Abstract: The present disclosure relates to an anode active material comprising a composite of a core-shell structure, a lithium secondary battery comprising the same, and a method of manufacturing the anode active material. According to an aspect of the present disclosure, there is provided an anode active material of a core-shell structure comprising a core including alloyed (quasi)metal oxide-Li (MOx—Liy) and a shell including a carbon material coated on a surface of the core. According to another aspect of the present disclosure, there is provided a method of manufacturing the anode active material of the core-shell structure. According to an aspect of the present disclosure, an anode active material with high capacity, excellent cycle characteristics and volume expansion control capacity, and high initial efficiency is provided.

Abstract: There is provided a non-aqueous electrolytic solution comprising an electrolyte salt, a specific fluorine-containing solvent and a fluorine-containing cyclic carbonate represented by the formula (A1): wherein X1 to X4 are the same or different and each is —H, —F, —CF3, —CHF2, —CH2F, —CF2CF3, —CH2CF3 or —CH2OCH2CF2CF3; at least one of X1 to X4 is —F, —CF3, —CF2CF3, —CH2CF3 or —CH2OCH2CF2CF3, and the non-aqueous electrolytic solution has further excellent noncombustibility and is suitable for lithium secondary batteries.

Abstract: A positive active material includes first and second lithium nickel complex oxides. A positive electrode and lithium battery include the positive active material. The positive active material, and the lithium battery including the positive active material have increased filling density, are thermally stable, and have improved capacity.

Abstract: This invention relates to a negative electrode material for lithium-ion batteries comprising silicon and having a chemically treated or coated surface influencing the zeta potential of the surface. The active material consists of particles or particles and wires comprising a core (11) comprising silicon, wherein the particles have a positive zeta potential in an interval between pH 3.5 and 9.5, and preferably between pH 4 and 9.5. The core is either chemically treated with an amino-functional metal oxide, or the core is at least partly covered with OySiHx groups, with 1<x<3, 1<y<3, and x>y, or is covered by adsorbed inorganic nanoparticles or cationic multivalent metal ions or oxides.

Abstract: Current collectors and methods are provided that relate to electrodes that are useful in electrochemical cells. The provided current collectors include a metallic substrate, a substantially uniform nano-scale carbon coating, and an active electrode material. The coating has a maximum thickness of less than about 200 nanometers.

Abstract: A rechargeable lithium-sulfur cell comprising an anode, a separator and/or electrolyte, a sulfur cathode, an optional anode current collector, and an optional cathode current collector, wherein the cathode comprises (a) exfoliated graphite worms that are interconnected to form a porous, conductive graphite flake network comprising pores having a size smaller than 100 nm; and (b) nano-scaled powder or coating of sulfur, sulfur compound, or lithium polysulfide disposed in the pores or coated on graphite flake surfaces wherein the powder or coating has a dimension less than 100 nm. The exfoliated graphite worm amount is in the range of 1% to 90% by weight and the amount of powder or coating is in the range of 99% to 10% by weight based on the total weight of exfoliated graphite worms and sulfur (sulfur compound or lithium polysulfide) combined. The cell exhibits an exceptionally high specific energy and a long cycle life.

Abstract: A system and method for stabilizing electrodes against dissolution and/or hydrolysis including use of cosolvents in liquid electrolyte batteries for three purposes: the extension of the calendar and cycle life time of electrodes that are partially soluble in liquid electrolytes, the purpose of limiting the rate of electrolysis of water into hydrogen and oxygen as a side reaction during battery operation, and for the purpose of cost reduction.

