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A facile synthesis of three-dimensional (3D) network of copper confined nitrogen-doped graphene (NG)/carbon nanotube (CNT) with high atomic percentage of nitrogen (10.1 at.%) has been reported. The homogenous intercalation of the CNT network in-between the graphene layers decorated with copper nanoparticles take place which inhibits the self-agglomeration within the lattice and enhance the volumetric storage capability. The composite electrode demonstrates exceptionally high specific capacitance of 1250 mA h/g obtained at a current density of 0.1 A/g which is 3.4 times greater than the theoretical capacity of graphite (372 mA h/g). The discharge-charge profiles (from 0.002 to 3 V) with reversible battery capacity exhibit a stable state of the lithium-ion batteries which were observed at high rate capability of 420 mA h/g at a current density of 1 A/g even after 500 cycles. The enhancement of the electrochemical performance could be attributed to the 3D electrically conductive networks of copper confined nitrogen-doped graphene/carbon nanotubes (Cu@[N-Gr/CNT])., QC 20201027

A three-dimensional nanostructured nitrogen-doped graphene/carbon nanotube composite has been synthesized via a thermal annealing process, using the high surface attachment properties of uric acid (solid nitrogen precursor) with graphene oxide and oxidized multiwalled carbon nanotube. In the synthesis procedures, the attachment of uric acid to graphene oxide surfaces and the oxidized multiwalled carbon nanotubes via hydrogen bonding and electrostatic forces in the solution leads to a lamellar nanostructure during thermal annealing by the proper insertion of carbon nanotubes in graphene layers with nitrogen doping. The resultant composite has good atomic percentage of N (11.2 at. %) and shows superior electrochemical energy storage and conversion properties compared with nitrogen-doped graphene only and physically mixed nitrogen-doped graphene and nitrogen-doped carbon nanotube samples. The composite exhibits high gravimetric and volumetric capacitance (324 F g -1 at a current density of 1 A g -1 ) as electrode in solid-state supercapacitors, superior capacitive deionization (440 F g -1 at a current density of 1 A g -1 ) in 1 M sodium chloride solution, and as high-performance anode in lithium-ion batteries (1150 mAh g -1 at 0.1 A g -1 ) with long-term cycling stability. In addition, the composite demonstrates efficient metal-free bifunctional electrocatalysis toward the oxygen reduction and evolution reactions, comparable with the commercial electrocatalysts.

A multifunctional nano-heterostructured electrocatalyst of transition metal/metal oxide (nickel/nickel oxide) embedded on nitrogen-doped graphene is reported. The hybrid composite of N-doped graphene nanosheets with a high atomic percentage of nitrogen (8.2 at%) and embedded with highly distributed nickel/nickel oxide nanoparticles inside the graphene layers is synthesized by a one pot thermal annealing process. The resultant composite demonstrates excellent electrocatalytic activity utilizing the superior electrocatalytic properties of nickel/nickel oxide nanoparticles supported on nitrogen-doped graphene. The hybrid exhibits efficient oxygen reduction reaction (ORR) properties comparable with state-of-the-art electrode Pt/C with a four-electron transfer pathway and superior oxygen evolution reaction (OER) compared to the state-of-the-art electrode for the OER, Ru/C. Alternatively, this composite acts as an excellent electrode material for the hydrogen evolution reaction (HER) both in acidic and alkaline media. Nevertheless, this composite facilitates the hydrogen peroxide oxidation reaction (HPOR) in the presence of hydrogen peroxide, which is crucial for developing reversible fuel cells and fuel cells with liquid oxidant.

A free-standing, 3D, macro/microstructured atomic-cobalt/cobalt-oxide-reduced-graphene-oxide (Co/Co3O4-Gr) composite has been developed for complete water splitting. The self-assembled porous morphology associated with the metal/metal oxide active sites makes the whole surface of the electrode conducive toward catalyzing hydrogen and oxygen evolution in alkaline media at a low onset potential. The liquid-crystal-mediated free-standing electrocatalyst shows oxygen evolution at the onset potential of 1.38 V and at the potential of 1.66 V for a current density of 10 mA cm−2. These potentials are comparable to the corresponding values for Ru/C (1.46 and 1.62 V, respectively). In addition, the promising hydrogen evolution performance of our composite compared to Pt/C in alkaline media makes it an efficient bifunctional electrocatalyst for comprehensive water splitting, as well as provides guidance for future electrochemical energy material technologies.

