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A kind of znmn2o4 hollow rod and its preparation method and application

A technology of hollow rods and zinc salts, applied in chemical instruments and methods, manganate/permanganate, structural parts, etc., can solve the problems of poor conductivity of transition metal oxides, pulverization of electrode active materials, and specific capacity of graphite materials Low-level problems, to achieve the effect of alleviating the volume expansion problem, good lithium storage capacity, and multiple active sites

Active Publication Date: 2022-06-03
UNIV OF JINAN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, commercial lithium-ion batteries mostly use graphite anode materials, but graphite materials have the disadvantage of low specific capacity, and its theoretical capacity is only 372mAh g -1
Transition metal oxides, as anode materials for lithium-ion batteries, have the advantage of high theoretical specific capacity for lithium storage, but transition metal oxides have poor conductivity and severe volume expansion during charging and discharging, resulting in powdering and falling off of electrode active materials. Therefore, the cycle stability of batteries using transition metal oxides as anodes is generally poor.

Method used

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  • A kind of znmn2o4 hollow rod and its preparation method and application
  • A kind of znmn2o4 hollow rod and its preparation method and application
  • A kind of znmn2o4 hollow rod and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] (1) Add 0.75 mmol of oxalic acid dihydrate to a mixed solution of 20 ml of absolute ethanol, 60 ml of polyethylene glycol 400 and 10 ml of deionized water, and the concentration of the oxalic acid solution is 0.008 mol / L.

[0029] (2) Take 0.5 mmol of ZnCl 2 and 1 mmol of MnCl 2 ·4H 2 O was added to the above mixed solution. Stir at room temperature for 6 h.

[0030] (3) The obtained liquid was centrifuged with a centrifuge to collect the precipitate, washed three times with water and twice with ethanol, and dried in an oven at 60 °C for 12 h to obtain a hollow rod precursor.

[0031] (4) The precursor was calcined in a muffle furnace, 1 °C / min, heated to 400 °C, and held for 2 h to obtain the target product ZnMn 2 O 4 Hollow rod.

Embodiment 2

[0033] (1) Add 1.5 mmol of oxalic acid dihydrate to a mixed solution of 20 ml of absolute ethanol, 30 ml of polyethylene glycol 400 and 10 ml of deionized water, and the concentration of the oxalic acid solution is 0.025 mol / L at this time.

[0034] (2) Take 0.5 mmol of Zn(NO 3 ) 2 ·6H 2 O and 1 mmol of MnCl 2 ·4H 2 O was added to the above mixed solution. Stir at room temperature for 6 h.

[0035] (3) The obtained liquid was centrifuged with a centrifuge to collect the precipitate, washed three times with water and twice with ethanol, and dried in an oven at 60 °C for 12 h to obtain a hollow rod precursor.

[0036] (4) The precursor was calcined in a muffle furnace, heated at 1 °C / min to 400 °C, and kept for 2 h to obtain the target product ZnMn 2 O 4 Hollow rod.

Embodiment 3

[0038] (1) Add 2.25 mmol of oxalic acid dihydrate to a mixed solution of 20 ml of absolute ethanol, 10 ml of polyethylene glycol 400 and 10 ml of deionized water, and the concentration of the oxalic acid solution is 0.056 mol / L.

[0039] (2) Take 0.5 mmol of Zn(CH 3 COO) 2 ·2H 2 O and 1 mmol of MnCl 2 ·4H 2 O was added to the above mixed solution. Stir at room temperature for 6 h.

[0040] (3) The obtained liquid was centrifuged with a centrifuge to collect the precipitate, washed three times with water and twice with ethanol, and dried in an oven at 60 °C for 12 h to obtain a hollow rod precursor.

[0041] (4) The precursor was calcined in a muffle furnace, heated at 1 °C / min to 450 °C, and kept for 2 h to obtain the target product ZnMn 2 O 4 Hollow rod.

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Abstract

A kind of utilizing coprecipitation method to prepare ZnMn 2 o 4 The hollow rod method and its application belong to the technical fields of new functional materials and new energy sources. In this method, a mixed solution of absolute ethanol, deionized water and polyethylene glycol 400 is used as a solvent, oxalic acid dihydrate, zinc salt and manganese salt are added to the mixed solution, stirred at room temperature until the reaction is complete, and the method of washing by centrifugation The resulting precipitate is collected and completely dried to form a hollow rod-shaped precursor, which is calcined in an air atmosphere to obtain ZnMn 2 o 4 Hollow rod. Compared with other methods for preparing hollow structures, the present invention is simple and easy, and the obtained hollow structures not only have a larger specific surface area, but also can provide more active sites, and can also alleviate the volume expansion caused by the lithium-deintercalation process problem, has better lithium storage capacity.

Description

technical field [0001] The invention belongs to the technical field of preparation of anode materials for new energy lithium ion batteries, and in particular relates to a ZnMn 2 O 4 Hollow rod and its preparation method and application. Background technique [0002] Lithium-ion batteries have the advantages of high energy density, high operating voltage, long cycle life, and no memory. They have been widely used in digital, energy storage, electric vehicles and other fields, becoming the most promising high-energy battery system. At present, most commercial lithium-ion batteries use graphite anode materials, but graphite materials have the disadvantage of low specific capacity, and their theoretical capacity is only 372mAh g -1 . As anode materials for lithium-ion batteries, transition metal oxides have the advantage of high theoretical specific capacity for lithium storage, but transition metal oxides have poor conductivity and severe volume expansion during charge and d...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G45/12H01M4/485H01M10/0525
CPCC01G45/1242H01M4/485H01M2004/021H01M2004/027H01M10/0525C01P2004/30C01P2002/72C01P2004/03C01P2004/04C01P2006/40Y02E60/10
Inventor 侯林瑞徐森炀秦理原长洲
Owner UNIV OF JINAN