56results about How to "Improve discharge capacity" patented technology

The invention discloses a graphite negative electrode material and a preparation method thereof. The invention provides a carbon nano tube / silicon carbide composite material which comprises silicon carbide particles and carbon nano tubes, and the carbon nano tubes are coated on the silicon carbide particles. According to the carbon nano tube / silicon carbide composite material and the carbon nano tube / silicon carbide-graphite matrix composite material disclosed by the invention, a graphite negative electrode material with a stable overall structure and high capacity is obtained by adopting a new coating mode and a new coating process, and the graphite negative electrode material can be used for an artificial graphite negative electrode.

The invention discloses a modified MOFs filler, a preparation method and a composite solid electrolyte of a lithium ion battery, and the preparation method of the modified MOFs filler comprises the following steps: adding cerium salt during preparation of an MOF material to obtain a cerium-doped MOF material; or after the MOF material is prepared, the MOF material is etched, and the etched MOF material is obtained. The preparation method of the composite solid electrolyte comprises the following steps: dispersing the prepared MOF material in a solvent under the protection of inert gas, adding an electrolyte lithium salt and PEO, stirring to obtain a colloidal suspension, pouring the colloidal suspension into a mold, and drying and molding. After the obtained modified MOFs filler is added into the composite solid electrolyte, the conductivity of the composite solid electrolyte can be effectively improved, the composite solid electrolyte has a wide electrochemical stability window, and an assembled lithium ion battery shows excellent electrochemical performance.

The invention provides a metal particle doped self-supporting carbon-based material as well as a preparation method and application thereof. The metal particles comprise metal elementary substance particles, and in the self-supporting carbon-based material doped with the metal particles, the loading capacity of the metal elementary substance particles is 15-55 wt%; the preparation method comprises the following steps: firstly, mixing a polymer, metal salt and a solvent, and preparing a carbon-based material precursor through electrostatic spinning; then sequentially carrying out pre-oxidation and calcination on the carbon-based material precursor; wherein the types of metal salts and the conditions of pre-oxidation and calcination are defined. According to the preparation method, by limiting the gas components in the calcination process and the temperature and time ranges in the pre-oxidation and calcination processes, the loading capacity of the metal elementary substance particles is remarkably improved, the precursor is fully carbonized to form the carbon fibers, and the prepared self-supporting carbon-based material is good in discharge capacity and cycle performance.

The invention belongs to the technical field of sodium ion batteries, and relates to a positive electrode sodium supplementing agent NaxFeyNizO4 (at) C, a preparation method thereof and an application of the positive electrode sodium supplementing agent NaxFeyNizO4 (at) C in a sodium ion battery. The preparation method of the positive electrode sodium supplementing agent comprises the following steps: S1, mixing a sodium source, an iron source, a nickel source and an organic solvent, and calcining to obtain a compound NFNC; and S2, the compound NFNC obtained in the step S1 and a carbon source are mixed and calcined to obtain the positive sodium supplement NaxFeyNizO4 (at) C, and x: y: z = (2-4): (0.5-2): 1. The preparation method is characterized in that a sodium source, an iron source, a nickel source and an organic solvent are mixed and then subjected to first calcination treatment to obtain a compound NFNC, and then the compound NFNC and a carbon source are mixed and then subjected to second calcination treatment, so that the obtained positive electrode sodium supplementing agent NaxFeyNizO4 (at) C can reduce gas production of a sodium ion battery after a formation stage; and the sodium ion battery has excellent discharge capacity and cycle performance in a working voltage range.

The invention relates to a preparation method and application of an organic coating material, in particular to a preparation method and application of a thiolated 3-chloropropanesulfonyl (trifluoromethanesulfonyl) lithium imide-triallyl phosphite organic coating material. In order to solve the problem of high reactivity of SC-NCM, a novel organic coating material, namely thiolated 3-chloropropanesulfonyl (trifluoromethanesulfonyl) lithium imide-triallyl phosphate (SH-LiCPSI-TLP), is provided by combining the influence of the type of the coating material and the form of a coating layer on the performance of the positive electrode material; as the Young modulus of an organic material is generally lower than that of an inorganic material, a uniform coating layer can be formed on the surface of the positive electrode material by adopting a simple wet coating method. An electrochemical test shows that after SH-LiCPSI-TLP is coated, the capacity diving phenomenon of the SC-NCM811 can be effectively inhibited, and under the 1C multiplying power, the capacity retention ratio is still 52.78% even if the SH-LiCPSI-TLP is circulated for 600 circles.

