Abstract: The present disclosure provides a method for manufacturing a positive electrode for a secondary battery, the method including forming a positive electrode mixture layer including a positive electrode active material on a positive electrode current collector, and forming a metal oxide coating layer on the positive electrode mixture layer by atomic layer deposition, wherein the positive electrode active material includes lithium composite transition metal oxide particles and a boron-containing coating layer formed on the lithium composite transition metal oxide particles, and the lithium composite transition metal oxide particles include nickel (Ni), cobalt (Co), and manganese (Mn), wherein the nickel (Ni) is 60 mol % or greater of all metals excluding lithium.

Abstract: A method and a system for predicting battery health based on distance driven on a full battery load with machine learning model are provided. The method includes: obtaining historical vehicle telematics of vehicles, wherein the historical vehicle telematics comprise at least one of the following: odometer readings, battery SOC, vehicle speed, battery-module temperatures, and battery-cell voltages; creating a distance driven model according to a relationship between a distance driven on a full battery load of vehicles and the historical vehicle telematics; obtaining a distance driven on a full battery load of a vehicle based on the distance driven model by using real-time vehicle telematics of the vehicle as model input; predicting battery health of the vehicle by comparing the obtained distance with a reference distance value.

Abstract: A lithium-ion battery includes an electrode with a plurality of channels formed at least partially through its thickness. Each channel has a diameter in a range from 5 ?m to 100 ?m and/or is spaced apart from another channel by a distance in a range from 10 ?m to 200 ?m as measured between centerlines of the channels. The electrode may be an anode and includes carbonaceous material such as graphite and/or additional electrochemically active lithium host materials. The battery can be charged at a C-rate greater than 2 C.

Abstract: The invention relates to a process for the preparation of carbon-deposited alkali metal oxyanion and the use thereof as cathode material in lithium secondary batteries wherein the process comprises synthesis of partially reacted alkali metal oxyanion, a wet-based nanomilling step, a drying step and a subsequent carbon deposition step performed by a thermal CVD process. The invention also relates to carbon deposited alkali metal oxyanion with less than 80 ppm of sulfur impurities for the preparation of a cathode of lithium secondary batteries with exceptional high-temperature electrochemical properties.

Abstract: A lithium ion secondary battery with increased durability and capacity includes a positive electrode, a negative electrode, and a separator. The positive electrode includes a current collector foil and an electrode mixture layer disposed on a surface of the current collector foil. The positive electrode mixture layer includes a superficial layer portion and a deep layer portion. The superficial layer portion opposes the negative electrode via the separator. The deep layer portion is disposed between the superficial layer portion and the current collector foil. The superficial layer portion contains positive electrode active material particles having an average particle diameter larger than an average particle diameter of positive electrode active material particles contained in the deep layer portion.

Abstract: The present application relates to a secondary battery, which includes: a cathode sheet, an anode sheet, and an electrolyte; the cathode sheet includes a cathode film layer containing a cathode active material, and the anode sheet includes an anode film layer containing an anode active material; and the secondary battery meets a following function relationship: 0.22?3×(A1/A2)×(B2?B1)/(B1+B2)?1.55, the parameters are referred to the description; and an electrical device including the secondary battery. The secondary battery in the present application has both good cycle life and excellent fast charging capacity.

Abstract: The present application relates to a secondary battery, a process for preparing the same and an apparatus containing the secondary battery.

Abstract: A battery 2 includes an outer can 10 and an electrode group 22 that is housed in the outer can 10 together with an alkaline electrolytic solution, in which a positive electrode 24 included in the electrode group 22 includes a positive electrode substrate and a positive electrode mixture supported on the positive electrode substrate, the positive electrode mixture includes nickel hydroxide, yttrium oxide serving as a first additive, and niobium oxide or titanium oxide serving as a second additive, a total amount of the first additive and the second additive is 0.1 parts by mass or more and 2.5 parts by mass or less per 100 parts by mass of the nickel hydroxide, a mass ratio of the first additive and the second additive is in a relationship of 1:0.2 to 5, and the positive electrode mixture after an activation treatment has a resistivity of 1 ?·m or more and 10 ?·m or less.

Abstract: A crosslinkable copolymer is provided. The crosslinkable copolymer has pendant cationic nitrogen-containing groups with some, but not all, of these pendant groups further including a (meth)acryloyl group. The (meth)acryloyl groups can react to form a crosslinked copolymer that is ionically conductive. The crosslinked copolymer can be used to provide an anion exchange membrane that can be used in electrochemical cells such as fuel cells, electrolyzers, batteries, and electrodialysis cells.

Abstract: The present disclosure provides a lithium manganate positive electrode active material, comprising a lithium manganate matrix and a cladding layer, where the cladding layer comprises an organic bonding material, one or more A-type salts, and one or more B-type salts. The lithium manganate positive electrode active material of the present disclosure significantly reduces the content of transition metal manganese ions within a battery through combined action of the organic bonding material, the A-type salts, and the B-type salts, thereby slowing down the decomposition and consumption of the SEI film (solid electrolyte interphase) by transition metal manganese, and improving the capacity retention rate and impedance performance of the battery.

