287results about How to "Does not affect conductivity" patented technology

The invention discloses a supercapacitor electrode corrosion-resistant conductive coating, which comprises the following components in percentage by weight: 10 to 35 percent of conductive agent, 0.1 to 3.5 percent of dispersing agent, 2.0 to 15 percent of binder, 0.1 to 8.0 percent of pH regulator, and 50 to 70 percent of pure water. The supercapacitor electrode corrosion-resistant conductive coating is prepared by the following steps of: fully mixing and uniformly stirring the components, adding the components into a ball mill for peptizing and dispersing, and discharging to obtain the supercapacitor electrode corrosion-resistant conductive coating. Compared with the conventional like products at home and abroad, the supercapacitor electrode corrosion-resistant conductive coating has the advantages of greatly improving the acid and alkali corrosion resistance, having no bubbles, falling off, corrosion and other phenomena after being soaked in alkaline solution for 120 hours and in acid solution for 32 hours, and improving the conductivity, adhesiveness and drying speed. The product can be diluted and adjusted according to need during use.

The invention discloses conductive graphite cream and a preparation method thereof, which solve the technical problem of improving dispersibility of graphite cream. The conductive graphite cream comprises materials including, in weight percent, 10-30% of conductive graphite, 1-30% of matrix resin, 0.1-5% of conductive polymer auxiliaries, 0.1-5% of dispersing auxiliaries and the balance solvents. The preparation method includes the steps: adding the conductive polymer auxiliaries into the solvents to obtain solution 1; adding the matrix resin into the solvents to obtain solution 2; adding the conductive graphite into the solution 2; adding the dispersing auxiliaries into the solution 2 for ball-milling; adding the solution 1 into solution 3; and performing ultrasonic oscillation, high-pressure dispersion and stirring to obtain the conductive graphite cream. Compared with the prior art, the conductive graphite cream and the preparation method have the advantages that nano carbon materials are added, ball-milling, ultrasonic oscillation and high-pressure dispersion are performed for assisting so that the conductive graphite cream is uniformly dispersed, and the preparation method is simple and low-cost.

The invention relates to an ultrathin film of a transparent high-strength and high-conductivity electrical self-supporting carbon nano-tube and a preparation method thereof. The ultrathin film mainly comprises a network consisting of interweaved carbon nano-tubes, and the application amount of the carbon nano-tubes is 0.01-0.7 mg/cm<2>; and the thickness of the film is more than 10nm, the light transmittance of the film is 50-97%, the electrical conductivity of the film is 30-500 MS/m, the tensile strength of the film can be as high as 2000MPa, and the ultrathin film has a larger area. The ultrathin film is prepared from single-walled and/or double-walled and/or multi-walled carbon nano-tubes through the steps of filtering, printing, coating and the like so as to form films, and then stripping from the formed films so as to from self-supporting films. The ultrathin film of the self-supporting carbon nano-tube provided by the invention has ultrahigh mechanical properties and excellent electronic and optical properties, therefore, the ultrathin film can be widely applied to the technical field of photoelectricity; and meanwhile, the ultrathin film is simple in process, easy to operate, good in controllability, safe and environmental-friendly, and can be prepared by using merchant carbon nano-tubes as raw materials, therefore, the ultrathin film is wide in material source and low in cost and is suitable for the industrial production on large-batch and large-area ultrathin film preparation.

The invention relates to an improved method for manufacturing a solid electrolyte/aluminum electrolytic capacitor. The method comprises the following steps: 1, electrolytic papers between an anode formation aluminium foil and a cathode foil are reeled to form core bags, wherein the cathode foil faces outwards and wraps the electrolytic papers, a high-temperature rubber belt is used for clinging and fixing both in a ring manner, and sealing rubber covers are mounted on the core bags; 2, the core bags are immersed into formation liquid to be subjected to repair processing, and the repaired core bags are subjected to carbonization processing, wherein the step 2 is repeated about 2-10 times; 3; the core bags are immersed into the formation liquid again to be subjected to formation and repair processing; 4, the carbonized core bags are immersed into an oxide-film protection liquid and then are dried at the temperature of 50-150 DEG C; and 5, firstly, the core bags are respectively placed into monomers and oxidant for immersion and heating convergence, then the processed core bags are mounted in an aluminum shell and a sealing procedure is performed, and lastly, the produced products are subjected to ageing processing.

