Showing papers in "Nano Research in 2011"

One-dimensional ZnO nanostructures: Solution growth and functional properties

Abstract: One-dimensional (1D) ZnO nanostructures have been studied intensively and extensively over the last decade not only for their remarkable chemical and physical properties, but also for their current and future diverse technological applications. This article gives a comprehensive overview of the progress that has been made within the context of 1D ZnO nanostructures synthesized via wet chemical methods. We will cover the synthetic methodologies and corresponding growth mechanisms, different structures, doping and alloying, position-controlled growth on substrates, and finally, their functional properties as catalysts, hydrophobic surfaces, sensors, and in nanoelectronic, optical, optoelectronic, and energy harvesting devices.

Magnetite/reduced graphene oxide nanocomposites: One step solvothermal synthesis and use as a novel platform for removal of dye pollutants

Abstract: A simple one step solvothermal strategy using non-toxic and cost-effective precursors has been developed to prepare magnetite/reduced graphene oxide (MRGO) nanocomposites for removal of dye pollutants. Taking advantage of the combined benefits of graphene and magnetic nanoparticles, these MRGO nanocomposites exhibit excellent removal efficiency (over 91% for rhodamine B and over 94% for malachite green) and rapid separation from aqueous solution by an external magnetic field. Interestingly, the performance of the MRGO composites is strongly dependent on both the loading of Fe3O4 and the pH value. In addition, the adsorption behavior of this new adsorbent fits well with the Freundlich isotherm and the pseudo-second-order kinetic model. In further applications, real samples—including industrial waste water and lake water—have been treated using the MRGO composites. All the results demonstrate that the MRGO composites are effective adsorbents for removal of dye pollutants and thus could provide a new platform for dye decontamination.

Fabrication of silver nanowire transparent electrodes at room temperature

Abstract: Silver nanowires (AgNWs) surrounded by insulating poly(vinylpyrrolidone) have been synthesized by a polyol process and employed as transparent electrodes. The AgNW transparent electrodes can be fabricated by heat-treatment at about 200 °C which forms connecting junctions between AgNWs. Such a heating process is, however, one of the drawbacks of the fabrication of AgNW electrodes on heat-sensitive substrates. Here it has been demonstrated that the electrical conductivity of AgNW electrodes can be improved by mechanical pressing at 25 MPa for 5 s at room temperature. This simple process results in a low sheet resistance of 8.6 Ω/square and a transparency of 80.0%, equivalent to the properties of the AgNW electrodes heated at 200 °C. This technique makes it possible to fabricate AgNW transparent electrodes on heat-sensitive substrates. The AgNW electrodes on poly(ethylene terephthalate) films exhibited high stability of their electrical conductivities against the repeated bending test. In addition, the surface roughness of the pressed AgNW electrodes is one-third of that of the heat-treated electrode because the AgNW junctions are mechanically compressed. As a result, an organic solar cell fabricated on the pressed AgNW electrodes exhibited a power conversion as much as those fabricated on indium tin oxide electrodes. These findings enable continuous roll-to-roll processing at room temperature, resulting in relatively simple, inexpensive, and scalable processing that is suitable for forthcoming technologies such as organic solar cells, flexible displays, and touch screens. Open image in new window

Graphene-based conducting inks for direct inkjet printing of flexible conductive patterns and their applications in electric circuits and chemical sensors

Abstract: A series of inkjet printing processes have been studied using graphene-based inks. Under optimized conditions, using water-soluble single-layered graphene oxide (GO) and few-layered graphene oxide (FGO), various high image quality patterns could be printed on diverse flexible substrates, including paper, poly(ethylene terephthalate) (PET) and polyimide (PI), with a simple and low-cost inkjet printing technique. The graphene-based patterns printed on plastic substrates demonstrated a high electrical conductivity after thermal reduction, and more importantly, they retained the same conductivity over severe bending cycles. Accordingly, flexible electric circuits and a hydrogen peroxide chemical sensor were fabricated and showed excellent performances, demonstrating the applications of this simple and practical inkjet printing technique using graphene inks. The results show that graphene materials-which can be easily produced on a large scale and possess outstanding electronic properties-have great potential for the convenient fabrication of flexible and low-cost graphene-based electronic devices, by using a simple inkjet printing technique.

