A composite particulate for a lithium battery, wherein the composite particulate has a diameter from 10 nm to 50 μm and comprises one or more than one anode active material particles that are dispersed in a high-elasticity polymer matrix or encapsulated by a high-elasticity polymer shell, wherein said high-elasticity polymer matrix or shell has a recoverable elastic tensile strain no less than 5%, when measured without an additive or reinforcement dispersed therein, and a lithium ion conductivity no less than 10.sup.−8 S/cm at room temperature and wherein the high-elasticity polymer comprises a crosslinked polymer network of chains derived from a phosphazene compound.

The disclosure provides a preparation method of a vanadium selenide/carbon cellulose composite, belonging to the technical fields of electrode materials of potassium ion batteries and preparation technologies thereof. Through compounding of carbon, carbon cellulose and vanadium diselenide (VSe.sub.2), a synergistic effect occurs between two components, and carbon cellulose-carbon coating is capable of increasing electron conductivity and potassium ion diffusion rate of a material while inhibiting the agglomeration of vanadium diselenide (VSe.sub.2). Therefore, the prepared vanadium selenide/carbon cellulose composite has excellent electrochemical performance and exhibits outstanding rate performance and cycling stability. The method is simple in process, low in cost, environmentally friendly, and suitable for large-scale industrial production.

Process for making an electrode active material according to general formula Li.sub.1+xTM.sub.1−xO.sub.2, wherein TM is a combination of Ni and Co and Zr and at least one metal selected from Mn and Al, and, optionally, at least one of Mg, Ti, and W, wherein GC at least 60 mole-% is Ni, referring to the sum of Ni, Co and, if applicable, Mn and Al, and x is in the range of from zero to 0.2, said process comprising the following steps: (a) mixing (A) a mixed oxide or oxyhydroxide of Ni, Co and, if applicable, Mn, (B) at least one lithium compound selected from lithium hydroxide, lithium oxide and lithium carbonate, and (C) at least one oxide or hydroxide or oxyhydroxide of Zr with an average diameter D50 in the range of from 1 to 7 μm, and in compounds (C) that are selected from oxides of Zr, their crystallite size is in the range of from 5 to 20 nm and (b) Subjecting said mixture to heat treatment at a temperature in the range of from 700 to 1000° C.

Provided is an apparatus for producing a positive electrode active material precursor. The apparatus includes: a reactor into which a reaction solution is introduced; a stirrer being inserted into the reactor and stirring the reaction solution; and a filter type baffle being inserted into the reactor and including a filter.

A method for preparing a cathode active material precursor for a secondary battery, including: moving a co-precipitation filtrate generated after a co-precipitation reaction to a co-precipitation filtrate storage tank; removing a metal hydroxide by passing the co-precipitation filtrate through a filter; reacting the co-precipitation filtrate from which the metal hydroxide is removed with sulfuric acid or nitric acid to produce an ammonium sulfate or an ammonium nitrate while removing ammonia from the co-precipitation filtrate from which the metal hydroxide is removed; cooling and crystallizing the co-precipitation filtrate from which the metal hydroxide and ammonia are removed to precipitate a sodium sulfate; filtering the precipitated sodium sulfate to separate the precipitated sodium sulfate from the co-precipitation filtrate from which the metal hydroxide and ammonia are removed; drying the sodium sulfate separated from the co-precipitation filtrate and moving the co-precipitation filtrate separated from the sodium sulfate to a circulation concentration tank; and heating the co-precipitation filtrate stored in the circulation concentration tank to a predetermined temperature for recycling and performing N.sub.2 purging or bubbling, is provided.

The present application describes the use of a solid electrolyte interphase (SEI) fluorinating precursor and/or an SEI fluorinating compound to coat an electrode material and create an artificial SEI layer. These modifications may increase surface passivation of the electrodes, SEI robustness, and structural stability of the silicon-containing electrodes.

Provided is a rechargeable alkali metal-sulfur cell comprising an anode active material layer, a cathode active material layer, a discrete anode-protecting layer disposed between the anode active material layer and the cathode active material layer, and an electrolyte (but no porous separator), wherein the anode-protecting layer has a thickness from 1 nm to 100 μm and comprises an elastomer having a fully recoverable tensile elastic strain from 2% to 1,000% and a lithium ion conductivity from 10.sup.−8 S/cm to 5×10.sup.−2 S/cm when measure at room temperature. The cathode layer comprises a sulfur-containing material selected from a sulfur-carbon hybrid, sulfur-graphite hybrid, sulfur-graphene hybrid, conducting polymer-sulfur hybrid, metal sulfide, sulfur compound, or a combination thereof. This battery exhibits an excellent combination of high sulfur content, high sulfur utilization efficiency, high energy density, no known dendrite issue, no dead lithium or dead sodium issue, and a long cycle life.

A cobalt oxide for a lithium secondary battery, a method of preparing the cobalt oxide; a lithium cobalt oxide for a lithium secondary battery formed from the cobalt oxide; and a lithium secondary battery having a positive electrode including the lithium cobalt oxide, the cobalt oxide having a tap density of about 2.8 g/cc to about 3.0 g/cc, and an intensity ratio of about 0.8 to about 1.2 of a second peak at 2θ of about 31.3±1° to a first peak at 2θ of about 19±1° in X-ray diffraction spectra, as analyzed by X-ray diffraction.

The present invention discloses a method for rapidly preparing a Prussian blue analogue with a monoclinic crystal structure. The Prussian blue analogue with a monoclinic crystal structure has a chemical formula of Na.sub.xM[Fe(CN).sub.6].sub.y.Math.zH.sub.2O, where M=Mn or Fe, 1.5 <<2, and 0.5<y<1. In this method, a mixture of sodium ferrocyanide and sodium chloride is adopted as a solution A, and a solution of manganese salt or iron salt in water is adopted as a solution B; the solutions A and B are continuously and rapidly mixed by a micromixer, and the precipitation reaction is conducted to obtain a nano-precursor slurry; and the nano-precursor slurry is aged at 80 C. to 160 C. for 3 min to 2 h to obtain a Prussian blue analogue with a monoclinic crystal structure that has a particle diameter of 200 nm to 2,000 nm.

The present application describes the use of a solid electrolyte interphase (SEI) fluorinating precursor and/or an SEI fluorinating compound to coat an electrode material and create an artificial SEI layer. These modifications may increase surface passivation of the electrodes, SEI robustness, and structural stability of the silicon-containing electrodes.