Quantitative analysis of the synergistic effect of Au nanoparticles on SnO2-rGO nanocomposites for room temperature hydrogen sensing.

Hydrogen detection devices based on gold-tin oxide/reduced graphene oxide (Au-SnO2/rGO) nanohybrids were fabricated by combining a hydrothermal method with sputter coating. The gas sensing performance of the Au-SnO2/rGO sensor was investigated under different concentrations of hydrogen from 0.04% to 1% at room temperature, which indicated a notable sensitive response even for 0.04% hydrogen. The activation energies of hydrogen adsorption/desorption were extracted via Arrhenius analysis which revealed the acceleration effect of gold dopants. This acceleration led to a faster response and recovery during hydrogen sensing. The activation energy analysis provided a more comprehensive understanding on the gas sensing mechanism. A hydrogen detection handheld device is demonstrated by integrating the sensor chip with a portable digital meter for direct readout of test results.

Resonance-Frequency Modulation for Rapid, Point-of-Care Ebola-Glycoprotein Diagnosis with a Graphene-Based Field-Effect Biotransistor.

Recent outbreaks of Ebola-virus infections in several countries demand a rapid point-of-care (POC)-detection strategy. This paper reports on an innovative pathway founded on electronic-resonance-frequency modulation to detect Ebola glycoprotein (GP), on the basis of a carrier-injection-trapping-release-transfer mechanism and the standard antibody-antigen-interaction principle within a dielectric-gated reduced graphene oxide (rGO) field-effect transistor (GFET). The sensitivity of Ebola detection can be significantly enhanced by monitoring the device's electronic-resonance frequency, such as its inflection frequency ( fi), where the phase angle reaches a maximum (θmax). In addition to excellent selectivity, a sensitivity of ∼36-160% and ∼17-40% for 0.001-3.401 mg/L Ebola GP can be achieved at high and low inflection-resonance frequencies, respectively, which are several orders of magnitude higher than the sensitivity from other electronic parameters (e.g., resistance-based sensitivity). Using equivalent circuit modeling for contributions from channel and contact, analytical equations for resonance shifts have been generalized. When matching with the incoming ac-measurement signal, electronic resonance from the phase-angle spectrum evolves from various relaxation processes (e.g., trap and release of injected charges at surface-trap sites of the channel-gate oxide and channel-source or drain interfaces) that are associated with a characteristic emission frequency. Using charge-relaxation dynamics, a high-performance bio-FET sensing platform for healthcare and bioelectronic applications is realized through resonance shifting.

Impedimetric phosphorene field-effect transistors for rapid detection of lead ions.

Stimuli-responsive field-effect transistors (FETs) based on 2D nanomaterials have been considered as attractive candidates for sensing applications due to their rapid response, high sensitivity, and real-time monitoring capabilities. Here we report on an impedance spectroscopy technique for FET sensor applications with ultra-high sensitivity and good reproducibility. An alumina-gated FET, using an ultra-thin black phosphorus flake as the channel material, shows significantly improved stability and ultra-high sensitivity to lead ions in water. In addition, the phase angle in the low frequency region was found to change significantly in the presence of lead ion solutions, whereas it was almost unchanged in the high frequency region. The dominant sensing performance was found at low frequency phase spectrum around 50 Hz and a systematic change in the phase angle in different lead ion concentrations was found. Applying the impedance spectroscopy technique to insulator-gated FET sensors could open a new avenue for real-world sensor applications.

Two-dimensional nanomaterial-based field-effect transistors for chemical and biological sensing.

Meeting the increasing demand for sensors with high sensitivity, high selectivity, and rapid detection presents many challenges. In the last decade, electronic sensors based on field-effect transistors (FETs) have been widely studied due to their high sensitivity, rapid detection, and simple test procedure. Among these sensors, two-dimensional (2D) nanomaterial-based FET sensors have been demonstrated with tremendous potential for the detection of a wide range of analytes which is attributed to the unique structural and electronic properties of 2D nanomaterials. This comprehensive review discusses the recent progress in graphene-, 2D transition metal dichalcogenide-, and 2D black phosphorus-based FET sensors, with an emphasis on rapid and low-concentration detection of gases, biomolecules, and water contaminants.