Abstract: A compound comprising a composition Ax(M?1?aM?a)y(XD4)z, Ax(M?1?aM?a)y(DXD4)z, or Ax(M?1?aM?a)y(X2D7)z, (A1?aM?a)xM?y(XD4)z, (A1?aM?a)xM?y(DXD4)z, or (A1?aM?a)xM?y(X2D7)z. In the compound, A is at least one of an alkali metal and hydrogen, M? is a first-row transition metal, X is at least one of phosphorus, sulfur, arsenic, molybdenum, and tungsten, M? any of a Group IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB, IVB, VB, and VIB metal, D is at least one of oxygen, nitrogen, carbon, or a halogen, 0.0001<a?0.1, and x, y, and z are greater than zero. The compound can be used in an electrochemical device including electrodes and storage batteries.

Abstract: According to one embodiment, there is provided an active substance. The active substance contains active material particles. The active material particles comprise a compound represented by the formula: Ti1-xM1xNb2-yM2yO7. The active material particles has a peak A attributed to a (110) plane which appears at 2? ranging from 23.74 to 24.14°, a peak B attributed to a (003) plane which appears at 2? ranging from 25.81 to 26.21° and a peak C attributed to a (?602) plane which appears at 2? ranging from 26.14 to 26.54° in an X-ray diffraction pattern of the active material particles. An intensity IA of the peak A, an intensity IB of the peak B, and an intensity IC of the peak C satisfy the relation (1): 0.80?IB/IA?1.12; and the relation (2) IC/IB?0.80.

Abstract: Some batteries can exhibit greatly improved performance by utilizing electrodes having randomly arranged graphene nanosheets forming a network of channels defining continuous flow paths through the electrode. The network of channels can provide a diffusion pathway for the liquid electrolyte and/or for reactant gases. Metal-air batteries can benefit from such electrodes. In particular Li-air batteries show extremely high capacities, wherein the network of channels allow oxygen to diffuse through the electrode and mesopores in the electrode can store discharge products.

Abstract: An anode, a lithium battery including the anode, and a method of manufacturing the anode. The anode includes: an anode active material including a metal alloyable with lithium; and a metal-carbon composite conducting agent having a density of 3.0 grams per cubic centimeter or greater.

Abstract: Provided is a metal oxygen battery 1 including a positive electrode 2 having oxygen as an active material, a negative electrode 3 having metallic lithium as an active material, and an electrolyte layer 4 interposed between the positive electrode 2 and negative electrode 3. The positive electrode 2 contains oxygen storage material including mixed crystal of hexagonal composite metal oxide expressed by the general formula AxByOz (in which, A is one type of metal selected from a group of Y, Sc, La, Sr, Ba, Zr, Au, Ag, Pt, Pd, B is one type of metal selected from a group of Mn, Ti, Ru, Zr, Ni, Cr, and x=1, 1?y?2, 1?z?7, provided that a case where both A and B are Zr is excluded) and one or more non-hexagonal composite metal oxide expressed by the general formula AxByOz.

Abstract: The positive electrode of a lithium ion secondary battery includes active material particles represented by LixNi1?yMyMezO2+?, and the active material particles include a lithium composite oxide represented by LixNi1?yMyO2, (where 0.95?x?1.1, 0<y?0.75, 0.001?z?0.05). The element M is selected from the group consisting of alkaline-earth elements, transition elements, rare-earth elements, IIIb group elements and IVb group elements. The element Me is selected from the group consisting of Mn, W. Nb, Ta, In, Mo, Zr and Sn, and the element Me is included in a surface portion of the active material particles. The lithium content x in the lithium composite oxide in an end-of-discharge state when a constant current discharge is performed at a temperature of 25° C. with a current value of 1C and an end-of-discharge voltage of 2.5 V satisfies 0.85?x??0.013Ln(z)+0.871.

Abstract: Disclosed is a cathode active material comprising a lithium-free metal oxide and a material with high irreversible capacity. A novel lithium ion battery system using the cathode active material is also disclosed. The battery, comprising a cathode using a mixture of a Li-free metal oxide and a material with high irreversible capacity, and an anode comprising carbon instead of Li metal, shows excellent safety compared to a conventional battery using lithium metal as an anode. Additionally, the novel battery system has a higher charge/discharge capacity compared to a battery using a conventional cathode active material such as lithium cobalt oxide, lithium nickel oxide or lithium manganese oxide.