Synthesis of Pd Nanocrystals Enclosed by {100} Facets and with Sizes < 10 nm for Application in CO Oxidation

Abstract: The catalytic activity of noble-metal nanocrystals is mainly determined by their sizes and the facets exposed on the surface. For single crystals, it has been demonstrated that the Pd(100) surface is catalytically more active than both Pd(110) and Pd(111) surfaces for the CO oxidation reaction. Here we report the synthesis of Pd nanocrystals enclosed by {100} facets with controllable sizes in the range of 6–18 nm by manipulating the rate of reduction of the precursor. UV-vis spectroscopy studies indicate that the rate of reduction of Na2PdCl4 can be controlled by adjusting the concentrations of Br− and Cl− ions added to the reaction mixture. Pd nanocrystals with different sizes were immobilized on ZnO nanowires and evaluated as catalysts for CO oxidation. We found that the activity of this catalytic system for CO oxidation showed a strong dependence on the nanocrystal size. When the size of the Pd nanocrystals was reduced from 18 nm to 6 nm, the maximum conversion rate was significantly enhanced by a factor of ∼10 and the corresponding maximum conversion temperature was lowered by ∼80 °C.

Monolayer Graphene as a Saturable Absorber in a Mode-Locked Laser

Abstract: We demonstrate that the intrinsic properties of monolayer graphene allow it to act as a more effective saturable absorber for mode-locking fiber lasers when compared to multilayer graphene. The absorption of monolayer graphene can be saturated at lower excitation intensity compared to multilayer graphene, graphene with wrinkle-like defects, or functionalized graphene. Monolayer graphene has a remarkably large modulation depth of 65.9%, whereas the modulation depth of multilayer graphene is greatly reduced due to nonsaturable absorption and scattering loss. Picosecond ultrafast laser pulses (1.23 ps) can be generated using monolayer graphene as a saturable absorber. Due to the ultrafast relaxation time, larger modulation depth and lower scattering loss of monolayer graphene, it performs better than multilayer graphene in terms of pulse shaping ability, pulse stability, and output energy.

Advanced asymmetrical supercapacitors based on graphene hybrid materials

Abstract: Supercapacitors operating in aqueous solutions are low cost energy storage devices with high cycling stability and fast charging and discharging capabilities, but generally suffer from low energy densities. Here, we grow Ni(OH)2 nanoplates and RuO2 nanoparticles on high quality graphene sheets in order to maximize the specific capacitances of these materials. We then pair up a Ni(OH)2/graphene electrode with a RuO2/graphene electrode to afford a high performance asymmetrical supercapacitor with high energy and power density operating in aqueous solutions at a voltage of ∼1.5 V. The asymmetrical supercapacitor exhibits significantly higher energy densities than symmetrical RuO2-RuO2 supercapacitors or asymmetrical supercapacitors based on either RuO2-carbon or Ni(OH)2-carbon electrode pairs. A high energy density of ∼48 W·h/kg at a power density of ∼0.23 kW/kg, and a high power density of ∼21 kW/kg at an energy density of ∼14 W·h/kg have been achieved with our Ni(OH)2/graphene and RuO2/graphene asymmetrical supercapacitor. Thus, pairing up metal-oxide/graphene and metal-hydroxide/graphene hybrid materials for asymmetrical supercapacitors represents a new approach to high performance energy storage.

