5544 results about "Electronic conductivity" patented technology

A field effect transistor in which a continuous semiconductor layer comprises:

• • a) an organic semiconductor; and,
  • b) an organic binder which has an inherent conductivity of less than 10⁻⁶Scm⁻¹ and a permittivity at 1,000 Hz of less than 3.3

and a process for its production comprising:

coating a substrate with a liquid layer which comprises the organic semiconductor and a material capable of reacting to form the binder; and,

converting the liquid layer to a solid layer comprising the semiconductor and the binder by reacting the material to form the binder.

Redox flow devices are described in which at least one of the positive electrode or negative electrode-active materials is a semi-solid or is a condensed ion-storing electroactive material, and in which at least one of the electrode-active materials is transported to and from an assembly at which the electrochemical reaction occurs, producing electrical energy. The electronic conductivity of the semi-solid is increased by the addition of conductive particles to suspensions and/or via the surface modification of the solid in semi-solids (e.g., by coating the solid with a more electron conductive coating material to increase the power of the device). High energy density and high power redox flow devices are disclosed. The redox flow devices described herein can also include one or more inventive design features. In addition, inventive chemistries for use in redox flow devices are also described.

By providing contact plugs having a lower plug portion, formed on the basis of well-established tungsten-based technologies, and an upper plug portion, which may comprise a highly conductive material such as copper or a copper alloy, a significant increase in conductivity of the contact structure may be achieved. For this purpose, after the deposition of a first dielectric layer of the inter-layer stack, a planarization process may be performed so as to allow the formation of the lower plug portions on the basis of tungsten, while, after the deposition of the second dielectric layer, a corresponding copper-based technology may be used for forming the upper plug portions of significantly enhanced conductivity.

Nanoscale ion storage materials are provided that exhibit unique properties measurably distinct from their larger scale counterparts. For example, the nanoscale materials can exhibit increased electronic conductivity, improved electromechanical stability, increased rate of intercalation, and/or an extended range of solid solution. Useful nanoscale materials include alkaline transition metal phosphates, such as LiMPO₄, where M is one or more transition metals. The nanoscale ion storage materials are useful for producing devices such as high energy and high power storage batteries, battery-capacitor hybrid devices, and high rate electrochromic devices.

The invention discloses a preparation method of a silicon and carbon-coated graphene composite cathode material. The technical problem to be solved is to enhance the electronic conductivity of the silicon-based cathode material, buffer the volume effect produced in the process of deintercalation of the lithium in the silicon-based cathode material and enhance the structure stability in the circulation process of the material at the same time. The material is prepared by using a spray drying-thermally decomposing treatment process in the invention. The preparation method comprises the following steps of: evenly dispersing nano silicon and graphite micro powder in a dispersion solution of oxidized graphene, carrying out thermal treatment under an inert protection atmosphere after spray drying, subsequently cooling along a furnace to obtain the silicon and carbon-coated graphene composite cathode material. The extra binder does not need to add in the process of manufacturing balls in the invention and the outer oxidized graphene is thermally reduced in situ to graphene in the thermal treatment process of the composite precursor, so that the process is simple and easy to operate; and the practical degree is high. The prepared composite material has the advantages of great reversible capacity, designable capacity, good cycling performance and high-current discharging performance, high tap density and the like.

The invention relates to organic-inorganic all-solid-state composite electrolyte as well as preparation and application methods thereof, belonging to the field of lithium ion batteries. According to the organic-inorganic all-solid-state composite electrolyte, a highly-ordered three-dimensional connection network skeleton is formed by an inorganic fast lithium ion conductor, and a three-dimensional connection network is filled with a polymer and lithium salt. The organic-inorganic all-solid-state composite electrolyte which is flexible and has a controllable three-dimensional connection network structure is prepared. The electrolyte is high in lithium ion conductivity, wide in electrochemical window, good in mechanical property and stable to lithium metal. A lithium ion secondary battery assembled by a composite electrolyte membrane prepared by the method is high in capacity, stable in cycle performance, low in interface impedance and good in interface stability.

