Ultrahigh-Desalination-Capacity Dual-Ion Electrochemical Deionization Device Based on Na3V2(PO4)3@C-AgCl Electrodes.

Seawater desalination is a promising way to alleviate water scarcity nowadays. Present capacitive desalination methods have limitation of salt removal capacity. Herein, a new dual-ion electrochemical desalination system with an ultrahigh desalination capacity is reported. It is composed of Na3V2(PO4)3@C wires as a sodium ion Faradaic electrode, AgCl as a chloride ion Faradaic electrode, and salt feed solution as the electrolyte. When a constant current is applied, redox reactions occur on electrodes, releasing or removing sodium ions and chloride ions. Na3V2(PO4)3 has a high sodium specific capacity, and as a sodium superionic conductor, Na3V2(PO4)3@C wires form an ion conductor network, providing high sodium ion mobility. Additionally, both the wire structure and carbon shell enhance the electrical conductivity of Na3V2(PO4)3. Benefiting from these, outstanding desalination performance, rate capability, and cycle capability have been achieved with the Na3V2(PO4)3@C wire-AgCl device. An ultrahigh desalination capacity of 98.0 mg/g is obtained at a current density of 100 mA/g for more than 50 cycles. This system provides a viable dual-ion electrochemical desalination strategy, which outperforms most of the existing desalination methods.

Correction: A dual-ion electrochemistry deionization system based on AgCl-Na0.44MnO2 electrodes.

Correction for 'A dual-ion electrochemistry deionization system based on AgCl-Na0.44MnO2 electrodes' by Fuming Chen et al., Nanoscale, 2017, 9, 10101-10108.

A Prussian blue anode for high performance electrochemical deionization promoted by the faradaic mechanism.

Desalination is a sustainable process that removes sodium and chloride ions from seawater. Herein, we demonstrate a faradaic mechanism to promote the capacity of capacitive deionization in highly concentrated salt water via an electrochemical deionization device. In this system, ion removal is achieved by the faradaic mechanism via a constant current operation mode, which is improved based on the constant voltage operation mode used in the conventional CDI operation. Benefiting from the high capacity and excellent rate performance of Prussian blue as an active electrochemical reaction material, the designed unit has revealed a superior removal capacity with an ultrafast ion removal rate. A high removal capacity of 101.7 mg g-1 has been obtained with proper flow rate and current density. To further improve the performance of the EDI, a reduced graphene oxide with nanopores and Prussian blue composite has been synthesized. The PB@NPG has demonstrated a high salt removal capacity of 120.0 mg g-1 at 1 C with an energy consumption of 6.76 kT per ion removed, which is much lower than most CDI methods. A particularly high rate performance of 0.5430 mg g-1 s-1 has been achieved at 40 C. The faradaic mechanism promoted EDI has provided a new insight into the design and selection of host materials for highly concentrated salt water desalination.

A dual-ion electrochemistry deionization system based on AgCl-Na0.44MnO2 electrodes.

Novel desalination technologies with high ion removal capacity and low energy consumption are desirable to tackle the water shortage challenge. Herein, we report a dual-ion electrochemistry deionization (DEDI) system with silver chloride as the electrochemical chloride release/capture anode, sodium manganese oxide as the electrochemical sodium release/capture cathode, and flow salt solution as the electrolyte. Sodium and chloride ions are synergistically released to the flow electrolyte feed at an applied positive current. Under negative current conditions, the two ions are extracted from the flow electrolyte feed to their corresponding electrodes at the same time, which can cause a conductivity decrease indicating salt removal. The salt absorption/desorption capacity of the novel deionization system is stable and reversible, up to 57.4 mg g-1 for 100 cycles, which is much higher than that obtained by conventional or hybrid capacitive deionization devices. The charge efficiency is 0.979/0.956 during the salt desorption/absorption process. This research will be of great significance for high efficiency and low energy consumption seawater desalination.

A Microfluidic DNA Sensor Based on Three-Dimensional (3D) Hierarchical MoS2/Carbon Nanotube Nanocomposites.

In this work, we present a novel microfluidic biosensor for sensitive fluorescence detection of DNA based on 3D architectural MoS2/multi-walled carbon nanotube (MWCNT) nanocomposites. The proposed platform exhibits a high sensitivity, selectivity, and stability with a visible manner and operation simplicity. The excellent fluorescence quenching stability of a MoS2/MWCNT aqueous solution coupled with microfluidics will greatly simplify experimental steps and reduce time for large-scale DNA detection.