Microbial Reduction of Graphene Oxide by Shewanella

Abstract: Graphene oxide (GO) can be reduced to graphene in a normal aerobic setup under ambient conditions as mediated by microbial respiration of Shewanella cells. The microbially-reduced graphene (MRG) exhibited excellent electrochemical properties. Extracellular electron transfer pathways at the cell/GO interface were systematically investigated, suggesting both direct electron transfer and electron mediators are involved in the GO reduction.

The origin of wrinkles on transferred graphene

Abstract: When two-dimensional graphene is exfoliated from three-dimensional highly oriented pyrolytic graphite (HOPG), ripples or corrugations always exist due to the intrinsic thermal fluctuations. Surface-grown graphenes also exhibit wrinkles, which are larger in dimension and are thought to be caused by the difference in thermal expansion coefficients between graphene and the underlying substrate in the cooling process after high temperature growth. For further characterization and applications, it is necessary to transfer the surface-grown graphenes onto dielectric substrates, and other wrinkles are generated during this process. Here, we focus on the wrinkles of transferred graphene and demonstrate that the surface morphology of the growth substrate is the origin of the new wrinkles which arise in the surface-to-surface transfer process; we call these morphology-induced wrinkles. Based on a careful statistical analysis of thousands of atomic force microscopy (AFM) topographic data, we have concluded that these wrinkles on transferred few-layer graphene (typically 1–3 layers) are determined by both the growth substrate morphology and the transfer process. Depending on the transfer medium and conditions, most of the wrinkles can be either erased or preserved. Our work suggests a new route for graphene engineering involving structuring the growth substrate and tailoring the transfer process. Open image in new window

Multicolor Luminescent Carbon Nanoparticles: Synthesis, Supramolecular Assembly with Porphyrin, Intrinsic Peroxidase-Like Catalytic Activity and Applications

Abstract: Luminescent carbon nanoparticles (CNPs) are newcomers to the world of nanomaterials and have shown great impact in health and environmental applications as well as being promising building blocks for future nanodevices because of their fascinating photoluminescence and potential to serve as nontoxic replacements for traditional heavy-metals-based quantum dots. Herein, fluorescent CNPs have been prepared from candle soot by refluxing with HNO3 and subsequently separated by a single centrifugation. The CNPs can be represented by the empirical formula C1H0.677O0.586N0.015Na0.069, and have a size of 20–100 nm, height of 3.0 nm, lifetime of 7.31 ns ± 0.06 ns and quantum yield of ∼1.7%. Further studies demonstrate that: (1) the as-prepared CNPs exhibit excellent stability in biological media and their luminescence intensity does not change with ionic strength or pH in the physiological and pathological range of pH 4.5–8.8; (2) CNPs can act as electron donors and transporters and porphyrin can assemble onto CNPs through electrostatic and π-stacking interactions to form porphyrin-CNPs supramolecular composites; (3) CNPs have strong intrinsic peroxidase-like activity. Based on this intrinsic peroxidase activity, a simple, cheap, and highly selective and sensitive colorimetric and quantitative assay has been developed for the detection of glucose levels. This assay has been used to analyze real samples, such as diluted blood and fruit juice. Open image in new window

Catalyst-Free Growth of Nanographene Films on Various Substrates

Abstract: We have developed a new method to grow uniform graphene films directly on various substrates, such as insulators, semiconductors, and even metals, without using any catalyst. The growth was carried out using a remote plasma enhancement chemical vapor deposition (r-PECVD) system at relatively low temperatures, enabling the deposition of graphene films up to 4-inch wafer scale. Scanning tunneling microscopy (STM) confirmed that the films are made up of nanocrystalline graphene particles of tens of nanometers in lateral size. The growth mechanism for the nanographene is analogous to that for diamond grown by PECVD methods, in spite of sp2 carbon atoms being formed in the case of graphene rather than sp3 carbon atoms as in diamond. This growth approach is simple, low-cost, and scalable, and might have potential applications in fields such as thin film resistors, gas sensors, electrode materials, and transparent conductive films.

