Showing papers on "Graphene oxide paper published in 2014"

Laser-induced porous graphene films from commercial polymers

Abstract: The straightforward and scalable synthesis and patterning of graphene-based nanomaterials remains a technological challenge. Here, the authors use a CO2 infrared laser, under ambient conditions, to directly produce and pattern porous graphene films with three-dimensional networks from commercial polymer films.

Exfoliation of Graphite into Graphene in Aqueous Solutions of Inorganic Salts

Abstract: Mass production of high-quality graphene sheets is essential for their practical application in electronics, optoelectronics, composite materials, and energy-storage devices. Here we report a prompt electrochemical exfoliation of graphene sheets into aqueous solutions of different inorganic salts ((NH4)2SO4, Na2SO4, K2SO4, etc.). Exfoliation in these electrolytes leads to graphene with a high yield (>85%, ≤3 layers), large lateral size (up to 44 μm), low oxidation degree (a C/O ratio of 17.2), and a remarkable hole mobility of 310 cm2 V–1 s–1. Further, highly conductive graphene films (11 Ω sq–1) are readily fabricated on an A4-size paper by applying brush painting of a concentrated graphene ink (10 mg mL–1, in N,N′-dimethylformamide). All-solid-state flexible supercapacitors manufactured on the basis of such graphene films deliver a high area capacitance of 11.3 mF cm–2 and an excellent rate capability of 5000 mV s–1. The described electrochemical exfoliation shows great promise for the industrial-scale ...

Graphene via sonication assisted liquid-phase exfoliation

Abstract: Graphene, the 2D form of carbon based material existing as a single layer of atoms arranged in a honeycomb lattice, has set the science and technology sectors alight with interest in the last decade in view of its astounding electrical and thermal properties, combined with its mechanical stiffness, strength and elasticity. Two distinct strategies have been undertaken for graphene production, i.e. the bottom-up and the top-down. The former relies on the generation of graphene from suitably designed molecular building blocks undergoing chemical reaction to form covalently linked 2D networks. The latter occurs via exfoliation of graphite into graphene. Bottom-up techniques, based on the organic syntheses starting from small molecular modules, when performed in liquid media, are both size limited, because macromolecules become more and more insoluble with increasing size, and suffer from the occurrence of side reactions with increasing molecular weight. Because of these reasons such a synthesis has been performed more and more on a solid (ideally catalytically active) surface. Substrate-based growth of single layers can be done also by chemical vapor deposition (CVD) or via reduction of silicon carbide, which unfortunately relies on the ability to follow a narrow thermodynamic path. Top-down approaches can be accomplished under different environmental conditions. Alongside the mechanical cleavage based on the scotch tape approach, liquid-phase exfoliation (LPE) methods are becoming more and more interesting because they are extremely versatile, potentially up-scalable, and can be used to deposit graphene in a variety of environments and on different substrates not available using mechanical cleavage or growth methods. Interestingly, LPE can be applied to produce different layered systems exhibiting different compositions such as BN, MoS2, WS2, NbSe2, and TaS2, thereby enabling the tuning of numerous physico-chemical properties of the material. Furthermore, LPE can be employed to produce graphene-based composites or films, which are key components for many applications, such as thin-film transistors, conductive transparent electrodes for indium tin oxide replacement, e.g. in light-emitting diodes, or photovoltaics. In this review, we highlight the recent progress that has led to successful production of high quality graphene by means of LPE of graphite. In particular, we discuss the mechanisms of exfoliation and methods that are employed for graphene characterization. We then describe a variety of successful liquid-phase exfoliation methods by categorizing them into two major classes, i.e. surfactant-free and surfactant-assisted LPE. Furthermore, exfoliation in aqueous and organic solutions is presented and discussed separately.

Layered SnS2-Reduced Graphene Oxide Composite – A High-Capacity, High-Rate, and Long-Cycle Life Sodium-Ion Battery Anode Material

Abstract: Author(s): Qu, Baihua; Ma, Chuze; Ji, Ge; Xu, Chaohe; Xu, Jing; Meng, Ying Shirley; Wang, Taihong; Lee, Jim Yang | Abstract: A layered SnS2-reduced graphene oxide (SnS2-RGO) composite is prepared by a facile hydrothermal route and evaluated as an anode material for sodium-ion batteries (NIBs). The measured electrochemical properties are a high charge specific capacity (630 mAh g-1 at 0.2 A g-1) coupled to a good rate performance (544 mAh g-1 at 2 A g-1) and long cycle-life (500 mAh g-1 at 1 A g -1 for 400 cycles). © 2014 WILEY-VCH Verlag GmbH a Co. KGaA, Weinheim.

