Tomich Anton W, Chen Jianjun, Carta Veronica, Guo Juchen, Lavallo Vincent
Department of Chemistry University of California, Riverside, Riverside, California 92521, United States.
Department of Chemical and Environmental Engineering University of California, Riverside, Riverside, California 92521, United States.
ACS Cent Sci. 2024 Jan 12;10(2):264-271. doi: 10.1021/acscentsci.3c01176. eCollection 2024 Feb 28.
To realize an energy storage transition beyond Li-ion competitive technologies, earth-abundant elements, such as Mg, are needed. Carborane anions are particularly well-suited to realizing magnesium-ion batteries (MIBs), as their inert and weakly coordinating properties beget excellent electrolyte performance. However, utilizing these materials in actual electrochemical cells has been hampered by the reliance on the Mg salts of the commercially available [HCBH] anion, which is not soluble in more weakly binding solvents apart from the higher glymes. Herein, we demonstrate it is possible to iteratively engineer the [HCBH] anion surface synthetically to address previous solubility issues and yield a highly conductive (up to 7.33 mS cm) and electrochemically stable (up to +4.2 V vs Mg) magnesium electrolyte that surpasses the state of the art. This novel non-nucleophilic electrolyte exhibits highly dissociative behavior regardless of concentration and is tolerant of prolonged periods of cycling in symmetric cells at high current densities (up to 2.0 mA cm, 400 h). The hydrocarbon functionalized carborane electrolyte presented here demonstrates >96% Coulombic efficiency when paired with a MoS cathode. This approach realizes a needed candidate to discover next-generation cathode materials that can enable the design of practical and commercially viable Mg batteries.
为了实现超越锂离子电池的储能技术转型,需要地球上储量丰富的元素,如镁。碳硼烷阴离子特别适合用于实现镁离子电池(MIB),因为它们的惰性和弱配位特性带来了优异的电解质性能。然而,在实际的电化学电池中使用这些材料受到了限制,这是由于依赖市售的[HCBH]阴离子的镁盐,除了较高的乙二醇二甲醚外,该镁盐在更弱结合的溶剂中不溶。在此,我们证明可以通过合成方法迭代地设计[HCBH]阴离子表面,以解决先前的溶解性问题,并产生一种高导电性(高达7.33 mS cm)和电化学稳定(相对于镁高达+4.2 V)的镁电解质,其性能超越了现有技术水平。这种新型的非亲核电解质无论浓度如何都表现出高度离解行为,并且在高电流密度(高达2.0 mA cm,400 h)下在对称电池中能够耐受长时间循环。本文提出的碳硼烷烃功能化电解质与MoS阴极配对时,库仑效率>96%。这种方法实现了一种所需的候选材料,可用于发现下一代阴极材料,从而推动实用且具有商业可行性的镁电池的设计。