3034 results about "Electro conductivity" patented technology

The invention provides nitrogen mixed grapheme hydrogel of which the water content is 90 to 99.5 percent, the electric conductivity is 10-3-100 S/m, and the molar ratio of N and C is 1 to 25 percent. The invention further provides nitrogen mixed aerogel of which the molar ratio of N and C is 2 to 20 percent, the molar ratio of C and O is 15 to 5, nitrogen atoms existing in the form of amidogen nitrogen accounts for 40 to 70 percent, pyridine type nitrogen accounts for 10 to 40 percent, graphite type nitrogen accounts for 10 to 30 percent, the specific area is 300 to 1500 m<2>/g, the apertures which are micropore account for 10 to 20 percent, the apertures which are mesoporous 20 to 50 percent, the apertures which are macropore 30 to 70 percent, the apparent density is 0.01 to 0.2 g/cm<3>, the pore volume is 5 to 20 cm<3>/g, and the electric conductivity is 1 to 1000 S/m. The nitrogen mixed grapheme hydrogel or aerogel and preparation method thereof provided by the invention has the characteristics that the operation is simple, the equipment requirement is low, the production efficiency is high, the scale-up of the technology is easy, the nitrogen mixed content is controllable and the compounding with other functional substances is simple.

Improvements in the sensor array are disclosed for an array used in a module for preventing unauthorized use of a firearm or other device. The module to which the invention is applicable of the type including a plurality of pressure sensors for sensing a user's handgrip on the device; comparator means for comparing a pressure signature profile compiled from an output from said pressure sensors with at least one pressure signature profile in storage; and means for preventing operation of the device when the compared profiles do not match. The improved sensor array comprises a first set of spaced electrically conductive lines formed on the gripping surface; a thin layer of (preferably) piezoresistive material overlying the first set of conductive lines; and a second set of spaced electrically conductive lines formed over the piezoresistive layer. The lines of the second set are orthogonal to the lines of the first set, to establish a grid-like pattern of conductive lines sandwiching the piezoresistive layer. The projected intersections between the lines of the first and second sets (i.e., the grid crossing points) thereby define with the intervening portion of the piezoresistive layer, an array of sensors which are responsive to pressure applied against the gripping surface by a user of the device. Such pressure changes the electrical conductivity in the path including the intersecting lines and intervening piezoresistive material. Signal outputs from the electrical paths including the array of sensors serve to define the pressure signal profile.

Provided is lithium secondary battery comprising a cathode, an anode, and an electrolyte or separator-electrolyte assembly disposed between the cathode and the anode, wherein the anode comprises: (a) a foil or coating of lithium or lithium alloy as an anode active material; and (b) a thin layer of a high-elasticity polymer having a recoverable tensile strain no less than 5%, a lithium ion conductivity no less than 10⁻⁶ S/cm at room temperature, and a thickness from 1 nm to 10 μm, wherein the high-elasticity polymer contains an ultrahigh molecular weight polymer having a molecular weight from 0.5×10⁶ to 9×10⁶ g/mole and is disposed between the lithium or lithium alloy and the electrolyte or separator-electrolyte assembly.

This invention provides a method of producing a highly electrically conductive sheet molding compound (SMC) composition and a fuel cell flow field plate or bipolar plate made from such a composition. The plate exhibits a conductivity typically greater than 100 S/cm and more typically greater than 200 S/cm. In one preferred embodiment, the method comprises: (a) providing a continuous sheet of a substrate material (bottom sheet) and a continuous sheet of flexible graphite (top sheet) from respective rollers; (b) feeding a resin mixture (comprising a thermoset resin and a conductive filler) to a space between the top sheet and the bottom sheet in such a way that the resin mixture forms a uniform core layer sandwiched between the two sheets to obtain a laminated structure; (c) compressing the laminated structure to obtain a SMC composition having two opposite outer surfaces; and (e) impressing a fluid flow channel to either or both of the outer surfaces (e.g., via embossing or matched-die molding) and curing the thermoset resin to obtain the plate.