Dispersion behaviour of graphene oxide and reduced graphene oxide

Abstract: The dispersion behaviour of graphene oxide (GO) and chemically reduced GO (rGO) has been investigated in a wide range of organic solvents. The effect of the reduction process on the GO solubility in eighteen different solvents was examined and analysed, taking into consideration the solvent polarity, the surface tension and the Hansen and Hildebrand solubility parameters. rGO concentrations up to ∼9 μg/mL in chlorinated solvents were achieved, demonstrating an efficient solubilization strategy, extending the scope for scalable liquid-phase processing of conductive rGO inks for the development of printed flexible electronics.

Selective ionic transport through tunable subnanometer pores in single-layer graphene membranes.

Abstract: We report selective ionic transport through controlled, high-density, subnanometer diameter pores in macroscopic single-layer graphene membranes. Isolated, reactive defects were first introduced into the graphene lattice through ion bombardment and subsequently enlarged by oxidative etching into permeable pores with diameters of 0.40 ± 0.24 nm and densities exceeding 1012 cm–2, while retaining structural integrity of the graphene. Transport measurements across ion-irradiated graphene membranes subjected to in situ etching revealed that the created pores were cation-selective at short oxidation times, consistent with electrostatic repulsion from negatively charged functional groups terminating the pore edges. At longer oxidation times, the pores allowed transport of salt but prevented the transport of a larger organic molecule, indicative of steric size exclusion. The ability to tune the selectivity of graphene through controlled generation of subnanometer pores addresses a significant challenge in the dev...

Mechanism of graphene oxide formation.

Abstract: Despite intensive research, the mechanism of graphene oxide (GO) formation remains unclear. The role of interfacial interactions between solid graphite and the liquid reaction medium, and transport of the oxidizing agent into the graphite, has not been well-addressed. In this work, we show that formation of GO from graphite constitutes three distinct independent steps. The reaction can be stopped at each step, and the corresponding intermediate products can be isolated, characterized, and stored under appropriate conditions. The first step is conversion of graphite into a stage-1 graphite intercalation compound (GIC). The second step is conversion of the stage-1 GIC into oxidized graphite, which we define as pristine graphite oxide (PGO). This step involves diffusion of the oxidizing agent into the preoccupied graphite galleries. This rate-determining step makes the entire process diffusive-controlled. The third step is conversion of PGO into conventional GO after exposure to water, which involves hydroly...

Space-Confined Growth of MoS2 Nanosheets within Graphite: The Layered Hybrid of MoS2 and Graphene as an Active Catalyst for Hydrogen Evolution Reaction

Abstract: Since the electrocatalytic activity of layered molybdenum disulfide (MoS2) for hydrogen evolution reaction (HER) closely depends on its exposed edges, the morphology and size of the material are critically important. Herein, we introduce a novel solvent-evaporation-assisted intercalation method to fabricate the hybrid of alternating MoS2 sheets and reduced graphene oxide layers, in which the nanosize of the MoS2 nanosheets can be effectively controlled by leveraging the confinement effect within the two-dimensional graphene layers. Significantly, the resulting MoS2/reduced graphene oxide (RGO) composite shows excellent catalytic activity for HER characterized by higher current densities and lower onset potentials than the conventional pre-exfoliated RGO supported MoS2 nanosheets. Further experiments on the effect of oxidation degree of graphene, the crystallinity of MoS2, and the exposed active site density on the HER performance of the MoS2/RGO composites show that there is an optimum condition for the c...

Unstacked double-layer templated graphene for high-rate lithium–sulphur batteries

Abstract: Graphene is often used as parts of electrodes in batteries and stacking of graphene layers is problematic. Here, Zhao et al. synthesize graphene on mesoporous layered double oxide flakes so that the stacking is effectively prevented, and show high-rate performance when used in Li–S batteries.

Nitrogen and Sulfur Codoped Graphene: Multifunctional Electrode Materials for High‐Performance Li‐Ion Batteries and Oxygen Reduction Reaction

Abstract: N and S codoping of graphene is realized by a novel approach: covalent functionalization of graphene oxide using 2-aminothiophenol as a source of both N and S followed by thermal treatment. The resulting N- and S-codoped graphene has potential applications in high-performance lithium-ion batteries and as a metal-free catalyst for oxygen reduction reaction.

