A class of compositions that are inclusive of a lithium metal oxide or oxyfluoride compound having a general formula: LiTM[n]OF where TM[n] represents a number of transition metal species inclusive of transitional metal species differentiated by charge or d.sup.0 electron shell conformation, with [n] being at least 4 of said transitional metal species, and wherein said lithium metal oxide or oxyfluoride has a cation-disordered rocksalt (DRX) structure and a mitigated SRO via a high entropy DRX design strategy. Also featured is a method of synthesizing the high entropy DRX lithium metal oxide or oxyfluoride compounds, as well as usage of the same in Li-ion batteries, with particular utility in cathodes of such Li-ion batteries.

The present invention pertains to a positive electrode active material for a lithium secondary battery, the positive electrode active material having a layered structure and containing lithium, transition metals, fluorine (F), and oxygen, wherein the layered structure includes a lithium layer consisting solely of lithium and a transition metal layer consisting solely of transition metals including nickel, the nickel includes Ni.sup.3+ and Ni.sup.2+ in terms of oxidation number, and the ratio (Ni.sup.2+/Ni.sup.3+) of Ni.sup.2+ to Ni.sup.3+ increases as the fluorine content increases.

Methods and systems for the electrochemical conversion of halogenated compounds are provided. In some embodiments, a method comprises converting a halogenated compound (e.g., fluorinated gas) to relatively non-hazardous products via one or more electrochemical reactions. The electrochemical reaction(s) may occur under relatively mild conditions (e.g., low temperature) and/or without the aid of a catalyst. In some embodiments, the electrochemical reaction may produce a relatively large amount of energy. In some such cases, systems, described herein, may be designed to facilitate the conversion of the halogenated compound (e.g., SF.sub.6, NF.sub.3) while harnessing (e.g., storing, converting) the energy associated with the electrochemical reaction. System and methods described herein may be used in a wide variety of applications, including waste management (e.g., environmental remediation, greenhouse gas mitigation), energy recovery (e.g., industrial energy recovery), and primary batteries (e.g., metal-gas batteries).

The present disclosure relates to fluoride ion batteries and structures of metal based electrode materials for various fluoride ion batteries. The structures of the metal based electrode materials comprise one or more shells or interfaces, enabling the electrodes to operate at room temperature with a liquid electrolyte.

An object is to provide an electrode active material that can provide an alkali metal battery having a longer charge/discharge life and a higher capacity. The problem is solved by means of an electrode active material for an alkali metal battery, represented by formula: A.sub.a1MS.sub.a2X.sub.a3 wherein A is selected from Li and Na; M is selected from V, Nb, Ta, Ti, Zr, Hf, Cr, Mo, and W which are group 4 to 6 elements; X is selected from F, Cl, Br, I, CO.sub.3, SO.sub.4, NO.sub.3, BH.sub.4, BF.sub.4, PF.sub.6, ClO.sub.4, CF.sub.3SO.sub.3, (CF.sub.3SO.sub.2).sub.2N, (C.sub.2F.sub.5SO.sub.2).sub.2N, (FSO.sub.2).sub.2N, and [B(C.sub.2O.sub.4).sub.2]; a1 is 1 to 9; a2 is 2 to 6; when a3 is 3 and a3 is 0, a2 is not 4; and when M does not include V, a3>0.

This positive electrode active material for a non-aqueous electrolyte secondary battery contains a lithium-transition metal composite compound. The lithium-transition metal composite compound is represented by general formula Li.sub.xMn.sub.yNi.sub.zMe.sub.αO.sub.aF.sub.b (in the formula, 1≤x≤1.2, 0.4≤y≤0.8; 0≤z≤0.4, x+y+z=2, 0<α<0.05, 1.8≤a≤2, and 1.8≤a±b≤2.2 are satisfied, and Me represents at least two kinds of elements selected from metal elements other than Li, Mn, and Ni) and Me includes at least one kind of element having an ion radius of 0.6 Å or more.

A process of synthesizing a solid state lithium ion conductor includes mechanically milling at least two precursors so as to form crystalline Li.sub.6MgBr.sub.8. For instance, the mechanical milling can be carried out using a planetary mill. Moreover, in a practical application, the precursors include LiBr and MgBr.sub.2.

Transition-metal doped Li-rich anti-perovskite cathode compositions are provided herein. The Li-rich anti-perovskite cathode compositions have a chemical formula of Li.sub.(3-δ)M5/.sub.mBA, wherein 0<δ<3m/(m+1) and δ=3m/(m+1) is the maximum value for the transition metals doping, a chemical formula of Li.sub.4-δMs.sub.δ/mPC.sub.4A, wherein 0<δ≦4m/(m+1) and δ=4m/(m+1) is the maximum value for the transition metals doping, or a combination thereof, wherein M is a transition metal, B is a divalent anion, and A is a monovalent anion. Also provided herein, are methods of making the Li-rich anti-perovskite cathode compositions, and uses of the Li-rich anti-perovskite cathode compositions.

A method for manufacturing an electrode having a porosity of between 20% and 60% by volume and pores with an average diameter of less than 50 nm. In the method, provision is made of a substrate and a colloidal suspension of aggregates or agglomerates of monodisperse primary nanoparticles of an active electrode material, having an average primary diameter D.sub.50 of between 2 and 100 nm, the aggregates or agglomerates having an average diameter D.sub.50 of between 50 nm and 300 nm. A layer is deposited from said colloidal suspension on the substrate. The deposited layer is then dried and consolidated to obtain a mesoporous layer. A coating of an electronically conductive material is then deposited on and inside the pores of the porous layer. Such a porous electrode can be used in lithium-ion microbatteries.

A coated cathode active material, a method of preparing the same, and a cathode and a non-aqueous electrolyte secondary battery, each including the same, the coated cathode active material including: a cathode active material particle and a coating layer on a surface of the cathode active material particle, the coating layer including LiAlF.sub.4, LiF, and Li.sub.3AlF.sub.6.