A graphene oxide Janus nanosheets relative permeability modifier (RPM) for carbonate formations. The graphene oxide Janus nanosheets RPM may be used to treat a water and hydrocarbon producing carbonate formation to reduce water permeability in the formation and increase the production of hydrocarbons. The graphene oxide Janus nanosheet RPM includes a first side having negatively charged functional groups and a second side having alkyl groups. The alkyl groups may include C8 to C30 alkyls. The negatively charged functional groups may include carboxyl groups, epoxy groups, and hydroxyl groups. Methods of reducing water permeability of a carbonate formation using the graphene oxide Janus nanosheets RPM and methods of manufacturing the graphene oxide Janus nanosheets RPM are also provided.

The present disclosure provides a method of graphene exfoliation and/or stabilization. Both graphene and silica are mixed in an organic solvent to form a liquid precursor, which is then directed through an orifice formed by a metal cylinder and a flat metal plate. The metal cylinder is pressed against the flat metal plate by a high pressure. The high shear between the metal cylinder and the flat metal plate breaks down the thick layers of graphene to thin layers, which are stably dispersed in the gel formed by the silica.

An array of graphene sheets configured to generate electricity from a flow of an ion-containing fluid, wherein the array comprises a plurality of graphene sheets, each graphene sheet comprising first and second electrical contacts, having a surface extending between the first and second electrical contacts for contacting the flow of ion-containing fluid, and wherein each graphene sheet is in electrical contact with at least a further graphene sheet.

Processes and materials are provided for use in Si-based anodes that can improve or extend the cycle life of a battery while also lowering production costs. A composite material design is provided as a porous silicon-graphene-carbon (SiGC) composite particle that is a composed of submicron silicon wrapped with graphene, particulate, flexible conductive additives, and an outer conductive shell or coating made for the purpose of acting as anode material in an electrochemical cell (battery). The tailored composite particle addresses common failure modes to improve cycling performance of silicon by combining multiple mitigation strategies; incorporating intimate graphene coatings to accommodate expansion and protect from solid-electrolyte interphase (SEI) formation; porosity to accommodate expansion; flexible conductive additives to maintain contact during expansion/retraction of the silicon particles and protect the surface from SEI formation; an outer protective shell to hold the composite material together during expansion/retraction; and submicron silicon to prevent pulverization during expansion/retraction.

Provided herein are nanoparticle compositions comprising an organophosphate compound and pharmaceutically acceptable carriers.

Presently disclosed is a multi-layered carbon-based scaffolded structure having a conductive substrate. A first film is deposited on the conductive substrate and includes: a first concentration of three-dimensional (3D) carbon-based particles comprising: a plurality of conductive 3D aggregates formed of graphene sheets that are sintered together to define a 3D hierarchical open porous structure with mesoscale structuring in combination with micron-scale fractal structuring that is also configured to provide conduction between contact points of the graphene sheets. A porous arrangement is formed in the 3D hierarchical open porous structure and contains a liquid electrolyte configured to provide ion transport through a plurality of interconnected porous channels. The first film is configured to provide a first conductivity. A second film is deposited on the first film and comprising a second concentration of 3D carbon-based particles. The second film configured to provide a second conductivity lower than the first conductivity.

Proposed is a method of preparing an independent free-standing graphene film. The graphene film is obtained by means of suction filtration of graphene oxide into a film, solid phase transfer, chemical reduction and the like steps. The graphene film is formed by means of physical cross-linking of a single layer of oxidized/reduced graphene oxide. The graphene film has a thickness of 10-2000 atomic layers. The graphene oxide film has a small thickness and a large number of defects inside, so that it has good transparency and excellent flexibility. On the basis of the transfer film-forming method above, an independent free-standing wrinkled graphene film having a nanoscale thickness is prepared by using a poor solvent and a special high temperature annealing process, and an independent free-standing foamed graphene film having a nanoscale thickness is obtained by using a film-forming thickness and a special high temperature annealing process.

A multilayer body includes a base portion and a graphene film. In an ion mass distribution versus depth of the multilayer body determined by time-of-flight secondary ion mass spectrometry, detection intensities of C.sub.6 ions have a maximum value at a depth of greater than 0 nm and 2.5 nm or less from an exposed surface. Detection intensities of C.sub.3 ions have a maximum value at a depth of greater than 0 nm and 3.0 nm or less from the exposed surface. Detection intensities of SiC.sub.4 ions have a maximum value at a depth of 0.5 nm or greater and 5.0 nm or less from the exposed surface. Detection intensities of SiC ions have a maximum value at a depth of 0.5 nm or greater and 10.0 nm or less from the exposed surface. Detection intensities of Si.sub.2 ions have a maximum value at a depth of 0.5 nm or greater and 10.0 nm or less from the exposed surface. A value obtained by dividing the maximum value of the detection intensities of SiC.sub.4 ions by an average of detection intensities of SiC.sub.4 ions associated with a region of the multilayer body is 1 or greater and 3.5 or less, the region having distances from the exposed surface in a thickness direction of the multilayer body of equal to or greater than 8 nm and 12 nm or less.

A method for preparing a large-area continuous flexible free-standing electrode is provided. The method includes: mixing a reduced graphene oxide, porous carbon particles and a solvent, and dispersing the resulting mixture to obtain a mixed slurry; coating the mixed slurry onto a hydrophobic substrate, and drying, to prepare the large-area continuous flexible free-standing electrode.

Apparatus and methods of fabrication and use of highly effective laser-induced graphene (LIG) electrodes including for electrochemical sensing and catalysis. One example is a sensitive and label-free laser-induced graphene (LIG) electrode functionalized for a specific application. One example of functionalization with antibodies, an enzyme, or an ionophore to electrochemically quantify a target species The LIG electrodes were produced by laser induction on film having a carbon precursor (e.g. polyimide) in ambient conditions, and hence circumvent the need for high-temperature, vacuum environment, and metal seed catalysts commonly associated with graphene-based electrodes fabricated via chemical vapor deposition processes. These results demonstrate how LIG-based electrodes can be used for electrochemical sensing in general. Other examples of applications include, but are not limited to, ion-sensing, pesticide monitoring and detection, and water splitting, using the LIG-based electrode(s) adapted for those purposes.