Abstract: A nonaqueous electrolyte battery includes a positive electrode, a negative electrode and a nonaqueous electrolyte. The negative electrode contains a lithium compound and a negative electrode current collector supporting the lithium compound. A log differential intrusion curve obtained when a pore size diameter of the negative electrode is measured by mercury porosimetry has a peak in a pore size diameter range of 0.03 to 0.2 ?m and attenuates with a decrease in pore size diameter from an apex of the peak. A specific surface area (excluding a weight of the negative electrode current collector) of pores of the negative electrode found by mercury porosimetry is 6 to 100 m2/g. A ratio of a volume of pores having a pore size diameter of 0.05 ?m or less to a total pore volume is 20% or more.

Abstract: Hetero-nanostructure materials for use in energy-storage devices are disclosed. In some embodiments, a hetero-nanostructure material (100) includes a silicide nanoplatform (110), ionic host nanoparticles (120) disposed on the silicide nanoplatform (110) and in electrical communication with the silicide nanoplatform (110), and a protective coating (130) disposed on the silicide nanoplatform (110) between the ionic host nanoparticles (120). In some embodiments, the silicide nanoplatform (110) includes a plurality of connected and spaced-apart nanobeams comprising a silicide core (110), ionic host nanoparticles (120) formed on the silicide core, and a protective coating (130) formed on the silicide core (110) between the ionic host nanoparticles (120).

Abstract: A positive electrode for a nonaqueous electrolyte battery includes a collector, and a positive electrode active material layer. The positive electrode active material layer includes a positive electrode active material, and also includes a heteropoly acid and/or heteropoly acid compound and phosphorous acid as additives.

Abstract: An active material composition includes a porous graphene nanocage and a source material. The source material may be a sulfur material. The source material may be an anodic material. A lithium-sulfur battery is provided that includes a cathode, an anode, a lithium salt, and an electrolyte, where the cathode of the lithium-sulfur battery includes a porous graphene nanocage and a sulfur material and at least a portion of the sulfur material is entrapped within the porous graphene nanocage. Also provided is a lithium-air battery that includes a cathode, an anode, a lithium salt, and an electrolyte, where the cathode includes a porous graphene nanocage and where the cathode may be free of a cathodic metal catalyst.

Abstract: A composition for use in a battery electrode including lithium-sulfur particles coated with a transition metal species bonded to a sulfur species. Methods and materials for preparing such a composition. Use of such a compound in a battery.

Abstract: An electrode for an electrochemical energy store, including an active material layer having an active material, a protective layer being at least partially applied to the active material, and the protective layer at least partially including a fluorophosphate-based material. Such an electrode offers a particularly high stability, even when high voltages are present. Also described is a method for manufacturing an electrode, to an electrochemical energy store and to the use of a fluorophosphate-based material for generating a protective layer for an active material of an electrode of an electrochemical energy store.

Abstract: A method of forming an electrode active material by reacting a metal fluoride and a reactant. The reactant can be a metal oxide, metal phosphate, metal fluoride, or a precursors expected to decompose to oxides. The method includes a milling step and an annealing step. The method can alternately include a solution coating step. Also included is the composition formed following the method.

Abstract: This invention provides lithium-rich compounds as precursors for positive electrodes for lithium cells and batteries. The precursors comprise a Li2O-containing compound as one component, and a second charged or partially-charged component, selected preferably from a metal oxide, a lithium-metal-oxide, a metal phosphate or metal sulfate compound. Li2O is extracted from the above-mentioned electrode precursors to activate the electrode either by electrochemical methods or by chemical methods. The invention also extends to methods for synthesizing and activating the precursor electrodes and to cells and batteries containing such electrodes.

