Forero-Saboya Juan, Hosseini-Bab-Anari Elham, Abdelhamid Muhammad E, Moth-Poulsen Kasper, Johansson Patrik
Department of Physics, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus UAB, E-08193 Bellaterra, Catalonia, Spain.
J Phys Chem Lett. 2019 Sep 5;10(17):4942-4946. doi: 10.1021/acs.jpclett.9b01467. Epub 2019 Aug 14.
Water-in-salt and water-in-bisalt electrolytes have recently attracted much attention due to their expanded electrochemical stability windows. The concentration limit of such electrolytes is constrained by the solubility of the lithium salts employed, ca. 21 m (mol kg) for LiTFSI (lithium bis(trifluoromethanesulfonyl)imide). By adding a second lithium salt, the total salt concentration can be increased, but the hydrogen evolution keeps limiting the application of such systems in batteries with low potential anodes. Herein we report a water-in-bisalt electrolyte with a record salt concentration (31.4 m LiTFSI + 7.9 m Li[N(CH)((CH)SO)((CH)SO)]) in which the bulky anion completely prevents the crystallization, even at such low water contents. Although the hydrogen evolution reaction is not completely suppressed, the expanded electrochemical stability window allows for low potential reactions such as aluminum-lithium alloying. The high salt concentration favors the formation of a suitable passivation layer that can be further engineered by modifying the anion structure.
盐包水和双盐包水电解质由于其扩展的电化学稳定窗口,最近备受关注。此类电解质的浓度极限受所用锂盐溶解度的限制,对于双(三氟甲磺酰)亚胺锂(LiTFSI)约为21 m(mol/kg)。通过添加第二种锂盐,总盐浓度可以提高,但析氢反应仍然限制了此类体系在低电位阳极电池中的应用。在此,我们报道了一种双盐包水电解质,其盐浓度创纪录(31.4 m LiTFSI + 7.9 m Li[N(CH)((CH)SO)((CH)SO)]),其中即使在如此低的含水量下,庞大的阴离子也能完全防止结晶。尽管析氢反应没有被完全抑制,但扩展的电化学稳定窗口允许进行低电位反应,如铝锂合金化。高盐浓度有利于形成合适的钝化层,可通过修饰阴离子结构进一步优化。