A high performance cobalt-doped ZnO visible light photocatalyst and its photogenerated charge transfer properties

Abstract: Highly photocatalytically active cobalt-doped ZnO (ZnO:Co) nanorods have been prepared by a facile hydrothermal process. X-ray diffraction, X-ray photoelectron spectroscopy, Raman scattering and UV-vis diffuse reflectance spectroscopy confirmed that the dopant ions substitute for some of the lattice zinc ions, and furthermore, that Co2+ and Co3+ ions coexist. The as-prepared ZnO:Co samples have an extended light absorption range compared with pure ZnO and showed highly efficient photocatalytic activity, only requiring 60 min to decompose ∼93% of alizarin red dye under visible light irradiation (λ > 420 nm). The photophysical mechanism of the visible photocatalytic activity was investigated with the help of surface photovoltage spectroscopy. The results indicated that a strong electronic interaction between the Co and ZnO was present, and that the incorporation of Co promoted the charge separation and enhanced the charge transfer ability and, at the same time, effectively inhibited the recombination of photogenerated charge carriers in ZnO, resulting in high visible light photocatalytic activity. Open image in new window

Generation and photocatalytic activities of Bi@Bi2O3 microspheres

Abstract: Composite Bi@Bi2O3 microspheres have been synthesized via a microwave-assisted solvothermal route. The Bi@Bi2O3 microspheres had a narrow size distribution in the range 1.2–2.8 mm. Glucose was selected as the reductant, BiCl3 as the bismuth source, and ethylene glycol (EG) as the solvent in the synthesis system. The as-synthesized sample was characterized by X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), particle diameter distribution, energy dispersive X-ray spectroscopy (EDS), ultraviolet-visible (UV-vis) spectroscopy, and photoluminescence (PL) spectroscopy. The photocatalytic activities of the Bi@Bi2O3 microspheres were evaluated by the photodegradation of rhodamine B (RhB) and methyl orange (MO) dyes under UV light irradiation. The degradation reached ∼96.6% for RhB and 100% for MO after 4 h reaction in the presence of the as-synthesized Bi@Bi2O3 microspheres.

A facile one-step synthesis of TiO2/graphene composites for photodegradation of methyl orange

Abstract: TiO2/graphene composite photocatalysts have been prepared by a simple liquid phase deposition method using titanium tetrafluoride and electron beam (EB) irradiation-pretreated graphene as the raw materials. The products were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The effects of varying the synthesis parameters such as graphene content, concentration of titanium tetrafluoride solution and irradiation dose were investigated. It was found that the preparation conditions had a significant effect on the structure and properties of the final products. The irradiated graphene was covered with petal-like anatase TiO2 nanoparticles, which were more uniform and smaller in size than those in products synthesized without EB irradiation-pretreated graphene. The photocatalytic activities of the products were evaluated using the photocatalytic degradation of methyl orange as a probe reaction. The results showed that the products synthesized using EB irradiation-pretreated graphene exhibited higher photocatalytic activities than those using graphene without EB irradiation pretreatment.

Binder-free activated carbon/carbon nanotube paper electrodes for use in supercapacitors

Abstract: Novel inexpensive, light, flexible, and even rollup or wearable devices are required for multi-functional portable electronics and developing new versatile and flexible electrode materials as alternatives to the materials used in contemporary batteries and supercapacitors is a key challenge. Here, binder-free activated carbon (AC)/carbon nanotube (CNT) paper electrodes for use in advanced supercapacitors have been fabricated based on low-cost, industrial-grade aligned CNTs. By a two-step shearing strategy, aligned CNTs were dispersed into individual long CNTs, and then 90 wt%–99 wt% of AC powder was incorporated into the CNT pulp and the AC/CNT paper electrode was fabricated by deposition on a filter. The specific capacity, rate performance, and power density of the AC/CNT paper electrode were better than the corresponding values for an AC/acetylene black electrode. The capacity reached a maximum value of 267.6 F/g with a CNT loading of 5 wt%, and the energy density and power density were 22.5 W·h/kg and 7.3 kW/kg at a high current density of 20 A/g. The AC/CNT paper electrode also showed a good cycle performance, with 97.5% of the original capacity retained after 5000 cycles at a scan rate of 200 mV/s. This method affords not only a promising paper-like nanocomposite for use in low-cost and flexible supercapacitors, but also a general way of fabricating multi-functional paper-like CNT-based nanocomposites for use in devices such as flexible lithium ion batteries and solar cells. Open image in new window