Two dimensional atomically thin MoS2 nanosheets and their sensing applications.

The extraordinary properties of layered graphene and its successful applications in electronics, sensors, and energy devices have inspired and renewed interest in other two-dimensional (2D) layered materials. Particularly, a semiconducting analogue of graphene, molybdenum disulfide (MoS2), has attracted huge attention in the last few years. With efforts in exfoliation and synthetic techniques, atomically thin films of MoS2 (single- and few-layer) have been recently prepared and characterized. 2D MoS2 nanosheets have properties that are distinct and complementary to those of graphene, making it more appealing for various applications. Unlike graphene with an indirect bandgap, the direct bandgap of single-layer MoS2 results in better semiconductor behavior as well as photoluminescence, suggesting its great suitability for electronic and optoelectronic applications. Compared to their applications in energy storage and optoelectronic devices, the use of MoS2 nanosheets as a sensing platform, especially for biosensing, is still largely unexplored. Here, we present a review of the preparation of 2D atomically thin MoS2 nanosheets, with an emphasis on their use in various sensing applications.

DNA single-base mismatch study using graphene oxide nanosheets-based fluorometric biosensors.

Single nucleotide polymorphisms (SNPs) are frequently associated with various gene-related human diseases, whose determination has attracted great interest. Herein, we report a graphene oxide (GO) nanosheets-based fluorometric DNA biosensor to study the type and location of the single-base mismatch, as well as the influence of the length of the strands. The results indicated that both short and long targets led to much lower fluorescence signals than the perfectly complementary target, while the type of mismatched base had negligible influence on the results. Furthermore, targets with mismatch location near the 5' end led to higher fluorescence intensity than those near the 3' end when the dye was tagged at the 5' end of the probe.

A novel single-layered MoS2 nanosheet based microfluidic biosensor for ultrasensitive detection of DNA.

Recently, MoS2 nanosheets were demonstrated to be able to spontaneously adsorb single-stranded DNA, acting as efficient dye quenchers. We herein report a novel microfluidic biosensor for fluorescent DNA detection based on single-layered MoS2 nanosheets. The proposed platform is simple, rapid and visible with high sensitivity and selectivity.

3D graphene-cobalt oxide electrode for high-performance supercapacitor and enzymeless glucose detection.

Using a simple hydrothermal procedure, cobalt oxide (Co(3)O(4)) nanowires were in situ synthesized on three-dimensional (3D) graphene foam grown by chemical vapor deposition. The structure and morphology of the resulting 3D graphene/Co(3)O(4) composites were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Raman spectroscopy. The 3D graphene/Co(3)O(4) composite was used as the monolithic free-standing electrode for supercapacitor application and for enzymeless electrochemical detection of glucose. We demonstrate that it is capable of delivering high specific capacitance of ∼1100 F g(-1) at a current density of 10 A g(-1) with excellent cycling stability, and it can detect glucose with a ultrahigh sensitivity of 3.39 mA mM(-1) cm(-2) and a remarkable lower detection limit of <25 nM (S/N = 8.5).

A graphene nanoribbon network and its biosensing application.

Graphene oxide nanoribbons (GONRs) have been prepared by chemically unzipping multiwalled carbon nanotubes (MWCNTs). Thin-film networks of GONRs were fabricated by spray-coating, followed by a chemical or thermal reduction to form reduced graphene oxide nanoribbons (rGONRs). Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations indicate that the thermal reduction in the presence of ethanol vapor effectively restores the graphitic structure of the GONR as compared to chemical reduction with hydrazine vapor. Electrical measurements under a liquid-gate configuration demonstrates that rGONR network field-effect transistors exhibit much higher on/off ratios than a network of microsized reduced graphene oxides (rGOs) or a continuous film of single-layered pristine or chemical vapor deposited (CVD) graphene. Furthermore, we demonstrated the potential applications of rGONR networks for biosensing, specifically, the real-time and sensitive detection of adenosine triphosphate (ATP) molecules.

Ultra-sensitive and wide-dynamic-range sensors based on dense arrays of carbon nanotube tips.

Electrochemical electrodes based on dense and vertically aligned arrays of multi-walled carbon nanotubes (MWCNTs) were produced. The open tips of individual hollow nanotubes are exposed as active sites while the entangled nanotube stems encapsulated in epoxy collectively provide multiplexed and highly conductive pathways for charge transport. This unique structure together with the extraordinary electrical and electrochemical properties of MWCNTs offers a high signal-to-noise ratio (thus high sensitivity) and a large detection range, compared with other carbon-based electrodes. Our electrodes can detect K(3)FeCN(6) and dopamine at concentrations as low as 5 nM and 10 nM, respectively, and are responsive in a large dynamic range that spans almost 5 orders of magnitude.

