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Preparation method of carbon-coated sodium titanium phosphate composite material and preparation method of negative pole piece

A technology for carbon-coated sodium titanium phosphate and composite materials, which is applied in the fields of nanomaterial technology and electrochemistry, can solve problems such as increasing environmental pollution, consuming large energy, increasing equipment complexity and production cost, and achieves a green and environmentally friendly process route. The effect of the simple process route

Inactive Publication Date: 2021-11-26
JIANGSU UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Currently existing laboratory preparation techniques such as hydrothermal method or sol-gel method are not suitable for large-scale production. Even if some technologies can achieve large-scale production, there are the following problems: 1. Almost all technologies use ammonium dihydrogen phosphate or phosphoric acid Ammonium and other decomposable phosphates are phosphorus sources, which will produce a large amount of corrosive and harmful tail gas—ammonia gas. The production of ammonia gas will not only increase the risk of environmental pollution, but also greatly increase the complexity of equipment and production after treatment. cost; 2. At present, many technologies use the process of wet grinding, dispersing and drying raw materials in the production process. The existing spray drying technology needs to consume a lot of energy; 3. Although phosphoric acid is cheap and the by-products produced by decomposition are only Water is in line with the concept of green production, but because phosphoric acid itself is a viscous liquid, it cannot be prepared into a powder precursor with other raw materials. At present, it is impossible to use phosphoric acid as a phosphorus source to achieve large-scale preparation of sodium titanium phosphate
Electrode pole pieces prepared with ordinary water-based glue cannot be used in batteries with aqueous solution as the electrolyte, because when the electrode pole piece encounters the aqueous electrolyte again, it will expand, causing the active material to be released from the current collector. Falling off, affecting battery performance and cycle life

Method used

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  • Preparation method of carbon-coated sodium titanium phosphate composite material and preparation method of negative pole piece

Examples

Experimental program
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Effect test

Embodiment 1

[0035] A preparation method of sodium titanium phosphate, comprising the steps of:

[0036](1) Add 1450g of sodium dihydrogen phosphate (sodium source), 2250g of phosphoric acid (phosphorus source) and 1940g of metatitanic acid (titanium source) into 25L of deionized water (dispersant) and stir evenly to obtain a slurry;

[0037] (2) Stir and reflux the obtained slurry at 100°C for 5 hours, remove about 2 / 3 of the deionized water under reduced pressure, then transfer it to a rake-type vacuum dryer, and obtain a powdery precursor after drying;

[0038] (3) The obtained powdery precursor was pressed into a rough billet, and then placed in a tubular atmosphere furnace, fed with nitrogen, with an air flow rate of 50 mL / min, and first heated to 350 °C for 2 hours at a rate of 5 °C / min for calcination, and then Then heat up to 800°C, heat-preserve and calcinate for 4 hours, cool to room temperature, stop ventilation, and obtain white product sodium titanium phosphate (NaTi 2 (PO 4...

Embodiment 2

[0040] A preparation method of carbon-coated sodium titanium phosphate composite material, comprising the steps of:

[0041] (1) Add 900g glucose (carbon source), 1450g sodium dihydrogen phosphate (sodium source), 2250g phosphoric acid (phosphorus source) and 1940g metatitanic acid (titanium source) to 25L deionized water (dispersant) and stir evenly , get slurry;

[0042] (2) Stir and reflux the obtained slurry at 100°C for 5 hours, remove about 2 / 3 of the deionized water under reduced pressure, then transfer it to a rake-type vacuum dryer, and obtain a powdery precursor after drying;

[0043] (3) The obtained powdery precursor was pressed into a rough billet, and then placed in a tubular atmosphere furnace, fed with nitrogen, with an air flow rate of 50 mL / min, and first heated to 350 °C for 2 hours at a rate of 5 °C / min for calcination, and then Then heat up to 800°C, heat-preserve and calcinate for 4 hours, cool to room temperature, stop ventilation, and obtain a black po...

Embodiment 3

[0047] A preparation method of carbon-coated sodium titanium phosphate composite material, comprising the steps of:

[0048] (1) Add 900g glucose (carbon source), 50g polyvinyl alcohol (carbon source), 1450g sodium dihydrogen phosphate (sodium source), 2250g phosphoric acid (phosphorus source) and 1940g metatitanic acid (titanium source) to 25L deionized water (dispersant) and stir evenly to obtain a slurry;

[0049] (2) Stir and reflux the obtained slurry at 100°C for 5 hours, remove about 2 / 3 of the deionized water under reduced pressure, then transfer it to a rake-type vacuum dryer, and obtain a powdery precursor after drying;

[0050] (3) The obtained powdery precursor was pressed into a rough billet, and then placed in a tubular atmosphere furnace, fed with nitrogen, with an air flow rate of 50 mL / min, and first heated to 350 °C for 2 hours at a rate of 5 °C / min for calcination, and then Then heat up to 800°C, heat-preserve and calcinate for 4 hours, cool to room tempera...

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Abstract

The invention discloses a preparation method of a carbon-coated sodium titanium phosphate composite material and a preparation method of a negative pole piece. The preparation method of the carbon-coated sodium titanium phosphate composite material comprises the following steps: (1) adding a carbon source, a sodium source, a phosphorus source and a titanium source into a dispersing agent, and stirring to obtain slurry; (2) stirring and refluxing the slurry, removing part of the dispersing agent under reduced pressure, and drying to obtain a powdery precursor; and (3) pressing the precursor into a rough blank, calcining in an inert atmosphere, and cooling to obtain the carbon-coated sodium titanium phosphate composite material. The preparation method of a carbon-coated sodium titanium phosphate negative pole piece comprises the following steps: S1, mixing water-based conductive slurry, water-based glue and a solvent, adding a conductive agent and the carbon-coated sodium titanium phosphate composite material, and uniformly stirring to obtain water-based coating slurry; and S2, coating a hydrophobic carbon-coated aluminum foil with the water-based coating slurry, drying, compacting and slitting to obtain the carbon-coated sodium titanium phosphate negative pole piece. According to the methods, no harmful or corrosive gas is discharged, the methods are green and environment-friendly production processes, and the used raw materials are common and cheap.

Description

technical field [0001] The invention relates to the field of nanomaterial technology and electrochemistry, and in particular to a carbon-coated sodium titanium phosphate composite material and a method for preparing a carbon-coated sodium titanium phosphate negative pole piece. Background technique [0002] Secondary batteries play an important role in the transformation of old and new energy forms and the utilization and development of new energy. At present, although lead-acid batteries and lithium-ion batteries have been widely used in mobile power sources, energy storage and other fields, due to their respective defects, new battery systems are beginning to develop rapidly, and emerging water-based batteries have attracted much attention. [0003] Sodium titanium phosphate (NaTi 2 (PO 4 ) 3 ), is a polyanionic material whose three-dimensional polyanionic framework has the advantages of high ion conductivity and high structural stability. As a negative electrode mater...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B25/45C01B32/05H01M4/04H01M4/1397H01M4/36H01M4/58H01M4/62H01M4/66
CPCC01B25/45C01B32/05H01M4/366H01M4/5825H01M4/625H01M4/1397H01M4/0404H01M4/661H01M4/662H01M4/667C01P2002/72Y02E60/10
Inventor 毛武涛贺畅鲍克燕钱逸泰
Owner JIANGSU UNIV OF TECH
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