The invention discloses a manganese dioxide/graphene lithium ion battery cathode material and a preparation method thereof, which belongs to the new energy and material fields. The preparation method comprises the following steps: 1)preparing three-dimensional graphene bubble; 2)adding potassium permanganate and manganese sulfate monohydrate in ultrapure water and uniformly stirring to obtain a mixing solution; 3)adding the three-dimensional graphene bubble and the mixing solution in an inner container of a high temperature-resistance enclosed stainless steel reaction vessel, tightly screwing the stainless steel reaction vessel and placing in a program control baking oven for heating treatment, separating to obtain a compound; and 4)washing, drying under vacuum and annealing under constant temperature to obtain the manganese dioxide/graphene lithium ion battery cathode material. According to the invention, the method has no damage on graphene, excellent conductivity of graphene can be influenced; the product can be directly used for assembling a battery, no extra current collector is required, and no binder and conductive agent is added; the preparation process is simple, and operationality is strong.

The invention discloses a film bulk acoustic resonator and a manufacturing method thereof. The film bulk acoustic resonator is characterized in that out of a cavity overlapping region and outside an electrode overlapping region, a first electrode plate body and a second electrode plate body respectively comprise a first vibration buffer strip and a second vibration buffer strip, so that the rigidity in the horizontal direction can be effectively reduced (the flexibility is enhanced) while the rigidity in the vertical direction is less influenced, and a buffering effect is achieved for horizontal elastic waves propagating along the electrode plate in the horizontal direction, so that the strength of elastic reflection waves is reduced. Besides, a piezoelectric induction oscillation plate clamped between the first electrode plate body and the second electrode plate body is integrally arranged in the cavity overlapping area, and the boundary of the piezoelectric induction oscillation plate is a polygon without any parallel opposite sides; and additional standing wave oscillation which becomes clutter in the horizontal direction is eliminated, and meanwhile energy consumed by transverse parasitic waves is reduced to the maximum extent. A corresponding manufacturing method is also disclosed.

The invention relates to a bonding copper wire and a preparation method thereof. The bonding copper wire comprises the following components in percentage by mass: 0.0003 percent to 0.003 percent of lithium, 0.0002 percent to 0.002 percent of calcium, 0.0002 percent to 0.001 percent of aluminium, 0.0005 percent to 0.005 percent of cerium and/or yttrium, 0.0001 percent to 0.001 percent of other inevitable impurity elements and the balance of copper. The preparation method of the bonding copper wire comprises the following steps of: preparing a middle alloy, preparing an alloy cast ingot, annealing uniformly, heat extrusion, stress relief annealing, drawing, final annealing, winding for multiple coils, packaging, and final protective packaging, wherein in a drawing process, middle stress relief annealing can be performed according to practical needs. The bonding copper wire has better inoxidizability while keeping better conduction and radiation properties; in the preparation process of the bonding copper wire, the uniform annealing is added and the middle stress relief annealing is performed, so that the mechanical property of the prepared bonding copper wire is better.

The invention relates to a high-conductivity, stretchable, compressible and repairable zwitterionic gel polymer electrolyte as well as preparation and application thereof. Zwitterionic SBMA, and monomers HEMA and LiCl which can enhance mechanical properties and do not affect electric conductivity are utilized, and the gel polymer electrolyte with good performance is prepared through an in-situ polymerization reaction. The P(HEMA-SBMA) electrolyte has good tensile compression performance, and the strain and stress can be adjusted by regulating the monomer ratio and the content of LiCl, so thatthe desired electrolyte with super-tensile strength or high strength is obtained. 50% compression cycle tests can be carried out for 50 times. The good adhesion provides the capability of maintainingthe shape of equipment when the assembled energy storage equipment bears deformation, and the electric conductivity is responsive during stretching and compression.