Detecting metabolic activities of bacteria using a simple carbon nanotube device for high-throughput screening of anti-bacterial drugs.

In this contribution, we demonstrate a simple carbon nanotube device to electrically detect the presence of bacteria (Escherichai coli) with high sensitivity (<100 cfu/mL) and the glucose triggered metabolic activities of bacteria in real-time. As proof-of-concept demonstration, we also show that this nanoelectronic approach can be employed for high-throughput screening of anti-bacterial drugs.

Nanoelectronic detection of triggered secretion of pro-inflammatory cytokines using CMOS compatible silicon nanowires.

Nanotechnology, such as nanoelectronic biosensors, is bringing new opportunities and tools to the studies of cell biology, clinical applications, and drug discovery. In this study, crystalline silicon nanowire based field-effect transistors fabricated using top-down approach were employed to parallelly detect pro-inflammatory cytokines in the complex biological fluids (cell culture medium and blood samples) with high specificity and femtomolar sensitivity. Using this technique, the dynamic secretion of TNF-alpha and IL6 was revealed during the immune response of macrophages and rats to the stimulation of bacteria endotoxin. This technique could provide a unique platform to examine the profile of complex immune responses for fundamental studies and diagnosis.

Nanoelectronic biosensors based on CVD grown graphene.

Graphene, a single-atom-thick and two-dimensional carbon material, has attracted great attention recently. Because of its unique electrical, physical, and optical properties, graphene has great potential to be a novel alternative to carbon nanotubes in biosensing. We demonstrate the use of large-sized CVD grown graphene films configured as field-effect transistors for real-time biomolecular sensing. Glucose or glutamate molecules were detected by the conductance change of the graphene transistor as the molecules are oxidized by the specific redox enzyme (glucose oxidase or glutamic dehydrogenase) functionalized onto the graphene film. This study indicates that graphene is a promising candidate for the development of real-time nanoelectronic biosensors.

Integrating carbon nanotubes and lipid bilayer for biosensing.

Membrane proteins, which are the target of most drugs, are implicated in many critical cellular functions such as signal transduction, bioelectricity, exocytosis and endocytosis. Therefore, developing techniques to investigate the functions of membrane proteins is obviously important. Here, we have developed a novel system by integrating artificial lipid bilayer (biomimetic membrane) with single-walled carbon nanotube networks (SWNT-net) based field-effect transistor (FET), and demonstrated that such hybrid nanoelectronic biosensors can specifically and electronically detect the presence and dynamic activities of ionophores (specifically, gramicidin and calcimycin) in their native lipid environment. This technique can potentially be used to examine other membrane proteins (e.g. ligand-gated ion channels, receptors, membrane insertion toxins, and antibacterial peptides) for the purposes of biosensing, fundamental studies, or high throughput drug screening.

Symmetry breaking of graphene monolayers by molecular decoration.

Aromatic molecules can effectively exfoliate graphite into graphene monolayers, and the resulting graphene monolayers sandwiched by the aromatic molecules exhibit a pronounced Raman G-band splitting, similar to that observed in single-walled carbon nanotubes. Raman measurements and calculations based on the force-constant model demonstrate that the absorbed aromatic molecules are responsible for the G-band splitting by removing the energy degeneracy of in-plane longitudinal and transverse optical phonons at the Gamma point.

Label-free detection of ATP release from living astrocytes with high temporal resolution using carbon nanotube network.

Owing to its unique combination of electrical, physiochemical, and one-dimension structural properties, single-walled carbon nanotube (SWNT) has recently emerged as a novel nanoelectronic biosensor for biomolecular detection with extraordinary sensitivity and simple detection scheme. All the realizations so far, however, are limited to static in vitro measurement. Dynamic detection of biomolecule release from living cells which may occur in millisecond timescale has yet to be demonstrated. In the present work, SWNT network was utilized to directly interface with living neuroglial astrocytes and label-freely detect the triggered release of adenosine triphosphate (ATP) from these cells with high temporal resolution. The secreted ATP molecules diffuse into the narrow interface gap between the SWNT-net and the astrocyte, and interact with the nanotubes. Highly charged ATP molecules electrostatically modulate the SWNT conductance leading to measurable current response. This technique provides a novel platform to study ATP release and signaling which play important roles in astrocyte-neuron crosstalk and other essential cellular functions.