C01G53/51

POSITIVE ELECTRODE ACTIVE MATERIAL, PREPARATION METHOD THEREOF, AND POSITIVE ELECTRODE PLATE, BATTERY CELL, BATTERY, AND ELECTRIC DEVICE CONTAINING SAME

The present application provides a positive electrode active material, a preparation method thereof, and a positive electrode plate, a battery cell, a battery, and an electric device containing the same, where the positive electrode active material includes a matrix and a sodium-rich layer formed in situ on the surface of the matrix, the matrix includes a sodium-containing layered transition metal oxide, and the sodium-rich layer includes one or more of sodium salts represented by Formula (I) and Formula (II), where m represents an integer from 1 to 8, and n represents an integer from 2 to 20.

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POSITIVE ELECTRODE ACTIVE MATERIAL AND PREPARATION METHOD THEREOF, POSITIVE ELECTRODE PLATE, BATTERY, AND ELECTRIC DEVICE

A positive electrode active material and a preparation method thereof, a positive electrode plate, a battery, and an electric device. The positive electrode active material includes: Na.sub.xMn.sub.aFe.sub.bM.sub.cN.sub.dO.sub.2+eF.sub.e, where 0.5x1.1, a0, b0, c0, d>0, a+b +c+d=1, 0.10.1, and e0; M ions include at least one of Ni.sup.2+, Ni.sup.3+, Cu.sup.2+, Cu.sup.+, Zn.sup.2+, Mg.sup.2+, Y.sup.3+, La.sup.3+, In.sup.3+, Sb.sup.3+, Li+, Sn.sup.2+, and Ag.sup.+; B.sub.iI.sub.i.sup.41500 .sup.4, where B.sub.i is a molar fraction of cations, I.sub.i is an ionic potential of the cations, in unit of .sup.1, and the cations include manganese ions, iron ions, M ions, and N ions; and the ionic potential of the N ions is greater than or equal to 5 .sup.1.

POSITIVE ELECTRODE ACTIVE MATERIAL AND PREPARATION METHOD THEREOF, POSITIVE ELECTRODE PLATE, BATTERY, AND ELECTRIC DEVICE

A positive electrode active material and a preparation method thereof, a positive electrode plate, a battery, and an electric device. The positive electrode active material includes: Na.sub.xMn.sub.aFe.sub.bM.sub.cN.sub.dO.sub.2+eF.sub.e, where 0.5x1.1, a0, b0, c0, d>0, a+b +c+d=1, 0.10.1, and e0; M ions include at least one of Ni.sup.2+, Ni.sup.3+, Cu.sup.2+, Cu.sup.+, Zn.sup.2+, Mg.sup.2+, Y.sup.3+, La.sup.3+, In.sup.3+, Sb.sup.3+, Li+, Sn.sup.2+, and Ag.sup.+; B.sub.iI.sub.i.sup.41500 .sup.4, where B.sub.i is a molar fraction of cations, I.sub.i is an ionic potential of the cations, in unit of .sup.1, and the cations include manganese ions, iron ions, M ions, and N ions; and the ionic potential of the N ions is greater than or equal to 5 .sup.1.

SODIUM LAYERED METAL OXIDE AND PREPARATION METHOD THEREOF, SECONDARY BATTERY, AND ELECTRIC APPARATUS
20260045496 · 2026-02-12 ·

A sodium layered metal oxide, a preparation method thereof, a secondary battery, and an electric apparatus are disclosed. The sodium layered metal oxide has a general chemical formula of Na.sub.1-xA.sub.xC.sub.M.sub.1-O.sub.2, where M includes a transition metal element, A includes at least one of a Group IIA element, a Group V metal element, a Group VIA metal element, or a Group IIIB element with an ionic radius greater than that of M, and C includes at least one of a third-period, fourth-period, or fifth-period metal element with a valence less than or equal to that of M. The parameters satisfy 0.001x0.150 and 0.001y0.500. Doping the sodium layered metal oxide with A and C suppresses layer sliding in a desodiated state, reduces phase transitions, and improves structural stability, thereby enhancing cycle performance and extending the service life of the battery.

