Abstract: A positive electrode material consists of composite particles. Each of the composite particles includes a base material particle, a film, and a carbon nanotube. The film covers at least a part of a surface of the base material particle. The base material particle includes a positive electrode active material. The film includes a boron oxide. The carbon nanotube includes a first portion and a second portion. The first portion is buried in the film. The second portion is exposed on a surface of the film.

Abstract: Resin-adhered graphite particles are obtained by causing a modified novolac-type phenolic resin to adhere to graphite particles. At least part of surfaces of the graphite particles is coated with a carbonaceous coating by heating the resin-adhered graphite particles in a non-oxidizing atmosphere at 900 to 1,500° C. to carbonize the modified novolac-type phenolic resin. Arylene groups having hydroxy groups account for 5 to 95 mol % of arylene groups constituting the modified novolac-type phenolic resin. The obtained carbonaceous substance-coated graphite particles exhibit excellent battery properties when used as a negative electrode material for a lithium ion secondary battery.

Abstract: The present application provides a positive electrode and a lithium-ion battery. The positive electrode comprises a current collector; a first active material layer comprising a first active material; and a second active material layer; wherein the first active material layer is arranged between the current collector and the second active material layer, the first active material layer comprises a first active material, and the first active material is at least one selected from a group consisting of a modified lithium transition metal oxide positive electrode material and a modified lithium iron phosphate. The positive electrode of the present application helps to improve the thermal stability of the lithium-ion battery, and the improvement of the thermal stability may reduce the proportion of the thermal runaway when the lithium-ion battery is internally short-circuited so that the safety performance of the lithium-ion battery is improved.

Abstract: Aspects of a modular clip for an electric battery module, a battery module comprising multiple such modular clips, and a battery pack comprising multiple battery modules are provided. The modular clip includes a housing configured to receive a plurality of battery cells. The modular clip may further comprise at least one interconnect plate. The modular clip may further comprise a retainer plate including a plurality of top cell recesses, each of the plurality of top cell recesses may comprise an opening to enable wire bonds between electrical terminals of a battery cell and the at least one interconnect plate. The battery module may comprise a plurality of wire bonds between at least one voltage sensing PCB and the at least one interconnect plate.

Abstract: Provided are a positive current collector, a preparation method thereof, a positive electrode sheet, a cell and a battery. The positive current collector. The positive current collector includes a substrate film and a functional layer arranged on a surface of the substrate film. The substrate film has a first surface and a second surface opposite to the first surface. The first surface has a first functional layer provided thereon, and the second surface has a second functional layer provided thereon. The first functional layer includes a bonding layer, a current conducting layer, and a protective layer that are stacked sequentially. The bonding layer is arranged on the first surface. The first functional layer is divided to have a first functional segment and a second functional segment in a direction parallel to the first surface. The first functional segment has a thickness greater than a thickness of the second functional segment.

Abstract: Disclosed is a negative electrode active material which includes: a silicon oxide composite including i) Si, ii) a silicon oxide represented by SiOx (0<x?2), and iii) magnesium silicate containing Si and Mg; and a carbon coating layer positioned on the surface of the silicon oxide composite and including a carbonaceous material, wherein X-ray diffractometry of the negative electrode active material shows peaks of Mg2SiO4 and MgSiO3 at the same time and shows no peak of MgO; the ratio of peak intensity, I (Mg2SiO4)/I (MgSiO3), which is intensity I (Mg2SiO4) of peaks that belong to Mg2SiO4 to intensity I (MgSiO3) of peaks that belong to MgSiO3 is smaller than 1, the peaks that belong to Mg2SiO4 are observed at 2?=32.2±0.2°, and the peaks that belong to MgSiO3 are observed at 2?=30.9±0.2°.

