C01G45/006

Transition metal cyanide coordination compounds having multiple reactions

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 according to Formula III—An electrochemical cell including a system having an anode, a cathode, and an electrolyte wherein the anode includes a material, including the material including at least one composition represented by Formula III: A.sub.xMn.sub.y[Mn(CN).sub.(6)].sub.z(Vac).sub.(1-z).n(H.sub.2O)m(Che) wherein, in Formula III, A includes one or more alkali metals including Na; and wherein 0<j≤4, 0≤k≤0.1, 1.2<x≤4, 0<y≤1, 0.8<z≤1, 0<n≤4; 0≤m≤0.2 and wherein x+2y−4z=0.

MANUFACTURING METHOD OF COMPOSITE OXIDE AND MANUFACTURING METHOD OF POWER STORAGE DEVICE
20220199998 · 2022-06-23 ·

An object is to reduce variation in shape of crystals that are to be formed. Solutions containing respective raw materials are made in an environment where an oxygen concentration is lower than that in air, the solutions containing the respective raw materials are mixed in an environment where an oxygen concentration is lower than that in air to form a mixture solution, and with use of the mixture solution, a composite oxide is formed by a hydrothermal method.

METAL OXIDE, OXYGEN ADSORPTION AND DESORPTION DEVICE, OXYGEN CONCENTRATING DEVICE, AND METHOD FOR PRODUCING METAL OXIDE

Provided is a metal oxide containing a brownmillerite-type manganese oxide represented by (Ca.sub.2-xA.sub.x)(Mn.sub.yAl.sub.zE.sub.2-y-z).sub.wO.sub.5+δ (in the formula, A represents one or more alkaline earth metal elements other than Ca; E represents one or more 3d transition metal elements or earth metal elements other than Mn and Al; and x, y, z, δ, and w satisfy 0≤x≤2, 0<y≤2, 0≤z<2, 0<y+z≤2, 0≤δ≤0.5, and 0.8≤w≤1.2), wherein the metal oxide has a defect in a (020) plane of a crystal of the brownmillerite-type manganese oxide.

Near infrared-reflective black pigment and method for producing same

Provided is a method for producing a near infrared-reflective black pigment containing at least the element calcium, the element titanium, and the element manganese, wherein the method produces a pigment that exhibits little of the elution of the element calcium and the element manganese that is caused by contact with acid. At least a calcium compound, a titanium compound, and a manganese compound are mixed by a wet grinding method and are calcined to provide a BET specific surface area of at least 1.0 m.sup.2/g and less than 3.0 m.sup.2/g. In another method, the element bismuth and/or the element aluminum is incorporated in a near infrared-reflective black pigment containing at least the element calcium, the element titanium, and the element manganese.

Battery

A battery includes a positive electrode including a positive electrode active material, a negative electrode, and an electrolytic solution including a lithium hexafluorophosphate and an additive. The positive electrode active material includes a compound having a crystal structure belonging to a space group FM3-M and represented by Compositional Formula (1): Li.sub.xMe.sub.yO.sub.αF.sub.β. The additive is at least one selected from the group consisting of difluorophosphates, tetrafluoroborates, bis(oxalate)borate salts, bis(trifluoromethanesulfonyl)imide salts, and bis(fluorosulfonyl)imide salts.

Cation-disordered rocksalt lithium manganese oxides or oxyfluorides

A class of compositions in the Li—Mn—O—F chemical space for Li-ion cathode materials. The compositions are cobalt-free, high-capacity Li-ion battery cathode materials synthesized with cation-disordered rocksalt (DRX) oxide or oxyfluorides, with the general formula Li.sub.xMn.sub.2-xO.sub.2-yF.sub.y (1.1≤x≤1.3333; 0≤y≤0.6667). The compositions are characterized by: (i) high capacities (e.g., >240 mAh/g); (ii) high energy densities (e.g., >750 Wh/kg between 1.5-4.8V); (iii) favorable cyclability; and (iv) low cost.

Modified black spinel pigments for glass and ceramic enamel applications

Modified copper chromite spinel pigments exhibit lower coefficients of thermal expansion than unmodified structures. Three methods exist to modify the pigments: (1) the incorporation of secondary modifiers into the pigment core composition, (2) control of the pigment firing profile, including both the temperature and the soak time, and (3) control of the pigment core composition.

Raw material of electrolyte solution, method for manufacturing electrolyte solution and method for manufacturing redox flow battery

A raw material of an electrolyte solution that is to be dissolved in a solvent to form an electrolyte solution, and the raw material of an electrolyte solution is a raw material of an electrolyte solution that is a solid or semisolid that contains Ti in an amount of 2 mass % to 83 mass % inclusive, Mn in an amount of 3 mass % to 86 mass % inclusive, and S in an amount of 6 mass % to 91 mass % inclusive.

High-capacity lithium metal oxyfluorides with combined metal and oxygen redox for Li-ion battery cathodes

A lithium metal oxide suitable for use as a cathode material in a rechargeable battery having a general formula of: Li.sub.xM.sub.zM′.sub.zO.sub.uF.sub.y, where x is 1.80<x<2.20, y=1, and more specifically 1.90<x<2.10, with 1.80<u<2.20. Preferably, 1.90<u<2.10, and 0.80<y<1.20, or more specifically, 0.90<y<1.10. The lithium metal oxide has a cation-disordered rocksalt structure, wherein M is a transition metal selected from a first group consisting of Ni, Mn, Co, Fe, and combinations thereof. M′ is a transition metal selected from a second group consisting of Ti, Zr, Nb, Mo, Sn, Hf, Te, Sb, and combinations thereof. M has a first oxidation state q and M′ has a second oxidation state q′, with (q/z)+(q′/z′)=+3, preferably +2.7≤q/z)+(q′/z′)≤+3.3.

METHOD OF MAKING HIGH CAPACITY ELECTRODE MATERIAL

A method of manufacturing lithium-metal nitride including suspending a lithium—metal-oxide-powder (LMOP) within a gaseous mixture, incrementally heating the suspended LMOP to a holding temperature of between 400 and 800 degrees Celsius such that the LMOP reaches the holding temperature, and maintaining the LMOP at the holding temperature for a time period in order for the gaseous mixture and the LMOP to react to form a lithium-metal nitride powder (LMNP).