Patent classifications
C01G49/0027
Composite metal oxide, method for producing composite metal oxide, and sodium secondary battery
An object of the present invention or a problem to be solved by the present invention is to provide, as a material for use as a positive electrode of a sodium secondary battery, a novel material that allows the resulting battery to have capacity characteristics superior to those of conventional batteries. The composite metal oxide of the present invention has a composition represented by the general formula Na.sub.xMe.sub.yO.sub.2, where Me is at least one selected from the group consisting of Fe, Mn, and Ni, x satisfies 0.8<x≦1.0, and y satisfies 0.95≦y<1.05, and consists of a P2 structure. The sodium secondary battery of the present invention includes: a positive electrode (13) containing the composite metal oxide of the present invention; a negative electrode (16) containing a material capable of absorbing and desorbing Na ions; and an electrolyte containing Na ions and anions.
Battery with Novel Components
A battery cell having an anode or cathode comprising an acidified metal oxide (“AMO”) material, preferably in monodisperse nanoparticulate form 20 nm or less in size, having a pH<7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0>−12, at least on its surface.
POSITIVE ELECTRODE ACTIVE MATERIAL AND PREPARATION METHOD THEREFOR, SODIUM ION BATTERY, AND APPARATUS COMPRISING SODIUM ION BATTERY
The present application discloses a positive electrode active material satisfying the chemical formula L.sub.xNa.sub.yM.sub.zCu.sub.αFe.sub.βMn.sub.γO.sub.2+δ−0.5ηX.sub.η and a preparation method therefor, a sodium ion battery and an apparatus including such battery, wherein L is a doping element at alkali metal site, M is a doping element at transition metal site, and X is a doping element at oxygen site, 0≤x<0.35, 0.65≤y≤1, 0<α≤0.3, 0<β≤0.5, 0<γ≤0.5, −0.03≤δ≤0.03, 0≤η≤0.1, z+α+β+γ=1, mx+y+nz+2α+3β+4γ=2(2+δ), m is the valence state of L, and n is the valence state of M; and the pH of the positive electrode active material is 10.5-13, wherein L is a doping element at alkali metal site, M is a doping element at transition metal site, and X is a doping element at oxygen site.
Mixed conductor, electrochemical device including the same, and method of preparing the mixed conductor
A mixed conductor represented by Formula 1:
A.sub.1±xM.sub.2±yO.sub.4−δ Formula 1
wherein, in Formula 1, A is a monovalent cation, and M is at least one of a monovalent cation, a divalent cation, a trivalent cation, a tetravalent cation, a pentavalent cation, or a hexavalent cation, 0≤x≤1, 0≤y≤2, and 0≤δ≤1, with the proviso that when M includes vanadium, 0<δ≤1, and wherein the mixed conductor has an inverse spinel crystal structure.
ACTIVE MATERIAL, NONAQUEOUS ELECTROLYTE BATTERY, BATTERY PACK, AND VEHICLE
According to one embodiment, an active material is provided. This active material includes active material particles containing orthorhombic Na-containing niobium titanium composite oxide, and satisfies the following formula (1):
1≦A5/A0 (1) where A5 is a mole content ratio of a Li mole content L5 to a total of a Ti mole content T5 and a Nb mole content N5, and A0 is a mole content ratio of a Li mole content L0 to a total of a Ti mole content T0 and a Nb mole content N0.
Method for efficiently preparing ferrate based on nascent interfacial activity
A method for efficiently preparing ferrate based on nascent state interfacial activity. The method is as follows: (a) preparing nascent iron solution; (b) adding an oxidizing agent to the iron solution of step (a); (c) adding alkali solution or alkali particles to the mixed solution of step (b), mixing by stirring, and carrying out solid-liquid separation; (d) adding a stabilizing agent to the liquid separated out in step (c), and thus obtaining ferrate solution. The yield is 78-98%. The prepared ferrate solution is stable and can be stored for 3-15 days.
DESODIATED SODIUM TRANSITION METAL OXIDES FOR PRIMARY BATTERIES
The invention provides primary batteries that incorporate a desodiated sodium transition metal oxide into the positive electrode (a cathode). Batteries of the invention using a desodiated sodium transition metal oxide in the cathode exhibit discharge voltages, battery capacities, and energy densities higher than a traditional Zn—MnO.sub.2 dry cell battery, such as a commercially available AA battery. These batteries are also advantageous over comparable lithium ion batteries due to the high abundance and low cost of sodium precursor materials with similar electrical performance.
BATTERY CELL WITH ANODE OR CATHODE WITH NANOMATERIAL INCLUDING ACIDIC SURFACE
A battery comprising an acidified metal oxide (“AMO”) material, preferably in monodispersed nanoparticulate form 20 nm or less in size, having a pH<7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0>−12, at least on its surface.
Battery with novel components
A battery cell having an anode or cathode comprising an acidified metal oxide (“AMO”) material, preferably in monodisperse nanoparticulate form 20 nm or less in size, having a pH<7 when suspended in a 5 wt % aqueous solution and a Hammett function H.sub.0>−12, at least on its surface.
POSITIVE ELECTRODE ACTIVE MATERIAL AND ITS PREPARATION METHOD, SODIUM ION BATTERY AND APPARATUS CONTAINING THE SODIUM ION BATTERY
The present application discloses a positive electrode active material and its preparation method, a sodium ion battery and an apparatus containing the sodium ion battery. The positive electrode active material satisfies a chemical formula of Na.sub.1-xCu.sub.hFe.sub.kMn.sub.lM.sub.mO.sub.2-y wherein M is one or more selected from Li, Be, B, Mg, Al, K, Ca, Ti, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, In, Sn, and Ba, 0<x≤0.33, 0<h≤0.24, 0≤k≤0.32, 0<l≤0.68, 0≤m≤0.1, h+k+l+m=1, 0≤y≤0.2, and the positive electrode active material has a water content of 6000 ppm or less.