Development of Novel Supported Gold Catalysts: A Materials Perspective

Abstract: Since Haruta et al. discovered that small gold nanoparticles finely dispersed on certain metal oxide supports can exhibit surprisingly high activity in CO oxidation below room temperature, heterogeneous catalysis by supported gold nanoparticles has attracted tremendous attention. The majority of publications deal with the preparation and characterization of conventional gold catalysts (e.g., Au/TiO2), the use of gold catalysts in various catalytic reactions, as well as elucidation of the nature of the active sites and reaction mechanisms. In this overview, we highlight the development of novel supported gold catalysts from a materials perspective. Examples, mostly from those reported by our group, are given concerning the development of simple gold catalysts with single metal-support interfaces and heterostructured gold catalysts with complicated interfacial structures. Catalysts in the first category include active Au/SiO2 and Au/metal phosphate catalysts, and those in the second category include catalysts prepared by pre-modification of supports before loading gold, by post-modification of supported gold catalysts, or by simultaneous dispersion of gold and an inorganic component onto a support. CO oxidation has generally been employed as a probe reaction to screen the activities of these catalysts. These novel gold catalysts not only provide possibilities for applied catalysis, but also furnish grounds for fundamental research.

Stable ultrahigh specific capacitance of NiO nanorod arrays

Abstract: Previously reported examples of electrochemical pseudocapacitors based on cheap metal oxides have suffered from the need to compromise between specific capacitance, rate capacitance, and reversibility. Here we show that NiO nanorod arrays on Ni foam have a combination of ultrahigh specific capacitance (2018 F/g at 2.27 A/g), high power density (1536 F/g at 22.7 A/g), and good cycling stability (only 8% of capacitance was lost in the first 100 cycles with no further change in the subsequent 400 cycles). This resulted in an improvement in the reversible capacitance record for NiO by 50% or more, reaching 80% of the theoretical value, and demonstrated that a three-dimensional regular porous array structure can afford all of these virtues in a supercapacitor. The excellent performance can be attributed to the slim (< 20 nm) rod morphology, high crystallinity, regularly aligned array structure and strong bonding of the nanorods to the metallic Ni substrate, as revealed by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD).

Electrochemical performance and ex situ analysis of ZnMn2O4 nanowires as anode materials for lithium rechargeable batteries

Abstract: One-dimensional ZnMn2O4 nanowires have been prepared and investigated as anode materials in Li rechargeable batteries. The highly crystalline ZnMn2O4 nanowires about 15 nm in width and 500 nm in length showed a high specific capacity of about 650 mAh·g−1 at a current rate of 100 mA·g−1 after 40 cycles. They also exhibited high power capability at elevated current rates, i.e., 450 and 350 mAh·g−1 at current rates of 500 and 1000 mA·g−1, respectively. Formation of Mn3O4 and ZnO phases was identified by ex situ X-ray diffraction (XRD) and transmission electron microscopy (TEM) studies after the initial discharge-charge cycle, which indicates that the ZnMn2O4 phase was converted to a nanocomposite of Mn3O4 and ZnO phases immediately after the electrochemical conversion reaction.

