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Preparation method and application of three-dimensional dendritic metal-carbon nanofibers

A technology of carbon nanofibers and dendrites, which is applied in the field of preparation of three-dimensional dendritic metal-carbon nanofibers, and achieves the effects of simple preparation method, good rate discharge performance and low price

Inactive Publication Date: 2020-07-10
XUZHOU NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the problem of Li dendrite growth and volume expansion caused by heterogeneous Li reaction current density remains a major challenge.

Method used

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  • Preparation method and application of three-dimensional dendritic metal-carbon nanofibers
  • Preparation method and application of three-dimensional dendritic metal-carbon nanofibers
  • Preparation method and application of three-dimensional dendritic metal-carbon nanofibers

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] (1) metal salts of iron acetylacetonate, nickel acetylacetonate, cobalt acetylacetonate (Co(acac) 2 ) and polyacrylonitrile (PAN) were mixed at 55°C for 24h at a mass ratio of 1:5, and three metal salts were reacted as separate raw materials in this example;

[0019] (2) Using the electrospinning method, the mixture obtained in step (1) is packed into a syringe, the needle is kept at a high voltage of 13.5KV, and the mixture is advanced at 1.5ml / h, and collected by a rotating collector with a rotating speed of 2000 rpm Iron-carbon (Fe / CNFs), nickel-carbon (Ni / CNFs), cobalt-carbon nanofiber (Co / CNFs) precursors;

[0020] (3) Place the metal-carbon nanofiber precursor obtained in step (2) in air at 290°C for 2h, then calcinate in stages in nitrogen, raise the temperature to 300°C at a rate of 2° / min, calcinate for 2h, and then Raise the temperature to 800°C at a rate of 5°C / min, and calcine for 2 hours. The metal raw materials in it can induce the growth of nano-branches...

Embodiment 2

[0027] (1) metal salts of iron acetylacetonate, nickel acetylacetonate, cobalt acetylacetonate (Co(acac) 2 ) and polyacrylonitrile (PAN) were mixed at 55°C for 24h at a mass ratio of 3:5, and three metal salts were reacted as separate raw materials in this example;

[0028] (2) Using the electrospinning method, the mixture obtained in step (1) is packed into a syringe, the needle is kept at a high voltage of 13.5KV, and the mixture is advanced at 1.5ml / h, and collected by a rotating collector with a rotating speed of 2000 rpm Iron-carbon (Fe / CNFs), nickel-carbon (Ni / CNFs), cobalt-carbon nanofiber (Co / CNFs) precursors;

[0029] (3) Place the metal-carbon nanofiber precursor obtained in step (2) in air at 290°C for 2h, then calcinate in stages in nitrogen, raise the temperature to 300°C at a rate of 2° / min, calcinate for 2h, and then Raise the temperature to 800°C at a rate of 5°C / min, and calcine for 2 hours. The metal raw materials in it can induce the growth of nano-branches...

Embodiment 3

[0031] (1) metal salts of iron acetylacetonate, nickel acetylacetonate, cobalt acetylacetonate (Co(acac) 2 ) and polyacrylonitrile (PAN) were mixed at 55°C for 24h at a mass ratio of 1:5, and three metal salts were reacted as separate raw materials in this example;

[0032] (2) Using the electrospinning method, the mixture obtained in step (1) is packed into a syringe, the needle is kept at a high voltage of 13.5KV, and the mixture is advanced at 1.5ml / h, and collected by a rotating collector with a rotating speed of 2000 rpm Iron-carbon (Fe / CNFs), nickel-carbon (Ni / CNFs), cobalt-carbon nanofiber (Co / CNFs) precursors;

[0033] (3) Place the metal-carbon nanofiber precursor obtained in step (2) in air at 290°C for 2h, then calcinate in stages in nitrogen, raise the temperature to 300°C at a rate of 2° / min, calcinate for 2h, and then Raise the temperature to 900°C at a rate of 5°C / min, and calcine for 2h. The metal raw materials in it can induce the growth of nano-branches on t...

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Abstract

The invention discloses a preparation method and application of three-dimensional dendritic metal-carbon nanofibers, and belongs to the technical field of lithium metal batteries. The preparation method comprises the following steps: uniformly mixing a metal salt and polyacrylonitrile (PAN), obtaining a metal-carbon nanofiber precursor (metal being iron, cobalt, nickel or a mixture thereof) by adopting an electrostatic spinning method, and after the precursor is stabilized in air, carrying out staged calcination to obtain the three-dimensional dendritic metal-carbon nanofibers. The three-dimensional dendritic metal-carbon nanofibers prepared by the method are used for preparing the lithium metal composite negative electrode, so that the problems existing in a lithium electrode are effectively avoided, and compared with other negative electrode materials, the three-dimensional dendritic metal-carbon nanofibers have good high-rate discharge performance while the cycle performance of thematerial is maintained; and meanwhile, the preparation method is simple and low in cost, can realize large-scale production and has a practical prospect.

Description

technical field [0001] The invention belongs to the technical field of lithium metal batteries, and in particular relates to a method for preparing three-dimensional dendritic metal-carbon nanofibers for lithium metal negative electrodes. Background technique [0002] With the rapid development of the global economy, the application of lithium-ion batteries has transitioned from portable electronics to electric vehicles. Li-ion batteries with high power density, low cost and long life have become the focus of development. Li metal anode has long been considered as the "holy grail" of energy storage systems, however, the low lifetime, poor rate performance and serious safety issues of Li metal electrodes limit their wide application. [0003] The main reasons for these problems are the high reactivity of Li metal with the electrolyte and the uneven reaction current density at the electrode surface. Freshly deposited Li metal is highly reactive towards most organic electroly...

Claims

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Application Information

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IPC IPC(8): H01M4/36H01M4/38H01M4/583H01M10/052
CPCH01M4/362H01M4/382H01M4/38H01M4/583H01M10/052H01M2004/022H01M2004/027Y02E60/10
Inventor 赖超刘新华孙闯
Owner XUZHOU NORMAL UNIVERSITY