Abstract: A negative active material for a rechargeable lithium battery includes a core including an active material being capable of performing reversible electrochemical oxidation and reduction, and a coating layer on the surface of the core. The coating layer includes a reticular structure including —O-M-O— wherein M is selected Si, Ti, Zr, Al, or combinations thereof and an organic functional group linked to the M as a side chain. The organic functional group is selected from the group consisting of an alkyl group, a haloalkyl group, a substituted or unsubstituted aryl group, and combinations thereof. The negative active material for a rechargeable lithium battery according to the present invention can be applied along with an aqueous binder, and improve high capacity, good cycle-life, and particularly high capacity during charge and discharge at a high rate.

Abstract: Negative active materials and rechargeable lithium batteries including the negative active materials are provided. The negative active material includes an intermetallic compound of Si and a metal, and a metal matrix including Cu and Al. The negative active material may provide a rechargeable lithium battery having high capacity and excellent cycle-life and cell efficiency.

Abstract: It is an object to provide a cathode active material and a cathode which can attain a lithium ion secondary battery with high capacity and high security, and further to provide the lithium ion secondary battery with high capacity and high security. According to the present invention, the cathode active material is represented by the following composition formula: Li1.1+xNiaM1bM2cO2 wherein M1 represents Co, or Co and Mn; M2 represents Mo, W or Nb; ?0.07?x?0.1; 0.6?a?0.9; 0.05?b?0.38; and 0.02?c?0.06.

Abstract: A process of electroless plating a tin or tin-alloy active material onto a metal substrate for the negative electrode of a rechargeable lithium battery comprising steps of (1) immersing the metal substrate in an aqueous plating solution containing metal ions to be plated, (2) plating tin or tin-alloy active material onto the metal substrate by contacting the metal substrate with a reducing metal by swiping one on the other, and (3) removing the plated metal substrate from the plating bath and rinsing with deionized water. A rechargeable lithium battery using tin or tin-alloy as the anode active material.

Abstract: The described embodiments provide an energy storage device that includes a positive electrode including a material that stores and releases ion, a negative electrode including Nb-doped TiO2(B), and a non-aqueous electrolyte containing lithium ions. The described embodiments provide a method including the steps of combining at least one titanium compound and at least one niobium compound in ethylene glycol to form a precursor solution, adding water into the precursor solution to induce hydrolysis and condensation reactions, thereby forming a reaction solution, heating the reaction solution to form crystallized particles, collecting the particles, drying the collected particles, and applying a thermal treatment at a temperature >350° C. to the dried particles to obtain Nb-doped TiO2(B) particles.

Abstract: An object of the invention is to provide a lithium secondary battery using a fused salt at ambient temperature where a high capacity is able to be maintained even when it is stored at a high temperature environment or even when it is subjected to charge and discharge repeatedly and also to provide an electrode for a nonaqueous electrolytic lithium secondary battery. There is disclosed a lithium secondary battery using at least a fused salt at ambient temperature having ionic conductivity in which at least one of the positive and negative electrode contains a powder which solely comprises an inorganic solid electrolyte having lithium ionic conductivity. There is also disclosed an electrode for a lithium secondary battery using, at least, a ionic liquid having ionic conductivity which contains a powder solely comprising inorganic solid electrolyte having lithium ionic conductivity.

Abstract: An active material capable of forming an electrochemical device excellent in its discharge capacity and rate characteristic is provided. The active material in accordance with a first aspect of the present invention comprises a compound particle containing a compound having a composition represented by the following chemical formula (1), a carbon layer covering the compound particle, and a carbon particle. The active material in accordance with a second aspect of the present invention comprises a carbon particle and a compound particle having an average primary particle size of 0.03 to 1.4 ?m, being carried by the carbon particle, and containing a compound represented by the following chemical formula (1): LiaMXO4??(1) where a satisfies 0.9?a?2, M denotes one species selected from the group consisting of Fe, Mn, Co, Ni, and VO, and X denotes one species selected from the group consisting of P, Si, S, V, and Ti.