According to the SCR device, the process method and the chip, compared with a traditional LVTSCR device, the trigger voltage of the SCR device is lower, the maintaining voltage is higher, the deep hysteresis phenomenon can be avoided, the application scene of the SCR device is expanded, and the SCR device can be applied to a high-working-voltage port. In addition, the SCR device can also form a plurality of ESD current discharge paths, so that the ESD current discharge capacity of the chip in unit area is higher, the SCR device has the characteristic of low on-resistance, the area of the chip is effectively saved, and the production cost of the chip is reduced; in addition, the distribution of the ESD current in the SCR device is more uniform due to the plurality of ESD current discharge paths, and the discharge path robustness of the SCR device under large current is effectively improved.

The application relates to the technical field of sodium ion battery positive electrode materials, in particular to a Na2Fe2(SO4)3@Na3Fe2(SO4)3F@CNT positive electrode material.The Na2Fe2(SO4)3 and Na3Fe2(SO4)3F precursors are mixed and sintered, and are coated by CNT, so that the electrochemical performance of the Na2Fe2(SO4)3 is remarkably improved, the conductivity of the material is improved, the material can be used as a sodium ion battery positive electrode material, has a high discharge specific capacity, and has cycle performance and rate performance.

The invention belongs to the technical field of lithium ion battery positive electrode materials, and particularly discloses a composite positive electrode material of a solid electrolyte epitaxial coating, which comprises an inner-layer positive electrode active material and an epitaxial layer coated outside the inner-layer positive electrode active material, the inner-layer positive electrode active material is a configuration entropy ultrahigh nickel positive electrode material, and the general formula of the configuration entropy ultrahigh nickel positive electrode material is LiNi < x > Co < y > M < 1-x-y > O < 2 >. The disorder degree and inherent strain of the positive electrode material can be relieved through the chloride solid electrolyte epitaxial coating, the consistency and interface compatibility between an electrode and an electrolyte are enhanced, the electrochemical performance of the configuration entropy ultrahigh nickel positive electrode material LiNi < x > Co < y > Mn < 1-x-y > O < 2 > is improved, and therefore the composite positive electrode material with high stability and long service life is constructed.

The invention provides a porous hollow carbon sphere composite material, a preparation method thereof and a sodium ion battery, and belongs to the technical field of sodium ion batteries. The composite material is mesoporous hollow carbon nanospheres co-doped with nitrogen element, phosphorus element and sulfur element. According to the composite material, mesoporous hollow nano carbon spheres capable of providing negative electrode capacity are designed, and a hollow nano structure is used for providing a space for electrode volume expansion after circulation, so that the discharge capacity and the circulation stability in a sodium ion battery are improved; meanwhile, due to the mesoporous structure on the surface of the mesoporous hollow carbon nanosphere, the diffusion path of sodium ions is greatly shortened, and the separation and embedding of the sodium ions are promoted, so that the specific capacity of the negative electrode material is improved; in addition, by utilizing the synergistic effect of nitrogen, phosphorus and sulfur co-doping, the carbon layer spacing of the mesoporous hollow carbon nanospheres can be obviously enlarged, the active sites can be increased, and the rate capability and the cycling stability can be optimized.

The invention discloses a lithium carbon fluoride battery electrolyte, a preparation method thereof and a lithium carbon fluoride battery, and belongs to the technical field of lithium / carbon fluoride primary batteries. The lithium carbon fluoride battery electrolyte comprises a lithium salt and a monofluoro-substituted short-chain ether solvent. Compared with a non-fluorinated ether solvent, the monofluoroether solvent has good compatibility with a carbon fluoride positive electrode and a metal lithium negative electrode, so that the battery has good discharge performance. Compared with a polyfluoro-substituted ether solvent, the monofluoro substituent group (-CH2F) obviously improves the ionic conductivity of the lithium carbon fluoride battery electrolyte at low temperature, and meanwhile, the monofluoro substituent group (-CH2F) has weak solvation energy at low temperature, so that the discharge platform of the battery at low temperature is obviously improved, and the discharge capacity of the battery is improved.