Scalable graphene sensor array for real-time toxins monitoring in flowing water.

Risk management for drinking water often requires continuous monitoring of various toxins in flowing water. While they can be readily integrated with existing water infrastructure, two-dimensional (2D) electronic sensors often suffer from device-to-device variations due to the lack of an effective strategy for identifying faulty devices from preselected uniform devices based on electronic properties alone, resulting in sensor inaccuracy and thus slowing down their real-world applications. Here, we report the combination of wet transfer, impedance and noise measurements, and machine learning to facilitate the scalable nanofabrication of graphene-based field-effect transistor (GFET) sensor arrays and the efficient identification of faulty devices. Our sensors were able to perform real-time detection of heavy-metal ions (lead and mercury) and E. coli bacteria simultaneously in flowing tap water. This study offers a reliable quality control protocol to increase the potential of electronic sensors for monitoring pollutants in flowing water.

Hg(II) ion detection using thermally reduced graphene oxide decorated with functionalized gold nanoparticles.

Fast and accurate detection of aqueous contaminants is of significant importance as these contaminants raise serious risks for human health and the environment. Mercury and its compounds are highly toxic and can cause various illnesses; however, current mercury detectors suffer from several disadvantages, such as slow response, high cost, and lack of portability. Here, we report field-effect transistor (FET) sensors based on thermally reduced graphene oxide (rGO) with thioglycolic acid (TGA) functionalized gold nanoparticles (Au NPs) (or rGO/TGA-AuNP hybrid structures) for detecting mercury(II) ions in aqueous solutions. The lowest mercury(II) ion concentration detected by the sensor is 2.5 × 10(-8) M. The drain current shows rapid response within less than 10 s after the solution containing Hg(2+) ions was added to the active area of the rGO/TGA-AuNP hybrid sensors. Our work suggests that rGO/TGA-AuNP hybrid structures are promising for low-cost, portable, real-time, heavy metal ion detectors.

Ordered assembly of sorted single-walled carbon nanotubes by drying an aqueous droplet on a meshed substrate.

We report on the ordered assembly of sorted single-walled carbon nanotubes (SWCNTs) (95% semiconducting tubes) by drying aqueous droplets on meshed grids with an enhanced evaporation rate. Besides the commonly observed "coffee ring" deposit of aligned SWCNTs on the droplet contact line after water evaporation, tubes self-organized in the central area of a grid and covered up to -1/3 of the whole surface area of a grid. In addition, parallel-aligned and straightened SWCNTs were seen to span across cracks in the SWCNT-surfactant film. The evaporation-driven assembly of sorted SWCNTs has the potential to produce ordered SWCNT structures that are attractive for the fabrication of electronic devices comprising mostly semiconducting or metallic tubes.

Nanoscale discharge electrode for minimizing ozone emission from indoor corona devices.

Ground-level ozone emitted from indoor corona devices poses serious health risks to the human respiratory system and the lung function. Federal regulations call for effective techniques to minimize the indoor ozone production. In this work, stable atmospheric corona discharges from nanomaterials are demonstrated using horizontally suspended carbon nanotubes (CNTs) as the discharge electrode. Compared with the conventional discharges employing micro- or macroscale electrodes, the corona discharge from CNTs could initiate and operate at a much lower voltage due to the small electrode diameter, and is thus energy-efficient. Most importantly, the reported discharge is environmentally friendly since no ozone (below the detection limit of 0.5 ppb) was detected for area current densities up to 0.744 A/m(2) due to the significantly reduced number of electrons and plasma volume generated by CNT discharges. The resulting discharge current density depends on the CNT loading. Contrary to the conventional wisdom, negative CNT discharges should be used to enhance the current density owing to the efficient field emission of electrons from the CNT surface.

