The present disclosure belongs to the technical field of lithium battery cathode materials, and discloses a preparation method of multiple carbon-coated high-compaction lithium iron manganese phosphate, comprising the following steps: (1) synthesizing a carbon and vanadium co-doped ferromanganese phosphate precursor through a co-precipitation method, sintering, and removing crystal water to obtain an anhydrous ferromanganese phosphate precursor; (2) adding lithium phosphate, a supplemental phosphorus source, an organic carbon source, a dopant and deionized water, and performing ball milling, wet sanding, spray drying and sintering to obtain an intermediate material; and (3) adding deionized water and the organic carbon source, then performing ball milling, sanding, spray drying, sintering and air jet pulverization to obtain multiple carbon-coated high-compaction lithium iron manganese phosphate.

A method for forming a treated sintered composition includes: providing a slurry precursor including a lithium-, sodium-, or magnesium-based compound; tape casting the slurry precursor to form a green tape; sintering the green tape at a temperature in a range of 500° C. to 1350° C. for a time in a range of less than 60 min to form a sintered composition; and heat treating the sintered composition at a temperature in a range of 700° C. to 1100° C. for a time in a range of 1 min to 2 hrs in an oxygen-containing atmosphere to form the treated sintered composition.

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.

The present disclosure relates to a lithium-sulfur battery cathode. The lithium-sulfur battery cathode comprises a carbon nanotube sponge and a plurality of sulfur nanoparticles. Wherein the carbon nanotube sponge comprises a plurality of micropores. The plurality of sulfur nanoparticles are uniformly distributed in the plurality of micropores. The present disclosure also relates a method for making the lithium-sulfur battery cathode and a lithium-sulfur battery using the lithium-sulfur battery cathode.

Solid-state lithium ion electrolytes of lithium metal nitride based compounds are provided which contain an anionic framework capable of conducting lithium ions. Materials of specific formulae are provided and methods to alter the materials with inclusion of aliovalent ions shown. Lithium batteries containing the composite lithium ion electrolytes are provided. Electrodes containing the lithium metal nitride based composites are also provided.

Solid-state lithium ion electrolytes of lithium metal nitride based compounds are provided which contain an anionic framework capable of conducting lithium ions. Materials of specific formulae are provided and methods to alter the materials with inclusion of aliovalent ions shown. Lithium batteries containing the composite lithium ion electrolytes are provided. Electrodes containing the lithium metal nitride based composites are also provided.

The process of making a lithium ion battery cathode comprises the step of forming a slurry of an active material, a nano-size conductive agent, a binder polymer, a solvent and a dispersant. The solvent consists essentially of one or more of a compound of Formula 1, 2, or 3, and the dispersant comprises an ethyl cellulose.

A lithium cobalt-based oxide cathode active material powder having: —a primary phase comprising Li, Co, and O, and —a secondary phase comprising LiNaSO.sub.4, wherein the content of said LiNaSO.sub.4 secondary phase in said powder is of at least 0.4 wt. % and inferior or equal to 1.1 wt. % with respect to a total weight of the cathode active material powder, said cathode active material powder being characterized in that it has a S/Na atomic ratio superior or equal to 0.80 and inferior or equal to 1.20.

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.