To provide a hydroxide precursor having a high density, a method for producing a lithium transition metal composite oxide using the precursor, a positive active material having a large discharge capacity per unit volume, which uses the composite oxide, an electrode for nonaqueous electrolyte secondary battery, and a nonaqueous electrolyte secondary battery. A method for producing a transition metal hydroxide precursor for use in production of a lithium transition metal composite oxide, including adding a solution containing a transition metal (Me) into a reaction tank in which a water solvent of dissolution of a complexing agent and a reducing agent has been charged in advance to coprecipitate a transition metal hydroxide that includes Mn and Ni, or Mn, Ni and Co, and has a mole ratio Mn/Me of larger than 0.5 and a mole ratio Co/Me of 0.15 or less. Further, a lithium transition metal composite oxide having an α-NaFeO.sub.2-type crystal structure, in which a mole ratio Li/Me is larger than 1, the mole ratios of Mn and Co are as described above, and which has an X-ray diffraction pattern attributable to R3-m, a ratio (FWHM (003)/FWHM (114)) of a full width at half maximum of a diffraction peak of a (003) plane to a full width at half maximum of a diffraction peak of a (104) plane of 0.72 or less, and a peak differential pore volume of 0.50 mm.sup.3/(g.Math.nm) or less as determined by a BJH method from an adsorption isotherm using a nitrogen gas adsorption method.

A metal-air battery and a component air cathode including a solid ionically conductive polymer material.

A metal-air battery and a component air cathode including a solid ionically conductive polymer material.

Disclosed is a method for improving the performance of a layered electrode material. An interlayer spacing of the layered electrode material is measured and donated as (b). A salt compound is selected and added into a solvent with a molecular diameter of (c) to prepare an electrolytic solution, where a diameter (a) of a cation in the salt compound is smaller than the interlayer spacing (b), and c>b−a. The electrolytic solution is used as the working electrolytic solution for the layered electrode material.

Disclosed is a method for improving the performance of a layered electrode material. An interlayer spacing of the layered electrode material is measured and donated as (b). A salt compound is selected and added into a solvent with a molecular diameter of (c) to prepare an electrolytic solution, where a diameter (a) of a cation in the salt compound is smaller than the interlayer spacing (b), and c>b−a. The electrolytic solution is used as the working electrolytic solution for the layered electrode material.

Rechargeable, non-aqueous lithium batteries which contain, as active anode material, either lithium metal or a lithium alloy, an active cathode material with a redox potential in the range of between 1.5 and 3.4 V vs Li/Li.sup.+ and lithium rhodanide (LiSCN) as electrolyte component. One or more related methods for providing overcharge protection are also described herein.

A new type of battery electrode plate preparation method is described. The method can include the following steps: a) a mixing process; b) a milling and polishing process; c) an extrusion shearing and extending process; d) cutting to obtain an electrode membrane; and e) pressing at a high temperature and a high pressure to obtain a battery electrode plate. The method can adopt the active material of different electrochemical batteries as the main body to prepare a thick type battery electrode plate with a high conductivity, a high capacity and a high active material loading, which has a viscoelastic body. The electrode plate can have a flexible organic network structure and an excellent mechanical strength, and can still exist in a variety of electrolytes after hundreds of times or even thousands of times of deep charge and discharge cycles. The thick electrode plate prepared by using the method can be applied to a variety of batteries such as lead-acid battery positive and negative electrode plates, a lead carbon battery electrode plate, a lithium ion battery electrode plate, a supercapacitor electrode plate, a Ni-MH battery electrode plate, and others.

A new type of battery electrode plate preparation method is described. The method can include the following steps: a) a mixing process; b) a milling and polishing process; c) an extrusion shearing and extending process; d) cutting to obtain an electrode membrane; and e) pressing at a high temperature and a high pressure to obtain a battery electrode plate. The method can adopt the active material of different electrochemical batteries as the main body to prepare a thick type battery electrode plate with a high conductivity, a high capacity and a high active material loading, which has a viscoelastic body. The electrode plate can have a flexible organic network structure and an excellent mechanical strength, and can still exist in a variety of electrolytes after hundreds of times or even thousands of times of deep charge and discharge cycles. The thick electrode plate prepared by using the method can be applied to a variety of batteries such as lead-acid battery positive and negative electrode plates, a lead carbon battery electrode plate, a lithium ion battery electrode plate, a supercapacitor electrode plate, a Ni-MH battery electrode plate, and others.

An alkaline electrochemical cell includes a cathode; a gelled anode having an anode active material and an electrolyte; and a separator disposed between the cathode and the anode; wherein the separator includes a non-conductive, porous material having a mean pore size of about 1 micron to about 5 microns, a maximum pore size of about 19 microns, and an air permeability of about 0.5 cc/cm.sup.2/s to about 3.8 cc/cm.sup.2/s at 125 Pa.

An alkaline battery, and a component cathode including a solid ionically conducting polymer material.