4.8 Article

Significantly improved interface between PVDF-based polymer electrolyte and lithium metal via thermal-electrochemical treatment

Journal

ENERGY STORAGE MATERIALS
Volume 46, Issue -, Pages 452-460

Publisher

ELSEVIER
DOI: 10.1016/j.ensm.2022.01.034

Keywords

Thermal stability; Thermal-electrochemical treatment; Solid-state battery; Lithium metal; Poly(vinylidene fluoride)

Funding

  1. basic science center program of National Natural Science Foundation of China [51788104]

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Polymer-based solid-state electrolytes have shown great potential for solid-state lithium batteries due to their flexibility, low cost, and good interfacial contact with electrodes. This study thoroughly investigates the thermal response and interfacial stability between a PVDF-based polymer electrolyte and Li metal. A thermal-electrochemical treatment method is proposed to improve the interfacial stability and enhance the cycle performance of Li symmetric cells.
Polymer-based solid-state electrolytes have attracted much attention for their potential applications in solid-state lithium (Li) metal batteries due to their flexibility, good interfacial contact with electrodes, low cost, and easy scale-up. However, the thermal response of polymer-based electrolytes is still one of the main concerns. Here, we thoroughly investigated the thermal response of the interfacial stability between a poly(vinylidene fluoride) (PVDF)-based polymer electrolyte and Li metal and found that the Li symmetric cells cycled at 60 degrees C presented a low polarization voltage and long life due to the balance between the interfacial diffusion kinetics and electrochemical reaction rate at a current density of 0.3, 0.5 or 1 mA cm(-2). The interface layer between the PVDF-based electrolyte and Li metal formed at 60 degrees C was uniformly thin and had a smooth surface, whereas the ones formed at 30 or 90 degrees C were unevenly thick or showed cracks. Based on the findings in the temperature dependency of the interface layer, we proposed a thermal-electrochemical treatment method through which a stable interface was in-situ formed at 60 degrees C and 0.3 mA cm(-2), rendering an ultralong cycle life, such as 2600 h at a current density of 0.3 mA cm(-2) and 30 degrees C, to the Li symmetric cell with the PVDF-based polymer electrolyte. The thermal-electrochemical treatment improved the cycle performance of LiFePO4 parallel to PVDF parallel to Li solid-state batteries. This work provides a strategy to effectively enhance the interfacial stability between the PVDF-based electrolyte and Li metal through rational thermal-electrochemical treatment.

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