Provided are a secondary battery and an electronic device, the secondary battery comprising: a housing comprising a shell and a cover plate, one end of the shell forming an opening, the cover plate covering the opening and being connected to the shell, the cover plate being provided with an explosion-proof valve; the electrode assembly is accommodated in the shell, and the electrode assembly comprises a tab facing the cover plate; the current collecting component is in welded connection with the tabs; the flow collecting component is provided with an annular first weak part and a plurality of second weak parts, the projection of the anti-explosion valve in the axial direction of the flow collecting component is located in an area surrounded by the first weak part, the second weak parts are arranged around the center of the flow collecting component, and each second weak part longitudinally extends in the radial direction of the flow collecting component. The annular first weak part surrounds the second weak parts, and the strength of the second weak parts is larger than that of the annular first weak part. According to the technical scheme, at least the central area of the current collecting component can be effectively opened during pressure relief, and the pressure is sprayed out along with the anti-explosion valve, so that the safety performance of the battery is improved.

An object of the present application is to provide a battery active material capable of maintaining good initial coulombic efficiency and cycle characteristics and increasing discharge capacity to, for example, 800 mAh / g or more, a battery composite active material containing the battery active material, and a secondary battery containing these materials in a negative electrode. The battery active material of the present application is an amorphous silicon-based material composed of elements including Si, O, and C, and has a solid solution structure in which Si, O, and C are mixed at the atomic level. The battery active material of the present application is characterized by having a specific surface area of 0.1 m2 / g or more and less than 20 m2 / g, a pore volume of 0.01 cm3 / g or more and less than 0.5 cm3 / g, and a pore diameter of 2 nm or more and less than 20 nm. 29 The ratio (A / B) of the total value A of the integral values of the respective peaks attributed to SiO2C2 and SiO3C to the integral value B of the peak attributed to SiO4 in the range of chemical shifts 20 ppm to -150 ppm of the Si-NMR spectrum is 0.5 or more and 5.0 or less.

The invention discloses a modified acrylate polymer as well as a preparation method and application thereof, and belongs to the technical field of lithium ion battery materials. The modified acrylate polymer provided by the invention is simple in preparation method, easy to synthesize, high in reaction product yield, low in preparation cost and excellent in environmental protection performance, a lithium ion battery diaphragm coating prepared from the modified acrylate polymer provided by the invention has good electrolyte infiltration performance, the internal resistance of a battery can be reduced, and the service life of the battery is prolonged. The rate capability and the discharge capacity of the battery are improved; meanwhile, the high-temperature-resistant performance is good, and the safety and the reliability of the battery in a high-temperature environment or when the battery is overheated can be improved.

In one embodiment of the present invention, the porous carbon particles used in the positive electrode of an air battery for forming a porous carbon film satisfy all of the following a) to g): a) The full width at half maximum (FWHM) of the D band peak in the Raman spectrum is 30 cm. ‑1 Above and 60cm ‑1 Below; b) The full width at half maximum (FWHM) of the G-band peak in the Raman spectrum is 32 cm. ‑1 Above and 80cm ‑1 The following are examples: c) The ratio of the intensity of the D band peak to the intensity of the G band peak in the Raman spectrum, i.e., an R value of 0.8 or higher; d) The surface spacing of the (002) plane of carbon based on X-ray diffraction (XRD) is d 002 e) The portion with a diameter greater than 0.336 nm and less than 0.355 nm; e) The volume of pores with a diameter greater than 1 nm and less than 1000 nm, determined by the BJH method from the adsorption isotherm obtained by nitrogen adsorption, is 1.5 cm³. 3 / g or more and 10.0cm 3 / g or less; f) The volume of pores with a diameter of 1 nm or more and less than 100 nm, determined by the BJH method from the adsorption isotherm obtained by nitrogen adsorption, is 1.0 cm³. 3 / g or more and 8.0cm 3 / g or less; g) The specific surface area obtained by the BET method from the adsorption isotherm obtained by nitrogen adsorption is 500 cm². 2 / g or more and 2000cm 2 / g or less.

