32148results about "Cell electrodes" patented technology

The invention relates to a method for preparing a lithium iron phosphate / carbon composite material of a lithium ion battery, which belongs to the technical field of lithium ion batteries. The method for preparing the lithium iron phosphate / carbon composite material of the lithium ion battery comprises the following steps of: 1) preparing a suspending graphene-dispersed aqueous solution system, namely, crushing graphite to 1 to 5 microns, adding the crushed graphite into distilled water or purified water, adding 0.1 to 5 percent of surfactant, heating with stirring the mixed solution to 180 to 250 DEG C in a sealing way, performing stirring for 2 to 6 hours and reducing the temperature; 2) crushing lithium iron phosphate to the particle size of 1 to 5 microns, adding the crushed lithium iron phosphate into the distilled water or the purified water, adding with stirring 0.01 to 1 percent of coupling agent, performing uniform stirring, adding the graphene-dispersed aqueous solution, and performing stirring and filtration; and 3) vacuum-drying solid powder obtained by the filtration, and calcinating the dried solid powder for 2 to 12 hours to obtain the graphene-coated lithium iron phosphate cathode material. The method has the advantages of simple process, high material performance, high conductivity, high bulk density, high compacted density and the like.

Systems, methods, and articles for a portable power case are disclosed. The portable power case is comprised of at least one battery and at least one PCB. The portable power case has at least one USB port and at least two access ports, at least two leads, or at least one access port and at least one lead. The portable power case is operable to supply power to an amplifier, a radio, a wearable battery, a mobile phone, and a tablet. The portable power case is operable to be charged using solar panels, vehicle batteries, AC adapters, non-rechargeable batteries, and generators. The portable power case provides for modularity that allows the user to disassemble and selectively remove the batteries installed within the portable power case housing.

Improved performance ion exchange membranes for use in REM, AEM and DMFC fuel cells, buffered fuel cells, hydrolysis, other applications comprise a molecular matrix of homopolymers, di-monomer, heteropolymers, copolymers, or block-polymers of fluorocarbon and hydrocarbon compounds combined with (i) skeletal support grid to improve durability, handling, reduce membrane swelling, and sequester dopants and nanoparticles from leakage; (ii) microporous membrane formed using a sacrificial filler process enhancing conductivity and limiting fuel crossover; (iii) hetero-ionomeric matrix of two-or-more membrane-bound acids e.g. sulphonic and phosphonic acid expanding usable range; (iv) permanent fillers enhancing conductivity and porosity including nanoparticles, metal-oxides, zeolites, silicates, GOs, CNTs, MOFs, POSS, and others; (v) ionic liquid doping to enhance membrane conductivity; (vi) membrane nanocoating preventing H2O2 diffusion; and / or (vii) catalytic nanocoating with metals, metal-oxides, and MOFs preventing atmospheric toxin catalyst poisoning. Combined with a heterogenous GDI, the IEM is integrated into iBFC power blade and energy bank applications.

The invention relates to the field of lithium battery negative electrode materials, and particularly discloses a silicon-carbon composite negative electrode material for a lithium ion battery and a preparation method of the silicon-carbon composite negative electrode material. The method comprises the following steps: preparing a porous carbon substrate, and depositing silicon nanoparticles in pores and on the surface of the porous carbon substrate by adopting a fluidized bed chemical vapor deposition process and taking silane as a silicon source to obtain a silicon-carbon core material; continuously carrying out carbon coating on the surface of the silicon-carbon core material in the fluidized bed by taking acetylene as a carbon source to form a carbon coating layer; and leading out the obtained material from the fluidized bed, taking acetylene as a carbon source, and carrying out carbon coating on the surface of the primary carbon coating layer again by adopting the rotary furnace to form a secondary carbon coating layer. According to the preparation method, a porous carbon matrix and double-layer functional carbon coating process is adopted, so that the volume expansion of silicon in the circulation process is remarkably inhibited, the interface side reaction is reduced, and the circulation stability of the material is effectively improved.