Impermeable barrier films and protective coatings based on reduced graphene oxide

Abstract: Flexible barrier films preventing permeation of gases and moistures are important for many industries ranging from food to medical and from chemical to electronic. From this perspective, graphene has recently attracted particular interest because its defect-free monolayers are impermeable to all atoms and molecules. However, it has been proved to be challenging to develop large-area defectless graphene films suitable for industrial use. Here we report barrier properties of multilayer graphitic films made by gentle chemical reduction of graphene oxide laminates with hydroiodic and ascorbic acids. They are found to be highly impermeable to all gases, liquids and aggressive chemicals including, for example, hydrofluoric acid. The exceptional barrier properties are attributed to a high degree of graphitization of the laminates and little structural damage during reduction. This work indicates a close prospect of graphene-based flexible and inert barriers and protective coatings, which can be of interest for numerous applications.

Electronic Properties of Graphene Encapsulated with Different Two-Dimensional Atomic Crystals

Abstract: Hexagonal boron nitride is the only substrate that has so far allowed graphene devices exhibiting micrometer-scale ballistic transport. Can other atomically flat crystals be used as substrates for making quality graphene heterostructures? Here we report on our search for alternative substrates. The devices fabricated by encapsulating graphene with molybdenum or tungsten disulfides and hBN are found to exhibit consistently high carrier mobilities of about 60 000 cm(2) V(-1) s(-1). In contrast, encapsulation with atomically flat layered oxides such as mica, bismuth strontium calcium copper oxide, and vanadium pentoxide results in exceptionally low quality of graphene devices with mobilities of ∼1000 cm(2) V(-1) s(-1). We attribute the difference mainly to self-cleansing that takes place at interfaces between graphene, hBN, and transition metal dichalcogenides. Surface contamination assembles into large pockets allowing the rest of the interface to become atomically clean. The cleansing process does not occur for graphene on atomically flat oxide substrates.

Thin-Film Composite Polyamide Membranes Functionalized with Biocidal Graphene Oxide Nanosheets

Abstract: Fouling of membranes by microorganisms is a major limiting factor in membrane separation processes. Novel strategies are therefore required to decrease the extent of bacterial growth on membranes. In this study, we confer strong antimicrobial properties to thin-film composite polyamide membranes by a simple graphene oxide surface functionalization. Using amide coupling between carboxyl groups of graphene oxide and carboxyl groups of the polyamide active layer, graphene oxide is irreversibly bound to the membrane. Surface binding of graphene oxide is demonstrated by scanning electron microscopy and Raman spectroscopy. Direct contact of bacteria with functionalized graphene oxide on the membrane surface results in 65% bacterial inactivation after 1 h of contact time. This bactericidal effect is imparted to the membrane without any detrimental effect to the intrinsic membrane transport properties. Our results suggest that functionalization of thin-film composite membranes with graphene oxide nanosheets is a ...

Three‐Dimensional Shape Engineered, Interfacial Gelation of Reduced Graphene Oxide for High Rate, Large Capacity Supercapacitors

Abstract: DOI: 10.1002/adma.201303503 Assembly of graphene into functional macroscopic objects, such as fi lms, [ 1 ] sheets, [ 2 ] fi bers, [ 3 ] foams, [ 4,5 ] and other complex architectures, [ 6 ] is of enormous research interest. How to attain desired structures in a cost effective and manufacturable manner is crucial for energy harvest/storage, catalysis, sensors and so on. Unlike fullerene or carbon nanotubes, whose assembly generally relies on weak van der Walls force or chemical modifi cation, two-dimensional graphene may straightforwardly exploit strong interlayer π – π stacking. Unfortunately, such a strong and directional interaction frequently results in graphitic stacking with minimal surface area. [ 7,8 ]

Multilayered Si nanoparticle/reduced graphene oxide hybrid as a high-performance lithium-ion battery anode.

Abstract: Multilayered Si/RGO anode nanostructures, featuring alternating Si nanoparticle (NP) and RGO layers, good mechanical stability, and high electrical conductivity, allow Si NPs to easily expand between RGO layers, thereby leading to high reversible capacity up to 2300 mAh g(-1) at 0.05 C (120 mA g(-1) ) and 87% capacity retention (up to 630 mAh g(-1) ) at 10 C after 152 cycles.

The global growth of graphene

Abstract: The large-scale production of graphene aimed at industrial applications has grown significantly in the past few years, especially since many companies in China have entered the market.