Abstract: A composite anode active material includes a first intermetallic compound, a second intermetallic compound, a metal that is incapable of alloy formation with lithium, and carbon. In the composite anode active material, an amorphous carbon is present between the first intermetallic compound and the second intermetallic compound, and the metal that is incapable of alloy formation with lithium is uniformly distributed throughout in the composite anode active material. The composite anode active material may be used as an anode of a lithium rechargeable battery.

Abstract: Disclosed are an anode active material for lithium secondary batteries and a method for manufacturing same, the anode active material comprising: a core part including a carbon-silicon complex and having a cavity therein; and a coated layer which is formed on the surface of the core part and includes a phosphor-based alloy.

Abstract: An aluminum ion battery includes an aluminum anode, a vanadium oxide material cathode and an ionic liquid electrolyte. In particular, the vanadium oxide material cathode comprises a monocrystalline orthorhombic vanadium oxide material. The aluminum ion battery has an enhanced electrical storage capacity. A metal sulfide material may alternatively or additionally be included in the cathode.

Abstract: Disclosed is a high-capacity electrochemical energy storage device in which a conversion reaction proceeds as the oxidation-reduction reaction, and the separation (hysteresis) between the electrode potentials for oxidation and reduction is small. The electrochemical energy storage device includes a first electrode including a first active material, a second electrode including a second active material, and a non-aqueous electrolyte interposed between the first and second electrodes. At least one of the first and second active materials is a metal salt having a polyatomic anion and a metal ion, and the metal salt is capable of oxidation-reduction reaction involving reversible release and acceptance of the polyatomic anion.

Abstract: A low-voltage, thin film battery and methods for making a low voltage battery. The battery includes a ceramic substrate having a first surface and a second surface. A cathode current collector is disposed adjacent to at least a portion of the first surface of the substrate. The current collector has a titanium layer and a gold layer. A high temperature annealed cathode is disposed adjacent to at least a portion of the gold cathode current collector and an electrolyte layer disposed adjacent to the annealed cathode. An annealed anode is disposed adjacent to at least a portion of the electrolyte, wherein the anode is electrically insulated from the cathode and the cathode current collectors by the electrolyte. An anode current collector is disposed adjacent to at least a portion of the anode.

Abstract: The present invention aims to provide a fuel cell anode, a membrane electrode assembly and a fuel cell, so as to obtain high electric power. The fuel cell anode has an electrode catalyst layer, and the electrode catalyst layer comprises a supported catalyst comprises electrically conductive carriers and fine catalytic particles supported thereon, a proton-conductive inorganic oxide supporting SiO2 on its surface, and a proton-conductive organic polymer binder. The SiO2 supported on the inorganic oxide prevents the oxide particles from growing, to ensure the high electric power. It is necessary to control the mixing ratios among the supported catalyst, the proton-conductive oxide and the proton-conductive binder in particular ranges.

Abstract: A composition including a first material and a metal or a metal oxide component for use in an electrochemical redox reaction is described. The first material is represented by a general formula M1xM2yXO4, wherein M1 represents an alkali metal element; M2 represents an transition metal element; X represents phosphorus; O represents oxygen; x is from 0.6 to 1.4; and y is from 0.6 to 1.4. Further, the metal or the metal oxide component includes at least two materials selected from the group consisting of transition metal elements, semimetal elements, group IIA elements, group IIIA elements, group IVA elements, alloys thereof and oxides of the above metal elements and alloys, wherein the two materials include different metal elements. Moreover, the first material and the metal or the metal oxide component are co-crystallized or physically combined, and the metal or the metal oxide component takes less than about 30% of the composition.

Abstract: A negative active material and a lithium battery are provided. The negative active material includes a composite core, and a coating layer formed on at least part of the composite core. The composite core includes a carbonaceous base and a metal/metalloid nanostructure disposed on the carbonaceous base. The coating layer includes a metal oxide coating layer and an amorphous carbonaceous coating layer.