The invention relates to the technical field of lithium ion battery materials, in particular to a chemical liquid phase deposition silicon-carbon negative electrode material and a preparation method and application thereof.The silicon-carbon negative electrode material comprises a porous carbon skeleton and nanometer silicon particles deposited on the surface and in pore channels of the porous carbon skeleton; the carbon source coating layer is used for coating the porous carbon skeleton and the nano silicon particles. The interior of the composite structure of the silicon-carbon negative electrode material is nanometer silicon particles deposited on the surface and in pore channels of a porous carbon skeleton, and the outer layer is a coating layer; porous carbon is used as a continuous and stable carbon skeleton to effectively relieve volume expansion and particle fragmentation of the silicon-based material, and the outermost coating layer improves the structural stability and conductivity of the composite material, so that the electrochemical cycle stability is improved; according to the structure of the silicon-carbon negative electrode material, the advantages of an embedded structure and a shell-core structure are combined, a stable carbon skeleton is provided for the silicon-carbon negative electrode material, a limited expansion space is provided for silicon particles, crushing is prevented, and the cycling stability of the negative electrode material is greatly improved.

The invention provides a doped and coated composite sodium battery positive electrode material as well as a preparation method and application thereof. The doped and coated composite sodium battery positive electrode material comprises an inner core and a coating layer on the surface of the inner core, the chemical general formula of the inner core is NabNixFeyMnzMjO2, x + y + z + j = 1, 0.2 < = x < = 0.6, 0.2 < = y < = 0.5, 0.2 < = z < = 0.5, 0 < j < = 0.2, 0.8 < = b < = 1.2; the coating layer comprises a ferric sodium pyrophosphate material; raw materials for preparing the doped and coated composite sodium battery positive electrode material comprise an inner core, a phosphoric acid ferric sodium pyrophosphate precursor material and a sodium source. The metal elements are doped in the inner core, and the surface is coated with the ferric sodium pyrophosphate material with relatively high stability, so that the inner core can be prevented from being in direct contact with an electrolyte, and the cycle performance of the sodium battery positive electrode material is improved.

The invention provides a secondary battery and an electric device. Particularly, the lithium ion secondary battery comprises a positive electrode plate, the positive electrode plate comprises a positive electrode current collector and a positive electrode film layer arranged on the positive electrode current collector and comprising a positive electrode active material, the positive electrode active material comprises a lithium-containing transition metal oxide and a lithium-containing transition metal phosphate, and the lithium-containing transition metal oxide and the lithium-containing transition metal phosphate are arranged on the positive electrode current collector. The lithium-containing transition metal oxide comprises a nickel element, a cobalt element, a manganese element and / or an aluminum element, and a silicon element; the average mass concentration ratio of silicon elements in an external area corresponding to the position where the surfaces of the primary particles of the lithium-containing transition metal oxide extend to the center by 1 / 4 radius is larger than the average mass concentration ratio of silicon elements in a core area corresponding to the position where the centers of the primary particles extend to the surfaces by 1 / 4 radius, and the lithium-containing transition metal phosphate comprises iron elements. The lithium-containing transition metal phosphate comprises secondary particles formed by agglomeration of primary particles.

The invention discloses a composite polycrystalline positive electrode material which is prepared by permeating and coating a polycrystalline positive electrode material with an oxyhalide solid electrolyte, and the oxyhalide solid electrolyte comprises one or more of Li-Ta-O-Cl, Li-Nb-O-Cl, Li-Zr-O-Cl and Li-Al-O-Cl. The specific oxyhalide electrolyte is adopted to carry out permeation coating on the polycrystalline positive electrode material, uniform coating on the surface of the polycrystalline positive electrode material and grain boundaries in particles is completed, capacity utilization in the particles of the polycrystalline positive electrode material is achieved, and the capacity utilization rate of the particles of the polycrystalline positive electrode material is improved through the coating effect of the oxyhalide with high ionic conductivity. Ion transmission inside and in gaps of the polycrystalline positive electrode material particles is regulated, interface impedance is reduced, energy density is improved, and the application prospect is wide.

