Textile article with a pattern comprising graphene, defining a surface with empty portions and full portions, with a percentage of coverage from 10 to 70% of the surface defined by the pattern, so as to forma thermal circuit for optimal management of the heat absorbed and of the breathability of the article, and the process for its preparation.

A material that can be used in a wide temperature range is provided. A graphene compound includes graphene or graphene oxide and a substituted or unsubstituted chain group, the chain group includes two or more ether bonds, and the chain group is bonded to the above graphene or graphene oxide through a Si atom. Alternatively, a method for forming a graphene compound includes a first step and a second step after the first step. In the first step, graphene oxide and a base are stirred under a nitrogen stream. In the second step, the mixture is cooled to room temperature, a silylating agent that has a group having two or more ether bonds is introduced into the mixture, and the obtained mixture is stirred. The base is butylamine, pentylamine, hexylamine, diethylamine, dipropylamine, dibutylamine, triethylamine, tripropylamine, or pyridine.

The invention relates to a heat spreading structure comprising: a first substrate layer; a second substrate layer; and a thermally conductive graphite film sandwiched between the first and second substrate layers, wherein the graphite film comprises a plurality of graphene layers having a turbostratic alignment between adjacent graphene layers. The invention also relates to a method for manufacturing a graphite film for a heat spreading structure.

Embodiments herein relate to methods and systems for applying a transfer material layer to graphene during a graphene fabrication process. In an embodiment, a method of producing a graphene sensor element is included. The method includes forming a graphene layer on a growth substrate and applying a fluoropolymer coating layer over the graphene layer. The method includes removing the growth substrate and transferring the graphene and fluoropolymer coating layers onto a transfer substrate, where the graphene layer is disposed on the transfer substrate and the fluoropolymer layer is disposed on the graphene layer. The method also includes removing the fluoropolymer coating layer. Other embodiments are also included herein.

The invention relates to a method for obtaining sheets of graphene, hexagonal boron nitride, molybdenum disulfide, tungsten disulfide or mixtures thereof from the powder of said materials. Said sheets consist of a set of strips, wherein said strips consist of between one and five layers. Said layers are layers of graphene, hexagonal boron nitride, molybdenum disulfide or tungsten disulfide having a monoatomic or monomolecular thickness. The invention also relates to a method for coating a surface with sheets of graphene, hexagonal boron nitride, molybdenum disulfide, tungsten disulfide or sheets of mixtures thereof.

The invention, belonging to the field of biological treatment of pollutants and functional materials, presents a non-dissolved redox mediator biofilm carrier and its preparation method. The graphene oxide and/or carbonylation modified graphene oxide are used as the non-dissolved redox mediator, which is called as the functional material, and the extrusion grade polyethylene/polypropylene particles are used as the basic material. The non-dissolved redox mediator biofilm carrier is prepared by the screw extrusion process, which is a simple, flexible and controllable method, and possesses strong adaptability. The reactor with these biofilm carriers has high removal efficiency of refractory organic pollutants.

The present disclosure relates to production of electrodes. The present disclosure particularly relates to production of graphene based transparent conducting electrode (TCE). The disclosure provides a simple and environmental friendly process for producing said graphene based TCE by coating of graphene on a modified or non-modified substrate. Said electrode provides large area metal network with reduced non-uniformity of conducting film, visible transparency and low or reduced sheet resistance. The disclosure further relates to a graphene based transparent conductive electrode (TCE).

Molecular Graphene (MG) of a physical size and bonding character that render the molecule suitable as a channel material in an electronic device, such as a tunnel field effect transistor (TFET). The molecular graphene may be a large polycyclic aromatic hydrocarbon (PAH) employed as a discrete element, or as a repeat unit, within an active or passive electronic device. In some embodiments, a functionalized PAH is disposed over a substrate surface and extending between a plurality of through-substrate vias. Heterogeneous surfaces on the substrate are employed to direct deposition of the functionalized PAH molecule to surface sites interstitial to the array of vias. Vias may be backfilled with conductive material as self-aligned source/drain contacts. Directed self-assembly techniques may be employed to form local interconnect lines coupled to the conductive via material. In some embodiments, graphene-based interconnects comprising a linear array of PAH molecules are formed over a substrate.

The impact of post-synthesis processing in, for example, graphene oxid or reduced graphene oxide materials for supercapacitor electrodes has been analyzed. A comparative study of vacuum, freeze and critical point drying was carried out for graphene oxide or hydrothermally reduced graphene oxide demonstrating that the optimization of the specific surface area and preservation of the porous network is important to maximize its properties such as supercapacitance performance. As described below, using a supercritical fluid as the drying medium, unprecedented values of specific surface area (e.g., 364 m.sup.2 g.sup.−1) and supercapacitance (e.g., 441 F g.sup.−1) for this class of materials were achieved.

The present invention is an improved method of production of graphenic materials used to store energy and the energy storage systems using such produced graphenic materials. Provided herein is a method of producing graphene oxide that includes oxidizing graphite powder in a mixture of H.sub.3PO.sub.4 and H.sub.2SO.sub.4 in the presence of KMnO.sub.4, wherein the ratio of graphite powder to KMnO.sub.4 is about 1:9 by weight and the ratio of H.sub.3PO.sub.4 to H.sub.2SO.sub.4 is about 1:9 by volume, to produce graphene oxide; dispersing the graphene oxide in water at an acidic pH (e.g., about 0) to form a solution; adjusting the solution to about a neutral pH; and isolating the graphene oxide. An energy storage device is provided herein that includes the graphene oxide made by the disclosed methods or that includes the population (plurality) of reduced graphene oxide particles having the properties disclosed herein, such as batteries and supercapacitors.