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Copper-doped vanadate electrode material as well as preparation method and application thereof

An electrode material, copper doping technology, applied in the direction of positive electrode, battery electrode, active material electrode, etc., can solve the problems of low voltage and small diffusion coefficient crystal structure of sodium ion battery

Inactive Publication Date: 2020-10-23
CHINA UNIV OF GEOSCIENCES (WUHAN)
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These together lead to the low voltage of the Na-ion battery, the small diffusion coefficient and the Na + Intercalation / deintercalation has a significant effect on the crystal structure of the electrode

Method used

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  • Copper-doped vanadate electrode material as well as preparation method and application thereof
  • Copper-doped vanadate electrode material as well as preparation method and application thereof
  • Copper-doped vanadate electrode material as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] A method for preparing a copper-doped vanadate electrode material with a three-dimensional network structure, comprising the following steps:

[0033] Step 1, put 1.0×10 -3 mol of NH 4 VO 3 , 5.0×10 -4 mol of Na 2 CO 3 and 1.0×10 -3 mol of Cu(NO 3 ) 2 ·3H 2 O was added to a beaker with 50 mL of distilled water, and stirred thoroughly until the mixture was dissolved to form a mixed solution;

[0034] Step 2, adding 3×10 -3 mol citric acid saturated solution of citric acid, then heated and stirred in a water bath at 80°C for 5 hours, and then put it into a ventilated drying oven at 80°C for 24 hours to form a xerogel precursor;

[0035] Step 3. Put the xerogel precursor into a muffle furnace for calcination. The calcination temperature is 500° C. and the calcination time is 6 hours to obtain a copper-doped vanadate electrode material with a three-dimensional network structure.

[0036] Carry out X-ray diffractometer test to the three-dimensional network structu...

Embodiment 2

[0040] This embodiment is basically the same as the steps in embodiment 1, the difference is that in step 1, the added VO 2 NO 3 1.5×10 -3 mol, NaHCO 3 1×10 -3 mol; in step 2, add 3.5×10 -3 mol citric acid citric acid solution, the temperature of hydrothermal reaction is 100°C, the time is 4h, the temperature of drying is 100°C, and the drying time is 18h.

[0041] The X-ray test, scanning electron microscope test, selected area electron diffraction and electrochemical performance test of the button cell were carried out on the three-dimensional network structure copper-doped vanadate electrode material. The X-ray test showed that the prepared product was Cu-doped NaVO 3 , Scanning electron microscope test shows that the obtained product is granular, and interconnected, interlaced to form a three-dimensional network structure, from the selected area electron diffraction (SAED) pattern, it can be clearly seen that the synthesized sample is a single crystal structure.

Embodiment 3

[0043] The steps in this embodiment are basically the same as in Example 1, the difference is that in step 1, the added (NH 4 ) 3 VO 4 1×10 -3 mol, NaHCO 3 1×10 -3 mol; in step 2, the calcination temperature is 400°C, and the calcination time is 7.5h.

[0044] The X-ray test, scanning electron microscope test, selected area electron diffraction and electrochemical performance test of the button cell were carried out on the three-dimensional network structure copper-doped vanadate electrode material. The X-ray test showed that the prepared product was Cu-doped NaVO 3 , Scanning electron microscope test shows that the obtained product is granular, and interconnected, interlaced to form a three-dimensional network structure, from the selected area electron diffraction (SAED) pattern, it can be clearly seen that the synthesized sample is a single crystal structure.

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Abstract

The invention discloses a preparation method of a copper-doped vanadate electrode material with a three-dimensional network structure, which comprises the following steps: step 1, dissolving a sodiumsource, a vanadium source and a copper source with water to obtain a mixed solution; 2, adding a citric acid saturated solution into the mixed solution, heating, and drying to obtain a xerogel precursor; 3, calcining the xerogel precursor to obtain the copper-doped vanadate electrode material with a three-dimensional network structure. The invention also provides the copper-doped vanadate electrode material with a three-dimensional network structure prepared by the preparation method, and also provides a sodium ion battery positive pole piece prepared from the copper-doped vanadate electrode material with a three-dimensional network structure. The preparation method has the beneficial effects of simple preparation process and good electrochemical performance.

Description

technical field [0001] The invention relates to the technical field of sodium ion battery materials. More specifically, the present invention relates to a copper-doped vanadate electrode material and its preparation method and application. Background technique [0002] Today, when resources are scarce, advanced energy storage technology has increasingly become one of the criteria for measuring a country's comprehensive national strength. In the current energy storage battery system, lithium-ion batteries have attracted much attention due to their high energy density and system flexibility, and have been widely used in various engineering fields such as electric vehicles and aerospace. However, lithium-ion batteries also have certain safety issues, coupled with high cost and insufficient resources will limit the application of lithium-ion batteries in the future, especially in large-scale energy storage systems. Therefore, it is particularly important to study battery syste...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01G31/00H01M4/58H01M10/054
CPCC01G31/00C01P2002/72C01P2004/03C01P2006/40H01M4/5825H01M10/054H01M2004/021H01M2004/028Y02E60/10
Inventor 袁勋龙董轶凡夏帆
Owner CHINA UNIV OF GEOSCIENCES (WUHAN)