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Lanthanum-aluminum-magnesium in-situ co-doped cobaltosic oxide material and preparation method thereof

A technology of cobalt tetroxide and co-doping, applied in chemical instruments and methods, cobalt oxide/cobalt hydroxide, inorganic chemistry, etc., to achieve the effects of slowing down the precipitation rate, improving structural stability, and improving diffusion efficiency

Pending Publication Date: 2020-12-01
GEM CO LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At this time, a single aluminum doping can no longer meet the higher requirements, and it is necessary to achieve the synergistic effect of various metals by doping bimetallic or even trimetallic, so as to not only improve the stability of the material structure, but also increase the electrical conductivity of the material and improve The migration efficiency of lithium ions during charging and discharging makes the final fired lithium cobalt oxide meet the product requirements of the next generation 4.48V and 4.5V

Method used

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  • Lanthanum-aluminum-magnesium in-situ co-doped cobaltosic oxide material and preparation method thereof
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preparation example Construction

[0026] The preparation method of the in-situ lanthanum-aluminum-magnesium co-doped cobalt tetroxide material of the present invention comprises the following steps:

[0027] (1) Cobalt salt solution is prepared; the cobalt salt in the cobalt salt solution is one or more of cobalt chloride, cobalt sulfate, and cobalt nitrate; the concentration of cobalt ions in the cobalt salt solution is 65g / L-195g / L.

[0028] (2) preparing aluminum salt solution; the aluminum salt in the aluminum salt solution is aluminum sulfate. The concentration of aluminum ions in the aluminum salt solution is 0.6g / L-6.0g / L.

[0029] (3) Prepare lanthanum salt solution and magnesium salt solution; the lanthanum salt in the lanthanum salt solution is lanthanum chloride, and the concentration of lanthanum ion in the lanthanum salt solution is 0.3g / L-1.2g / L. The magnesium salt in the magnesium salt solution is one or both of magnesium chloride and magnesium sulfate, and the concentration of magnesium ions i...

Embodiment 1

[0036] The lanthanum chloride solution that the lanthanum ion concentration is 1.2g / L and the magnesium chloride solution that the magnesium ion concentration is 1.2g / L are squeezed into the aluminum sulfate solution that the aluminum ion concentration is 3.6g / L by metering pump, the lanthanum chloride solution, The volume ratio of the magnesium chloride solution and the aluminum sulfate solution is 1:1:1 to obtain a mixed solution.

[0037] The cobalt chloride solution, the mixed solution and the ammonium bicarbonate solution with a cobalt ion concentration of 120g / L are respectively added to the reaction kettle with deionized water in parallel flow through a metering pump to carry out coprecipitation reaction, and the three metal-containing La-Al-Mg co-doped flake cobalt carbonate. The amount of deionized water added is 20% of the volume of the reactor, and the volume ratio of the cobalt chloride solution, mixed solution, and ammonium bicarbonate solution added to the reacto...

Embodiment 2

[0046] The lanthanum chloride solution that the lanthanum ion concentration is 0.3g / L and the magnesium chloride solution that the magnesium ion concentration is 0.3g / L are squeezed into the aluminum sulfate solution that the aluminum ion concentration is 1.2g / L by metering pump, the lanthanum chloride solution, The volume ratio of the magnesium chloride solution and the aluminum sulfate solution is 1:1:1 to obtain a mixed solution.

[0047] The cobalt chloride solution, the mixed solution, and the ammonium bicarbonate solution with a cobalt ion concentration of 80g / L are respectively added to a reaction kettle with deionized water in parallel flow through a metering pump to carry out a coprecipitation reaction to obtain La-Al-Mg co-doped flake cobalt carbonate. The amount of deionized water added is 30% of the volume of the reactor, and the volume ratio of the cobalt salt solution, mixed solution, and ammonium bicarbonate solution added to the reactor is 1.5:3:2; the concentr...

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Abstract

The invention relates to a lanthanum-aluminum-magnesium in-situ co-doped cobaltosic oxide material. The chemical formula of the material is LaxAlyMgzCoaOb, x is larger than 0.0015 and smaller than 0.004, y is larger than 0.035 and smaller than 0.1, z is larger than 0.01 and smaller than 0.02, a is larger than 2.876 and smaller than 2.954, and b is larger than 3.999 and smaller than 4.005. The preparation method of the material comprises the following steps: pumping a lanthanum salt solution and a magnesium salt solution into an aluminum salt solution through a metering pump to obtain a mixed solution; and adding the cobalt salt solution, the mixed solution and the ammonium bicarbonate solution into a reaction kettle with a base solution in a parallel flow manner, carrying out a co-precipitation reaction, and calcining the obtained lanthanum-aluminum-magnesium co-doped cobalt carbonate containing three metals to obtain the lanthanum-aluminum-magnesium co-doped cobaltosic oxide containing three metals. The material is good in uniformity and strong in structural stability, and lithium cobalt oxide prepared from the material has high specific capacity and excellent cycle performance under high voltage.

Description

technical field [0001] The invention relates to the field of production of battery material precursors, in particular to a lanthanum-aluminum-magnesium in-situ co-doped tricobalt tetroxide material and a preparation method thereof. Background technique [0002] Cobalt tetroxide is the main raw material of lithium cobalt oxide, which is mainly used in the field of 3C electronic products. The main problem with lithium cobalt oxide in current use is that the theoretical voltage is above 4.2V, but the current average is only 3.6V, the highest has not reached 4.0V, the theoretical specific capacity is 260hA / kg, the actual specific capacity is 130hA / kg, and Capacity decreases with increasing cycle times. In order to release higher energy in a smaller space, lithium cobaltate is developing towards a high voltage of 4.5-4.6V. Under high voltage, more lithium ions can be extracted from the crystal structure. At present, it can be obtained by doping The way to improve the structural...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01G51/04C01G51/00
CPCC01G51/04C01G51/42C01P2004/32
Inventor 许开华李晨威刘文泽杨航易全瑞
Owner GEM CO LTD