Sensitive field-effect transistor sensors with atomically thin black phosphorus nanosheets.

Atomically thin black phosphorus (BP) field-effect transistors have excellent potential for sensing applications. However, commercial scaling of PFET sensors is still in the early stage due to various technical challenges, such as tedious fabrication, low response% caused by rapid oxidation, non-ideal response output (spike/bidirectional), and large device variation due to poor control over layer thickness among devices. Attempts have been made to address these issues. First, a theoretical model for response% dependence on the number of layers is developed to show the role of atomically thin BP for better responses. A position-tracked, selected-area-exfoliation method has been developed to rapidly produce thin BP layers with a narrow distribution (∼1-7 layers), which can harness excellent gate control over the PFET channel. The typical current on/off ratio is in the range of ∼300-500. The cysteine-modified Al2O3-gated PFET sensors show high responses (∼30-900%) toward a wide detection range (∼1-400 ppb) of lead ions in water with a typical response time of ∼10-30 s. A strategy to minimize device variation is proposed by correlating PFETs' on/off ratio with sensitivity parameters. The thickness variation of the gate oxide is investigated to explain non-ideal and ideal response transient kinetics.

Reduced graphene oxide for room-temperature gas sensors.

We demonstrated high-performance gas sensors based on graphene oxide (GO) sheets partially reduced via low-temperature thermal treatments. Hydrophilic graphene oxide sheets uniformly suspended in water were first dispersed onto gold interdigitated electrodes. The partial reduction of the GO sheets was then achieved through low-temperature, multi-step annealing (100, 200, and 300 degrees C) or one-step heating (200 degrees C) of the device in argon flow at atmospheric pressure. The electrical conductance of GO was measured after each heating cycle to interpret the level of reduction. The thermally-reduced GO showed p-type semiconducting behavior in ambient conditions and was responsive to low-concentration NO2 and NH3 gases diluted in air at room temperature. The sensitivity can be attributed mainly to the electron transfer between the reduced GO and adsorbed gaseous molecules (NO2/NH3). Additionally, the contact between GO and the Au electrode is likely to contribute to the overall sensing response because of the adsorbates-induced Schottky barrier variation. A simplified model is used to explain the experimental observations.

Facile Synthesis of Highly Dispersed Co3O4 Nanoparticles on Expanded, Thin Black Phosphorus for a ppb-Level NO x Gas Sensor.

Expanded few-layer black phosphorus nanosheets (FL-BP NSs) were functionalized by branched polyethylenimine (PEI) using a simple noncovalent assembly to form air-stable overlayers (BP-PEI), and a Co3O4@BP-PEI composite was designed and synthesized using a hydrothermal method. The size of the highly dispersed Co3O4 nanoparticles (NPs) on the FL-BP NSs can be controlled. The BP-C5 (190 °C for 5 h) sensor, with 4-6 nm Co3O4 NPs on the FL-BP NSs, exhibited an ultrahigh sensitivity of 8.38 and a fast response of 0.67 s to 100 ppm of NO x at room temperature in air, which is 4 times faster than the response of the FL-BP NS sensor, and the lower detection limit reached 10 ppb. This study points to a promising method for tuning properties of BP-based composites by forming air-stable overlayers and highly dispersed metal oxide NPs for use in high-performance gas sensors.

Three-dimensional graphene-based composites for energy applications.

Three-dimensional (3D) graphene-based composites have drawn increasing attention for energy applications due to their unique structures and properties. By combining the merits of 3D graphene (3DG), e.g., a porous and interconnected network, a high electrical conductivity, a large accessible surface area, and excellent mechanical strength and thermal stability, with the high chemical/electrochemical activities of active materials, 3DG-based composites show great promise as high-performance electrode materials in various energy devices. This article reviews recent progress in 3DG-based composites and their applications in energy storage/conversion devices, i.e., supercapacitors, lithium-ion batteries, dye-sensitized solar cells, and fuel cells.