The application discloses modified tricobalt tetraoxide and a preparation method and application thereof, and belongs to the technical field of battery materials. The modified tricobalt tetraoxide is doped with rare earth elements and aluminum simultaneously; the total doping amount of the rare earth elements is not more than 0.5% in terms of mass percentage; and the doping amount of the aluminum is not more than 1.2%. The modified tricobalt tetraoxide has a relatively compact structure and high mechanical strength, is not easy to be broken during calcination, and has no surface floating powder phenomenon, so that the electrochemical performance of downstream product lithium cobaltate positive electrode material is improved.

This application provides a battery pack reconfiguration method, electronic device, storage medium, and program product. The method includes: acquiring battery pack-level data for each battery cluster in a target energy storage system, including the capacity retention rate and state of charge of the cells; calculating the capacity retention rate of each battery pack in the target energy storage system based on the "weakest link" principle; exchanging and reconfiguring the batteries in the target energy storage system to obtain the change in capacity retention rate of the target energy storage system after the exchange and reconfiguration; and determining the corresponding battery pack reconfiguration scheme for the target energy storage system based on the change in capacity retention rate. This method aims to fully utilize the energy storage capacity of existing batteries in the energy storage system without adding additional energy storage units, reducing the bottleneck effect, increasing the overall discharge capacity of the system, and improving the profitability of the power station. By exchanging and reconfiguring the batteries in the energy storage system, the difference in capacity retention rate is reduced, and the capacity retention rate of each level of the energy storage system is balanced.

The invention discloses a solid electrolyte, a solid-state battery and a preparation method and application thereof, and belongs to the technical field of solid-state batteries. The chemical formula of the solid electrolyte provided by the invention is Li < 2 + x > In < 2-x > / 3Cl4, and x is greater than or equal to 0 and less than or equal to 2. The ionic conductivity and the electrochemical performance of the solid electrolyte are improved mainly by optimizing the sintering temperature and the sintering time. According to the method, the transmission path of lithium ions in the solid electrolyte can be shortened, the energy density of the solid-state lithium ion battery is remarkably improved, and meanwhile, the solid-state lithium ion battery has relatively good cycling stability.

The present disclosure relates to a negative electrode and a method of manufacturing the same. The negative electrode includes a silicon-based negative electrode active material and a carbon-based negative electrode active material to have excellent charge / discharge capacity and energy density, and to have excellent fast charging performance and lifespan characteristics because the carbon-based negative electrode active material included in each negative electrode active layer is oriented to have a predetermined inclination with respect to a negative electrode current collector.

The present disclosure provides a coated ternary anode material, a preparation method therefor, and a lithium ion battery. The coated ternary anode material comprises an aluminum, zirconium, and fluorine co-doped ternary anode active material core and a coating layer coated on the surface of the core, the coating layer comprising zirconium hydrogen phosphate and a boron compound. The coated ternary anode material effectively solves the gas production problem and improves the safety performance. At the same time, the material has high discharge capacity, a high first effect, good cycle stability, and a good safety performance.

The invention provides a solid-state battery composite pole piece, a preparation method thereof and an all-solid-state battery. The preparation method comprises the steps that a pole piece and an electrolyte membrane are provided, the pole piece comprises a current collector and an active material layer attached to the current collector, the active material layer comprises a first binding agent, the electrolyte membrane comprises an electrolyte membrane, the electrolyte membrane comprises a second binding agent, the first binding agent and the second binding agent are thermal response type binding agents, and the first binding agent and the second binding agent are thermal response type binding agents; the pole piece and the electrolyte membrane are subjected to rolling compounding to form the solid-state battery composite pole piece, the pole piece and the electrolyte membrane are heated through infrared radiation before rolling compounding, so that the surface of the active substance layer and the surface of the electrolyte membrane are softened, and then the binding force between the pole piece and the electrolyte membrane is remarkably improved through rolling compounding; and the two are combined more tightly, so that the discharge capacity of the battery under high rate can be improved, the structural stability of the solid-state battery composite pole piece is improved, the cycle life of the battery is prolonged, and the safety of the battery is improved.