The invention provides a preparation method of a carbon-coated lithium iron manganese phosphate positive electrode material, and belongs to the technical field of battery positive electrode materials, and the preparation method comprises the following steps: co-precipitating a mixed solution of an iron source, a manganese source and a phosphorus source and a precipitant solution, and drying to obtain a manganese iron phosphate precursor; adding a lithium source, calcining in stages in an inert gas atmosphere, and grinding to obtain lithium manganese iron phosphate powder; the preparation method comprises the following steps: carrying out ball milling on lithium manganese iron phosphate powder and a fluxing agent, dispersing in a carbon source solution, uniformly wrapping a carbon source, drying, carrying out segmented calcination, and carrying out ball milling. The precursor nucleation coating uniformity is improved through segmented speed control reaction of a phosphorus source solution, a manganese source solution and an iron source solution; lithium source mixing and segmented calcination are adopted, and lithium volatilization is reduced; the modified nitrogen-doped porous carbon source is used for coating the lithium iron manganese phosphate powder to generate the lithium iron manganese phosphate positive electrode material, so that the conductivity of the lithium iron manganese phosphate positive electrode material is enhanced.

The invention provides a preparation method of a porous carbon-silicon composite negative electrode material of a lithium battery. The preparation method comprises the following steps: constructing a multi-stage template system; carrying out carbon precursor impregnation and gradient temperature carbonization on the multistage template system; removing the template to form a gradient porous carbon carrier; carrying out gradient temperature zone silane deposition; and plasma-assisted carbon coating and nitrogen doping are carried out. According to the method, a silicon dioxide sphere hard template is combined with cetyltrimethylammonium bromide and a block copolymer soft template to form a porous carbon carrier with a micropore-mesopore-macropore three-stage structure, and gradient distribution of silicon in porous carbon is realized by utilizing a three-temperature-zone fluidized bed reactor and a pulse type deposition technology, so that the silicon-based porous carbon composite material is obtained. The problem of volume expansion of the silicon material is effectively relieved and the material cycling stability is improved. The porous carbon-silicon composite negative electrode material prepared by the invention has high specific surface area, excellent ion transmission channel and good structural stability, and can be applied to a high-energy-density lithium ion battery.

Systems, methods, and articles for a wearable and lightweight portable power case are disclosed. The portable power case is comprised of a cylindrical housing, at least two battery elements connected to a printed circuit board (PCB), and at least one separating barrier between the at least two batteries and the PCB. The portable power case is operable to supply power to an amplifier, a radio, a wearable battery, a mobile phone, a tablet, a portable satellite dish and / or any other power consuming device. The portable power case is operable to be charged using solar panels, vehicle batteries, AC adapters, non-rechargeable batteries, and / or generators.

The invention provides a silicon-carbon negative electrode material and a preparation method thereof. The preparation method comprises the following steps: a) mixing a phenol monomer, an aldehyde solution, ammonia water and water, dropwise adding a boric acid solution for reaction, and curing to obtain boron-containing phenolic resin; b) carbonizing the boron-containing phenolic resin obtained in the step a), mixing with alkali, and activating to obtain boron-doped porous carbon; and c) carrying out silicon deposition on the boron-doped porous carbon obtained in the step b) by adopting a gaseous silicon source, carrying out carbon coating by adopting a gaseous carbon source, and cooling to obtain the silicon-carbon negative electrode material. Compared with the prior art, the preparation method provided by the invention has the advantages that a conductive network can be formed by doping the boron element, the electron concentration can be improved, the electron transfer rate is favorably improved, the conductivity of the material is effectively enhanced, and the rate capability of the negative electrode material is effectively improved; meanwhile, the residual carbon rate in the porous carbon preparation process can be greatly increased, and the cost of the whole silicon-carbon negative electrode material is effectively reduced.

The invention discloses a preparation method of a sodium ion battery coated hard carbon negative electrode material. The preparation method comprises the following steps: S1, precursor preparation: crushing and sieving a biomass raw material; s2, oxidation treatment: mixing the biomass precursor with an oxidizing agent for oxidation treatment; s3, pre-carbonization: carrying out pre-carbonization treatment on the oxidized precursor; s4, precursor mixing: mixing the pre-carbonized precursor with an activating agent; s5, activating treatment: performing low-temperature activation on the mixed precursor; s6, acid pickling treatment: performing acid pickling on the activated precursor, and performing centrifugal drying; s7, coating treatment: carrying out coating treatment on the dried activated material to obtain a coated activated material; and S8, carbonization treatment: carrying out carbonization treatment on the coated activated material to obtain the sodium-ion battery coated hard carbon negative electrode material. The material has the characteristics of good cycling stability, high reversible specific capacity and excellent processability.