Abstract: The present disclosure aims to provide a nonaqueous electrolyte secondary battery having excellent discharge load characteristics and excellent long-term cycle characteristics. A nonaqueous electrolyte secondary battery which is one example of an embodiment of the present disclosure includes a positive electrode, a negative electrode (30), separators, and a nonaqueous electrolyte. The negative electrode (30) includes a negative electrode collector (31) and a negative electrode mixture layer (32) formed on the negative electrode collector (31). The negative electrode mixture layer (32) includes a first mixture layer primarily composed of a carbon-coated graphite (35) and a second mixture layer (34) primarily composed of a graphite (36), the first mixture layer (33) is disposed at a surface side of the negative electrode mixture layer (32), and the second mixture layer (34) is disposed at a side of the negative electrode collector (31).

Abstract: A thermal formation sintering compound containing a binder, a sinterable powder material and a pore formation material, for formation into a predetermined shape in a thermal formation step, removal of the binder in a degreasing step, and sintering of the powder material in a sintering step is provided. The binder contains a low-temperature draining component which melts in the thermal formation step, begins draining at a temperature lower than a draining temperature of the pore formation material, and drains at a temperature lower than a temperature at which the pore formation material drains; and a high-temperature draining component which melts in the thermal formation step, begins draining after the pore formation material begins draining, and drains at a temperature higher than does the pore formation material.

Abstract: The embodiments of the present application relate to an electrode sheet and a battery cell including the same. The electrode sheet according to an embodiment comprises an electrode sheet body and a plurality of tabs connected to the electrode sheet body. The width of each of the plurality of tabs is different from one another; or the length of each of the plurality of tabs is different from one another. The electrode sheet and the battery cell provided in the embodiments of the present application ensure that each of the tabs in the electrode sheet can electrically conduct well with the tab lead. Thus, the battery cell provided in the present application has the advantage of good electrical conductivity.

Abstract: The disclosed principles provide techniques for 3D fabrication of sensing systems embedded inside battery cells and provide cell parameter data for a comprehensive and robust battery management system. The disclosed principles provide online and real-time monitoring battery state-of-health down to the individual cell level of each battery using embedded sensors on one or more of the internal layers of a cell, such as the dielectric separators found in such battery cells. The implementation of the disclosed principles in individual battery cells therefore provides an increased likelihood to mitigate catastrophic failures in batteries. In addition, the disclosed fabrication processes for printing sensors directly on one or more of the components or layers within each individual battery cell significantly reduce manufacturing steps required by conventional battery management systems.

Abstract: Provided is a solid electrolyte material represented by a composition formula Li3?3?Y1+??aMaCl6?x?yBrxIy, where M is at least one element selected from the group consisting of Al, Sc, Ga, and Bi; ?1<?<1; 0<a<2; 0<(1+??a); 0?x?6; 0?y?6; and (x+y)?6.

Abstract: Systems and methods for anisotropic expansion of silicon-dominant anodes may include a cathode, an electrolyte, and an anode, where the anode may include a current collector and an active material on the current collector. An expansion of the anode during operation may be configured by a thickness of the current collector. The expansion of the anode may be more anisotropic for thicker current collectors. A thicker current collector may be 10 ?m thick or greater. The expansion of the anode may be more anisotropic for more rigid materials used for the current collector. A more rigid current collector may include nickel and a less rigid current collector may include copper. The expansion of the anode may be more anisotropic for a rougher surface current collector.

Abstract: To provide a method for production of an all-solid-state battery in which cracking of the ends of the electrodes can be suppressed even if a negative electrode active material layer including lithium-titanium oxide is roll-pressed, provided is a method for the production of an all-solid-state battery, including roll-pressing to consolidate a negative electrode active material layer; wherein the all-solid-state battery has a structure including a laminate of a positive electrode current collector layer, a positive electrode active material layer, a solid electrolyte layer, the negative electrode active material layer, and a negative electrode current collector layer in this order, the negative electrode active material layer includes a lithium-titanium oxide as a negative electrode active material, and prior to the roll-pressing, a stress relaxation rate of the negative electrode active material layer is 32.5% or more.

