Preparation method and application of nitrogen-doped porous carbon negative electrode material

A negative electrode material and porous carbon technology, which is applied in the field of preparation of nitrogen-doped porous carbon negative electrode materials, can solve the problems of reduced battery life, insufficient specific capacity potential, and difficult lithium intercalation process, achieving easy preparation, good cycle stability, Structured Effects

CN107919461AInactive Publication Date: 2018-04-17NANJING UNIV OF TECH
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Publication Date
2018-04-17
Estimated Expiration
Not applicable · inactive patent

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Abstract

The invention belongs to the technical field of carbon material preparation, belongs to the category of alkali metal ion secondary energy storage and relates to a method for preparing nitrogen-doped porous carbon from perinone nitrogen-containing polycyclic aromatic hydrocarbon as a carbon source and an application of the nitrogen-doped porous carbon as a negative electrode or positive electrode material for an alkali metal ion secondary battery. According to the method, perinone nitrogen-containing conjugated polycyclic aromatic hydrocarbon is firstly mixed with a template or an activator andthermal decomposition carbonization is carried out at the temperature within a certain range to obtain a nitrogen-doped porous carbon negative electrode or positive electrode material. By adopting the perinone nitrogen-containing conjugated polycyclic aromatic hydrocarbon with large molecular weight as the carbon source, the loss of a nitrogen element in a thermal treatment process can be reduced, high-proportion nitrogen doping in the porous carbon is effectively achieved and electrochemical oxidation reduction sites are effectively increased. According to the method, the specific surface area of the porous carbon can be adjusted and controlled through the carbon source screening, thermal treatment carbonization temperature and the mass ratio of the template or the activator, the chargeexchange interface is increased and high energy storage is effectively achieved. The material has the advantages that (1) the structure is abundant and the perinone material is cheap and available; and (2) the material has relatively high energy density, magnification power density and cycling stability.
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Description

technical field

[0001] The invention specifically relates to a preparation method of nitrogen-doped porous carbon negative electrode materials, and relates to the steps and raw materials used in the preparation process of these materials. technical background

[0002] In the electronic information age, people's demand for portable, high-power, and highly intelligent power supply equipment is increasing day by day, making high-performance energy storage systems a common topic in the field of energy research and application that needs to be realized urgently. Driven by multiple objective forces such as the reduction of traditional energy reserves, global warming, and the increasing protection of the living environment, the way of energy production and use is changing to a new type of clean energy. Nowadays, the emergence of high-efficiency secondary energy storage devices and key technologies and materials provides the preferred option for convenient energy and power support f...

Examples

Embodiment 1

[0028] Mix and grind one of the carbon sources in 1-34 and sodium hydroxide at a mass ratio of 1:1 for 10 minutes; in a tube furnace, under an argon atmosphere of 20ml / min, at a heating rate of 1°C / min Raise the temperature to 600°C, carbonize for 2 hours, wash and dry with water, and obtain the nitrogen-doped porous carbon negative electrode material.

Embodiment 2

[0030] Mix and grind one of the carbon sources in 1-34 and sodium sulfate at a mass ratio of 1:1 for 10 minutes; in a tube furnace, raise the temperature at a rate of 1°C / min under an argon atmosphere of 20ml / min carbonization at 600°C for 2 hours, washed with water and dried to obtain nitrogen-doped porous carbon negative electrode material.

Embodiment 3

[0032] Mix and grind one of the carbon sources in 1-34 and sodium chloride at a mass ratio of 1:1 for 10 minutes; in a tube furnace, under an argon atmosphere of 20ml / min, at a heating rate of 1°C / min Raise the temperature to 600°C, carbonize for 2 hours, wash and dry with water, and obtain the nitrogen-doped porous carbon negative electrode material.