NAS), through π-π stacking interactions between the benzene ring tethered to the polymer and ERGO. After covalent immobilization of a primary antibody on the polymer-modified surfaces, sandwich ELISA was carried out for the detection of an antigen by use of a horseradish peroxidase (HRP)-labeled secondary antibody. Under the optimized experimental conditions, the developed electrochemical immunosensor exhibited a linear response over a wide range of antigen concentrations with a very low limit of detection (ca. 100 fg/mL, which corresponds to ca. 700 aM). The high sensitivity of the electrochemical immunosensor may be attributed not only to the enhanced electrocatalytic activity owing to ERGO but also to the minimized background current owing to the reduced nonspecific binding of proteins.

Synthesis and characterization of monomeric, oligomeric, and polymeric aluminum 8-hydroxyquinolines.

We report the synthesis and characterization of monomeric, oligomeric, and polymeric aluminum 8-hydroxyquinolines. The new structures of aluminum quinolate are contrived for expanding the application of AlQ(3) in the area of solution process by modifying AlQ(3) structure for improving solution processibility and crystallization resistance. Oligomeric aluminum 8-hydroxyquinoline (OALQ) was obtained using methylaluminoxane (MAO) and 8-hydroxyquinoline (8-HQ). Polymeric aluminum 8-hydroxyquinoline (PALQ) consists of 8-HQ and a polymeric Al-O backbone, simply prepared by stoichiometrically reacting 8-hydroxyquinoline, pentaerythritol propoxylate, and triethyl aluminum in the presence of chloroform. The absorption and emission spectra of OALQ and PALQ bear a clear resemblance to those of AlQ(3), and the molecular orbitals of OALQ and PALQ are virtually identical to those of AlQ(3). In the SEM images of AlQ(3) and OALQ, cylindrical rods of >100 microm in length and 5-10 microm in diameter for AlQ(3) and 20-100 microm in length and 1-5 microm in diameter for OALQ were observed, respectively. The size of the cylindrical rods of OALQ decreased compared with that of AlQ(3). As for the image of PALQ, an amorphous phase with bulge spots (ca. 5 microm) was observed. These microscope data correspond well to the X-ray powder pattern results. The chemical shifts (31.1, 57.0 ppm) and peak broadness of (27)Al NMR of AlQ(3) and its DFT calculation results present that mer- and fac-AlQ(3) appear in equilibrium through pentacoordinated intermediates. With the combination of DFT optimization and NMR calculation, models of OALQ and PALQ, hexa-, penta-, and tetracoordinated structures, were proposed, which exist in polymeric Al-O backbone and with inter- and intracoordination of Al-O bonds.