The composite particle for an electrode in accordance with the present invention contains an electrode active material, a conductive auxiliary agent having an electronic conductivity, and an oxidizing/reducing agent. Therefore, this composite particle can construct an effective conductive network, and effectively provide so-called oxidizing/reducing capacity due to the oxidizing/reducing agent. Hence, when the composite particle for an electrode in accordance with the present invention is used as a constituent material of an electrode in an electrochemical device, the electrochemical device can realize a higher capacity.

The invention discloses a hydrothermal synthesis method of lithium-ion battery anode material of lithium iron phosphate, relating two kinds of metal phosphate. The steps are as follows: lithium source and phosphorus source are dissolved in water or mixed with water, and added into the reaction autoclave, the quaternary cationic surfactants and the alkylphenols polyoxyethylene ethers nonionic surfactant is also added into the reaction autoclave, the air in the dead volume of the autoclave inside is purged by the inert gas, the autoclave is sealed and heated to 40-50 DEG C with stirring, a feed valve and an exhaust valve are opened, pure ferrous salting liquid is added into the autoclave, and then the autoclave is sealed for the reaction of the material at 140 to 180 DEG C for 30 to 480 minutes; the mixture ratio of the invention is set as follows: the molar ratio of Li, Fe and P is 3.0-3.15:1:1.0-1.15, and then the resultant is filtered, washed, dried and carbon-coated, thus the lithium iron phosphate is obtained. The lithium iron phosphate which is produced by the invention has the advantages that: the electrochemical performance is excellent, the particle size distribution of which the D50 is between 1.5 um to 2 um is even, the phase purity is above 99 percent and the electronic conductivity of the material is improved.

A nonaqueous secondary battery 10 of the invention has an active material compound layer 14 deposed over at least one face of a collector 12 made of metal foil and is equipped with a positive electrode 11 having a portion 13 in a part of which metal is exposed. The positive electrode 11 together with the exposed-metal portion 13 faces a negative electrode 17 through an interposed separator 23, and on that part of the exposed-metal portion 13 that faces the negative electrode 17 through the interposed separator 23 there is formed a protective layer 16 made of a material whose electronic conductivity is lower than that of the metal and which moreover is non-insulative. With such nonaqueous secondary battery 10, should part of an electrode pierce the separator and contact with the other electrode, the battery will be gently discharged, thereby averting abnormal heat generation by the battery and additionally enabling the battery's abnormality to be sensed by the equipment via the fall in battery voltage. Thus, there is provided a nonaqueous secondary battery of excellent safety that can prevent abnormal heat generation due to a short circuit caused by burr, powder or the like piercing the separator.

The invention discloses a method for preparing a graphite alkyne film. The method comprises that: a copper sheet or any one substrate the surface of which is covered with a copper film layer is used as a substrate; 6-alkynyl-benzene is subjected to coupling reaction in a solvent under the catalytic action of the copper to obtain the graphite alkyne film on the surface of the substrate. The method for preparing the graphite alkyne film, which is provided by the invention, has simple and convenient process, and can carry out large-scale preparation of the graphite alkyne film on the surface of the copper sheet or the substrate any surface of which is covered with the copper. The electrical conductivity of the graphite alkyne film is 2.516*10-4S/m. The film has uniform surface, can exist stably in the air, is a semiconductor with similar performances with silicon, and has potential application prospect in the fields of catalysis, electron, semiconductor, energy, material and the like.

The invention relates to solid-state electrolytes, in particular to a polycarbonate all-solid-state polymer electrolyte, an all-solid-state secondary lithium battery made of the same and preparation and application thereof. The all-solid-state polymer electrolyte is prepared from polycarbonate macromolecules, lithium salt and a porous supporting material; the thickness is 20-800 micrometers, the mechanical strength is 10-80 MPa, the room temperature ion conductivity is 2*10<-5>S/cm-1*10<-3>S/cm, and the electrochemical window is higher than 4V. The all-solid-state polymer electrolyte is easy to prepare and form, good in mechanical property, high in ion conductivity and wide in electrochemical window; meanwhile, the solid-state electrolyte effectively inhibits growth of negative electrode lithium dendrites and improves interface stability and long circulation performance.