The present invention provides a carbon-cladded composite composition for use as a fuel cell flow field plate or bipolar plate. In one preferred embodiment, the composition comprises a core composite layer sandwiched between two clad layers, wherein (a) the clad layer comprises a conductive carbon or graphite material (e.g., carbon nano-tubes, nano-scaled graphene plates, graphitic nano-fibers, and fine graphite particles); (b) the core composite layer comprises a matrix resin and a conductive filler present in a sufficient quantity to render the composite layer electrically conductive with an electrical conductivity no less than 1 S/cm (preferably no less than 100 S/cm); and (c) the composition has a planar outer surface on each clad side having formed therein a fluid flow channel.

The invention discloses a preparation method of an all-solid polymer electrolyte through in-situ ring opening polymerization of an epoxy compound, and an application of the all-solid polymer electrolyte in an all-solid battery. The preparation method is characterized in that a liquid-state epoxy compound, a lithium salt, a battery additive and the like are employed as precursors and are injected into between a positive pole sheet and a negative pole sheet of the battery, and under a heating condition, in-situ polymerization solidification is carried out to form the all-solid polymer electrolyte, and furthermore, the all-solid battery is produced. The ionic conductivity at room temperature of the all-solid polymer electrolyte can reach from 1*10<-5> S/cm to 9*10<-3> S/cm and electric potential window is 3.5-5 V. The all-solid polymer electrolyte is prepared through the in-situ copolymerization method, so that the all-solid polymer electrolyte has excellent contact with electrodes, thereby greatly improving interface compatibility of the solid-state battery, reducing interface wetting and modification steps of the solid-state battery, reducing production cost of the solid-state battery and improving performances of the solid-state battery. The invention also discloses an all-solid polymer lithium battery assembled from the all-solid polymer electrolyte.

A system/method allowing hydrophilicity alteration of a polymeric material (PM) is disclosed. The PM hydrophilicity alteration changes the PM characteristics by decreasing the PM refractive index, increasing the PM electrical conductivity, and increasing the PM weight. The system/method incorporates a laser radiation source that generates tightly focused laser pulses within a three-dimensional portion of the PM to affect these changes in PM properties. The system/method may be applied to the formation of customized intraocular lenses comprising material (PLM) wherein the lens created using the system/method is surgically positioned within the eye of the patient. The implanted lens refractive index may then be optionally altered in situ with laser pulses to change the optical properties of the implanted lens and thus achieve optimal corrected patient vision. This system/method permits numerous in situ modifications of an implanted lens as the patient's vision changes with age.

The invention discloses a thick electrode with a good electrochemical performance. The electrode comprises a current collector and an electrode membrane containing active substances and conductive substances. With a thickness greater than 300 micrometers, the electrode membrane includes an internal membrane layer close to the current collector and an external membrane layer far from the current collector. The conductivity of the electrode membrane decreases from the internal membrane layer to the external membrane layer, while the porosity of the electrode membrane increases from the internal membrane layer to the external membrane layer. The internal membrane layer has great conductivity which can make electrons at the current collector entering or separating from the internal membrane layer rapidly. With great porosity, the external membrane layer can adsorb a lot of electrolyte, thus solving the problem of poor electrolyte wettability of thick electrodes. In addition, the invention also discloses a preparation method of a thick electrode with a good electrochemical performance.