Metal@Silica yolk-shell nanostructures as versatile bifunctional nanocatalysts

Abstract: Recent developments in nanochemistry offer precise morphology control of nanomaterials, which has significant impacts in the field of heterogeneous catalysis. Rational design of bifunctional catalysts can influence various aspects of catalytic properties. In this review, a new class of bifunctional catalysts with a metal@silica yolk-shell nanostructure is introduced. This structure has many advantages as a heterogeneous catalyst since it ensures a homogeneous environment around each metal core, and particle sintering is effectively eliminated during high temperature reactions. The catalysts exhibit high activity and recyclability in gas- and solution-phase reactions. It is anticipated that appropriate selection of bifunctional components and optimal structural control will significantly further enhance the catalytic properties, and enable target reaction-oriented development of new catalysts.

Sodium citrate: A universal reducing agent for reduction / decoration of graphene oxide with au nanoparticles

Abstract: A facile method is proposed for the synthesis of reduced graphene oxide nanosheets (RGONS) and Au nanoparticle-reduced graphene oxide nanosheet (Au-RGONS) hybrid materials, using graphene oxide (GO) as precursor and sodium citrate as reductant and stabilizer. The resulting RGONS and Au-RGONS hybrid materials were characterized by UV-vis spectroscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, atomic force microscopy, transmission electron microscopy, and X-ray diffraction. It was found that the RGONS and Au-RGONS hybrid materials formed stable colloidal dispersions through hydrogen bonds between the residual oxygen-containing functionalities on the surface of RGONS and the hydroxyl/carboxyl groups of sodium citrate. The electrochemical responses of RGONS and Au-RGONS hybrid material-modified glassy carbon electrodes (GCE) to three kinds of biomolecules were investigated, and all of them showed a remarkable increase in electrochemical performance relative to a bare GCE.

Ionic liquid-assisted one-step hydrothermal synthesis of TiO2-reduced graphene oxide composites

Abstract: We have demonstrated a facile and efficient strategy for the fabrication of soluble reduced graphene oxide sheets (RGO) and the preparation of titanium oxide (TiO2) nanoparticle-RGO composites using a modified one-step hydrothermal method. It was found that graphene oxide could be easily reduced under solvothermal conditions with ascorbic acid as reductant, with concomitant growth of TiO2 particles on the RGO surface. The TiO2-RGO composite has been thoroughly characterized by Fourier transform infrared spectroscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and thermogravimetric analysis. Microscopy techniques (scanning electron microscopy, atomic force microscopy, and transmission electron microscopy) have been employed to probe the morphological characteristics as well as to investigate the exfoliation of RGO sheets. The TiO2-RGO composite exhibited excellent photocatalysis of hydrogen evolution. Open image in new window

Self-assembly and photocatalysis of mesoporous TiO2 nanocrystal clusters

Abstract: Mesoporous nanocrystal clusters of anatase TiO2 with large surface area and enhanced photocatalytic activity have been successfully synthesized. The synthesis involves the self-assembly of hydrophobic TiO2 nanocrystals into submicron clusters, coating of these clusters with a silica layer, thermal treatment to remove organic ligands and improve the crystallinity of the clusters, and finally removing silica to expose the mesoporous catalysts. With the help of the silica coating, the clusters not only maintain their small grain size but also keep their mesoporous structure after calcination at high temperatures (with BET surface area as high as 277 m2/g). The etching of SiO2 also results in the clusters having high dispersity in water. We have been able to identify the optimal calcination temperature to produce TiO2 nanocrystal clusters that possess both high crystallinity and large surface area, and therefore show excellent catalytic efficiency in the decomposition of organic molecules under illumination by UV light. Convenient doping with nitrogen converts these nanocrystal clusters into active photocatalysts in both visible light and natural sunlight. The strategy of forming well-defined mesoporous clusters using nanocrystals promises a versatile and useful method for designing photocatalysts with enhanced activity and stability.

