Department of Energy Engineering, Hanyang University , Seoul 133-791, Korea.
Advanced Batteries Research Center, Korea Electronics Technology Institute , Seongnam 463-816, Korea.
ACS Appl Mater Interfaces. 2015 Dec 16;7(49):27206-14. doi: 10.1021/acsami.5b08111. Epub 2015 Dec 4.
Room-temperature Na-metal-based rechargeable batteries, including Na-O2 and Na-S systems, have attracted attention due to their high energy density and the abundance of sodium resources. Although these systems show considerable promise, concerns regarding the use of Na metal should be addressed for their success. Here, we report dendrite-free Na-metal electrode for a Na rechargeable battery, engineered by employing nonflammable and highly Na(+)-conductive NaAlCl4·2SO2 inorganic electrolyte, as a result, showing superior electrochemical performances to those in conventional organic electrolytes. We have achieved a hard-to-acquire combination of nondendritic Na electrodeposition and highly stable solid electrolyte interphase at the Na-metal electrode, enabled by inducing polygonal growth of Na deposit using a highly concentrated Na(+)-conducting inorganic electrolyte and also creating highly dense passivation film mainly composed of NaCl on the surface of Na-metal electrode. These results are highly encouraging in the development of room-temperature Na rechargeable battery and provide another strategy for highly reliable Na-metal-based rechargeable batteries.
室温钠金属基可充电电池,包括 Na-O2 和 Na-S 体系,由于其高能量密度和丰富的钠资源而受到关注。尽管这些体系具有相当大的潜力,但为了它们的成功,应该解决使用钠金属的问题。在这里,我们报告了一种无枝晶钠金属电极,用于 Na 可充电电池,通过使用不可燃和高 Na(+)传导性的 NaAlCl4·2SO2 无机电解质来实现,结果表明,与传统有机电解质相比,具有优异的电化学性能。我们通过使用高浓度的 Na(+)传导性无机电解质诱导 Na 沉积物的多角形生长,并在 Na 金属电极表面形成主要由 NaCl 组成的高密度钝化膜,从而实现了难以获得的无枝晶 Na 沉积和高度稳定的固体电解质中间相的组合。这些结果对室温 Na 可充电电池的发展非常有希望,并为高可靠性的基于 Na 金属的可充电电池提供了另一种策略。