材料科学
超级电容器
电化学窗口
电解质
能量密度
化学工程
窗口(计算)
储能
电化学
共晶体系
水溶液
盐(化学)
离子电导率
工程物理
热力学
化学
电极
有机化学
微观结构
物理化学
复合材料
功率(物理)
工程类
物理
操作系统
计算机科学
作者
Xuejun Lu,R. J. Jiménez Riobóo,Dónal Leech,María C. Gutiérrez,M. Luisa Ferrer,Francisco del Monte
标识
DOI:10.1021/acsami.0c04011
摘要
Water-in-salt (WIS) electrolytes are gaining increased interest as an alternative to conventional aqueous or organic ones. WIS electrolytes offer an interesting combination of safety, thanks to their aqueous character, and extended electrochemical stability window, thanks to the strong coordination between water molecules and ion salt. Nonetheless, cost, the tendency of salt precipitation, and sluggish ionic transfer leading to poor rate performance of devices are some intrinsic drawbacks of WIS electrolytes that yet need to be addressed for their technological implementation. It is worth noting that the absence of "free'' water molecules could also be achieved via the addition of a certain cosolvent capable of coordinating with water. This is the case of the eutectic mixture formed between DMSO and H2O with a molar ratio of 1:2 and a melting point as low as -140 °C. Interestingly, addition of salts at near-saturation conditions also resulted in an increase of the boiling point of the resulting solution. Herein, we used a eutectic mixture of DMSO and H2O for dissolution of LiTFSI in the 1.1-8.8 molality range. The resulting electrolyte (e.g., the so-called aqueous-eutectic-in-salt) exhibited excellent energy and power densities when operating in a supercapacitor cell over a wide range of extreme ambient temperatures, from as low as -35 °C to as high as +65 °C.
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