Abstract: There is provided a prismatic power storage device having a reduced weight and ensuring a space for an electrode body that expands during charging, while the rigidity of an insulating sheet is ensured. A prismatic power storage device according to an aspect of the present disclosure includes: an electrode body (11) including a positive electrode plate, a negative electrode plate, and a separator disposed between the positive electrode plate and the negative electrode plate; an insulating holder (30) formed by shaping an insulating sheet (31) into a box shape and accommodating the electrode body (11); a prismatic outer case having an opening and accommodating the electrode body (11) and the insulating holder (30); and a sealing body sealing the opening of the outer case. The insulating sheet (31) includes a porous body.

Abstract: Aspects of the disclosure relate to electrode active materials for use in battery cells that include a lithium metal phosphate core having a more ionically conductive layer thereon. The layer of the ionic conducting material advantageously can increase lithium ion conduction of the active material by at least one order of magnitude relative to the core material alone. As such, electrodes may be fabricated with lower areal densities resulting in battery cells that have such electrodes with higher charge rates and potentially smaller physical dimensions.

Abstract: A battery maintenance system includes an enclosure including a plurality of walls. A plurality of battery cells are located in the enclosure and surrounded by electrolyte. An electrolyte agitator such as a piezoelectric device is attached to at least one of the walls of the enclosure and is configured to selectively agitate the electrolyte.

Abstract: A fast charging lithium-ion battery includes a positive electrode plate, a negative electrode plate, a separator, and an electrolyte. The positive electrode plate includes a positive current collector and a positive active material layers. The negative electrode plate includes a negative current collector and negative active material layers. The negative active material layers include titanium niobium oxide, lithium titanate, or a combination thereof. The separator is disposed between the positive electrode plate and the negative electrode plate. The electrolyte contacts the positive electrode plate and the negative electrode plate. The negative active material layers have an effective area corresponding to the positive electrode plate. The negative active material layers have a thickness on one surface of the negative current collector. A ratio of the effective area to the thickness is greater than 2×105 mm.

Abstract: A powderous positive electrode material for lithium ion batteries, comprising crystalline lithium transition metal-based oxide particles having a general formula Li1+a ((Niz (Ni0.5Mn0.5)y Cox)1?k Ak)1?a O2, wherein A is a dopant, ?0.030?a?0.025, 0.10?x?0.40, 0.25?z?0.52, x+y+z=1 and k?0.01, wherein the crystalline powder has a crystallite size less than 33 nm as determined by the Scherrer equation based on the peak of the (104) plane obtained from the X-ray diffraction pattern using a Cu K ? radiation source, and wherein the molar ratio MR(Ni) of Ni versus the total transition metal content in a cross section of a particle is higher in the surface area than in the center area of the particle, as determined by EDS analysis.

Abstract: According to one embodiment, a positive electrode active material for a non-aqueous electrolyte secondary battery contains a lithium/transition metal composite oxide that contains 80 mol % or more, relative to the total mol number of metal elements other than Li, of Ni and at least one kind of metal element selected from among Co, Mn, Al, W, Mg, Mo, Nb, Ti, Si and Zr. When a filtrate of a suspension, said suspension being prepared by adding 250 mg of the positive electrode active material to 10 mL of a 17.5 mass % aqueous solution of hydrochloric acid, dissolving by heating at 90° C. for 2 hours and then diluting to 50 mL, is analyzed by inductively coupled plasma mass spectrometry, the elution amount of S in the filtrate is 0.002 mmol or greater.

Abstract: A gel composition, in particular a gelled electrolyte, comprising: i) fumed alumina particles, wherein the mean primary particle size of the particle is from 5 to 50 nm and the BET specific surface area is from 40 to 400 m2/g; ii) at least two organic solvents; and iii) a lithium salt; wherein the amount of the alumina particles is 0.2-10% by weight based on the total weight of the gel composition. A method to prepare a gelled electrolyte, a Li-ion battery, a Li-ion battery and a device are also provided.

Abstract: A method for preparing a silicon monoxide composite material includes: a first stage: introducing a protective gas into a vapor deposition oven, and pre-heating a silicon monoxide raw material, such that a part of the silicon monoxide raw material is subjected to a disproportionation reaction; a second stage: continuously introducing the protective gas and introducing a carbon source gas, and subjecting the pre-heated silicon monoxide raw material to a chemical vapor deposition to form carbon nanotubes on a surface of silicon monoxide; and a third stage: after a predetermined time period, stopping introducing the carbon source gas, and stopping introducing the protective gas until the vapor deposition oven is cooled to room temperature, to prepare the silicon monoxide composite material. During the preparation process, no extra catalyst needs to be added, a product of the previous disproportionation reaction may act as a catalyst for the growth of the carbon nanotubes.

Abstract: A method comprises obtaining a stack for an energy storage device, the stack comprising a substrate, a first electrode layer, a second electrode layer, and an electrolyte layer between the first electrode layer and the second electrode layer. The method comprises laser ablating the stack to form a plurality of first grooves in the stack, each of the plurality of first grooves being through the first electrode layer and the electrolyte layer. The method comprises forming, in or on the stack, at least one registration feature, different from each of the plurality of first grooves. An apparatus and a stack for an energy storage device is also disclosed.

Abstract: Provided herein are battery cells comprising artificial solid-electrolyte interphase (SEI) layers used as protective coatings on electrodes. The SEI layers are produced by liquid-phase deposition (LDP). The battery cell may comprise an anode, a cathode, an electrolyte disposed between the anode and the cathode, a polymer separator disposed between the anode and the cathode, and a casing containing the anode, the cathode, the electrolyte, and the polymer separator, wherein at least one or the anode or cathode comprises an SEI layer produced by an LDP method.