Single Stage Simultaneous Electrochemical Exfoliation and Functionalization of Graphene

Development of applications for graphene are currently hampered by its poor dispersion in common, low boiling point solvents. Covalent functionalization is considered as one method for addressing this challenge. To date, approaches have tended to focus upon producing the graphene and functionalizing subsequently. Herein, we describe simultaneous electrochemical exfoliation and functionalization of graphite using diazonium salts at a single applied potential for the first time. Such an approach is advantageous, compared to postfunctionalization of premade graphene, as both functionalization and exfoliation occur at the same time, meaning that monolayer or few-layer graphene can be functionalized and stabilized <i>in situ</i> before they aggregate. Furthermore, the N₂ generated during <i>in situ</i> diazonium reduction is found to aid the separation of functionalized graphene sheets. The degree of graphene functionalization was controlled by varying the concentration of the diazonium species in the exfoliation solution. The formation of functionalized graphene was confirmed using Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, atomic force microscopy, and X-ray photoelectron spectroscopy. The functionalized graphene was soluble in aqueous systems, and its solubility was 2 orders of magnitude higher than the nonfunctionalized electrochemically exfoliated graphene sheets. Moreover, the functionalization enhanced the charge storage capacity when used as an electrode in supercapacitor devices with the specific capacitance being highly dependent on the degree of graphene functionalization. This simple method of <i>in situ</i> simultaneous exfoliation and functionaliztion may aid the processing of graphene for various applications

Mesoporous Vertical Co₃O₄ Nanosheet Arrays on Nitrogen-Doped Graphene Foam with Enhanced Charge-Storage Performance

A hierarchical electrode structure, consisting of cobalt oxide and nitrogen-doped graphene foam (NGF), has been fabricated with the aim of achieving enhanced charge-storage performance. Characterization of the material via electron microscopy and Raman spectroscopy demonstrates that the Co₃O₄ nanosheets grow vertically on NGF and the nanosheets are mesoporous with pore diameters between 3 and 8 nm. The Co₃O₄/NGF electrode shows an enhanced charge-storage performance, attributed to the 3D hierarchical structure and the synergistic effect of Co₃O₄ and NGF. The present study shows that specific capacitances as high as 451 F g^–1 can be obtained, indicating that high-performance electrochemical capacitors can be made using electrode materials with advanced structures. The present electrode design can be readily extended to other electroactive materials and their composites

Influence of Gas Phase Equilibria on the Chemical Vapor Deposition of Graphene

We have investigated the influence of gas phase chemistry on the chemical vapor deposition of graphene in a hot wall reactor. A new extended parameter space for graphene growth was defined through literature review and experimentation at low pressures (≥0.001 mbar). The deposited films were characterized by scanning electron microscopy, Raman spectroscopy, and dark field optical microscopy, with the latter showing promise as a rapid and nondestructive characterization technique for graphene films. The equilibrium gas compositions have been calculated across this parameter space. Correlations between the graphene films grown and prevalent species in the equilibrium gas phase revealed that deposition conditions associated with a high acetylene equilibrium concentration lead to good quality graphene deposition, and conditions that stabilize large hydrocarbon molecules in the gas phase result in films with multiple defects. The transition between lobed and hexagonal graphene islands was found to be linked to the concentration of the monatomic hydrogen radical, with low concentrations associated with hexagonal islands

Continuous Electrochemical Exfoliation of Micrometer-Sized Graphene Using Synergistic Ion Intercalations and Organic Solvents

A novel top-down electrochemical method is demonstrated to prepare gram quantities of few-layer graphene in a single-step, one-pot process. Potential-controlled cathodic reduction is used to intercalate graphite electrodes with alkali-substituted, ammonium- and dimethyl sulfoxide-solvated cations. In situ decomposition of the intercalated compounds breaks the π–π stacking of the graphene layers along the <i>c</i> axis of the graphite gallery, producing 1–20-μm-diameter few-layer graphene sheets, without the need for defect-inducing oxidative or sonication treatments. With a slight modification of the electrodes’ configuration, the process can run in a continuous manner, presenting a potentially scalable approach for few-layer graphene production