Synthesis of large-area, few-layer graphene on iron foil by chemical vapor deposition

Abstract: We demonstrate a simple and controllable way to synthesize large-area, few-layer graphene on iron substrates by an optimized chemical vapor deposition (CVD) method using a mixture of methane and hydrogen. Based on an analysis of the Fe-C phase diagram, a suitable procedure for the successful synthesis of graphene on Fe surfaces was designed. An appropriate temperature and cooling process were found to be very important in the synthesis of highly crystalline few-layer graphene. Graphene-based field-effect transistor (FET) devices were fabricated using the resulting few-layer graphene, and showed good quality with extracted mobilities of 300–1150 cm2/(V·s). Open image in new window

Ni3Si2O5(OH)4 multi-walled nanotubes with tunable magnetic properties and their application as anode materials for lithium batteries

Abstract: Highly crystalline and thermally stable pure multi-walled Ni3Si2O5(OH)4 nanotubes with a layered structure have been synthesized in water at a relatively low temperature of 200–210 °C using a facile and simple method. The nickel ions between the layers could be reduced in situ to form size-tunable Ni nanocrystals, which endowed these nanotubes with tunable magnetic properties. Additionally, when used as the anode material in a lithium ion battery, the layered structure of the Ni3Si2O5(OH)4 nanotubes provided favorable transport kinetics for lithium ions and the discharge capacity reached 226.7 mA·h·g−1 after 21 cycles at a rate of 20 mA·g−1. Furthermore, after the nanotubes were calcined (600 °C, 4 h) or reduced (180 °C, 10 h), the corresponding discharge capacities increased to 277.2 mA·h·g−1 and 308.5 mA·h·g−1, respectively. Open image in new window

Length-sorted semiconducting carbon nanotubes for high-mobility thin film transistors

Abstract: We have developed a process for chemical purification of carbon nanotubes for solution-processable thin-film transistors (TFTs) having high mobility. Films of the purified carbon nanotubes fabricated by simple drop coating showed carrier mobilities as high as 164 cm2V−1s−1, normalized transconductances of 0.78 Sm−1, and on/off current ratios of 106. Such high performance requires the preparation of a suspension of micrometer-long and highly purified semiconducting single-walled carbon nanotubes (SWCNTs). Our purification process includes length and electronic-type selective trapping of SWCNTs using recycling gel filtration with a mixture of surfactants. The results provide an important milestone toward printed high-speed and large-area electronics with roll-to-roll and ink-jet device fabrication. Open image in new window

Patterning nanoroads and quantum dots on fluorinated graphene

Abstract: Using ab initio methods we have investigated the fluorination of graphene and find that different stoichiometric phases can be formed without a nucleation barrier, with the complete “2D-Teflon” CF phase being thermodynamically most stable. The fluorinated graphene is an insulator and turns out to be a perfect matrix-host for patterning nanoroads and quantum dots of pristine graphene. The electronic and magnetic properties of the nanoroads can be tuned by varying the edge orientation and width. The energy gaps between the highest occupied and lowest unoccupied molecular orbitals (HOMO-LUMO) of quantum dots are size-dependent and show a confinement typical of Dirac fermions. Furthermore, we study the effect of different basic coverage of F on graphene (with stoichiometries CF and C4F) on the band gaps, and show the suitability of these materials to host quantum dots of graphene with unique electronic properties.

One-step electrochemical approach to the synthesis of Graphene/MnO 2 nanowall hybrids

Abstract: We have demonstrated a one-step and effective electrochemical method to synthesize graphene/MnO2 nanowall hybrids (GMHs). Graphene oxide (GO) was electrochemically reduced to graphene (GN), accompanied by the simultaneous formation of MnO2 with a nanowall morphology via cathodic electrochemical deposition. The morphology and structure of the GMHs were systematically characterized by scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Raman spectroscopy. The resulting GMHs combine the advantages of GN and the nanowall array morphology of MnO2 in providing a conductive network of amorphous nanocomposite, which shows good electrochemical capacitive behavior. This simple approach should find practical applications in the large-scale production of GMHs. Open image in new window

