There are provided a solid electrolyte material having high density and ion conductivity, and an all solid lithium ion secondary battery using the solid electrolyte material. The solid electrolyte material has a garnet-related structure which has a chemical composition represented by Li.sub.7-x-yLa.sub.3Zr.sub.2-x-yTa.sub.xNb.sub.yO.sub.12 (0x0.8, 0.2y1, and 0.2x+y1) and relative density of 99% or greater, and belongs to a cubic system. The solid electrolyte material has lithium ion conductivity which is equal to or greater than 1.010.sup.3 S/cm. The solid electrolyte material has a lattice constant a which satisfies 1.28 nma1.30 nm, and has a lithium ion which occupies only two or more 96h sites in a crystal structure. The all solid lithium ion secondary battery includes a positive electrode, a negative electrode, and a solid electrolyte. The solid electrolyte includes the solid electrolyte material.

The present invention is directed to solid state electrolytes that comprise a coating layer. The present invention is also directed to methods of making the solid state electrolyte materials and methods of using the solid state electrolyte materials in batteries and other electrochemical technologies.

An electrode for a secondary battery comprises a current collector; and an active material-containing layer has active materials which comprise titanium-containing composite oxide having an orthorhombic crystal structure and represented by a general formula Li.sub.2+aM1.sub.2bTi.sub.6cM2.sub.dO.sub.14+;

wherein the active material-containing layer has intensity ratio Ia/Ib in an X-ray diffraction pattern of the active material-containing layer, the Ia and the Ib are obtained by powder X-ray diffraction method using Cu-K ray, the intensity ratio is within a range of 0.5Ia/Ib2, the Ia is the strongest intensity of a diffraction peak among diffraction peaks appearing within a range of 42244, and the Ib is the strongest intensity of a diffraction peak among diffraction peaks appearing within a range of 44<248.

(M1 is at least one selected from the group consisting of Sr, Ba, Ca, Mg, Na, Cs, Rb and K, M2 is at least one selected from the group consisting of Zr, Sn, V, Nb, Ta, Mo, W, Y, Fe, Co, Cr, Mn, Ni and Al a is within a range of 0a6 b is within a range of 0b<2 c is within a range of 0c<6 d is within a range of 0d<6 is within a range of 0.50.5.)

According to one embodiment, a negative electrode active material includes particles and a carbon material. The particles is represented by Li.sub.2+aA.sub.dTi.sub.6bB.sub.bO.sub.14c, where A is at least one element selected from the group consisting of Na, K, Mg, Ca, Ba, and Sr; B is a metal element other than Ti; and a, b, c, and d respectively satisfy 0a5, 0b6, 0c0.6, and 0d3. The carbon material covers at least a part of surfaces of the particles.

Provided are an oxide semiconductor excellent in transparency, mobility, and weatherability, etc., and a semiconductor device having the oxide semiconductor, a p-type semiconductor being realizable in the oxide semiconductor. The oxide semiconductor consists of a composite oxide, which has a crystal structure including a foordite structure and contains Nb and Sn elements, and its holes become charge carriers by the condition that Sn.sup.4+/(Sn.sup.2++Sn.sup.4+) which is a ratio of Sn.sup.4+ to a total amount of Sn in the composite oxide is 0.006Sn.sup.4+/(Sn.sup.2++Sn.sup.4+)0.013.

Provided are an oxide semiconductor excellent in transparency, mobility, and weatherability, etc., and a semiconductor device having the oxide semiconductor, a p-type semiconductor being realizable in the oxide semiconductor. The oxide semiconductor consists of a composite oxide, which has a crystal structure including a pyrochlore structure, containing at least one or more kinds of elements selected from Nb and Ta, and containing Sn element, and its holes become charge carriers by the condition that Sn.sup.4+/(Sn.sup.2++Sn.sup.4+) which is a ratio of Sn.sup.4+ to a total amount of Sn in the composite oxide is 0.124Sn.sup.4+/(Sn.sup.2++Sn.sup.4+)0.148.

In an exemplary embodiment, a piezoelectric ceramic composition is an alkali niobate-based piezoelectric ceramic composition whose primary component is a compound expressed by the general formula Li.sub.xNa.sub.yK.sub.1xyNbO.sub.3 (where 0<x<1, 0<y<1, and x+y<1), and which contains 100 ppm or more but less than 1000 ppm of fluorine by mass. The alkali niobate-based piezoelectric ceramic composition demonstrates good properties even when sintered at low temperature.

To provide a piezoelectric body film and a piezoelectric element from which an excellent piezoelectric characteristic can be obtained even in a high-temperature environment and a method for manufacturing a piezoelectric element.

A piezoelectric body film of the present invention is a piezoelectric body film containing a perovskite-type oxide represented by Formula (1), in which a content q of Nb with respect to the number of all atoms in the perovskite-type oxide and a ratio r of a diffraction peak intensity from a (200) plane to a diffraction peak intensity from a (100) plane of the perovskite-type oxide, which is measured using an X-ray diffraction method, satisfy Formula (2), Formula (1) A.sub.1+[(Zr.sub.yTi.sub.1-y).sub.1-xNb.sub.x]O.sub.2, Formula (2) 0.35r/q<0.58, in this case, in Formula (1), A represents an A site element containing Pb, x and y each independently represent a numerical value of more than 0 and less than 1, standard values of and z each are 0 and 3, but these values may deviate from the standard values as long as the perovskite-type oxide has a perovskite structure, and, in Formula (2), a unit of q is atm %.

The present invention provides a titanium-niobium composite oxide, which includes titanium, niobium, dopant M and oxygen, and the molar ratio of the titanium, niobium and dopant M is 1:(2x):x, and x is 0.01 to 0.2; wherein the dopant M is doped in a crystal structure with a monoclinic crystal structure formed from the titanium, niobium and oxygen, and the dopant M is at least one metal element selected from the group consisting of Sn, Al and Zr. The present invention further provides a preparation method of the titanium-niobium composite oxide, an active material and a lithium ion secondary battery using the same. The titanium-niobium composite oxide produced by the present invention has better electrical performance than the existing negative electrode materials, so that the lithium ion secondary battery using it can exhibit longer cycle life, larger electric capacity and faster charging and discharging performance, thereby having a bright prospect of the application.

This disclosure provides systems, methods, and apparatus related to lithium metal oxyfluorides. In one aspect, a method for manufacturing a lithium metal oxyfluoride having a general formula Li.sub.1+x(MM).sub.zO.sub.2-yF.sub.y, with 0.6z0.95, 0<y0.67, and 0.05x0.4, the lithium metal oxyfluoride having a cation-disordered rocksalt structure, includes: providing at least one lithium-based precursor; providing at least one redox-active transition metal-based precursor; providing at least one redox-inactive transition metal-based precursor; providing at least one fluorine-based precursor comprising a fluoropolymer; and mixing the at least one lithium-based precursor, the at least one redox-active transition metal-based precursor, the at least redox-inactive transition metal-based precursor, and the at least one fluorine-based precursor comprising a fluoropolymer to form a mixture.