Characterization of MoS₂–Graphene Composites for High-Performance Coin Cell Supercapacitors

Two-dimensional materials, such as graphene and molybdenum disulfide (MoS₂), can greatly increase the performance of electrochemical energy storage devices because of the combination of high surface area and electrical conductivity. Here, we have investigated the performance of solution exfoliated MoS₂ thin flexible membranes as supercapacitor electrodes in a symmetrical coin cell arrangement using an aqueous electrolyte (Na₂SO₄). By adding highly conductive graphene to form nanocomposite membranes, it was possible to increase the specific capacitance by reducing the resistivity of the electrode and altering the morphology of the membrane. With continued charge/discharge cycles the performance of the membranes was found to increase significantly (up to 800%), because of partial re-exfoliation of the layered material with continued ion intercalation, as well as increasing the specific capacitance through intercalation pseudocapacitance. These results demonstrate a simple and scalable application of layered 2D materials toward electrochemical energy storage

Investigation of the Differential Capacitance of Highly Ordered Pyrolytic Graphite as a Model Material of Graphene

A study of the differences among the capacitances of freshly exfoliated highly ordered pyrolytic graphite (HOPG, sample denoted FEG), HOPG aged in air (denoted AAG), and HOPG aged in an inert atmosphere (hereafter IAG) is presented in this work. The FEG is found to be more hydrophilic than AAG and IAG because the aqueous electrolyte contact angle (CA) increases from 61.7° to 72.5° and 81.8° after aging in Ar and air, respectively. Electrochemical impedance spectroscopy shows the FEG has an intrinsic capacitance (6.0 μF cm^–2 at the potential of minimum capacitance) higher than those of AAG (4.3 μF cm^–2) and IAG (4.7 μF cm^–2). The observed changes in the electrochemical response are correlated with spectroscopic characterization (Raman spectroscopy and X-ray photoelectron spectroscopy), which show that the surface of HOPG was doped or contaminated after exposure to air. Taken together, these changes upon atmospheric exposure are attributed to oxygen molecule, moisture, and airborne organic contaminations: high-vacuum annealing was applied for the removal of the adsorbed contaminants. It was found that annealing the aged sample at 500 °C leads to partial removal of the contaminants, as gauged by the recovery of the measured capacitance. To the best of our knowledge, this is first study of the effect of the airborne contaminants on the capacitance of carbon-based materials

Controlling the Thermoelectric Behavior of La-Doped SrTiO₃ through Processing and Addition of Graphene Oxide

The addition of graphene has been reported as a potential route to enhance the thermoelectric performance of SrTiO3. However, the interplay between processing parameters and graphene addition complicates understanding this enhancement. Herein, we examine the effects of processing parameters and graphene addition on the thermoelectric performance of La-doped SrTiO3 (LSTO). Briefly, two types of graphene oxide (GO) at different oxidation degrees were used, while the LSTO pellets were densified under two conditions with different reducing strengths (with/without using oxygen-scavenging carbon powder bed muffling). Raman imaging of the LSTO green body and sintered pellets suggests that the added GO sacrificially reacts with the lattice oxygen, which creates more oxygen vacancies and improves electrical conductivity regardless of the processing conditions. The addition of mildly oxidized electrochemical GO (EGO) yields better performance than the conventional heavily oxidized chemical GO (CGO). Moreover, we found that muffling the green body with an oxygen-scavenging carbon powder bed during sintering is vital to achieving a single-crystal-like temperature dependence of electrical conductivity, implying that a highly reducing environment is critical for eliminating the grain boundary barriers. Combining 1.0 wt % EGO addition with a highly reducing environment leads to the highest electrical conductivity of 2395 S cm–1 and power factor of 2525μW m–1 K–2 at 300 K, with an improved average zT value across the operating temperature range of 300–867 K. STEM-EELS maps of the optimized sample show a pronounced depletion of Sr and evident deficiency of O and La at the grain boundary region. Theoretical modeling using a two-phase model implies that the addition of GO can effectively improve carrier mobility in the grain boundary phase. This work provides guidance for the development of high-performance thermoelectric ceramic oxides

