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Open Access

Preparation and performance of polymer/graphene composite solid electrolyte film

Xinghua LIANGa,b,Dongxue HUANGaLingxiao LANaSuo LIaYujuan NINGaYu ZHANGaPenggui WUaXiaofeng ZHANGb( )
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science and Technology, Liuzhou 545006, China
National Engineering Laboratory for Modern Materials Surface Engineering Technology, Guangdong Institute of New Materials, Guangdong Academy of Science, Guangzhou, 510650, China

Peer review under responsibility of Editorial Committee of JAMST

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Abstract

The polymer solid electrolyte has a simple preparation method, good film-forming performance, and good electrode-electrolyte interface contact. However, the low room temperature ionic conductivity, poor electrochemical stability, and the inability to match the cathode material with a wide voltage window limit the large-scale commercial application of polymer solid electrolytes; graphene has excellent mechanical, mechanical properties, photoelectric thermal properties and a large specific surface area, high ion conductivity and electron migration number, so it has strong electrical conductivity. In this paper, a typical polymer solid electrolyte polyethylene oxide (PEO) and graphene composite are selected to further enhance the electrochemical performance of the composite material. Experiments have found that the polymer/graphene composite solid electrolyte membrane with graphene added does not decompose significantly before 5 V, which clarifies that it has good electrochemical stability. And the first charge-discharge specific capacity of the composite solid electrolyte membrane is higher than that of the single polymer solid electrolyte membrane. Neither the diffraction peak nor the reduction peak shifted after 5 cycles, and the cycle life was still 99.449% after 100 cycles, indicating that it has good cycle stability. Therefore, the application of polymer/graphene composite solid electrolyte membranes in all-solid-state lithium batteries is feasible.

References

1

Ely T O, Kamzabek D, Chakraborty D. Batteries safety: Recent progress and current challenges. Frontiers in Energy Research 2019;7:71.

2

Bai LX, Xue WD, Li Y, et al. The interfacial behaviours of all-solid-state lithium ion batteries. Ceramics International 2018; 44(7): 7319-7328.

3

Zhang SZ, Xia XH, Xie D, et al. Facile interfacial modification via in-situ ultraviolet solidified gel polymer electrolyte for high-performance solid-state lithium ion batteries. Journal of Power Sources 2019;409:31-37.

4

Wang HC, Sheng L, Yasin G, et al. Reviewing the current status and development of polymer electrolytes for solid-state lithium batteries. Energy Storage Materials 2020;33:188-215.

5

Zeng Y, Wang H, Cheng HM. Research progress and potential applications for graphene/polymer composites. Carbon 2017;114:755.

6

Yu XW, Shi G-Q. Preparation and applications of graphene/polymer composite thin films. Acta Polymerica Sinica 2014; (7): 885-895(in Chinese).

7

Anwar Z, Kausar A, Muhammad B. Polymer and graphite-derived nanofiller composite: An overview of functional applications. Polymer-Plastics Technology and Engineering 2016;55(16):1765-1784.

8

Gao Y, Chen G-H. Recent progress in preparation method of the polymer/graphene composites and it's industrialization status. Acta Polymerica Sinica 2014;(10):1314-1327(in Chinese).

9

Cui G, Zhang CC, Wang AL, et al. Research progress on self-healing polymer/graphene anticorrosion coatings. Progress in Organic Coatings 2021; 155:106231.

10

Kausar A, Anwar Z, Muhammad B, et al. Overview of nonflammability characteristics of graphene and graphene oxide-based polymeric composite and essential flame retardancy techniques. Polymer-Plastics Technology and Engineering, 2016;56(5):488-505.

11

Chen WF, Lv G, Shen JL, et al. The preparation and application of polymer/graphene nanocomposites. Emerging Materials Research 2020;9(3):943-959.

12

Gao S, Zhong J, Xue G, et al. Ion conductivity improved polyethylene oxide/lithium perchlorate electrolyte membranes modified by graphene oxide. Journal of Membrane Science 2014; 470:316-322.

13

Liang X, Han D, Wang Y, et al. Preparation and performance study of a PVDF-LATP ceramic composite polymer electrolyte membrane for solid-state batteries. RSC Advances 2018;8(71):40498-40504.

14

Cheng J, Hou GM, Sun Q, et al. Cold-pressing PEO/LAGP composite electrolyte for integrated all-solid-state lithium metal battery. Solid State Ionics 2020;345:115156.

15

Park D-W, Caňas NA, Wagner N, et al. Novel solvent-free direct coating process for battery electrodes and their electrochemical performance. Journal of Power Sources 2016; 306:758-763.

16

Fu GP, Dempsey J, Izaki K, et al. Highly conductive solid polymer electrolyte membranes based on polyethylene glycol-bis-carbamate dimethacrylate networks. Journal of Power Sources 2017; 359:441-449.

Journal of Advanced Manufacturing Science and Technology
Cite this article:
LIANG X, HUANG D, LAN L, et al. Preparation and performance of polymer/graphene composite solid electrolyte film. Journal of Advanced Manufacturing Science and Technology, 2021, 1(4): 2021011. https://doi.org/10.51393/j.jamst.2021011

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Received: 01 October 2021
Revised: 05 November 2021
Accepted: 02 December 2021
Published: 15 October 2021
© 2021 JAMST All rights reserved.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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