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用于锂离子电池中普鲁士蓝类似物的阴极电解质界面工程

Cathode Electrolyte Interphase Engineering for Prussian Blue Analogues in Lithium-Ion Batteries.

作者信息

Wi Tae-Ung, Park Changhyun, Ko Sangho, Kim Taewon, Choi Ahreum, Muralidharan Vithiya, Choi Myeongjun, Lee Hyun-Wook

机构信息

School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.

Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas 77005, United States.

出版信息

Nano Lett. 2024 Jun 26;24(25):7783-7791. doi: 10.1021/acs.nanolett.4c01971. Epub 2024 Jun 13.

Abstract

The increasing use of low-cost lithium iron phosphate cathodes in low-end electric vehicles has sparked interest in Prussian blue analogues (PBAs) for lithium-ion batteries. A major challenge with iron hexacyanoferrate (FeHCFe), particularly in lithium-ion systems, is its slow kinetics in organic electrolytes and valence state inactivation in aqueous ones. We have addressed these issues by developing a polymeric cathode electrolyte interphase (CEI) layer through a ring-opening reaction of ethylene carbonate triggered by OH radicals from structural water. This facile approach considerably mitigates the sluggish electrochemical kinetics typically observed in organic electrolytes. As a result, FeHCFe has achieved a specific capacity of 125 mAh g with a stable lifetime over 500 cycles, thanks to the effective activation of Fe low-spin states and the structural integrity of the CEI layers. These advancements shed light on the potential of PBAs to be viable, durable, and efficient cathode materials for commercial use.

摘要

低端电动汽车中低成本磷酸铁锂阴极的使用日益增加,这引发了人们对用于锂离子电池的普鲁士蓝类似物(PBAs)的兴趣。六氰合铁酸铁(FeHCFe)面临的一个主要挑战,尤其是在锂离子系统中,是其在有机电解质中的动力学缓慢以及在水性电解质中的价态失活。我们通过由结构水产生的OH自由基引发碳酸亚乙酯的开环反应,开发了一种聚合物阴极电解质界面(CEI)层,从而解决了这些问题。这种简便的方法大大减轻了通常在有机电解质中观察到的缓慢电化学动力学。结果,由于Fe低自旋态的有效激活和CEI层的结构完整性,FeHCFe实现了125 mAh g的比容量,在500次循环中具有稳定的寿命。这些进展揭示了PBAs成为可行、耐用且高效的商业用阴极材料的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e679/11216687/47b617d6a330/nl4c01971_0001.jpg

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