The invention relates to a preparation method and application of a manganese ion doped modified ferric sodium pyrophosphate positive electrode material, and belongs to the technical field of sodium ion battery positive electrodes. The preparation method comprises the following steps: adding a sodium source, a phosphorus source and a carbon source into ethanol, uniformly mixing to form a mixed solution, sequentially adding an iron source and a manganese source into the mixed solution, uniformly mixing to form slurry, and drying the slurry to obtain precursor powder; calcining in a protective atmosphere to obtain a manganese-doped carbon-coated ferric pyrophosphate sodium material; the calcining conditions are as follows: heating to the temperature of 300-350 DEG C at the heating rate of 2-3 DEG C / min, carrying out first-stage constant-temperature calcination for 2-3 hours, heating to the temperature of 500-550 DEG C at the heating rate of 5-8 DEG C / min, and carrying out second-stage constant-temperature calcination for 10-12 hours. By doping the manganese ions, the electronic conductivity and the ion diffusivity of the ferric sodium phosphate pyrophosphate composite material are improved, so that the discharge capacity of the ferric sodium phosphate pyrophosphate composite material at high rate is improved, and the battery has relatively high cycle stability.

The invention discloses a silicon-carbon negative electrode material, porous carbon and a preparation method, the porous carbon is prepared by mixing ammonium fluoride and a pre-carbonized material to prepare a premix; and putting the premix in an inert atmosphere, and carrying out pre-activation, drying, carbonization, activation and crushing treatment to obtain the composite material. And uniformly depositing the nano silicon particles into the porous carbon skeleton through a mature CVD (Chemical Vapor Deposition) process to obtain the silicon-carbon composite material. Fluorine and nitrogen co-doping modification can increase the defect degree of a carbon skeleton, efficiently relieve mechanical stress accompanied by lithium storage volume expansion of the silicon negative electrode in a micro scale, provide abundant lithium ion transport and mass transfer channels and enhance the conductivity of porous carbon, and ammonium fluoride is used as a supplementary activator besides water vapor, so that the porosity of the porous carbon is further improved, and the conductivity of the porous carbon is improved. An effective space is provided for uniform deposition of silicon, the fluorine-containing carbon layer can induce formation of a high-stability SEI film rich in LiF on the surface of the nano silicon material, and the interface stability and coulombic efficiency of the silicon negative electrode are further improved.

The present invention discloses a silicon-carbon negative electrode material with a gradient silicon concentration for lithium-ion batteries and a preparation method thereof. The silicon-carbon negative electrode material comprises graded porous carbon, nano-silicon and a coating layer. The graded porous carbon comprises an inner core porous carbon and an outer layer porous carbon. The pores of the inner core porous carbon are micropores, and the pores of the outer layer porous carbon are mesopores. Nano-silicon is distributed on the graded porous carbon in a gradient manner to form a silicon-carbon composite. The silicon concentration in the mesopores of the outer layer porous carbon is less than the silicon concentration in the micropores of the inner core porous carbon. The coating layer is a carbon layer, which is coated on the surface of the silicon-carbon composite. This gradient distribution of silicon concentration can effectively limit the volume expansion of silicon during battery cycling, reduce side reactions with electrolytes, and avoid the problem of silicon shells being easily generated on the porous carbon surface in a silicon-rich system. In addition, the dense carbon film on the outermost layer of the silicon-carbon negative electrode material further reduces the specific surface area of ​​the material and reduces the formation of SEI film.

