Park Jooha, Xu Zheng-Long, Kang Kisuk
Department of Materials Science and Engineering, Research Institute of Advanced Materials (RIAM), Seoul National University, Seoul, South Korea.
Department of Industrial and Systems Engineering, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Front Chem. 2020 May 21;8:432. doi: 10.3389/fchem.2020.00432. eCollection 2020.
Reversible intercalation of guest ions in graphite is the key feature utilized in modern battery technology. In particular, the capability of Li-ion insertion into graphite enabled the successful launch of commercial Li-ion batteries 30 years ago. On the road to explore graphite as a universal anode for post Li-ion batteries, the conventional intercalation chemistry is being revisited, and recent findings indicate that an alternative intercalation chemistry involving the insertion of solvated ions, designated as co-intercalation, could overcome some of the obstacles presented by the conventional intercalation of graphite. As an example, the intercalation of Na ions into graphite for Na-ion batteries has been perceived as being thermodynamically impossible; however, recent work has revealed that a large amount of Na ions can be reversibly inserted in graphite through solvated-Na-ion co-intercalation reactions. More recently, it has been extensively demonstrated that with appropriate electrolyte selection, not only Na ions but also other ions such as Li, K, Mg, and Ca ions can be co-intercalated into a graphite electrode, resulting in high capacities and power capabilities. The co-intercalation reaction shares a lot in common with the conventional intercalation chemistry but also differs in many respects, which has attracted tremendous research efforts in terms of both fundamentals and practical applications. Herein, we aim to review the progress made in understanding the solvated-ion intercalation mechanisms in graphite and to comprehensively summarize the state-of-the-art achievements by surveying the correlations among the guest ions, co-intercalation conditions, and electrochemical performance of batteries. In addition, the advantages and challenges related to the practical application of graphite undergoing co-intercalation reactions are presented.
客体离子在石墨中的可逆嵌入是现代电池技术所利用的关键特性。特别是,锂离子插入石墨的能力使得30年前商用锂离子电池得以成功推出。在探索将石墨作为锂离子电池后通用负极的道路上,传统的嵌入化学正在被重新审视,最近的研究结果表明,一种涉及溶剂化离子插入的替代嵌入化学(称为共嵌入)可以克服石墨传统嵌入所带来的一些障碍。例如,钠离子插入石墨用于钠离子电池曾被认为在热力学上是不可能的;然而,最近的研究表明,大量钠离子可以通过溶剂化钠离子共嵌入反应可逆地插入石墨中。最近,大量研究表明,通过适当选择电解质,不仅钠离子,而且锂、钾、镁和钙离子等其他离子也可以共嵌入石墨电极,从而实现高容量和高功率性能。共嵌入反应与传统嵌入化学有许多共同之处,但在许多方面也有所不同,这在基础研究和实际应用方面都吸引了大量的研究工作。在此,我们旨在回顾在理解石墨中溶剂化离子嵌入机制方面取得的进展,并通过研究客体离子、共嵌入条件和电池电化学性能之间的相关性,全面总结当前的研究成果。此外,还介绍了与石墨共嵌入反应实际应用相关的优势和挑战。