Abstract: A novel hybrid lithium-ion anode material based on coaxially coated Si shells on vertically aligned carbon nanofiber (CNF) arrays. The unique cup-stacking graphitic microstructure makes the bare vertically aligned CNF array an effective Li+ intercalation medium. Highly reversible Li+ intercalation and extraction were observed at high power rates. More importantly, the highly conductive and mechanically stable CNF core optionally supports a coaxially coated amorphous Si shell which has much higher theoretical specific capacity by forming fully lithiated alloy. Addition of surface effect dominant sites in close proximity to the intercalation medium results in a hybrid device that includes advantages of both batteries and capacitors.

Abstract: A novel hybrid lithium-ion anode material based on coaxially coated Si shells on vertically aligned carbon nanofiber (CNF) arrays. The unique cup-stacking graphitic microstructure makes the bare vertically aligned CNF array an effective Li+ intercalation medium. Highly reversible Li+ intercalation and extraction were observed at high power rates. More importantly, the highly conductive and mechanically stable CNF core optionally supports a coaxially coated amorphous Si shell which has much higher theoretical specific capacity by forming fully lithiated alloy. Addition of surface effect dominant sites in close proximity to the intercalation medium results in a hybrid device that includes advantages of both batteries and capacitors.

Abstract: A novel hybrid lithium-ion anode material based on coaxially coated Si shells on vertically aligned carbon nanofiber (CNF) arrays. The unique cup-stacking graphitic microstructure makes the bare vertically aligned CNF array an effective Li+ intercalation medium. Highly reversible Li+ intercalation and extraction were observed at high power rates. More importantly, the highly conductive and mechanically stable CNF core optionally supports a coaxially coated amorphous Si shell which has much higher theoretical specific capacity by forming fully lithiated alloy. Addition of surface effect dominant sites in close proximity to the intercalation medium results in a hybrid device that includes advantages of both batteries and capacitors.

Abstract: A negative active material includes a conductive unit bound in island-like form to silicon-based nanowires on a carbonaceous base. Such negative active material may improve the electrical conductivity of the silicon-based nanowires, and suppress separation of the silicon-based nanowires caused from volume expansion, and thus may improve lifetime characteristics of a lithium battery.

Abstract: With a small amount of a conductive additive, an electrode for a storage battery including an active material layer which is highly filled with an active material is provided. The use of the electrode enables fabrication of a storage battery having high capacity per unit volume of the electrode. By using graphene as a conductive additive in an electrode for a storage battery including a positive electrode active material, a network for electron conduction through graphene is formed. Consequently, the electrode can include an active material layer in which particles of an active material are electrically connected to each other by graphene. Therefore, graphene is used as a conductive additive in an electrode for a sodium-ion secondary battery including an active material with low electric conductivity, for example, an active material with a band gap of 3.0 eV or more.

Abstract: The rechargeable lithium battery includes a positive electrode which includes a positive active material, a negative electrode, and an electrolyte which includes a non-aqueous organic solvent and a lithium salt. The positive active material includes a core including at least one of a compound represented by Formula 1 and a compound represented by Formula 2, and a surface-treatment layer which is formed on the core and includes a compound represented by Formula 3. The lithium salt includes LiPF6 and a lithium imide-based compound. LiaNibCocMndMeO2??(1) LihMn2MiO4??(2) M?xPyOz??(3) wherein each of M and M? is independently selected from the group consisting of an alkali metal, an alkaline-earth metal, a Group 13 element, a Group 14 element, a transition element, a rare earth element, and combinations thereof, 0.95?a?1.1, 0?b?0.999, 0?c?0.999, 0?d?0.999, 0.001?e?0.2, 0.95?h?1.1, 0.001?i?0.2, 1?y?4, 0?y?7, and 2?z?30.