The invention relates to a high-voltage-resistant deep eutectic-based in-situ polymerization solid electrolyte as well as preparation and application thereof. The in-situ polymerization solid electrolyte is obtained through an in-situ polymerization reaction of a precursor solution comprising 30-80 wt% of a deep eutectic solution, 10-50 wt% of a polymerizable monomer, 1-30 wt% of an additive and 0.05-10 wt% of an initiator; the deep eutectic solution comprises a lithium salt and a hydrogen bond donor organic solvent; the hydrogen bond donor organic solvent comprises a nitrile solvent and a non-nitrile solvent; the polymerizable monomer comprises a monomer for free radical-initiated polymerization or ring-opening polymerization; the additive comprises lithium nitrate and fluoroethylene carbonate. The high-voltage-resistant in-situ polymerization solid electrolyte formed by in-situ compounding of an organic framework formed by in-situ polymerization of a deep eutectic solution, an additive and a monomer has the excellent characteristics of wide electrochemical window, high ionic conductivity, high mechanical strength, good flame retardance, wide-temperature applicability and the like, and can be suitable for a high-voltage system of 4.6 V or above; the solid-solid contact problem of a solid-state battery interface is effectively solved, and the side reaction between the electrolyte and the lithium metal negative electrode is reduced.

Systems, methods, and articles for a wearable and lightweight portable power case are disclosed. The portable power case is comprised of a cylindrical housing, at least two battery elements connected to a printed circuit board (PCB), and at least one separating barrier between the at least two batteries and the PCB. The portable power case is operable to supply power to an amplifier, a radio, a wearable battery, a mobile phone, a tablet, a portable satellite dish and / or any other power consuming device. The portable power case is operable to be charged using solar panels, vehicle batteries, AC adapters, non-rechargeable batteries, and / or generators.

The invention provides a lithium iron manganese phosphate positive electrode material and a preparation method and application thereof, the lithium iron manganese phosphate positive electrode material comprises a doped type iron manganese phosphate inner core and a coating layer coating the surface of the doped type iron manganese phosphate inner core, and the coating layer is a lithium-containing carbon layer; the doped iron manganese phosphate inner core comprises doped ions, and in the particles of the doped iron manganese phosphate inner core from inside to outside, the content gradient of manganese ions and iron ions is reduced, and the content gradient of the doped ions is increased. According to the lithium manganese iron phosphate positive electrode material with the structure, a series of problems caused by poor phase structure stability, poor conductivity and Jahn-Teller effect and manganese dissolution of the material in the lithium manganese iron phosphate positive electrode material can be effectively improved; further, the conductivity of the lithium manganese iron phosphate positive electrode material and the comprehensive performance of gram volume, cycling stability and the like when the lithium manganese iron phosphate positive electrode material is applied to a battery are improved.

The invention discloses a positive electrode material for a zinc-bromine flow battery and a preparation method and application thereof, and belongs to the technical field of zinc-bromine flow batteries, the preparation method comprises the following steps: crushing and sieving an active carbon source, adding the active carbon source into a graphene oxide aqueous dispersion, stirring, centrifuging, removing supernate, drying, mixing with an activating agent, and activating in an inert atmosphere; washing to be neutral, drying and sieving to obtain a graphene / activated carbon composite material; and attaching the graphene / activated carbon composite material to a carbon-plastic bipolar plate to obtain the positive electrode material for the zinc-bromine flow battery. A graphene / activated carbon composite system is combined with a high-conductivity network, graded holes and surface functional groups, so that the reaction kinetics bottleneck of a traditional carbon material Br2 is broken through.

The invention provides a lithium iron phosphate material and a preparation method thereof, a positive pole piece and a secondary battery, and relates to the field of positive pole materials. The lithium iron phosphate material meets the condition that sigma b / sigma f is larger than or equal to 1.10 and smaller than or equal to 5.00, sigma b is the sample standard deviation of the circularity C of large-particle lithium iron phosphate, sigma f is the sample standard deviation of the circularity C of small-particle lithium iron phosphate, and the large-particle lithium iron phosphate and the small-particle lithium iron phosphate with different morphologies are matched with each other through the difference of the sample standard deviation of the circularity of the large-particle lithium iron phosphate and the sample standard deviation of the circularity of the small-particle lithium iron phosphate. Therefore, the lithium iron phosphate material has good tap density and specific surface area. According to the preparation method of the lithium iron phosphate material, the large-particle-size iron phosphate seed crystal partially coated with polydopamine is subjected to vacuum dehydration to obtain the modified iron phosphate seed crystal with the dehydrated surface layer, the morphology of the large-particle iron phosphate prepared by precipitation reaction is influenced, and the iron phosphate material is obtained by utilizing the large and small seed crystals through a coprecipitation method. And finally, the lithium iron phosphate material with good tap density and specific surface area is prepared.

