Sodium metal is considered a promising candidate as an anode to maximize the energy density of sodium secondary batteries. The use of β"-alumina solid electrolyte (BASE) is a viable approach to ensure the safe operation of sodium metal batteries.1, 2 Although sodium metal batteries utilizing BASE have gained success at elevated temperatures (e.g. 250 °C), exhibiting stable and efficient cycling performance, even beyond 1000 mA cm−2,3 they are prone to short circuits above certain current densities, which is underscored by a crucial metric referred to the critical current density (CCD). The CCD of BASE typically varies from 0.1 to 10 mA cm−2 at room temperature,1 possibly due to insufficient contact between the rigid surface of BASE and solid sodium metal. This research focuses on the deposition and dissolution behavior of sodium metal anodes in both liquid and solid states, particularly at slight temperature differences near the melting point of sodium. The CCDs were assessed in a symmetric Na/BASE/Na cell configuration at 90 and 105 °C for solid and liquid sodium (m.p. of sodium 98 °C), respectively. The cell failure was verified by electrochemical impedance spectroscopy after each cycle. Post-test morphological characterizations of the BASE were investigated through scanning electron microscopy. Moreover, rate and cycle performance was assessed using a Na//Na3V2(PO4)3 configuration at two different temperatures. In conclusion, a slight increase in temperature to maintain sodium in the liquid state significantly bolsters the performance of the Na anode, enabling prolonged cycle duration without the dendrite formation causing cell degradation.
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