Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4. Additional compositional modification to include Si increases the cycle life and greatly improved the coulombic efficiency to between 97-100% at a C/3 cycle rate.

Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4. Additional compositional modification to include Si increases the cycle life and greatly improved the coulombic efficiency to between 97-100% at a C/3 cycle rate.

Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4. Additional compositional modification to include Si increases the cycle life and greatly improved the coulombic efficiency to between 97-100% at a C/3 cycle rate.

Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4. Additional compositional modification to include Si increases the cycle life and greatly improved the coulombic efficiency to between 97-100% at a C/3 cycle rate.

Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4. Additional compositional modification to include Si increases the cycle life and greatly improved the coulombic efficiency to between 97-100% at a C/3 cycle rate.

Abstract: A lithiated metal phosphate material substituted by divalent atoms at the M2 site and trivalent atoms, a portion of which are present at both the M2 and the M1 sites. The substituted material has the general formula of Li1-3tM2+1-t-dTt3+Dd2+PO4, wherein M is selected from the group consisting of Mn2+, Co2+, Ni2+ and combinations thereof; T is selected from the group consisting of Fe3+, Al3+ and Ga3+ and a portion of said T resides at the M2 sites, said portion being greater than 0 and no more than 99 percent of the total T atoms; D is selected from the group consisting of Fe2+, Mn2+, Co2+, Ni2+, Mg2+, Zn2+, Ca2+ and combinations thereof; d has a value greater than 0 and no more than 0.3; and t has a value in the range of 0 to 0.3. Also disclosed are electrodes which incorporate the substituted metal phosphate material and are disposed in electrochemical cells as well as batteries, including rechargeable lithium ion batteries.

Abstract: A positive electrode material having a nominal stoichiometry Li1+y/2Co1?x?y?z?dSizFexMyM?d(PO4)1+y/2 where M is a trivalent cation selected from at least one of Cr, Ti, Al, Mn, Ni, V, Sc, La and/or Ga, M? is a divalent cation selected from at least one of Mn, Ni, Zn, Sr, Cu, Ca and/or Mg, y is within a range of 0<y?0.10 and x is within a range of 0?x?0.2. The use of double compositional modification to LiCoPO4 increases the discharge capacity from ˜100 mAh/g to about 130 mAh/g while retaining the discharge capacity retention of the singly Fe-substituted LiCoPO4.

Abstract: A non-aqueous rechargeable electrochemical cell includes an electrolyte composition produced through the dissolution of a thermally stable lithium salt in a lactone solvent. The resulting cell has stable performance in a wide temperature range between ?40° C. and 80° C. The resulting cell operates across this wide temperature range with a commercially acceptable capacity retention, power loss characteristics, and safety characteristics across this temperature range.

Abstract: A lithiated metal phosphate material substituted by divalent atoms at the M2 site and trivalent atoms, a portion of which are present at both the M2 and the M1 sites. The substituted material has the general formula of Li1-3tM2+1-t-dT3+Dd2+PO4, wherein M is selected from the group consisting of Mn2+, Co2+, Ni2+ and combinations thereof; T is selected from the group consisting of Fe3+, Al3+ and Ga3+ and a portion of said T resides at the M2 sites, said portion being greater than 0 and no more than 99 percent of the total T atoms; D is selected from the group consisting of Fe2+, Mn2+, Co2+, Ni2+, Mg2-+, Zn2+, Ca2+ and combinations thereof; d has a value greater than 0 and no more than 0.3; and t has a value in the range of 0 to 0.3. Also disclosed are electrodes which incorporate the substituted metal phosphate material and are disposed in electrochemical cells as well as batteries, including rechargeable lithium ion batteries.

Abstract: An electrochemical system is provided by the present invention which includes a positive electrode; a negative electrode; an electrolyte containing a lithium salt dissolved in a non-aqueous solvent; and a nitrile component in the electrolyte. A preferred nitrile component is an aromatic nitrile. Also described is a process for inhibiting electrolyte decomposition wherein an initial cycle is performed on an inventive electrochemical system such that a solid-electrolyte interphase forms on the anode, inhibiting electrolyte decomposition.

Abstract: A composition is provided as a salt having the formula MBF3X where M is an alkali metal cation and X is the halide fluoride, bromide or iodide. A lithium salt has several characteristics making the composition well suited for inclusion within a lithium-ion battery. A process for forming an alkali metal trifluorohaloborate salt includes the preparation of a boron trifluoride etherate in an organic solvent. An alkali metal halide salt where the halide is chloride, bromide or iodide is suspended in the solution and reacted with boron trifluoride etherate to form an alkali metal trifluorohaloborate. The alkali metal trifluorohaloborate so produced is collected as a solid from the solution. The process is simple and yields alkali metal trifluorohaloborate of sufficient purity to be used directly in battery applications.

