Zhao Wei, Wang Chunting, Cheng Zhenjie, Zheng Cheng, Yao Qian, Pan Jun, Ma Xiaojian, Yang Jian
Key Laboratory of Colloid and Interface Chemistry Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University Jinan 250100 P. R. China.
School of Physical and Mathematical Sciences, Nanyang Technological University Singapore 637371 Singapore
Chem Sci. 2024 Apr 5;15(17):6500-6506. doi: 10.1039/d3sc06640a. eCollection 2024 May 1.
The thermodynamic instability of Na-intercalated compounds is an important factor limiting the application of graphite anodes in sodium-ion batteries. Although solvent co-intercalation is recognized as a simple and effective strategy, the challenge lies in the lack of durable electrolytes. Herein, we successfully apply low-concentration imidazole-based electrolytes to graphite anodes for sodium-ion batteries. Specifically, low concentrations ensure high ionic conductivity while saving on costs. Methylimidazole molecules can be co-intercalated with Na, and a small amount of unreleased solvated Na serves the dual purpose of providing support to the graphite layer and preventing peeling off. The interphase formed in imidazole is more uniform and dense compared with that in ether electrolytes, which reduces side reactions and the risk of internal short circuits. The obtained battery demonstrates a long cycle life of 1800 cycles with a capacity retention of 84.6%. This success extends to other imidazole-based solvents such as 1-propylimidazole and 1-butylimidazole.
钠插层化合物的热力学不稳定性是限制石墨负极在钠离子电池中应用的一个重要因素。尽管溶剂共插层被认为是一种简单有效的策略,但挑战在于缺乏耐用的电解质。在此,我们成功地将低浓度咪唑基电解质应用于钠离子电池的石墨负极。具体而言,低浓度可确保高离子电导率,同时节省成本。甲基咪唑分子可与钠共插层,少量未释放的溶剂化钠起到支撑石墨层和防止剥离的双重作用。与醚类电解质相比,咪唑中形成的界面更均匀、致密,这减少了副反应和内部短路的风险。所制备的电池展现出1800次循环的长循环寿命,容量保持率为84.6%。这一成功也适用于其他咪唑基溶剂,如1-丙基咪唑和1-丁基咪唑。