Abstract: The present invention relates to an electrolytic copper foil for a secondary battery, and a method of producing the same. The electrolytic copper foil for a secondary battery exhibits a little change in a physical property caused by a difference in a crosshead speed when tensile strength and an elongation percentage of the electrolytic copper foil are measured, thereby achieving excellent charging and discharging characteristics of a battery and preventing exfoliation of an active material. The electrolytic copper foil for a secondary battery is produced from a plating solution containing Total Organic Carbon (TOC), cobalt, and iron by using a drum, in which a ratio of the TOC to the cobalt and the iron contained in the electrolytic copper foil follows Formula 1 below. TOC/(cobalt+iron)=1.3 to 1.

Abstract: Provided are an all-solid-state battery and a preparation method thereof. The all-solid-state battery includes a positive electrode, a negative electrode, and a solid-state electrolyte located between the positive electrode and the negative electrode. The negative electrode includes a first negative electrode and a second negative electrode. The second negative electrode is located on a side of the first negative electrode. The solid-state electrolyte includes a first solid-state electrolyte and a second solid-state electrolyte. The first solid-state electrolyte is located between the positive electrode and the first negative electrode. The second solid-state electrolyte is located between the positive electrode and the second negative electrode. The roughness of the second solid-state electrolyte is greater than the roughness of the first solid-state electrolyte.

Abstract: Embodiments described herein relate to divided energy electrochemical cells and electrochemical cell systems. Divided energy electrochemical cells and electrochemical cell systems include a first electrochemical cell and a second electrochemical cell connected in parallel. Both electrochemical cells include a cathode disposed on a cathode current collector, an anode disposed on an anode current collector, and a separator disposed between the anode and the cathode. In some embodiments, the first electrochemical cell can have different performance properties from the second electrochemical cell. For example, the first electrochemical cell can have a high energy density while the second electrochemical cell can have a high power density. In some embodiments, the first electrochemical cell can have a battery chemistry, thickness, or any other physical/chemical property different from those properties of the second electrochemical cell.

Abstract: This disclosure provides a battery including a cathode, an anode positioned opposite the cathode and a carbon interface layer. The carbon interface layer includes an electrically insulating flaky carbon layer conformally encapsulating the anode. A plurality of carbon nano-onions (CNOs) defining a plurality of interstitial pore volumes are interspersed throughout the electrically insulating flaky carbon layer. An electrolyte is in contact with the carbon interface layer and the cathode. A separator is positioned between the anode and the cathode. The electrically insulating flaky carbon layer can include graphene oxide (GO). The plurality of interstitial pore volumes can be configured to transport lithium (Li) ions between the anode and the cathode via the plurality of interstitial pore volumes in a bulk phase of the electrolyte. The carbon interface layer can be configured to inhibit growth of Li dendritic structures from the anode towards the cathode.

Abstract: A negative electrode for a nonaqueous electrolyte secondary battery, which is an example of embodiments, comprises a negative electrode core body and a negative electrode mixture layer provided on the surface of the negative electrode core body. The negative electrode mixture layer includes graphite and fibrous carbon. The BET specific surface area of the graphite included in the first region is smaller than the BET specific surface area of the graphite included in the second region. In addition, the average length of the fibrous carbon included in the second region is longer than the average length of the fibrous carbon included in the first region.

Abstract: A negative electrode for a nonaqueous electrolyte secondary battery, which is an example of embodiments, comprises a negative electrode core body and a negative electrode mixture layer provided on the surface of the negative electrode core body. The negative electrode mixture layer includes graphite and fibrous carbon. The BET specific surface area of the graphite included in the first region is smaller than the BET specific surface area of the graphite included in the second region. In addition, the average length of the fibrous carbon included in the first region is longer than the average length of the fibrous carbon included in the second region.

Abstract: Systems and methods for anisotropic expansion of silicon-dominant anodes may include a cathode, an electrolyte, and an anode, where the anode may include a current collector and an active material on the current collector. An expansion of the anode during operation may be configured by a metal used for the current collector, and/or a lamination process that adheres the active material to the current collector. The expansion of the anode may be more anisotropic for thicker current collectors. A thicker current collector may be 10 ?m thick or greater. The expansion of the anode may be more anisotropic for more rigid materials used for the current collector. A more rigid current collector may include nickel and a less rigid current collector may include copper. The expansion of the anode may be more anisotropic for a rougher surface current collector.