The present invention discloses a process for the preparation of metal sulphide quantum dots by using a very low cost sulphur precursor as a sulphur source. The metal sulphide quantum dots finds application in optical devices selected from photovoltaic cells, photodetectors and light-emission devices.

The present invention discloses a process for the preparation of metal sulphide quantum dots by using a very low cost sulphur precursor as a sulphur source. The metal sulphide quantum dots finds application in optical devices selected from photovoltaic cells, photodetectors and light-emission devices.

A manganese nickel composite hydroxide which serves as a starting material for positive electrode active materials for secondary batteries, and the secondary battery having low resistance and high output characteristics. A manganese nickel composite hydroxide according to the present invention is represented by general formula (A) Mn.sub.1xyNi.sub.xM.sub.y(OH).sub.2+(wherein 00.27, 0y0.05, 00.5, and M represents at least one element selected from among Mg, Al, Ca, Ba, Sr, Ti, V, Fe, Cr, Co, Cu, Zr, Nb, Mo and W), and has an SO.sub.4 content of 0.90% by weight or less, an Na content of 0.04% by weight or less, a BET specific surface area of from 40 m.sup.2/g to 70 m.sup.2/g (inclusive), and a value obtained by [(d.sub.90-d.sub.10)/(average particle diameter)] of 0.90 or less, said value being an index indicating the expanse of the particle size distribution.

A positive-electrode active material contains a lithium composite oxide containing at least one selected from the group consisting of F, Cl, N, and S. The crystal structure of the lithium composite oxide belongs to a space group C2/m. An XRD pattern of the lithium composite oxide comprises a first peak within the first range of 44 degrees to 46 degrees of a diffraction angle 2 and a second peak within the second range of 18 degrees to 20 degrees of the diffraction angle 2. The ratio of the second integrated intensity of the second peak to the first integrated intensity of the first peak is within a range of 0.05 to 0.90.

A system, method, and articles of manufacture for a surface-modified transition metal cyanide coordination compound (TMCCC) composition, an improved electrode including the composition, and a manufacturing method for the composition which may include multiple chelation species (Che x). The composition, compound, device, and uses thereof according to A.sub.xMn.sub.(y-k)M.sup.j.sub.k[Mn.sup.m(CN).sub.(6-p-q)(NC).sub.p(Che_I).sup.r.sub.q].sub.z. CHE_GROUP (Vac).sub.(1-z).nH.sub.2O, wherein CHE_GROUP includes one or more chelation materials selected from the group consisting of (Che_I).sup.r.sub.w, (Che_II).sup.s.sub.v, and combinations thereof, and wherein 0<j4, 0k0.1, 0(p+q)6, 0<x4, 0<y1, 0<z1, 0<w0.2; 3r3; 0<v0.2; 3s3; and 0n6; wherein x+2(yk)+jk+(m+(r+1)q6)z+wr+vs=0.

A system, method, and articles of manufacture for a surface-modified transition metal cyanide coordination compound (TMCCC) composition, an improved electrode including the composition, and a manufacturing method for the composition which may include multiple chelation species (Che_x). The composition, compound, device, and uses thereof according to A.sub.xMn.sub.(y-k)M.sup.j.sub.k[Mn.sup.m(CN).sub.(6-p-q)(NC).sub.p(Che_I).sup.r.sub.q].sub.z. CHE_GROUP (Vac).sub.(1-z).nH.sub.2O, wherein CHE_GROUP includes one or more chelation materials selected from the group consisting of (Che_I).sup.r.sub.w, (Che_II).sup.s.sub.v, and combinations thereof, and wherein 0<j4, 0k0.1, 0(p+q)6, 0<x4, 0<y1, 0<z1, 0<w0.2; 3r3; 0<v0.2; 3s3; and 0n6; wherein x+2(yk)+jk+(m+(r+1)q6)z+wr+vs=0.

The present invention provides a positive-electrode active material for non-aqueous secondary battery comprising a sodium transition metal composite oxide represented by Formula:
Na.sub.xFe.sub.1-yM.sub.yO.sub.2, wherein 0.4x0.7, 0.25y<1.0, and M is at least one element selected from the group consisting of manganese, cobalt and nickel, the sodium transition metal composite oxide having a crystal structure substantially composed of P6.sub.3/mmc alone.

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.

Process for precipitating a carbonate or (oxy)hydroxide comprising nickel from an aqueous solution of a nickel salt wherein such process is carried out in a vessel comprising (A) a vessel body, (B) one or more elements that control the hydraulic flow of the slurry formed during the precipitation and that induce a loop-type circulation flow, and (C) a stirrer whose stirrer element is in the vessel but located separately from the element(s) (B).

A battery according to the present disclosure includes a positive electrode, a negative electrode, and an electrolyte layer positioned between the positive electrode and the negative electrode. The positive electrode includes a positive electrode material. The positive electrode material includes a positive electrode active material and a first solid electrolyte material. The positive electrode active material includes Li.sub.xMn.sub.yO.sub.2, where 0?x??1.05 and 0.9?y?1.1 are satisfied. The negative electrode includes Bi as a main component of a negative electrode active material.