Preparation method of high-capacity linear supercapacitor electrode based on MXene/PANI

A supercapacitor and high-capacity technology, which is applied in the manufacture of hybrid capacitor electrodes and hybrid/electric double-layer capacitors, etc., can solve the problems of limiting rate performance, reducing the specific surface area of ​​electrodes, and poor mechanical properties, so as to achieve good electrochemical performance and improve Active surface area, favorable transport effect

Active Publication Date: 2020-06-02
CHANGZHOU UNIV +1
View PDF13 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] From the perspective of electrode materials, materials with good electrochemical performance while maintaining light weight, flexibility and wear resistance are the first choice for flexible wearable energy storage devices, such as two-dimensional transition metal carbide (MXene). As well as graphene-based materials, in previous studies, MXene was used as an electrode material for supercapacitors, mainly because of its good conductivity and the ability to exhibit additional pseudocapacitance in acidic electrolytes, but it can be used as a flexible electrode Said that its mechanical properties are poor, and the MXene film prepared by the conventional vacuum filtration method does not have good toughness, which limits its use as an electrode material for flexible devices.
Graphene-based materials have good flexibility, but the key to limiting their performance is that they cannot provide high capacity, which requires higher mass or larger area per unit capacitance, which is not in line with the lightweight need
Therefore, it is necessary to combine the advantages of the two. For example, CN 107680824 A constructed a MXene / rGO composite electrode. The patent pointed out that the flexibility of the composite material becomes better as the proportion of reduced graphene oxide is increased, but the capacity will be serious as the proportion of rGO increases. Decrease, the ratio of MXene:rGO decreased from 9:1 to 7:1 volume ratio capacitance decreased by 75% (600Fcm -3 to 200F cm -3 )
[0004] In order to solve the problem of low capacity, CN 109273273 A utilizes PANI, GO, PEDOT compound, in order to utilize PANI, the extra pseudocapacitance of PEDOT this kind of conductive elastomer material in acidic electrolyte improves the overall specific capacity, but from its CV (cycle It can be seen from the graph that the rate performance of the material is extremely poor, because at 5mV s -1 The material has completely lost its rectangular-like shape at a scan rate of 100, and does not show the redox reaction peak of the pseudocapacitive reaction.
[0005] Since MXene is brittle after film formation and has poor mechanical properties, the twisting process of the film may break the film, so wet spinning is used to prepare fiber electrodes such as CN 107680824 A, which can be seen from the scanning electron microscope image The internal structure of the wet-spun fiber electrode is very compact, which also reduces the specific surface area of ​​the electrode, increases the difficulty of ion diffusion inside the electrode, and limits its rate performance.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of high-capacity linear supercapacitor electrode based on MXene/PANI
  • Preparation method of high-capacity linear supercapacitor electrode based on MXene/PANI
  • Preparation method of high-capacity linear supercapacitor electrode based on MXene/PANI

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] (1) Take 1g of lithium fluoride, add 20ml of hydrochloric acid with a concentration of 9mol / L and stir evenly, then slowly add 1g of precursor V 2 AlC, stirred at 40°C for 24 hours, washed and dried to obtain V 2 C MXene powder, the resulting powder was added to deionized water to form a 10mg / ml suspension, and the resulting solution was centrifuged after ultrasonic pulverization at 700W under an argon protective atmosphere and an ice bath environment, and the supernatant was taken to obtain V 2 C MXene Monodispersion.

[0027] (2) Add aniline 10% by volume to 1mol / L dilute hydrochloric acid, stir and mix evenly, and then add V with a concentration of 2mg / ml obtained in step (1). 2 C MXene monodisperse, V 2 The volume ratio of C MXene monodispersion to the hydrochloric acid solution of aniline is 1:2 (33% MXene). After stirring at 0°C for 4 hours, the MXene / PANI precipitate was obtained. The precipitate was repeatedly washed with deionized water and dried. Obtain MXe...