Abstract: A method of preparing a composite cathode active material having superior cell characteristics includes mixing and milling starting material, carbon and an organic complexing agent. The mixture is heated at a first temperature in an inert atmosphere to form a composite precursor, and then the precursor is ground and heated at a second temperature in an inert atmosphere to produce a carbon-containing composite cathode material having high electronic conductivity. The said composite cathode has a general formula of LiFe1?xMxPO4—C, within 0?x<1, M is selected from the group consisting of Co, Ni, V, Cr, Mn and a mixture thereof.

Abstract: The carboxyl borate represents a novel liquid that upon reaction with lithium halide produces a lithium ion electrochemical device electrolyte upon dissolution in an aprotic solvent mixture.

Abstract: An electrolyte compound has the formula where p is an integer from 1 to 3 inclusive; and Yp+ is a metal ion, onium species, or proton; j is an integer value between 0 and 4 inclusive; k is an integer between 1 and 3 inclusive; and the sum 2k and j equals 6; Z is independently in each occurrence CR1R2 or C(O); R1 and R2 are independently in each occurrence H, F or CH3. A process for preparing an oxyfluorophosphate is also provided.

Abstract: A non-aqueous rechargeable electrochemical cell includes an electrolyte composition produced through the dissolution of a thermally stable lithium salt in a lactone solvent. The resulting cell has stable performance in a wide temperature range between ?40° C. and 80° C. The resulting cell operates across this wide temperature range with a commercially acceptable capacity retention, power loss characteristics, and safety characteristics across this temperature range.

Abstract: A lithiated metal phosphate material is doped by a portion of the lithium atoms which are present at the M2 sites of the material. The doped material has the general formula: Li1+xM1?x?dDdPO4. In the formula, M is a divalent ion of one or more of Fe, Mn, Co and Ni. D is a divalent metal ion which is one or more of Mg, Ca, Zn, and Ti. It is present in an amount represented by the subscript d which has a value ranging from 0 to 0.1. The portion of the lithium which is present at the M2 octahedral sites of the material is represented by the subscript x and is greater than 0 and no more than 0.07. Also disclosed are electrodes which incorporate the material as well as batteries, including lithium ion batteries, which include cathodes fabricated from the doped, lithiated metal phosphate materials.

Abstract: A method for enhancing the performance characteristics of a battery through the use of the electrolyte composition comprised of a non-aqueous solvent, and a salt mixture. The salt mixture includes an alkali metal electrolyte salt and an additive salt having an anion of a mixed anhydride of oxalic acid and boric acid. Specific additive salts include lithium bis(oxalato) borate and lithium oxalyldifluoroborate. Particular electrolyte salts comprise LiPF6 and LiBF4. The additive salt is present in an amount of 0.1-60 mole percent of the total of the additive salt and electrolyte salt content of the electrolyte.

Abstract: A non-aqueous electrolyte solution for lithium or a lithium ion cell, which improves lithium ion cell capacity retention and enhances storage life thereof. The non-aqueous solution can be implemented in the context of an electrolyte system that includes a lithium salt dissolved in a solvent formed from a mixture of one or more cyclic esters, and/or one or more chain esters, and at least one lactam based solvent. Such a system is suited for use with electrochemical energy storage devices, which are based on non-aqueous electrolytes, such as high energy density batteries and/or high power electrochemical capacitors. Such an electrochemical storage devices is generally based on non-aqueous electrolytes that include lithium salt dissolved in a solvent system.

Abstract: A method of preparing a composite cathode active material having superior cell characteristics includes mixing and milling starting material, carbon and an organic complexing agent. The mixture is heated at a first temperature in an inert atmosphere to form a composite precursor, and then the precursor is ground and heated at a second temperature in an inert atmosphere to produce a carbon-containing composite cathode material having high electronic conductivity The said composite cathode has a general formula of LiFe1-xMxPO4—C, within 0?x<1, M is selected from the group consisting of Co, Ni, V, Cr, Mn and a mixture thereof.

Abstract: A lithium battery includes an electrolyte comprised of a non-aqueous solvent, and a salt mixture. The salt mixture includes an alkali metal electrolyte salt and an additive salt having an anion of a mixed anhydride of oxalic acid and boric acid. Specific additive salts include lithium bis(oxalato) borate and lithium oxalyldifluoroborate. Particular electrolyte salts comprise LiPF6 and LiBF4. The additive salt is present in an amount of 0.1–60 mole percent of the total of the additive salt and electrolyte salt content of the electrolyte. Also disclosed is a method for enhancing the performance characteristics of a lithium battery through the use of the electrolyte composition. Also disclosed is the compound lithium oxalyldifluoroborate.