A mixed conductor represented by Formula 1:
A.sub.4±xTi.sub.5−yG.sub.zO.sub.12−δ  Formula 1 wherein, in Formula 1, A is a monovalent cation, G is at least one of a monovalent cation, a divalent cation, a trivalent cation, a tetravalent cation, a pentavalent cation, or a hexavalent cation, with the proviso that G is not Ti or Cr, wherein 0<x<2, 0.3<y<5, 0<z<5, and 0<δ≤3.

Provided is a new 5 V-class spinel-type lithium-manganese-containing composite oxide capable of achieving both the expansion of a high potential capacity region and the suppression of gas generation. Proposed is the spinel-type lithium-manganese-containing composite oxide comprising Li, Mn, O and two or more other elements, and having an operating potential of 4.5 V or more at a metal Li reference potential, wherein a peak is present in a range of 14.0 to 16.5° at 2θ, in an X-ray diffraction pattern measured by a powder X-ray diffractometer (XRD) using CuKα1 ray.

Provided is a new 5 V class spinel-type lithium manganese-containing composite oxide which enables the expansion of a high potential capacity region and the suppression of gas generation. The 5 V class spinel-type lithium manganese-containing composite oxide has an operating potential of 4.5 V or more at a metal Li reference potential, and contains Li, Mn, O and two or more other elements. The spinel-type lithium manganese-containing composite oxide is characterized in that, in an electronic diffraction image from a transmission electron microscope (TEM), a diffraction spot observed in the Fd-3m structure as well as a diffraction spot not observed in the Fd-3m structure are confirmed.

A method of producing a particulate lithium metal oxide cathode material comprising the steps of providing an organic acid, providing a lithium compound, and providing a metal compound. The organic acid, the lithium compound, and the metal compound are mixed to form a mixture. The organic acid is melted to form a liquid organic acid, if the organic acid is provided as a solid. The mixture, including the liquid organic acid, is cCalcined in an atmosphere containing oxygen to form a lithium metal oxide. The lithium metal oxide is cooled and sized to produce the particulate lithium metal oxide having a predetermined average particle size.

The present disclosure relates to a positive electrode material including a spinel-structured lithium manganese-based first positive electrode active material and a lithium nickel-manganese-cobalt-based second positive electrode active material, wherein the first positive electrode active material includes a lithium manganese oxide represented by Formula 1 and a coating layer which is disposed on a surface of the lithium manganese oxide, the second positive electrode active material is represented by Formula 2, and an average particle diameter of the second positive electrode active material is greater than an average particle diameter of the first positive electrode active material, and a positive electrode and a lithium secondary battery which include the positive electrode material:
Li.sub.1+aMn.sub.2−bM.sup.1.sub.bO.sub.4−cA.sub.c  [Formula 1]
Li.sub.1+x[Ni.sub.yCo.sub.zMn.sub.wM.sup.2.sub.v]O.sub.2−pB.sub.p  [Formula 2]

A positive electrode active material has a small difference in a crystal structure between the charged state and the discharged state. For example, the crystal structure and volume of the positive electrode active material, which has a layered rock-salt crystal structure in the discharged state and a pseudo-spinel crystal structure in the charged state at a high voltage of approximately 4.6 V, are less likely to be changed by charging and discharging as compared with those of a known positive electrode active material. In order to form the positive electrode active material having the pseudo-spinel crystal structure in the charged state, it is preferable that a halogen source such as a fluorine and a magnesium source be mixed with particles of a composite oxide containing lithium, a transition metal, and oxygen, which is synthesized in advance, and then the mixture be heated at an appropriate temperature for an appropriate time.

A process for producing lithium titanate which includes the steps of synthesizing a lithium titanate hydrate intermediate via aqueous chemical processing, and thermally treating the lithium titanate hydrate intermediate to produce the lithium titanate. The lithium titanate hydrate is preferably (Li.sub.1.81H.sub.0.19)Ti.sub.2O<<2H.sub.2O. The lithium titanate is preferably Li.sub.4Ti.sub.5O.sub.12 (LTO). Synthesizing the lithium titanate hydrate intermediate may include mixing a titanium-containing compound with a lithium-containing compound in a solvent to produce a lithium-titanium precursor mixture. Preferably the titanium-containing compound includes titanium tetrachloride TiCl.sub.4. Also, a lithium titanate obtained according to the process and a lithium battery including the lithium titanate.

There is provided a Co-based 5-V spinel-type lithium manganese-containing complex oxide not only having an operating potential of 4.5 V or higher but also being capable of extending its capacity region of a 5.5 to 5.5 V region and being capable of enhancing its energy density as well. There is proposed a spinel-type lithium cobalt manganese-containing complex oxide having a crystal structure classified as a space group Fd-3m and being represented by the general formula [Li.sub.x(Co.sub.yMn.sub.3−x−y)O.sub.4−δ] (wherein 0.90≦x≦1.15 and 0.75≦y≦1.25), wherein the oxide has a crystallite size measured by a Rietveld method using the fundamental method of 100 nm to 200 nm, an interatomic distance of Li—O of 1.80 Å to 2.00 Å, and a strain of 0.20 to 0.50.

A method is provided in which a lithium titanate precursor structure is subjected to element selective sputtering to form a lithium titanate structure including a lithium titanate core and a conformal layer on the lithium titanate core, wherein the conformal layer includes titanium oxide. A method of preparing an electrode for a lithium ion battery, wherein the electrode includes lithium titanate structures, is also provided.

Disclosed is a lithium manganese (Mn)-based oxide including Mn as an essential transition metal and having a layered crystal structure, in which the amount of Mn is greater than that of other transition metal(s), the lithium manganese-based oxide exhibits flat level section characteristics in which release of oxygen occurs together with lithium deintercalation during first charging in a high voltage range of 4.4 V or higher, and at least one of a transition metal layer including Mn and an oxygen layer is substituted or doped with a pillar element.