Rational design of carbon network cross-linked Si-SiC hollow nanosphere as anode of lithium-ion batteries.

This study aims to realize controllable synthesis of Si-based nanostructures from common and easily accessible silica nanoparticles and to study their component/structure-dependent electrochemical performance as an anode of lithium-ion batteries (LIBs). To this end, a controllable route based on deliberate design has been developed to prepare hollow Si-based nanospheres with tunable composition and crystal structure at the nanoscale. The synthesis process started with coating silica nanoparticles with a carbonaceous polymer with a controllable thickness followed by magnesiothermic reduction. An Si-SiC-C composite was finally produced with a unique hollow sphere structure featuring Si-SiC nanoparticles encapsulated by a cross-linked carbon film network. In addition to the scalability of the synthetic route, the resulting composite exhibits a number of advantageous properties, including excellent electrical conductivity, highly accessible surfaces, structural coherence, and a favorable structure for the formation of a stable solid-electrolyte interphase, which makes it attractive and promising for advanced anode materials of LIBs.

Semiconducting graphene: converting graphene from semimetal to semiconductor.

Interest in graphene has grown extensively in the last decade or so, because of its extraordinary physical properties, chemical tunability, and potential for various applications. However, graphene is intrinsically a semimetal with a zero bandgap, which considerably impedes its use in many applications where a suitable bandgap is required. The transformation of graphene into a semiconductor has attracted significant attention, because the presence of a sizable bandgap in graphene can vastly promote its already-fascinating potential in an even wider range of applications. Here we review major advances in the pursuit of semiconducting graphene materials. We first briefly discuss the electronic properties of graphene and some theoretical background for manipulating the band structure of graphene. We then summarize many experimental approaches proposed in recent years for producing semiconducting graphene. Despite the relatively short history of research in semiconducting graphene, the progress has been remarkable and many significant developments are highly anticipated.

Ultrafast hydrogen sensing through hybrids of semiconducting single-walled carbon nanotubes and tin oxide nanocrystals.

We report an ultrafast and sensitive hydrogen (H(2)) sensing platform using semiconducting single-walled carbon nanotubes (SWCNTs) decorated with tin oxide (SnO(2)) nanocrystals (NCs). The hybrid SnO(2) NC-SWCNT platform shows a response time of 2-3 seconds to 1% H(2) under room temperature and can fully recover within a few minutes in air.

Controllable photoelectron transfer in CdSe nanocrystal-carbon nanotube hybrid structures.

Carbon nanotubes (CNTs) coated with nanocrystals (NCs) or quantum dots (QDs) form a new class of hybrid nanomaterials that could potentially display both the unique properties of NCs and those of CNTs. The photo-induced charge transfer within the hybrid nanostructure may either increase or decrease the CNT electrical conductivity. The use of a chemical vapor deposition method realizes direct assembly of CdSe NCs onto the external surfaces of single-walled CNTs without applying any organic linkers. The NC loading on the nanotubes can be tuned simply through deposition duration. Upon visible light excitation, photo-generated electrons are injected into CNTs from the excited states of CdSe NCs, which is monitored by the measurement of the photocurrent and field effect transistor (FET) characteristics. The direction of the electron transfer could be controlled with the NC coverage on CNTs and the gate voltage.

Modulating gas sensing properties of CuO nanowires through creation of discrete nanosized p-n junctions on their surfaces.

We report significant enhancement of CuO nanowire (NW) sensing performance at room temperature through the surface functionalization with SnO(2) nanocrystals (NCs). The sensitivity enhancement can be as high as ∼300% for detecting 1% NH(3) diluted in air. The improved sensitivity could be attributed to the electronic interaction between p-type CuO NWs and n-type SnO(2) NCs due to the formation of nanosized p-n junctions, which are highly sensitive to the surrounding gaseous environment and could effectively manipulate local charge carrier concentration. Our results suggest that the NC-NW structure is an attractive candidate for practical sensing applications, in view of its outstanding room-temperature sensitivity, excellent dynamic properties (rapid response and quick recovery), and flexibility in modulating the sensing performance (e.g., by adjusting the coverage of SnO(2) NCs on CuO NWs and doping of SnO(2) NCs).