Enhanced photocatalytic activity of TiO2 nanofibers and their flexible composite films: Decomposition of organic dyes and efficient H2 generation from ethanol-water mixtures

Abstract: TiO2 nanofibers decorated with Pt and Pd nanoparticles have been synthesized and studied in various photocatalytic processes. Excellent photocatalytic behavior in the decomposition of organic dyes in water, degradation of organic stains on the surface of flexible freestanding cellulose/catalyst composite films and in generation of hydrogen from ethanol using both suspended and immobilized catalysts are demonstrated. The performance of the nanofiber-based TiO2 materials is competitive with—and in some cases outperforms—their conventional nanoparticle-based counterparts. In all cases, Pd-decorated TiO2 nanoparticles and nanofibers proved to be more efficient than their Pt-based counterparts, which could be explained on the basis of the formation of nano-sized Schottky interfaces at the contacts between TiO2 and metal nanoparticles. The feasibility of forming cellulose/catalyst composites provides a novel way of utilizing photocatalyst materials in large-area coatings and freestanding films.

Controllable synthesis of Co3O4 from nanosize to microsize with large-scale exposure of active crystal planes and their excellent rate capability in supercapacitors based on the crystal plane effect

Abstract: Co3O4 nanorods, nanobelts, nanosheets and cubic/octahedral nanoparticles have been successfully synthesized with tunable size from the nanoscale to the microscale, accompanied by a variation in the nature of the exposed crystal planes. The products are formed by thermal treatment of Co(CO3)0.5(OH)·0.11H2O nanorod, nanobelt, nanosheet and nanocubic/nanooctahedral precursors at 250 °C. Detailed characterization, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photo-electron spectroscopy (XPS), and nitrogen adsorption and desorption isotherms, revealed that the as-prepared nanorods, nanobelts, and nanosheet Co3O4 samples are single crystalline and mesoporous in nature with a predominance of exposed high-energy (110) crystal planes. They exhibited excellent electrochemical properties in supercapacitors, showing higher capacitance and better rate capability than conventional cubic/octahedral Co3O4 nanoparticles having exposed low-energy (100) and (111) planes. No decay in capacitance was observed when the scan rate was increased from 5 mV/s to 100 mV/s, or from 1 A/g to 10 A/g. The maximum value of the specific capacitance was calculated to be 162.8 F/g and the capacitance retention reached as high as 90%. Their excellent performance in supercapacitors is believed to result from the large-area exposure of active (110) crystal planes. The Co3O4 nanosheets showed the best performance due to their larger surface area and ability to provide a better pathway for charge transfer, and are promising electrode materials for application in practical supercapacitors. Open image in new window

Facile and Scalable Synthesis of a Highly Hydroxylated Water-Soluble Fullerenol as a Single Nanoparticle

Abstract: A water-soluble polyhydroxylated fullerene, i.e. a fullerenol, with 44 hydroxyl groups and 8 secondary bound water molecules, C60(OH)44·8H2O (estimated average structure), has been synthesized in a facile one step reaction from pristine C60 by hydroxylation with hydrogen peroxide in the presence of a phase-transfer catalyst, tetra-n-butylammonium hydroxide (TBAH), under organic/aqueous bilayer conditions. The fullerenol exhibited high water solubility, up to 64.9 mg/mL, under neutral (pH = 7) conditions. Dynamic light-scattering (DLS) analysis showed a narrow particle size distribution, of 1–2 nm, indicating that the fullerenol had high dispersion properties in water. The results of particle size analyses, which both focused on a single nanoregion and were conducted using a novel induced grating (IG) method and a scanning probe microscope (SPM), were consistent with the DLS results. A plausible reaction mechanism, which includes fullerene oxide intermediates detected by liquid chromatography-mass spectrometry (LC-MS), has been proposed.