Optimizing the Reinforcement of Polymer-Based Nanocomposites by Graphene

The stress transfer between the internal layers of multilayer graphene within polymer-based nanocomposites has been investigated from the stress-induced shifts of the 2D Raman band. This has been undertaken through the study of the deformation of an ideal composite system where the graphene flakes were placed upon the surface of a polymer beam and then coated with an epoxy polymer. It is found that the rate of band shift per unit strain for a monolayer graphene flake is virtually independent of whether it has one or two polymer interfaces (<i>i</i>.<i>e</i>., with or without an epoxy top coating). In contrast, the rate of band shift is lower for an uncoated bilayer specimen than a coated one, indicating relatively poor stress transfer between the graphene layers. Mapping of the strain in the coated bilayer regions has shown that there is strain continuity between adjacent monolayer and bilayer regions, indicating that they give rise to similar levels of reinforcement. Strain-induced Raman band shifts have also been evaluated for separate flakes of graphene with different numbers of layers, and it is found that the band shift rate tends to decrease with an increase in the number of layers, indicating poor stress transfer between the inner graphene layers. This behavior has been modeled in terms of the efficiency of stress transfer between the inner graphene layers. Taking into account the packing geometry of polymer-based graphene nanocomposites and the need to accommodate the polymer coils, these findings enable the optimum number of graphene layers for the best reinforcement to be determined. It is demonstrated that, in general, multilayer graphene will give rise to higher levels of reinforcement than monolayer material, with the optimum number of layers depending upon the separation of the graphene flakes in the nanocomposite

Supercapacitor Electrodes from the in Situ Reaction between Two-Dimensional Sheets of Black Phosphorus and Graphene Oxide

Two-dimensional materials show considerable promise as high surface area electrodes for energy-storage applications such as supercapacitors. A single sheet of graphene possesses a large specific surface area because of its atomically thin thickness. However, to package this area efficiently in a device, it must be confined within a finite three-dimensional volume without restacking of the sheet faces. Herein, we present a method of maintaining the high surface area through the use of a hybrid thin film in which few-layer-exfoliated black phosphorus (BP) reduces graphene oxide (GO) flakes. When the film is exposed to moisture, a redox reaction between the BP and the GO forms an interpenetrating network of reduced GO (RGO) and a liquid electrolyte of intermediate phosphorus acids H_<i>x</i>PO_<i>y</i>. The presence of the liquid H_<i>x</i>PO_<i>y</i> electrolyte in the RGO/H_<i>x</i>PO_<i>y</i> film stabilizes and preserves an open-channel structure enabling rapid ion diffusion, leading to an excellent charging rate capability (up to 500 mV s^–1 and retaining 62.3% of initial capacitance at a large current density of 50 A g^–1) when used as electrodes in supercapacitors

Thermoelectric Power Generation from Lanthanum Strontium Titanium Oxide at Room Temperature through the Addition of Graphene

The applications of strontium titanium oxide based thermoelectric materials are currently limited by their high operating temperatures of >700 °C. Herein, we show that the thermal operating window of lanthanum strontium titanium oxide (LSTO) can be reduced to room temperature by the addition of a small amount of graphene. This increase in operating performance will enable future applications such as generators in vehicles and other sectors. The LSTO composites incorporated one percent or less of graphene and were sintered under an argon/hydrogen atmosphere. The resultant materials were reduced and possessed a multiphase structure with nanosized grains. The thermal conductivity of the nanocomposites decreased upon the addition of graphene, whereas the electrical conductivity and power factor both increased significantly. These factors, together with a moderate Seebeck coefficient, meant that a high power factor of ∼2500 μWm^–1K^–2 was reached at room temperature at a loading of 0.6 wt % graphene. The highest thermoelectric figure of merit (<i>ZT</i>) was achieved when 0.6 wt % graphene was added (<i>ZT</i> = 0.42 at room temperature and 0.36 at 750 °C), with >280% enhancement compared to that of pure LSTO. A preliminary 7-couple device was produced using bismuth strontium cobalt oxide/graphene-LSTO pucks. This device had a Seebeck coefficient of ∼1500 μV/K and an open voltage of 600 mV at a mean temperature of 219 °C