The invention discloses a method for preparing concavo-convex rod soil/zinc oxide nanometer composite materials, which comprises the following steps: purifying and dispersing the concavo-convex rod soil in water to prepare concavo-convex rod soil dispersion liquid; then adjusting the temperature of the concavo-convex rod soil dispersion liquid to 30 to 100 DEG C; agitating the concavo-convex rod soil dispersion liquid dispersion liquid and while adding zinc salt aqueous solution with the concentration of 0.3 to 3 mol.L<-1> and carbonate aqueous solution with the concentration of 0.3 to 2 mol.L<-1> to the concavo-convex rod soil dispersion liquid dispersion liquid; and keeping the pH value of mixed liquid within the range of 6.0 to 8.0. The prepared mixed serous fluid comprising the prepared nanometer concavo-convex rod soil and basic zinc carbonate is filtered; and a filter cake is washed by deionized water; when the electrical conductivity of filtrate is less than 300 MuS.cm<-1>, the washing is finished; and the filter bake obtained is dried at the temperature of below 100 DEG C, then baked for 1 to 10 hours at the temperature of 300 to 600 DEG C, and finally crushed. The invention is simple and has the advantages of low energy consumption and high safety; the load of the adsorbing material prepared is uniform and has good dispersibility, strong adsorbability and remarkable photo-catalyzed degradation property.

The invention relates to a high-strength and high-conductivity dispersion-strengthened alloy, which comprises a copper base, a ceramic dispersion-strengthening phase and a doping element, wherein the ceramic dispersion-strengthening phase may be one or several of ZrO2, Y2O3, MgO, Al2O3 and TiB2 which accounts for 0.1 to 2 mass percent of the copper alloy; and the doping element may be one or several of Ni, Y, Ag, Ti, Zr and Hf which accounts for 0.1 to 1 percent of the copper alloy. In the invention, the problems of ceramic particle agglomeration caused by low bonding performance of the copper and ceramic interface, the roughening of the ceramic particles in sintering and material conductivity reduction caused by the scattering of electrons at the copper and ceramic interface are solved, and the dispersion-strengthened alloy with higher hardness and higher conductivity is obtained. The invention also relates to a preparation method of the high-strength and high-conductivity dispersion-strengthened alloy.

The invention discloses an all-solid polymer electrolyte, and a preparation method and an application of the all-solid polymer electrolyte, and belongs to the field of lithium ion batteries. The all-solid polymer electrolyte comprises polyethylene oxide, lithium salt, inorganic nano particles and ion liquid, wherein a mass ratio of the lithium salt to polyethylene oxide is 0.1-0.5; the mass sum of the inorganic nano particles and the ion liquid is 10-30% of the mass of the all-solid polymer electrolyte; the lithium salt comprises one or several of bistrifluoromethane sulfonimide lithium salt, lithium tetrafluoroborate, lithium perchlorate, lithium hexafluorophosphate, lithium hexafluoroarsenate, lithium trifluoromethanesulfonate and lithium bis borate; and the inorganic nano particles comprise one or several of nano aluminum oxide, nano silicon oxide, nano zirconium oxide and nano barium titanate. The all-solid polymer electrolyte has better mechanical strength and higher ion conductivity. The method is simple in technology and low in cost; and raw materials are easy to obtain.

The invention belongs to the field of lithium batteries, and relates to an inorganic/organic composite porous lithium battery diaphragm and a preparation method thereof. The inorganic/organic composite porous lithium battery diaphragm comprises a base material layer and an inorganic/organic composite porous diaphragm layer arranged on the surface of the base material layer, wherein the base material layer adopts polypropylene non-woven fabrics; the inorganic/organic composite porous diaphragm layer adopts a polyvinylidene fluoride- hexafluoropropylene multipolymer containing inorganic nano grains and hydrophilizing agents; and the inorganic nano grains are silicon dioxide nano grains or coupling agent improved silicon dioxide nano grains. The inorganic/organic composite porous lithium battery diaphragm provided by the invention has the advantages that the production cost of the lithium battery diaphragm is lowered while high ion-conductivity, excellent electrochemical performance, high mechanical strength and low thermal shrinking percentage are ensured.