Tailoring the planar morphology of graphene and the generation of electron-dense active sites on its surface by heteroatom doping is one potential approach to enhance the charge storage performance of graphene based electrode materials. Herein, we have reported the preparation of a three-dimensional self-standing cellular architecture as sulfur-doped graphene foam (SGF) by using the simple self-assembly of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) polymer chains on graphene oxide followed by thermal treatment. Successful homogeneous sulfur doping in a three-dimensional (3D) framework of graphene allowed the material to have a large surface area with bulk electroactive regions on the surface for better interfacial contact with electrolyte ions and hence resulted in unprecedented energy storage capability in a flexible aqueous symmetric supercapacitor (367 F g-1 at 1 A g-1), a lithium ion battery (1697 mA h g-1 at 100 mA g-1), and a sodium ion battery (472 mA h g-1 at 50 mA g-1) as a binder-free electrode material. The outstanding electrochemical performance of the material demonstrates the potential of this synthesis approach for various heteroatom-doped self-standing nano-carbon monoliths on a small as well as a large scale for high-performance energy device fabrication for the advancement of modern electronic devices.

The capture and storage of CO2 have been suggested as an effective strategy to reduce the global emissions of greenhouse gases. Hence, in recent years, many studies have been carried out to develop highly efficient materials for capturing CO2. Until today, different types of porous materials, such as zeolites, porous carbons, N/B-doped porous carbons or metal-organic frameworks (MOFs), have been studied for CO2 capture. Herein, the CO2 capture performance of new hybrid materials, graphene-organic frameworks (GOFs) is described. The GOFs were synthesized under mild conditions through a solvothermal process using graphene oxide (GO) as a starting material and benzene 1,4-diboronic acid as an organic linker. Interestingly, the obtained GOF shows a high surface area (506 m2 g−1) which is around 11 times higher than that of GO (46 m2 g−1), indicating that the organic modification on the GO surface is an effective way of preparing a porous structure using GO. Our synthetic approach is quite simple, facile, and fast, compared with many other approaches reported previously. The synthesized GOF exhibits a very large CO2 capacity of 4.95 mmol g−1 at 298 K (1 bar), which is higher those of other porous materials or carbon-based materials, along with an excellent CO2/N2 selectivity of 48.8.

The topography of a biomaterial regulates cellular interactions and determine stem cell fate. A complete understanding of how topographical properties affect cell behavior will allow the rational design of material surfaces that elicit specified biological functions once placed in the body. To this end, we fabricate substrates with aligned or randomly organized fibrous nanostructured topographies. Culturing adipose-derived stem cells (ASCs), we explore the dynamic relationship between the alignment of topography, cell shape and cell differentiation to osteogenic and myogenic lineages. We show aligned topographies differentiate cells towards a satellite cell muscle progenitor state - a distinct cell myogenic lineage responsible for postnatal growth and repair of muscle. We analyze cell shape between the different topographies, using fluorescent time-lapse imaging over 21 days. In contrast to previous work, this allows the direct measurement of cell shape at a given time rather than defining the morphology of the underlying topography and neglecting cell shape. We report quantitative metrics of the time-based morphological behaviors of cell shape in response to differing topographies. This analysis offers insights into the relationship between topography, cell shape and cell differentiation. Cells differentiating towards a myogenic fate on aligned topographies adopt a characteristic elongated shape as well as the alignment of cells.