Face-to-face transfer of wafer-scale graphene films

Abstract: Graphene has attracted worldwide interest since its experimental discovery, but the preparation of large-area, continuous graphene film on SiO2/Si wafers, free from growth-related morphological defects or transfer-induced cracks and folds, remains a formidable challenge. Growth of graphene by chemical vapour deposition on Cu foils has emerged as a powerful technique owing to its compatibility with industrial-scale roll-to-roll technology. However, the polycrystalline nature and microscopic roughness of Cu foils means that such roll-to-roll transferred films are not devoid of cracks and folds. High-fidelity transfer or direct growth of high-quality graphene films on arbitrary substrates is needed to enable wide-ranging applications in photonics or electronics, which include devices such as optoelectronic modulators, transistors, on-chip biosensors and tunnelling barriers. The direct growth of graphene film on an insulating substrate, such as a SiO2/Si wafer, would be useful for this purpose, but current research efforts remain grounded at the proof-of-concept stage, where only discontinuous, nanometre-sized islands can be obtained. Here we develop a face-to-face transfer method for wafer-scale graphene films that is so far the only known way to accomplish both the growth and transfer steps on one wafer. This spontaneous transfer method relies on nascent gas bubbles and capillary bridges between the graphene film and the underlying substrate during etching of the metal catalyst, which is analogous to the method used by tree frogs to remain attached to submerged leaves. In contrast to the previous wet or dry transfer results, the face-to-face transfer does not have to be done by hand and is compatible with any size and shape of substrate; this approach also enjoys the benefit of a much reduced density of transfer defects compared with the conventional transfer method. Most importantly, the direct growth and spontaneous attachment of graphene on the underlying substrate is amenable to batch processing in a semiconductor production line, and thus will speed up the technological application of graphene.

Graphene and graphene oxide and their uses in barrier polymers

Abstract: Currently, there is great interest in graphene-based devices and applications because graphene has unique electronic and material properties, which can lead to enhanced material performance. Graphene may be used in a wide variety of potential applications from next-generation transistors to lightweight and high-strength polymeric composite materials. Graphene, which has atomic thickness and two-dimensional sizes in the tens of micrometer range or larger, has also been considered a promising nanomaterial in gas- or liquid-barrier applications because perfect graphene sheets do not allow diffusion of small gases or liquids through its plane. Recent molecular simulations and experiments have demonstrated that graphene and its derivatives can be used for barrier applications. In general, graphene and its derivatives can be applied via two major routes for barrier polymer applications. One is the transfer or coating of few-layered, ultrathin graphene and its derivatives, such as graphene oxide (GO) and reduced graphene oxide (rGO), on polymeric substrates. The other is the incorporation of fully exfoliated GO or rGO nanosheets into the polymeric matrix. In this article, we review the state-of-the-art research on the use of graphene, GO, and rGO for barrier applications, including few-layered graphene or its derivatives in coated polymeric films and polymer nanocomposites consisting of chemically exfoliated GO and rGO nanosheets, and their gas-barrier properties. As compared to other nanomaterials being used for barrier applications, the advantages and current limitations are discussed to highlight challenging issues for future research and the potential applications of graphene/polymer, GO/polymer, and rGO/polymer composites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 39628.

Large-area freestanding graphene paper for superior thermal management.

Abstract: Large-area freestanding graphene papers (GPs) are fabricated by electrospray deposition integrated with a continuous roll-to-roll process. Upon mechanical compaction and thermal annealing, GPs can achieve a thermal conductivity of as high as 1238.3-1434 W m(-1) K(-1) . The super-thermally conductive GPs display an outstanding heat-spread ability and are more efficient in removing hot spots than Cu and Al foils.

Graphene–nickel interfaces: a review

Abstract: Graphene on nickel is a prototypical example of an interface between graphene and a strongly interacting metal, as well as a special case of a lattice matched system. The chemical interaction between graphene and nickel is due to hybridization of the metal d-electrons with the π-orbitals of graphene. This interaction causes a smaller separation between the nickel surface and graphene (0.21 nm) than the typical van der Waals gap-distance between graphitic layers (0.33 nm). Furthermore, the physical properties of graphene are significantly altered. Main differences are the opening of a band gap in the electronic structure and a shifting of the π-band by ∼2 eV below the Fermi-level. Experimental evidence suggests that the ferromagnetic nickel induces a magnetic moment in the carbon. Substrate induced geometric and electronic changes alter the phonon dispersion. As a consequence, monolayer graphene on nickel does not exhibit a Raman spectrum. In addition to reviewing these fundamental physical properties of graphene on Ni(111), we also discuss the formation and thermal stability of graphene and a surface-confined nickel-carbide. The fundamental growth mechanisms of graphene by chemical vapor deposition are also described. Different growth modes depending on the sample temperature have been identified in ultra high vacuum surface science studies. Finally, we give a brief summary for the synthesis of more complex graphene and graphitic structures using nickel as catalyst and point out some potential applications for graphene–nickel interfaces.