The invention discloses a three-layer composite wave-absorbing film and a preparation method thereof. The three-layer composite wave-absorbing film consists of an impedance matching layer, an absorption layer and a reflection layer, wherein the impedance matching layer consists of a dielectric material and an organic carrier; the absorption layer consists of magnetic particles and the organic carrier; the reflection layer consists of a carbon material with better electro-conductivity and the organic carrier; the thickness of the impedance matching layer is 0.1 to 0.3 millimetre (mm); the thickness of the absorption layer is 0.2 to 0.4 mm; and the thickness of the reflection layer is 0.1 to 0.3 mm. The preparation method of the three-layer composite wave-absorbing film comprises the following steps of: firstly, processing organic particles; secondly, uniformly dispersing the organic particles in an organic phase in a certain mode, and spreading to form a film; and finally, after a solvent of a first layer is completely volatilized, spreading a second layer and a third layer to form the three-layer composite wave-absorbing film. The three-layer composite wave-absorbing film has the advantages of high efficiency, light weight and low thickness, can be applied to electromagnetic shielding materials, and has a wide application prospect in ultra-thin radar wave-absorbing materials.

The invention discloses a biomass-based grading porous carbon and a preparation method thereof. The method comprises the following steps of shearing and sieving the biomass raw materials to 20 to 80 meshes; adding the materials into a double-salt system water solution; performing stirring; performing low-temperature hydro-thermal method pre-carbonization treatment for 5 to 20h at 180 to 300 DEG C;performing washing and filtering to obtain a pre-carbonization product; then raising the temperature to 600 to 1000 DEG C in inert atmosphere; performing carbonization activation treatment for 0.5 to8h; performing acid washing, alkali washing or ultrasonic treatment on the obtained product; then washing the materials by water to the neutral state; performing drying to obtain the biomass-based grading porous carbon. The hydrothermal carbonization is performed during the pre-carbonization; the double-salt system is used as a salt template and a pre-hole-forming agent; the adverse conditions are provided for the subsequent carbonization activation for preparing the porous carbon; the obtained porous carbon has high specific surface area and the loose three-dimensional connection pore passage structures; high electrical conductivity and good capacitive characters are realized; the biomass-based grading porous carbon can be applied to supercapacitors as carbon electrodes.

The invention relates to an aluminium ion battery and a preparation method thereof and belongs to the field of aluminium ion batteries and preparation thereof. The aluminium ion battery comprises a positive electrode, a negative electrode and an aluminium ion electrolyte, wherein the positive electrode is made of transition metal oxide; the negative electrode is made of high purity aluminium; the battery comprises a diaphragm material when the aluminium ion electrolyte is in a liquid state. Since abundant aluminium elements are stored, the cost for the ion battery is greatly reduced; the safety performance is improved; the transition metal oxide is applicable to hypervalent ion batteries due to relative stability under the variable valence states and different valence states. The ion liquid serves as the electrolyte for the hypervalent ion battery, so that aluminium ion is high in conductivity, good in heat stability, broad in electrochemical window and high in chemical stability and almost incapable of reacting with the positive electrode materials, the negative electrode materials, a current collector, a binder and a diaphragm in a battery system and capable of maintaining the liquid state in a board temperature range. The aluminium ion battery can be applied to various fields, such as electronic industries, communication industries and electric vehicles and the like.

The invention relates to a method for preparing a nano-sulfur / graphene oxide composite material with high specific capacity and belongs to the field of cross application of material synthesis and electrochemical power supplies. The nano-sulfur / graphene oxide composite material is applicable to an electrode material of a lithium sulfur secondary battery with the high specific capacity. The method is characterized by comprising the following steps of: synthesizing nano-sulfur particles by using a simple chemical method under the protection of a surfactant; and uniformly attracting graphene oxide and a carbon material to the surfaces of the nano-sulfur particles by interaction of the surfactant and the graphene oxide to form a core-shell type nano-sulfur / graphene oxide composite material. The graphene oxide and the carbon material coat a sulfur surface, so a sulfur electrode material is stable in structure, high in electric conductivity and high in cycle performance. Environmentally-harmful materials are not employed, and the method can be implemented at low temperature, and is low in energy consumption in the synthesis process and low in equipment requirement. The synthesized material is high in charging/discharging capacity, non-toxic and harmless to a human body, and sulfur is abundant in nature, so the material has a good industrial prospect and can be applied to large-scale industrial production.