PCT No. PCT/JP97/02854 Sec. 371 Date Mar. 11, 1999 Sec. 102(e) Date Mar. 11, 1999 PCT Filed Aug. 19, 1997 PCT Pub. No. WO98/07772 PCT Pub. Date Feb. 26, 1998A polymer solid electrolyte obtained by blending (1) a polyether copolymer having a main chain derived form ethylene oxide and an oligooxyethylene side chain, (2) an electrolyte salt compound, and (3) a plasticizer of an aprotic organic solvent or a derivative or metal salt of a polyalkylene glycol having a number-average molecular weight of 200 to 5,000 or a metal salt of the derivative is superior in ionic conductivity and also superior in processability, moldability and mechanical strength to a conventional solid electrolyte. A secondary battery is constructed by using the polymer solid electrolyte in combination with a lithium metal negative electrode and a lithium cobaltate positive electrode.

Provided are an all-solid state battery with a better quality of contact among particles of an active material and with an enhanced discharge capacity; an electrode for an all-solid state battery; and a method of manufacturing the same. The all-solid state battery is manufactured through the steps of: causing a deliquescent solid electrolyte to deliquesce, the deliquescent solid electrolyte having ionic conductivity, electronic conductivity and a deliquescent property; preparing an electrode mixture by mixing the deliquescent solid electrolyte having deliquesced and an active material together; heat-treating and shaping the electrode mixture to produce an electrode; and bonding the thus-produced electrode and a solid electrolyte layer with the solid electrolyte layer interposed between the electrode and another electrode which are paired to serve as a positive electrode and a negative electrode.

Provided is anode active material layer for a lithium battery, comprising multiple particulates of an anode active material, wherein a particulate is composed of one or a plurality of particles of a high-capacity anode active material being embraced or encapsulated by a thin layer of a high-elasticity polymer having a recoverable tensile strain no less than 10% when measured without an additive or reinforcement, a lithium ion conductivity no less than 10^-5 S/cm at room temperature, and a thickness from 0.5 nm (or a molecular monolayer) to 10 μm (preferably less than 100 nm), and wherein the high-capacity anode active material has a specific lithium storage capacity greater than 372 mAh/g (e.g. Si, Ge, Sn, SnO₂, Co₃O₄, etc.).

The invention discloses a lithium titanate-carbon composite nano-material, a preparation method thereof and application thereof. The method comprises the following steps: 1) statically spinning lithium titanate sol, or lithium titanate sol doped with a conductive substance or lithium titanate sol doped with metal ions to obtain a thin film, wherein the conductive substance is conductive metal or conductive carbon; and 2) heat treating the thin film in inert atmosphere to obtain the lithium titanate-carbon composite nano-material. The lithium titanate-carbon composite nano-material provided by the invention has a standard one-dimensional morphological structure, high crystallinity, high conductivity and high safety performance, and has high lithium ion diffusion speed and high electronic conductivity when applied as the cathode material of the lithium ion battery. Moreover, the lithium titanate-carbon composite nano-material has high charge/discharge capacity, excellent high-current charge/discharge performance and stable cycling performance. The 10c charge/discharge capacity is 125mAh/g, the 40C charge/discharge capacity reaches 95mAh/g, and the retention rate of the high-current 40C charge/discharge capacity within 3000 times reaches 85 percent.