One‐Step Hydrothermal Synthesis of 2D Hexagonal Nanoplates of α‐Fe2O3/Graphene Composites with Enhanced Photocatalytic Activity

Abstract: There has been significant progress in the field of semiconductor photocatalysis, but it is still a challenge to fabricate low-cost and high-activity photocatalysts because of safety issues and nonsecondary pollution to the environment. Here, 2D hexagonal nanoplates of -Fe2O3/graphene composites with relatively good distribution are synthesized for the first time using a simple, one-step, template-free, hydrothermal method that achieves the effective reduction of the graphene oxide (GO) to graphene and intimate and large contact interfaces of the -Fe2O3 nanoplates with graphene. The - Fe2O3/graphene composites showed significantly enhancement in the photocatalytic activity compared with the pure -Fe2O3 nanoplates. At an optimal ratio of 5 wt% graphene, 98% of Rhodamine (RhB) is decomposed with 20 min of irradiation, and the rate constant of the composites is almost four times higher than that of pure -Fe2O3 nanoplates. The decisive factors in improving the photocatalytic performance are the intimate and large contact interfaces between 2D hexagonal -Fe2O3 nanoplates and graphene, in addition to the high electron withdrawing/storing ability and the highconductivity of reduced graphene oxide (RGO) formed during the hydrothermal reaction. The effective charge transfer from -Fe2O3 nanoplates to graphene sheets is demonstrated by the significant weakening of photoluminescence in -Fe2O3/graphene composites.

Graphene oxide nanosheet: an emerging star material for novel separation membranes

Abstract: Advanced membranes that enable ultrafast permeance are very important for processes such as water purification and desalination. Ideally, an efficient ultrafast membrane should be as thin as possible to maximize the permeance, be robust enough to withstand the applied pressure and have a narrow distribution of pore size for excellent selectivity. Graphene oxide nanosheets offer an encouraging opportunity to assemble a brand new class of ultrathin, high-flux and energy-efficient sieving membranes because of their unique two-dimensional and mono-atom thick structure, outstanding mechanical strength and good flexibility as well as their facile and large-scale production in solution. The current state-of-the-art in graphene oxide membranes will be reviewed based on their exceptional separation performance (gas, ions and small molecules). We will focus on the structure of nanochannels within the graphene oxide membranes, the permeance and rejection rate, and the interactions between graphene oxide sheets. The separation performance of graphene oxide membranes can be easily influenced by the state of oxygen-containing groups on the graphene oxide sheets, which provides much more straightforward strategies to tune the pore size of graphene oxide nanochannels when compared to other filtration membranes. We will illustrate in the review theoretical calculations to elucidate the potential of precisely controlling the ionic and small molecular sieving and water transport behaviour through graphene oxide nanochannels. This review will serve as a valuable platform to fully understand how the ions, small molecules and water are transported through the laminar graphene oxide membrane as well as the latest progress in graphene oxide separation membranes.

MoS2 nanoflower-decorated reduced graphene oxide paper for high-performance hydrogen evolution reaction

Abstract: A facile, one-pot solvothermal method is developed to synthesize MoS2 nanoflowers (MoS2NFs) coated on reduced graphene oxide (rGO) paper. The resulting MoS2NF/rGO paper serves as a freestanding, flexible and durable working electrode for hydrogen evolution reaction (HER), exhibiting an overpotential lowered to −0.19 V with a Tafel slope of ∼95 mV per decade.

Freestanding Graphene Paper Supported Three-Dimensional Porous Graphene–Polyaniline Nanocomposite Synthesized by Inkjet Printing and in Flexible All-Solid-State Supercapacitor

Abstract: Freestanding paper-like electrode materials have trigged significant research interest for their practical application in flexible and lightweight energy storage devices. In this work, we reported a new type of flexible nanohybrid paper electrode based on full inkjet printing synthesis of a freestanding graphene paper (GP) supported three-dimensional (3D) porous graphene hydrogel (GH)–polyaniline (PANI) nanocomposite, and explored its practical application in flexible all-solid-state supercapacitor (SC). The utilization of 3D porous GH scaffold to load nanostructured PANI dramatically enhances the electrical conductivity, the specific capacitance and the cycle stability of the GH–PANI nanocomposite. Additionally, GP can intimately interact with GH–PANI through π–π stacking to form a unique freestanding GP supported GH–PANI nanocomposite (GH–PANI/GP) with distinguishing mechanical, electrochemical and capacitive properties. These exceptional attributes, coupled with the merits of full inkjet printing strat...