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A lithium battery negative electrode material co 3 o 4 Preparation method of nanofiber

A negative electrode material and nanofiber technology, applied in the field of preparation of lithium battery negative electrode material Co3O4 nanofibers, can solve the problems of poor cycle durability, battery material falling off, hindering negative electrode materials, etc., to improve electrical conductivity, alleviate negative effects, and improve electrical conductivity. The effect of performance and energy density

Active Publication Date: 2021-07-30
阮绍徐
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, Co 3 o 4 As a lithium battery anode material, the conductivity is poor, and the cycle durability is poor, and the capacity decays sharply after many cycles, which largely hinders the Co 3 o 4 Practical applications of anode materials
This is mainly due to the volume expansion of the electrode material during the battery cycle, which causes the battery material to pulverize and fall off the current collector, eventually causing permanent damage to the electrode.

Method used

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  • A lithium battery negative electrode material co  <sub>3</sub> o  <sub>4</sub> Preparation method of nanofiber
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  • A lithium battery negative electrode material co  <sub>3</sub> o  <sub>4</sub> Preparation method of nanofiber

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Experimental program
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Effect test

Embodiment 1

[0024] Add 20mL N,N-dimethylformamide in the beaker as solvent, then add 1mmoL (0.2903g) trimethoprim (C 14 h 18 N 4 o 3 ) and 1mmoL (0.2491g) cobalt acetate tetrahydrate (C 4 h 6 CoO 4 4H 2 0), magnetic stirring 1h, solid is dissolved completely; In beaker, add 1.42g polyacrylonitrile (PAN) again as binding agent, magnetic stirring 2h, obtain the red spinning precursor solution; The red spinning precursor solution Loaded into a 10mL syringe, at a voltage of 18kV, the distance between the spinning needle and the receiver is 15cm, and the push flow rate is 1.1mL h -1, the temperature was 35°C, and the relative humidity of the cabinet was 35% for electrospinning. After spinning for 12 hours, the spinning product was collected and dried in a vacuum drying oven at 60°C for 1 hour to obtain the dried electrostatic spinning product; Add 60mL of methanol and 6mmol, 1.5g of cobalt acetate tetrahydrate into a 100mL beaker, and magnetically stir for 1 hour to completely dissolve ...

Embodiment 2

[0026] Add 20mL N,N-dimethylformamide in the beaker as solvent, then add 1mmoL (0.2903g) trimethoprim (C 14 h 18 N 4 o 3 ) and 1mmoL (0.2491g) cobalt acetate tetrahydrate (C 4 h 6 CoO 4 4H 2 0), magnetic stirring 1h, solid is dissolved completely; In beaker, add 1.42g polyacrylonitrile (PAN) again as binding agent, magnetic stirring 2h, obtain the red spinning precursor solution; The red spinning precursor solution Loaded into a 10mL syringe, at a voltage of 20kV, the distance between the spinning needle and the receiver is 25cm, and the push flow rate is 1.1mL h -1 , the temperature was 35°C, and the relative humidity of the cabinet was 35% for electrospinning. After spinning for 12 hours, the spinning product was collected and dried in a vacuum drying oven at 60°C for 1 hour to obtain the dried electrostatic spinning product; Add 60mL of methanol and 6mmol, 1.5g of cobalt acetate tetrahydrate into a 100mL beaker, and magnetically stir for 1 hour to completely dissolve...

Embodiment 3

[0028] Add 20mL N,N-dimethylformamide in the beaker as solvent, then add 1mmoL (0.2903g) trimethoprim (C 14 h 18 N 4 o 3 ) and 1mmoL (0.2491g) cobalt acetate tetrahydrate (C 4 h 6 COO 4 4H 2 0), magnetic stirring 1h, solid is dissolved completely; In beaker, add 1.42g polyacrylonitrile (PAN) again as binding agent, magnetic stirring 2h, obtain the red spinning precursor solution; The red spinning precursor solution Loaded into a 10mL syringe, at a voltage of 19kV, the distance between the spinning needle and the receiver is 20cm, and the push flow rate is 1.1mL h -1 , the temperature is 35 ℃, and the relative humidity of the cabinet is 35% to carry out electrospinning. After spinning for 12 hours, the spinning product is collected and dried in a vacuum drying oven at 60 ℃ for 1 hour to obtain the dried electrostatic spinning product; Add 60mL of methanol and 6mmol, 1.5g of cobalt acetate tetrahydrate into a 100mL beaker, and magnetically stir for 1 hour to completely di...

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Abstract

The invention discloses a lithium battery negative electrode material Co 3 o 4 The preparation method of nanofiber, the present invention uses trimethoprim (C 14 h 18 N 4 o 3 ) organic ligands, cobalt acetate tetrahydrate as the main raw materials, Co prepared by electrospinning and temperature-controlled sintering technology 3 o 4 Nanofibers, coated with a layer of carbon on the surface of cobalt trioxide nanocarbon fibers, improved the metal oxide in Li + The shortcomings of large volume expansion coefficient and poor conductivity during the deintercalation process have high reversible capacity; nanofibers have a quantum size effect, which increases the contact area between the material and the electrolyte, which is Li + Provides more active sites and shortens the Li + The transmission path improves the Li during the charging and discharging process + Deintercalation rate, stable structure, good reversible performance, high specific capacity, simple operation, low cost and low equipment investment in the whole preparation process, suitable for mass production.

Description

technical field [0001] The invention belongs to the field of material chemistry, and in particular relates to a lithium battery negative electrode material Co 3 o 4 Preparation methods of nanofibers. Background technique [0002] Lithium-ion batteries (LIBs) are a promising battery with light weight, high energy density, long cycle life, wide operating temperature range, no memory effect, and environmental friendliness. It has become an important direction for the development of secondary batteries and is widely used in electronic products, electric vehicles, military aerospace and other fields. The theoretical specific capacitance of graphite anode materials for traditional lithium batteries is 372 mAh g -1 (Chemical Communications, 2012, 48, 1201-1217), its theoretical specific capacity is low, and the reaction kinetics is poor. When discharged to a lower voltage, lithium dendrites will be generated, and the lithium dendrites will break to form dead lithium, thereby form...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/36H01M4/52H01M4/62H01M10/0525D01D5/00D01F9/08B82Y30/00B82Y40/00
CPCB82Y30/00B82Y40/00D01D5/003D01D5/0069D01D5/0092D01F9/08H01M4/366H01M4/523H01M4/62H01M4/625H01M4/628H01M10/0525Y02E60/10
Inventor 李星刘语舟黄水平
Owner 阮绍徐
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