SODIUM LAYERED METAL OXIDE AND PREPARATION METHOD THEREOF, SECONDARY BATTERY, AND ELECTRIC APPARATUS
20260045496 · 2026-02-12 ·

A sodium layered metal oxide, a preparation method thereof, a secondary battery, and an electric apparatus are disclosed. The sodium layered metal oxide has a general chemical formula of Na.sub.1-xA.sub.xC.sub.M.sub.1-O.sub.2, where M includes a transition metal element, A includes at least one of a Group IIA element, a Group V metal element, a Group VIA metal element, or a Group IIIB element with an ionic radius greater than that of M, and C includes at least one of a third-period, fourth-period, or fifth-period metal element with a valence less than or equal to that of M. The parameters satisfy 0.001x0.150 and 0.001y0.500. Doping the sodium layered metal oxide with A and C suppresses layer sliding in a desodiated state, reduces phase transitions, and improves structural stability, thereby enhancing cycle performance and extending the service life of the battery.

METHOD FOR PREPARING SODIUM-ION BATTERY CATHODE MATERIAL

A method for preparing a sodium-ion battery cathode material includes: compounding metal salt solutions to obtain a mixed metal salt solution, where metal sources include one or more of nickel, iron, and manganese; performing spray pyrolysis on the mixed metal salt solution to obtain a first precursor powder; mixing the first precursor powder with an isopropanol solvent to obtain a first mixed solution; dispersing nano-scale titanium dioxide into the first mixed solution to obtain a second mixed solution; drying the second mixed solution to obtain a second precursor powder; and mixing the second precursor powder with a sodium source for sintering to obtain a sodium-ion battery cathode material. A titanium-doped sodium-ion battery cathode material is prepared by adding a heterogeneous element titanium to suppress a phase change at the beginning of the charging, thereby improving the structure stability, output characteristic, and service life of the sodium-ion battery.

METHOD FOR PREPARING SODIUM-ION BATTERY CATHODE MATERIAL

A method for preparing a sodium-ion battery cathode material includes: compounding metal salt solutions to obtain a mixed metal salt solution, where metal sources include one or more of nickel, iron, and manganese; performing spray pyrolysis on the mixed metal salt solution to obtain a first precursor powder; mixing the first precursor powder with an isopropanol solvent to obtain a first mixed solution; dispersing nano-scale titanium dioxide into the first mixed solution to obtain a second mixed solution; drying the second mixed solution to obtain a second precursor powder; and mixing the second precursor powder with a sodium source for sintering to obtain a sodium-ion battery cathode material. A titanium-doped sodium-ion battery cathode material is prepared by adding a heterogeneous element titanium to suppress a phase change at the beginning of the charging, thereby improving the structure stability, output characteristic, and service life of the sodium-ion battery.

POSITIVE ELECTRODE ACTIVE MATERIAL, MANUFACTURING METHOD OF POSITIVE ELECTRODE ACTIVE MATERIAL, AND BATTERY
20260038824 · 2026-02-05 · ·

The disclosure relates to a positive electrode active material, a manufacturing method of a positive electrode active material, and a battery. The positive electrode active material of the present disclosure includes an Na-containing oxide. The Na-containing oxide has a P2-type structure. The Na-containing oxide includes, as constituent elements, at least: Na; Ca; at least one transition metal element among Mn, Ni, and Co; and O.

POSITIVE ELECTRODE ACTIVE MATERIAL, MANUFACTURING METHOD OF POSITIVE ELECTRODE ACTIVE MATERIAL, AND BATTERY
20260038824 · 2026-02-05 · ·

The disclosure relates to a positive electrode active material, a manufacturing method of a positive electrode active material, and a battery. The positive electrode active material of the present disclosure includes an Na-containing oxide. The Na-containing oxide has a P2-type structure. The Na-containing oxide includes, as constituent elements, at least: Na; Ca; at least one transition metal element among Mn, Ni, and Co; and O.

TUNGSTEN DOPED MULTI-IONIC CATHODE
20260070810 · 2026-03-12 ·

The present invention discloses to tungsten doped mixed cationic cathodes for energy devices notably non-aqueous re-chargeable alkali-ion electrochemical cells and batteries and to the process of preparation thereof. More particularly, the present invention discloses to doped cathode active materials of Formula (I) that show a higher capacity and which can able to retains their structure during the entire charging-discharging cycles.