Provided is a rechargeable alkali metal-sulfur cell comprising an anode active material layer, an electrolyte, and a cathode active material layer containing multiple particulates of a sulfur-containing material selected from a sulfur-carbon hybrid, sulfur-graphite hybrid, sulfur-graphene hybrid, conducting polymer-sulfur hybrid, metal sulfide, sulfur compound, or a combination thereof and wherein at least one of the particulates is composed of one or a plurality of sulfur-containing material particles being embraced or encapsulated by a thin layer of a high-elasticity polymer having a recoverable tensile strain no less than 10% when measured without an additive or reinforcement, a lithium ion conductivity no less than 10⁻⁵ S/cm at room temperature, and a thickness from 0.5 nm to 10 μm. This battery exhibits an excellent combination of high sulfur content, high sulfur utilization efficiency, high energy density, and long cycle life.

Techniques, arrangements and compositions are provided to incorporate nanostructured materials into electrodes for energy storage devices. Materials such as, for example, carbon nanotubes, silicon nanowires, silicon carbide nanowires, zinc nanowires, and other materials may be used to modify electrode properties such as electronic conductivity, thermal conductivity, or durability, for example. In some embodiments, nanostructured materials may be added to electrode formulations such as, for example, slurries or powders. Nanostructured materials may be deposited directly onto active material particles or electrode components. In some embodiments, coatings may be used to assist in deposition.

A NOT circuit realized using an atomic switch serving as a two terminal device and including a first electrode made of a compound conductive material having ionic conductivity and electronic conductivity and a second electrode made of a conductive substance. Ag₂S, Ag₂Se, Cu₂S, or Cu₂Se is preferably used as the compound conductive material.

An electronic cigarette includes an atomizer having a coil-less heating element. The coil-less heating element may include a heating section and two leads electrically connected to the heating section. The heating section is made of one or more fiber materials. The two leads may be made of conductive materials that can conduct liquid to the heating section. Alternatively, the heating element may include one or more fiber materials with two conductive sections, and a heating section between the conductive sections. The heating section has a significantly higher electrical resistance than the conductive sections. The different electrical resistances may be achieved by modifying the fiber materials with a material (e.g. metals) having higher electronic conductivity. Different electrical resistances may also be achieved by modifying the shape of the fiber materials to provide the conductive sections with a larger cross-section, and the heating section with a smaller cross-section.

The invention discloses a high voltage-resistant multi-stage structure composite solid-state electrolyte and its preparation method and use in a solid-state lithium battery. The lithium battery utilizes a multi-stage structure solid-state electrolyte containing different components. A polymer electrolyte with excellent electrode interface compatibility is used as an electrolyte in the negative electrode side. A high voltage-resistant polymer electrolyte is used as an electrolyte in the positive electrode side. A polymer electrolyte or an inorganic electrolyte with high ionic conductivity is used as a middle layer. The multi-stage structure solid-state electrolyte has advantages such as high mechanical properties, high ionic conductivity, a wide electrochemical window, excellent electrode interfacial compatibility and lithium dendrite growth inhibition of different components. Compared with the traditional liquid lithium ion battery, the battery with the multi-stage composite solid-state electrolyte has higher safety and higher energy density.

A precursor electro-catalyst composition for producing a fuel cell electrode. The precursor composition comprises (a) a molecular metal precursor dissolved or dispersed in a liquid medium and (b) a polymer dissolved or dispersed in the liquid medium, wherein the polymer is both ion-conductive and electron-conductive with an electronic conductivity no less than 10⁻⁴ S/cm (preferably greater than 10⁻² S/cm) and ionic conductivity no less than 10⁻⁵ S/cm (preferably greater than 10⁻³ S/cm). Also disclosed is an electro-catalyst composition derived from this precursor composition, wherein the molecular metal precursor is converted by heat and/or energy beam to form nanometer-scaled catalyst particles and the polymer forms a matrix that is in physical contact with the catalyst particles, coated on the catalyst particles, and/or surrounding the catalyst particles as a dispersing matrix with the catalyst particles dispersed therein when the liquid is removed. The fuel cell comprising such a composition in an electrode exhibits a superior power output.