期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 29, 页码 14528-14537出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta06024k
关键词
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资金
- Technology Development Program to Solve Climate Changes of the National Research Foundation (NRF) - Ministry of Science and ICT [2017M1A2A2044501]
- Royalty funding through Argonne National Laboratory
- U.S. Department of Energy [DE-ACO2-06CH11357]
- National Research Foundation of Korea [2017M1A2A2044501] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
In a conventional Na-ion battery system using liquid electrolyte, there are critical safety issues due to the instability of the liquid electrolyte. Na3Zr2Si2PO12(NASICON) solid electrolyte is a material that is sufficient to replace a liquid electrolyte as it has high ionic conductivity and thermal and electrochemical stability. However, as there is a large interfacial resistance in the NASICON solid electrolyte powder, even when used in combination with a polymer electrolyte, the advantageous effects of ceramics are not easily exhibited. In this study, we propose a top-down method of combining a polymer with a ceramic in which an ion transport channel is previously formed. In this method, a NASICON solid electrolyte is partially sintered to form ion transport channels. Then the NASICON solid electrolyte pores are filled with an epoxy polymer to increase the strength of the epoxy-NASICON composite electrolyte. This method demonstrates the possibility of our composite electrolyte being used as a thin and strong film. As a result of our methods, the ionic conductivity and thermal and electrochemical stability of NASICON were maintained, while the physical strength was enhanced by approximately 2 times. In addition, a capacity of 120 mA h g(-1)and stability of 20 cycles were confirmed in a half cell with a Na3V2(PO4)(3)cathode and Na metal. This method proposes a new direction for research regarding composite electrolytes created using an oxide-based solid electrolyte.
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