The utility model discloses a secondary battery, a battery pack and an energy storage cabinet, the secondary battery comprises a shell, a top cover and a naked battery cell, the naked battery cell is located in a containing cavity of the shell, the top cover covers an opening of the containing cavity, the naked battery cell comprises a plurality of stacked pole pieces, and the naked battery cell further comprises a bending area and a straight area. Each pole piece is provided with a first surface and a second surface along a first direction x, the first surface is provided with a first coating and a third coating, the second surface is provided with a second coating and a fourth coating, the first coating and the third coating as well as the second coating and the fourth coating are alternately distributed along a second direction y, and projections of the first coating and the second coating along the first direction x are at least partially overlapped. In the first direction x, the thickness of the first coating is larger than that of the third coating, and the thickness of the second coating is larger than that of the fourth coating; in the second direction y, the width of the first coating is smaller than that of the second coating and / or the width of the first coating and the width of the second coating are gradually increased; the first coating and the second coating are located in the bending area.

The invention discloses a method for preparing a hard carbon negative electrode material rich in micro-sodium pore structures by using a biological fermentation method and application, and relates to the technical field of sodium ion battery negative electrode materials. The microbial flora is added into the viscous pasty material, hyphae generated by fermentation of the microbial flora can effectively enter structural gaps of hard carbon, rich and uniform pores can be reserved after calcination, and it can be ensured that the hard carbon material rapidly achieves efficient transmission of ions and electrons. In addition, a double-layer carbon-coated hard carbon material formed by a calcination coating process is coated with pore inner-layer carbon and hard carbon outer-layer carbon. Wherein the porous carbon coating structure can ensure that the hard carbon material can quickly and efficiently realize high-efficiency transmission of ions and electrons, and the conductivity and the cycling stability of the material are greatly improved; the outer carbon-coated structure can improve the overall conductivity of the material, protect the structural integrity of the material, and prevent structural damage caused by volume expansion or shrinkage, thereby improving the cycling stability of the material.

The invention discloses a lithium-rich manganese-based positive electrode material compositely coated with an alpha-ZrP-conducting polymer, a preparation method of the lithium-rich manganese-based positive electrode material and application of a solid-state battery. According to the material, a bulk phase modified lithium-rich manganese-based material is used as a core, and a composite coating layer composed of a delaminated alpha-ZrP nanosheet and a conductive polymer is constructed on the surface of the lithium-rich manganese-based material. The composite coating layer can realize internal proton self-exchange response with the conductive polymer based on the solid acid characteristic of alpha-ZrP, and an overpass type rapid ion-electron dual-transmission channel is formed in the material body. Meanwhile, the coating layer is used as a compact physical and chemical barrier, and harmful side reactions between the positive electrode and the solid electrolyte are effectively blocked. When the prepared positive electrode material is applied to a solid-state battery, high first-circle coulombic efficiency and excellent cycling stability and rate capability are shown, and the two core problems of unstable interface and slow dynamics of a lithium-rich manganese-based material in the solid-state battery are effectively solved.

The application provides a preparation method of a thermal battery positive electrode active material, an antimony sulfide / carbon composite material, a positive electrode sheet and a thermal battery. The thermal battery positive electrode active material comprises antimony sulfide. The application adopts antimony sulfide (Sb2S3) as the positive electrode active material, and the antimony sulfide has excellent thermal stability and better high-voltage platform stability.

The application belongs to the technical field of lead-acid batteries, and particularly relates to a positive active plate of a flooded traction lead-acid battery and a manufacturing method thereof. The positive active plate of the flooded traction lead-acid battery comprises a positive grid with a plate lug, positive lead paste and a polyester heat-shrink bag. The positive grid is provided with horizontal ribs and vertical ribs. The positive lead paste is thickly coated in the positive grid. The polyester heat-shrink bag is wrapped outside the positive grid and the positive lead paste to bind the positive lead paste to the positive grid. The positive active plate of the flooded traction lead-acid battery avoids the falling of the lead paste by means of the over-coating of the lead paste and the wrapping of the polyester heat-shrink bag, improves the service life of the positive active plate, improves the working environment and reduces the investment cost of the production equipment. The application also provides a manufacturing method of the positive active plate of the flooded traction lead-acid battery, which is simple and easy to implement.