An electrode material of Fe¿CLi phosphate and its composite metal phosphate is electrode material of LiFePO4 and LiFePO4 / MxP in high density spherical shape with diameter of 2micro m. The electrode material of LiFePO4 and LiFePO4 / MxP can be prepared by low ¿C temperature controllable one ¿C stage atomizing process in short flow.

The invention discloses a method for flow-electrode capacitive deionization (FCDI)-based desalination and application. According to the method, a direct current voltage stabilization power supply, a flow electrode, a dual-channel peristaltic pump, an FCDI module unit, a small-size peristaltic pump, a conductivity meter, an organic glass fixing device, a stainless steel interface and an electrode connection splice are involved; one end of each of two pump pipes of the dual-channel peristaltic pump is arranged in each of anode chamber flow electrode liquid and cathode chamber flow electrode liquid, and the other end of the pump pipe is connected with the stainless steel interface in the lower part of the organic glass fixing device; the flow electrode enters the FCDI unit module through the stainless steel interface through pressure provided by the dual-channel peristaltic pump; incoming water is pumped into the FDCI unit module with a prepared sodium chloride solution with different concentration at certain flow speed through the small-size peristaltic pump; the conductivity meter is used for measuring the conductivity concentration of discharged water. A reaction device used in the method is simple in structure, low in operation cost and easy to operate, and no chemicals is fed; automatic control and on-line monitoring are easy to implement; the method is low in energy consumption, and the preparation cost of the electrode is lowered; the method can be applied to the technical field of environmental engineering and water treatment.

Belonging to the technical field of chemical material preparation, the invention relates to a preparation method of a Co3O4/graphene nanocomposite material. The method provided in the invention is characterized by: first employing a simple chemical method to synthesize Co3O4 nanoparticles under the protection of a surfactant, then adsorbing oxidized graphene on surfaces of the Co3O4 nanoparticles uniformly by means of the interaction between the surfactant and the oxidized graphene, and reducing the oxidized graphene, thus forming the uniform Co3O4/graphene nanocomposite material. Good electrical conductivity is achieved among Co3O4 nanoparticles through graphene, so that the electroconductibility of the composite material can be improved. The Co3O4 nanoparticles in the composite material have a size of 50-100 nanometers, and account for 60%-95% by weight. The method provided in the invention does not involve environmentally harmful materials, and the process is simple, practicable and easy to operate. The prepared Co3O4/graphene nanocomposite material has high specific capacity and capacitance, as well as good cycle performance, thus having good application prospects in the fields of lithium ion batteries and supercapacitors.

A light emitting device 100 of the invention is the one using a first main surface of a compound semiconductor layer portion, having a light emitting layer section 24 therein, as a light extraction surface, and having, on the second main surface side of the compound semiconductor layer, a device-substrate 7 bonded thereto while placing, in between, a main metal layer 10 having a reflective surface reflecting light from the light emitting layer section 24 towards the light extraction surface side, and is characterized in that the device-substrate 7 is composed of a Si substrate having a conductivity type of p type, and that the device-substrate 7 has, as being formed on the main surface thereof on the main metal layer 10 side, a contact layer 31 having Al as a major component. With respect to light emitting devices configured as having a structure in which a light emitting layer section and a device-substrate are bonded while placing a metal layer in between, the invention is successful in providing a light emitting device having a desirable electro-conductivity, and a method of fabricating the same.

A cathode active material for a metal-sulfur battery is provided. By using a cathode active material for a metal-sulfur battery comprising a sulfur-carbon composite composed of composited spherical sulfur compound particle and carbon material particle, electric conductivity of the cathode for a lithium-sulfur battery is increased to improve initial capacity close to theoretical capacity and polysulfide lost in the cathode during charging and discharging is minimized to increase sulfur utilization. Reaction between a metal anode and the polysulfide is minimized to increase life span and stability of the metal-sulfur battery.