Abstract: The present invention relates to a process for the preparation of compounds of general formula (I) Lia-bM1bV2-cM2c(PO4)x??(I) wherein M1, M2, a, b, c and x have the following meanings: M1: Na, K, Rb and/or Cs, M2: Ti, Zr, Nb, Cr, Mn, Fe, Co, Ni, Al, Mg and/or Sc, a: 1.5-4.5, b: 0-0.6, c: 0-1.98 and x: number to equalize the charge of Li and V and M1 and/or M2, if present, wherein a-b is >0, to a compound according to general formula (I) as defined above, to spherical agglomerates and/or particles comprising at least one compound of general formula (I) as defined above, to the use of such a compound for the preparation of a cathode of a lithium ion battery or an electrochemical cell, and to a cathode for a lithium ion battery, comprising at least one compound as defined above.

Abstract: The present invention relates to a process for the preparation of compounds of general formula (I) Lia-bM1bV2-cM2c(PO4)x??(I) wherein M1, M2, a, b, c and x have the following meanings: M1: Na, K, Rb and/or Cs, M2: Ti, Zr, Nb, Cr, Mn, Fe, Co, Ni, Al, Mg and/or Sc, a: 1.5-4.5, b: 0-0.6, c: 0-1.98 and x: number to equalize the charge of Li and V and M1 and/or M2, if present, wherein a-b is >0, to a compound according to general formula (I) as defined above, to spherical agglomerates and/or particles comprising at least one compound of general formula (I) as defined above, to the use of such a compound for the preparation of a cathode of a lithium ion battery or an electrochemical cell, and to a cathode for a lithium ion battery, comprising at least one compound as defined above.

Abstract: The rechargeable lithium battery of the present invention includes a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte. The positive active material includes a core and a coating layer formed on the core. The core is made of a material such as LiCo0.98M?0.02O2, and the coating layer is made of a material such as MxPyOz. The electrolyte solution includes a nitrile-based additive. The rechargeable lithium battery of the present invention shows higher cycle-life characteristics and longer continuous charging time at high temperature.

Abstract: Disclosed are a cathode active material for lithium secondary batteries, a method for preparing the same, and lithium secondary batteries comprising the same. The cathode active material for lithium secondary batteries comprises a lithium metal oxide secondary particle core formed by aggregation of a plurality of lithium metal oxide primary particles; a first shell formed by coating the surface of the secondary particle core with a plurality of barium titanate particles and a plurality of metal oxide particles; and a second shell formed by coating the surface of the first shell with a plurality of olivine-type lithium iron phosphate oxide particles and a plurality of conductive material particles. The cathode active material for lithium secondary batteries allows manufacture of lithium secondary batteries having excellent thermal stability, high-temperature durability and overcharge safety.

Abstract: The specification relates to a composite particle for storing lithium. The composite particle is used in an electrochemical cell. The composite particle includes a metal oxide on the surface of the composite particle, a major dimension that is approximately less than or equal to 40 microns and a formula of MM?Z, wherein M is from the group of Si and Sn, M? is from a group of Mn, Mg, Al, Mo, Bronze, Be, Ti, Cu, Ce, Li, Fe, Ni, Zn, Co, Zr, K, and Na, and Z is from the group of O, Cl, P, C, S, H, and F.

Abstract: A positive-electrode material includes lithium vanadium phosphate particles having an average primary particle diameter from 0.3 ?m to 2.6 ?m and crystallite sizes from 24 nm to 33 nm. The lithium vanadium phosphate particles are coated with a conductive carbon of a range of 0.5 mass % to 2.4 mass % with respect to a total lithium vanadium phosphate particles.

Abstract: A rechargeable lithium battery including a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte including a non-aqueous organic solvent and a lithium salt. The positive electrode has an active-mass density of about 3.7 to 4.1 g/cc, and the non-aqueous electrolyte includes a nitrile-based compound additive, a non-aqueous organic solvent, and a lithium salt.