The invention discloses perovskite solar cell conductive carbon paste which comprises organic solvents, binders and conductive filling materials. The conductive carbon paste further comprises inorganic additives. The inorganic additives are ZrO2 or NiO powder. By mass percent, the conductive carbon paste comprises 6%-15% of binders, 14%-20% of conductive filling materials and 3%-5% of inorganic additives. The invention further discloses a carbon counter electrode for a perovskite solar cell. The carbon counter electrode is prepared and acquired by adopting the above-mentioned conductive carbon paste in a screen printing means. The invention further discloses the perovskite solar cell comprising the above-mentioned carbon counter electrode. A method of preparing the conductive carbon paste is further disclosed. The conductive carbon paste which does not make a perovskite film corroded further increases the photoelectric conversion efficiency.

The invention discloses an electroencephalogram signal wireless collecting system which comprises a control module, a wireless electrode cap module and an electroencephalogram processing module.The control module, the wireless electrode cap module and the electroencephalogram processing module are each provided with a wireless signal transmission module.The wireless electrode cap module further comprises a microcurrent stimulator, a dry electrode and an electroencephalogram resistance detecting device.The microcurrent stimulator receives a control instruction wirelessly sent by the control module and simulates the electrode to output simulation current to act on scalp.The dry electrode collects an electroencephalogram signal fed back by the scalp and sends the signal to the electroencephalogram resistance detecting device, and the signal is processed and then transmitted to an amplifier through the corresponding wireless signal transmission module to be amplified.The dry electrode structure in the electroencephalogram signal wireless collecting system is improved, the dry electrode can make tighter contact with scalp, and the signal to noise ratio is higher.

The invention belongs to the technical field of energy materials and in particular relates to a trace Cu-doped Bi2S3-based thermoelectric material. In the thermoelectric material, metal simple substance Bi and Cu powder with the purity of 99.99 percent and simple substance S powder serve as raw materials, the thermoelectric material is prepared according to a chemical general formula of CuxBi2-xS3, wherein x is mole fraction of a Cu component and x is more than or equal to 0.001 and less than or equal to 0.05, and the thermoelectric material is prepared into a block material by combining a discharge plasma sintering technology and a mechanical alloying method. By the method, the trace Cu-doped Bi2S3-based block thermoelectric material can be easy and convenient to prepare, trace Cu is introduced into a Bi2S3 lattice, the carrier concentration of a sample is improved, a power factor is optimized, a Cu-S nano deposition coherent with a substrate structure is formed, and the thermal conductivity is greatly reduced; therefore, the thermoelectric performance of the Bi2S3-based block material can be greatly improved.

The invention relates to a water-based composite chromium-free passivation solution for a galvanized steel plate. The passivation solution contains 10-30g/L of sodium molybdate, 0-10g/L of sodium phosphate, 5-10g/L of organic phosphoric acid, 1-10g/L of fluotitanic acid, 5-15g/L of a silane coupling agent, 5-20g/L of sodium metasilicate, 0.1-1% of a wetting dispersant and the balance of deionized water. The passivation solution provided by the invention consists of an organic phosphoric acid-molybdate system in match with the modified hydrolysis type silane coupling agent and a nano-inorganic filler, does not contain a chromate and is in line with ROHS requirements; the passivation and drying curing time is short, the degree of stability is high, the quality of a film layer is good, the white rust area in a 72h salt fog test does not exceed 5%, the cost is relatively low, a passivation process device does not need to be changed, and continuous passivation can be realized by using a hexavalent chromium passivation device in early period.

The invention discloses lithium battery electrolyte. The electrolyte comprises solvent, lithium salt and flame retardant additive. The dosage of the lithium salt is 0.1-2.5mol/L. The dosage of the flame retardant additive is 0.1-30% of the total mass of the electrolyte. The flame retardant additive comprises polymerized phosphorus-nitrogen compounds. The lithium battery electrolyte provided by the invention is characterized in flame retardance, high chemical stability, high thermal stability and a high capacity retention ratio.