The present disclosure relates to the technical field of sodium-ion batteries, and in particular to an iron-based polyphosphate-type sodium-ion battery positive electrode material, a preparation method therefor and a use thereof. An organic ferrous source, a sodium source, a phosphorus source and a dopant are mixed and then ground until D50 is less than 180 nm, so that the reactivity of the material is improved, a solid-phase reaction is facilitated, and doped high-valence metal elements such as vanadium, niobium, titanium, zirconium and tin can be better doped into lattices of the iron-based polyphosphate-type sodium-ion battery positive electrode material (NFPP), so as to replace the iron site to form lattice defects such as vacancies, thereby improving the ionic conductivity of the material, inhibiting generation of NaFePO4 impurity phase, and improving the capacity and cycling stability of the material.

The invention provides a silicon-carbon material and a preparation method thereof, a porous carbon substrate, a negative electrode material and a battery, and relates to the technical field of battery materials. The core point provided by the invention is controllable synthesis of the porous carbon substrate in the silicon-carbon material, a phenolic monomer and an aldehyde monomer are polymerized in the presence of a catalyst and a dispersing agent, meanwhile, a doping agent and a pre-carbonized biomass carbon precursor are added into a solution, the phenolic resin formed by polymerization is of a spherical structure, and the silicon-carbon composite material is obtained. Homogeneous doping of elements is completed in the synthesis process, the added biomass carbon precursor is of a blocky structure, matching of carbon-based particles of different structures can better exert respective beneficial effects and complement each other, the battery performance is comprehensively improved, and the battery has excellent cycle performance and conductivity.

The invention discloses a silicon negative electrode material as well as a preparation method and application thereof, and belongs to the technical field of lithium ion batteries. The silicon negative electrode material comprises a silicon material substrate and a coating layer coating the surface of the silicon material substrate, the coating layer comprises cyclized polyacrylonitrile and a fast ion conductor. According to the silicon negative electrode material provided by the invention, a uniform cyclized polyacrylonitrile and fast ion conductor coating layer is constructed on the surface of a silicon material matrix. The good electronic conductivity and elasticity of the cyclized polyacrylonitrile and the excellent ionic conductivity of the fast ion conductor are beneficial to buffering the volume expansion of the silicon carbon material, accelerating the lithium ion transmission kinetics and effectively improving the rate capability of the negative electrode material; the cyclized polyacrylonitrile has high chemical stability and strong compatibility with the silicon material and the sulfide solid electrolyte, and is used as a buffer layer between the silicon material and the sulfide solid electrolyte to avoid direct contact between the silicon carbon material and the sulfide solid electrolyte, inhibit interface side reaction and effectively improve the cycle stability of the battery.

The invention relates to a silicon-carbon composite material and a preparation method and application thereof.The preparation method comprises the steps that a porous graphite raw material is subjected to acid pickling and smashing to obtain pretreated porous graphite, then the pretreated porous graphite is soaked in a carbon precursor solution in a vacuum mode, carbonization treatment is conducted after centrifugal separation, pores of the porous graphite are filled with carbides, physical activation is conducted, and the silicon-carbon composite material is obtained; the preparation method comprises the following steps: forming pores in a carbide to form a graded pore structure to obtain a porous graphite composite material, then carrying out silicon deposition in a fluidized bed to obtain a uniform nano silicon layer, and then carrying out carbon coating treatment to obtain a silicon-carbon composite material; the graphite with relatively low cost is adopted as a matrix, high capacity and long cycle performance of the graphite-based silicon-carbon negative electrode material are realized through hierarchical pore structure design, carbonization-activation synergistic pore forming and interface deposition process optimization, and the graphite-based silicon-carbon negative electrode material can be applied to the fields of power batteries and high-energy-density energy storage, especially the field of lithium ion batteries and has wide application prospects. The expansion rate of the battery can be reduced, and the specific capacity, cycling stability and safety of the lithium ion battery can be improved.