Embodiment 2

[0032] (1) Take 2g of lithium fluoride, add 20ml of hydrochloric acid with a concentration of 9mol / L and stir evenly, then slowly add 2g of precursor Ti 3 AlC 2 , stirred at 40°C for 24h, washed and dried to obtain Ti 3 C2 MXene powder, the obtained powder was added to deionized water to form a 10mg / ml suspension, and the obtained solution was ultrasonically pulverized at 900W under an argon atmosphere and an ice bath environment, and the resulting solution was centrifuged, and the supernatant was taken to obtain a MXene monodispersion.

[0033] (2) Add 5% of aniline to 1mol / L dilute hydrochloric acid by volume ratio, stir and mix evenly, and then add in the MXene monodispersion with a concentration of 4mg / ml obtained in step (1), the volume ratio of MXene monodispersion to aniline hydrochloric acid solution 1:1 (50% MXene), stirred at -5°C for 4 hours to obtain MXene / PANI precipitate, washed the precipitate repeatedly with deionized water and dried to obtain MXene / PANI powd...

Embodiment 3

[0038] (1) Take 1g of lithium fluoride, add 20ml of hydrochloric acid with a concentration of 9mol / L and stir evenly, and at the same time add 1g of precursor Ti 3 AlC 2 , stirred at 40°C for 24h, washed and dried to obtain Ti 3 C 2 MXene powder, the obtained powder was added to deionized water to form a 10mg / ml suspension, and the obtained solution was ultrasonically pulverized at 900W under an argon atmosphere and an ice bath environment, and the resulting solution was centrifuged, and the supernatant was taken to obtain a MXene monodispersion.

[0039] (2) Add aniline 5% by volume in 1mol / L dilute hydrochloric acid, stir and mix evenly and add in the MXene monodispersion with a concentration of 4mg / ml obtained in step (1), the volume of the hydrochloric acid solution of MXene monodispersion and aniline The ratio is 1:3 (25% MXene). After stirring at 0°C for 4 hours, the MXene / PANI precipitate was obtained. The precipitate was repeatedly washed with deionized water and dr...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention belongs to the field of flexible wearable energy storage equipment, and relates to a preparation method of a high-capacity linear supercapacitor electrode based on MXene / PANI. After thata MXene dispersion liquid is mixed with a hydrochloric acid solution of aniline in proportion, self-assembly is carried out at a low temperature to generate an MXene / PANI composite material, a smallamount of deionized water is added into the MXene / PANI composite material, ground into slurry, and coated on a glass plate to prepare a composite film, freeze drying is carried out, an adhesive tape is used to implement stripping, and a motor carries out twisting to prepare the film into a linear electrode. According to the linear supercapacitor, the MXene material and the PANI material can show extra pseudocapacitance in the acid electrolyte, and compared with an electrode structure which is too tight in wet spinning, the electrode has richer pores after mechanical twisting, and a higher active surface area is brought. In addition, the problems of high brittleness and poor mechanical properties after MXene film formation are solved.

Description

technical field [0001] The invention belongs to the field of flexible wearable energy storage devices, and in particular relates to a method for preparing a high-capacity linear supercapacitor electrode based on MXene / PANI. Background technique [0002] With the popularity of wearable electronic devices, the demand for traditional energy storage devices is also developing towards small size and light weight, such as fiber supercapacitors. As a traditional energy storage device, supercapacitors have the properties of fast charge and discharge capability, high power density and long life. As a flexible wearable device, it needs to have additional mechanical properties and the characteristics of being able to work normally in various outdoor environments under bending conditions. [0003] From the perspective of electrode materials, materials with good electrochemical performance while maintaining light weight, flexibility and wear resistance are the first choice for flexible ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): H01G11/86H01G11/30H01G11/26
CPCH01G11/86H01G11/30H01G11/26Y02E60/13
Inventor 袁宁一谈娟周小双鞠逸凡丁建宁徐江王茜
Owner CHANGZHOU UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products