The invention discloses UV light-cured resin applied to a silver nanowire conductive film and a preparation method of the UV light-cured resin. The UV light-cured resin is prepared from the raw materials: polyurethane acrylate, active monomers, a solvent, a light initiator, a silver stabilizer, graphene quantum dots and ATO. Compared with the existing polyurethane acrylate UV light-cured resin, the UV light-cured resin provided by the invention is greatly improved in the aspects of water resistance, bending resistance, surface hardness and solvent resistance, and is more suitable for the silver nanowire conductive film.

The invention discloses a method of preparing a carbon-coated metal nanowire conductive thin film. A certain amount of metal nanowires is dispersed in a glucose solution, and a hydro-thermal reaction is carried out in a condition of 160 to 200 DEG C for 1 to 5 hours. The metal nanowire is a gold, silver, copper and the like metal nanowire or an alloy and a mixture. The metal nanowire transparent conductive thin film can be prepared through spraying or a thin film transfer method. The method is simple and easy to operate, and the metal nanowire conductive thin film stability can be improved obviously, and the method can promote application of the metal nanowire transparent conductive thin film in the field of an optoelectronic device such as a solar cell.

The invention belongs to the technical field of carbon nano materials, and particularly to carbon nanotube paper. The carbon nanotube paper comprises carbon nanotubes and chemical fibers. The invention also relates to a preparation method of the carbon nanotube paper, and the preparation method comprises the following steps: step one, placing the carbon nanotubes in an alcohol solvent, conductingultrasonic dispersion, placing the chemical fibers in an alcohol solvent, and conducting high-speed dispersion; step two, mixing the chemical fiber dispersion liquid with the carbon nanotube dispersion liquid to obtain a uniform mixed solution; step three, placing the uniform mixed solution in a corresponding filter device, conducting filtering, and forming carbon nanotube wet paper with uniform thickness on a filter membrane; step four, placing the carbon nanotube wet paper and the filter membrane into a drying oven together, and carrying out baking; and step five, stripping dried carbon nanotube paper from the filter membrane, and carrying out roll pressing by using a roller press. The carbon nanotube paper provided by the invention is low in cost, high in purity, and convenient in transfer; and the preparation method has few preparation processes, and is suitable for large-scale production.

The invention discloses an LDMOS device and a forming method thereof. The LDMOS device comprises a semiconductor substrate, a drift region, a shallow trench isolation structure, a doping layer, a gate structure, a source region and a drain region. A well region is located in the semiconductor substrate. The drift region is located in the well region, and the doping type of the drift region is opposite to the doping type of the well region. The shallow trench isolation structure is placed in the drift region, and the depth of the shallow trench isolation structure is smaller than the depth of the drift region. The doping layer is placed at the bottom of the shallow trench isolation structure, and the doping type of the doping layer is opposite to the doping type of the drift region. The gate structure is placed on the semiconductor substrate, one end of the gate structure extends to the position above the well region, and the other end of the gate structure extends to the position above the shallow trench isolation structure. The source region is located in the well region on one side of the gate structure, and the drain region is located in the drift region on the other side of the gate structure. The breakdown voltage of the LDMOS device is kept unchanged, and meanwhile drive currents are increased.

The invention relates to a high barrier and high tolerance composite proton exchange membrane and a preparation method thereof, belonging to the technical field of proton exchange membranes. The composite proton exchange membrane is prepared from 95-99.5wt% of ion exchange resin and 0.5-5wt% of an orientation layer, wherein the ion exchange resin is one of perfluorosulfonic acid resin, sulfonatedpolyarylether, sulfonated polyaryletherketone, sulfonated polythioether ketone or sulfonated polyarylether sulfone ketone; the orientation layer component is one of reduced graphene oxide, single-walled carbon nanotubes or a modified montmorillonite. The composite proton exchange membrane prepared by the method has efficient proton conduction ability, high mechanical tolerance and high barrier property. The invention also provides the preparation method of the composite proton exchange membrane; the method comprises four steps, and is scientific and reasonable, simple and easy to implement, low in cost, safe and environmentally-friendly.