The invention discloses a difunctional filler synergistically enhanced polymer solid electrolyte and a solid-state battery, and belongs to the field of solid-state batteries. The electrolyte adopts a polymer matrix, a lithium salt and two functional fillers: the first filler has a high dielectric constant, and can accelerate dissociation of the lithium salt, fix negative ions of the lithium salt and improve the transference number of lithium ions under the action of self polarization; and the second filler has high electrochemical window and ionic conductivity, can inhibit high-voltage decomposition, and is adaptive to a high-voltage positive electrode material. Through cooperation and balance design of the two kinds of filler, ion transmission, interface stability and high-pressure compatibility can be considered at the same time. In addition, the invention further designs a composite negative pole piece, the surface of the negative pole piece is coated with the solid electrolyte, and the ion transmission kinetics in the pole piece can be remarkably improved. On the basis, the invention develops a high-performance solid-state battery which is excellent in electrochemical performance and can play an important role in the fields of consumer electronics, electric automobiles, energy storage systems, low-altitude flight and the like.

The invention discloses an asphalt-based hard carbon material as well as a pre-oxidation preparation method and application thereof. Belongs to the technical field of asphalt-based hard carbon materials. The pre-oxidation preparation method comprises the following steps: carrying out primary pre-oxidation treatment on asphalt at 250-400 DEG C in air flow of 50-500mL / min; crushing the obtained primary pre-oxidized asphalt, and then carrying out secondary pre-oxidation treatment at 250-400 DEG C in air flow of 50-500mL / min to obtain secondary pre-oxidized asphalt; and carrying out carbonization treatment on the secondary pre-oxidized asphalt. According to the method, the asphalt can be kept in a solid-phase state to be subjected to efficient and thorough oxidation cross-linking reaction, the production cost is reduced, the obtained asphalt-based hard carbon material has high first coulombic efficiency and high capacity, and powerful support is provided for commercial application of sodium-ion battery negative electrode materials and rapid development of an energy storage technology.

The invention discloses a zinc-iodine battery positive electrode material based on corn straw shell derived porous carbon and a preparation method of the zinc-iodine battery positive electrode material. According to the material, corn straw shells serve as the sole carbon source, an indigenous nitrogen-doped biomass charcoal carrier with a hierarchical pore structure is prepared through pre-carbonization and KOH activation processes, and the material is characterized in that the specific surface area is larger than or equal to 1500 m < 2 > / g, and the micropore proportion is larger than 90%. The iodine is loaded on the carrier (the iodine content is greater than or equal to 45wt%) through a vacuum sublimation method to form the indigenous nitrogen-doped biomass charcoal / iodine composite material. According to the positive electrode material, through the synergistic effect of physical confinement and pyridine nitrogen chemical adsorption, the multi-iodide shuttle effect is effectively inhibited, so that the capacity retention rate of the zinc-iodine battery is greater than or equal to 93% after 40000 cycles under the current density of 2A g <-1 >, and the capacity retention rate is greater than 45% under the rate of 10A / g. The method has double benefits of agricultural waste resource utilization and high-performance energy storage device development.

The invention relates to catalytically coated anion exchange membranes and their production. The catalytically active coated anion exchange membranes are used in electrochemical cells, in particular for water electrolysis. The object of the invention was to provide a process for producing an electrocatalytically active coated anion exchange membrane whose coating is porous and thus the electrocatalytically active centers located in the coating are easily accessible to the reactants. A basic idea of the process according to the invention is to incorporate particulate inorganic material into the catalyst coating as a placeholder, to solidify the coating, and then to leach the inorganic material out of the coating. The leaching converts the inorganic material into a water-soluble product that can be easily washed out of the coating.What remains are voids (pores) where the particulate inorganic material was previously located within the coating. The inorganic material therefore assumes the function of a structure-imparting agent within the coating composition, which is lost during the catalytically active coating process.

Systems, methods, and articles for a portable power case are disclosed. The portable power case is comprised of at least one battery and at least one PCB. The portable power case has at least one USB port and at least two access ports, at least two leads, or at least one access port and at least one lead. The portable power case is operable to supply power to an amplifier, a radio, a wearable battery, a mobile phone, and a tablet. The portable power case is operable to be charged using solar panels, vehicle batteries, AC adapters, non-rechargeable batteries, and generators. The portable power case provides for modularity that allows the user to disassemble and selectively remove the batteries installed within the portable power case housing.