A novel flexible three-dimensional (3D) architecture of nitrogen and sulfur codoped graphene has been successfully synthesized via thermal treatment of a liquid crystalline graphene oxide−doping agent composition, followed by a soft self-assembly approach. The high temperature process turns the layer-by-layer assembly into a high surface area macro- and nanoporous free-standing material with different atomic configurations of graphene. The interconnected 3D network exhibits excellent charge capacitive performance of 305 F g−1 (at 100 mV s−1), an unprecedented volumetric capacitance of 188 F cm−3 (at 1 A g−1), and outstanding energy density of 28.44 Wh kg−1 as well as cycle life of 10 000 cycles as a free-standing electrode for an aqueous electrolyte, symmetric supercapacitor device. Moreover, the resulting nitrogen/sulfur doped graphene architecture shows good electrocatalytic performance, long durability, and high selectivity when they are used as metal-free catalyst for the oxygen reduction reaction. This study demonstrates an efficient approach for the development of multifunctional as well as flexible 3D architectures for a series of heteroatom-doped graphene frameworks for modern energy storage as well as energy source applications.

Raman spectroscopy is among the primary techniques for the characterisation of graphene materials, as it provides insights into the quality of measured graphenes including their structure and conductivity as well as the presence of dopants. However, our ability to draw conclusions based on such spectra is limited by a lack of understanding regarding the origins of the peaks. Consequently, traditional characterisation techniques, which estimate the quality of the graphene material using the intensity ratio between the D and the G peaks, are unreliable for both GO and rGO. Herein we reanalyse the Raman spectra of graphenes and show that traditional methods rely upon an apparent G peak which is in fact a superposition of the G and D' peaks. We use this understanding to develop a new Raman characterisation method for graphenes that considers the D' peak by using its overtone the 2D'. We demonstrate the superiority and consistency of this method for calculating the oxygen content of graphenes, and use the relationship between the D' peak and graphene quality to define three regimes. This has important implications for purification techniques because, once GO is reduced beyond a critical threshold, further reduction offers limited gain in conductivity.

Recent developments in graphene oxide fibre (GO) processing include exciting demonstrations of hand woven textile structures. However, it is uncertain whether the fibres produced can meet the processing requirements of conventional textile manufacturing. This work reports for the first time the production of highly flexible and tough GO fibres that can be knitted using textile machinery. The GO fibres are made by using a dry-jet wet-spinning method, which allows drawing of the spinning solution (the GO dispersion) in several stages of the fibre spinning process. The coagulation composition and spinning conditions are evaluated in detail, which led to the production of densely packed fibres with near-circular cross-sections and highly ordered GO domains. The results are knittable GO fibres with Young's modulus of ~7.9 GPa, tensile strength of ~135.8 MPa, breaking strain of ~5.9%, and toughness of ~5.7 MJ m(-3). The combination of suitable spinning method, coagulation composition, and spinning conditions led to GO fibres with remarkable toughness; the key factor in their successful knitting. This work highlights important progress in realising the full potential of GO fibres as a new class of textile.

A novel method for nitrogen doping of graphene via solid-state impregnation was developed using graphene oxide (GO) as the raw substrate and aminoterephthalic acid as the doping agent via a facile thermal treatment at 750 °C. The structure, morphology and chemical composition of the synthesised N-doped graphene were characterised using XRD, SEM, EDS and XPS. The N-graphene product exhibits homogeneous doping with high nitrogen content (approx. 6 at%) in four configurations: pyridinic-N, pyrrolic-N, pyridinic-N-oxide and graphitic-N. The electric double layer capacitor (EDLC) fabricated using an N-doped graphene electrode attained a specific capacitance of 210 F g-1 (at a current density of 1 A g-1), which was greater than the values attained by pristine graphene and a GO electrode by factors of about two and six, respectively. Our synthesised N-graphene shows supercapacitance at a low electrolyte concentration compared to supercapacitors reported in the literature for high electrolyte concentrations with similar electrodes. The EDLC device we constructed based on N-graphene showed excellent charge-discharge stability for tests of up to 5000 cycles with high capacity retention (>90%). A comparison of the electrochemical performance of GO, graphene and N-graphene demonstrated that doping with nitrogen can dramatically enhance capacitance.