Grindal Andrew, Azimi Gisele
Department of Materials Science and Engineering, University of Toronto, 184 College Street, Toronto, ON, M5S3E4, Canada.
Laboratory for Strategic Materials, Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, ON, M5S3E5, Canada.
Sci Rep. 2024 Nov 18;14(1):28468. doi: 10.1038/s41598-024-78437-9.
Rechargeable aluminum-ion batteries (AIBs) stand out as a potential cornerstone for future battery technology, thanks to the widespread availability, affordability, and high charge capacity of aluminum. However, the efficacy of current AIBs on the market is significantly limited by the charge storage process within their graphite cathodes. To fully realize the capabilities of AIBs, the discovery of a new cathode material is essential. Transition metal sulfides present an attractive option for cathode materials, although there has been a variety of conflicting reports regarding the exact nature of their charge storage mechanisms. This paper investigates cobalt sulfide (CoS) cathodes in AIBs, with a particular focus on deciphering the mechanisms of charge storage. Through synthesis, electrochemical testing, and post-cycling characterization, we illuminate the roles of AlCl intercalation, cobalt sulfide to AlS conversion, and sulfur to AlS conversion in charge storage. As cycling progresses, AlS synthesis from segregated sulfur segments emerged as the predominant mechanism, showcasing its potential to fully leverage the high capacity of aluminum metal and propel AIBs towards higher energy densities. Despite these promising findings, the study also uncovered significant challenges, notably material loss, intra-cathode diffusion limitations, and irreversible reactions that precipitously diminish charge capacity over time. These issues highlight the critical need for enhanced electrode stability, improved electrolyte compatibility, and accelerated aluminum diffusion. The research paves the way for further exploration of transition metal sulfides as cathode materials in AIBs, highlighting the imperative for innovations that bolster mechanical and chemical stability while optimizing ion transport. This work not only contributes to the fundamental understanding of charge storage in AIBs but also charts a course for the development of more durable and efficient battery systems.
可充电铝离子电池(AIBs)因其铝的广泛可得性、可承受性和高电荷容量,成为未来电池技术的潜在基石。然而,目前市场上的AIBs的效能受到其石墨阴极内电荷存储过程的显著限制。为了充分实现AIBs的性能,发现一种新的阴极材料至关重要。过渡金属硫化物是阴极材料的一个有吸引力的选择,尽管关于其电荷存储机制的确切性质存在各种相互矛盾的报道。本文研究了AIBs中的硫化钴(CoS)阴极,特别关注电荷存储机制的破译。通过合成、电化学测试和循环后表征,我们阐明了AlCl嵌入、硫化钴向AlS转化以及硫向AlS转化在电荷存储中的作用。随着循环的进行,由分离的硫段合成AlS成为主要机制,展示了其充分利用铝金属高容量并推动AIBs向更高能量密度发展的潜力。尽管有这些有前景的发现,但该研究也发现了重大挑战,特别是材料损失、阴极内扩散限制以及随着时间推移急剧降低电荷容量的不可逆反应。这些问题凸显了增强电极稳定性、改善电解质兼容性和加速铝扩散的迫切需求。该研究为进一步探索过渡金属硫化物作为AIBs中的阴极材料铺平了道路,强调了创新的必要性,即在优化离子传输的同时增强机械和化学稳定性。这项工作不仅有助于对AIBs中电荷存储的基本理解,还为开发更耐用、高效的电池系统指明了方向。