The invention belongs to the field of design and manufacturing of semiconductors / integrated circuits, and particularly relates to a manufacturing method of a one-step adjustable bidirectional large-through-flow TVS (Transient Voltage Suppressor) device. A doped silicon substrate with specific crystal orientation and resistivity is selected, an epitaxial layer is generated, then an oxide layer is formed through thermal oxidation or chemical vapor deposition, a groove is formed through photoetching and etching, and doped polycrystalline silicon is filled and sealed. And then etching to remove surface doped silicon, performing high-temperature diffusion and junction pushing, depositing an oxide layer, forming a through hole, filling conductive metal, depositing metal, etching to form an electrode, and performing related operation of a back electrode on a specific TVS (Transient Voltage Suppressor). The required groove type device structure is formed in one step, the chip area can be reduced by more than 30% compared with a plane structure, meanwhile, the PN junction structure formed in one step can meet the requirement for consistent symmetry of breakdown voltage, the clamping voltage Vc can be accurately controlled, and meanwhile the surge current absorption capacity of the TVS can be improved.

The object of the present invention is to provide a thermal power generation battery with excellent battery characteristics. The above problem can be solved by a thermal power generation element that does not require a temperature gradient, wherein a first part comprising a semiconductor which produce thermally excited electron and hole, a second part comprising an electrolyte in which an charge transport ion pair can be moved therein, and a third part comprising a substance that is an electrode, are in contact with each other in this order, and wherein a valance band potential of the semiconductor of the first part is positive with respect to a redox potential of a charge transport ion pair; and an ion which is more susceptible to oxidation among the two ions is oxidized at an interface between the first part and the second part; and an ion which is more susceptible to reduction among the two ions is reduced at an interface between the third part and the second part; and wherein the thermal power generation element satisfies the following formula (I): L / IDT=1−20 wherein L is a "shortest distance between the first part and the third part", and IDT is "ion diffusion thickness."

The application relates to a preparation method of a lithium battery diaphragm and belongs to the technical field of lithium battery preparation. The method is as follows: epoxy resin, a diluent, a curing agent 1 and an oleophilic emulsifier are uniformly mixed to obtain dispersion liquid 1; an electrolyte solution is constantly dropped into the dispersion liquid 1, constant-temperature high-speed stirring is carried out, and a water-in-oil emulsion is obtained; under constant temperature, deionized water, a hydrophilic emulsifier and a curing agent 2 are uniformly mixed to obtain dispersion liquid 2; the water-in-oil emulsion is added into the dispersion liquid 2, high-speed emulsification is carried out, and a water-in-oil-in-water emulsion system is obtained; the water-in-oil-in-water emulsion system is subjected to temperature rising and curing; after curing, centrifugal separation, washing and drying are carried out, and a solid nanometer adhesive is obtained; the solid nanometer adhesive is ground, then is uniformly coated in a mold and is subjected to high-temperature treatment, and the lithium battery diaphragm is obtained. The electrolyte solution is selected as the inner water phase of the water-in-oil emulsion, the internal osmotic pressure of the emulsion can be increased, fusion between the emulsions can be prevented, and the particle size is increased.

The invention discloses a preparation method of artificial graphite, which comprises the following steps: uniformly mixing boric acid, water and anthracite, dipping, drying, uniformly mixing with a binder and nickel-plated carbon nanotubes, granulating, carbonizing, graphitizing, crushing and shaping to obtain the artificial graphite. The method is low in cost, low in energy consumption and high in graphitization degree, and the lithium ion battery prepared from the artificial graphite has good cycle performance.

This invention provides a lightning protection device for medium-wave transmitters, belonging to the technical field of medium-wave transmitters. It includes a cabinet structure with a vertically mounted grounding mechanism on the bottom surface. A lightning rod is installed at the top of the support, serving as the first line of lightning protection. A complete intelligent grounding system is constructed, with humidity detectors evenly distributed at multiple depths in the soil layer to monitor humidity changes at different depths in real time. When a decrease in soil moisture and an increase in grounding resistance are detected, maintenance personnel can inject water into the water storage box through the water injection pipe. The water seeps evenly into the soil layer through the injection holes, effectively reducing the grounding resistance and ensuring excellent lightning protection grounding performance even in dry seasons or arid regions. Multiple grounding rods are arranged in parallel, increasing the contact area with the soil and further improving the discharge capacity. This design fundamentally solves the technical problems of traditional grounding devices being greatly affected by soil moisture and having unstable grounding effects.