A general approach to one-pot fabrication of crumpled graphene-based nanohybrids for energy applications.

Crumpled graphene oxide (GO)/graphene is a new type of carbon nanostructure that has drawn growing attention due to its three-dimensional open structure and excellent stability in an aqueous solution. Here we report a general and one-step approach to produce crumpled graphene (CG)-nanocrystal hybrids, which are produced by direct aerosolization of a GO suspension mixed with precursor ions. Nanocrystals spontaneously grow from precursor ions and assemble on both external and internal surfaces of CG balls during the solvent evaporation and GO crumpling process. More importantly, CG-nanocrystal hybrids can be directly deposited onto various current-collecting substrates, enabling their tremendous potential for energy applications. As a proof of concept, we demonstrate the use of hybrid electrodes of CG-Mn(3)O(4) and CG-SnO(2) in an electrochemical supercapacitor and a lithium-ion battery, respectively. The performance of the resulting capacitor/battery is attractive and outperforms conventional flat graphene-based hybrid devices. This study provides a new and facile route to fabricating high-performance hybrid CG-nanocrystal electrodes for various energy systems.

Fast and selective room-temperature ammonia sensors using silver nanocrystal-functionalized carbon nanotubes.

We report a selective, room-temperature NH(3) gas-sensing platform with enhanced sensitivity, superfast response and recovery, and good stability, using Ag nanocrystal-functionalized multiwalled carbon nanotubes (Ag NC-MWCNTs). Ag NCs were synthesized by a simple mini-arc plasma method and directly assembled on MWCNTs using an electrostatic force-directed assembly process. The nanotubes were assembled onto gold electrodes with both ends in Ohmic contact. The addition of Ag NCs on MWCNTs resulted in dramatically improved sensitivity toward NH(3). Upon exposure to 1% NH(3) at room temperature, Ag NC-MWCNTs showed enhanced sensitivity (~9%), very fast response (~7 s), and full recovery within several minutes in air. Through density functional theory calculations, we found that the fully oxidized Ag surface plays a critical role in the sensor response. Ammonia molecules are adsorbed at Ag hollow sites on the AgO surface with H pointing toward Ag. A net charge transfer from NH(3) to the Ag NC-MWCNTs hybrid leads to the conductance change in the hybrid.

Ag nanocrystal as a promoter for carbon nanotube-based room-temperature gas sensors.

We have investigated the room-temperature sensing enhancement of Ag nanoparticles (NPs) for multiwalled carbon nanotube (MWCNT)-based gas sensors using electrical measurements, in situ infrared (IR) microspectroscopy, and density functional theory (DFT) calculations. Multiple hybrid nanosensors with structures of MWCNTs/SnO(2)/Ag and MWCNTs/Ag have been synthesized using a process that combines a simple mini-arc plasma with electrostatic force directed assembly, and characterized by electron microscopy techniques. Ag NPs were found to enhance the sensing behavior through the "electronic sensitization" mechanism. In contrast to sensors based on bare MWCNTs and MWCNTs/SnO(2), sensors with Ag NPs show not only higher sensitivity and faster response to NO(2) but also significantly enhanced sensitivity to NH(3). Our DFT calculations indicate that the increased sensitivity to NO(2) is attributed to the formation of a NO(3) complex with oxygen on the Ag surface accompanying a charge rearrangement and a net electron transfer from the hybrid to NO(2). The significant response to NH(3) is predicted to arise because NH(3) is attracted to hollow sites on the oxidized Ag surface with the H atoms pointing towards Ag atoms and electron donation from H to the hybrid sensor.