An Imidazole-Based Electrolyte Additive for Enhancing the Cyclability of Graphite||LiFePO4 Batteries

材料科学 电解质 咪唑 石墨 化学工程 无机化学 纳米技术 有机化学 冶金 电极 物理化学 化学 工程类
作者
Ziyu Wu,Jianing Duan,Congcong Sun,Jianming Zheng,Dan Sun,Maochun Hong
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:17 (24): 35372-35381 被引量:4
标识
DOI:10.1021/acsami.5c01749
摘要

Graphite||LiFePO4 (Gr||LFP) lithium-ion batteries (LIBs) are extensively utilized in stationary energy storage systems, particularly for photovoltaic and wind power generation. Nevertheless, the lifetime of Gr||LFP batteries remains inadequate for fulfilling long-term energy storage demands. In this study, through molecular structure design, an imidazole-based molecule, N,N′-carbonyldiimidazole (CDI), is applied as an innovative solid electrolyte interphase (SEI)-forming additive for Gr||LFP batteries. This molecular design aims to construct a dense and chemically stable SEI on a graphite anode. CDI is characterized by a low energy level of the lowest unoccupied molecular orbital and strong adsorption energy on the graphite surface, attributed to its dual-ring structure. It can be preferentially reduced at 1.58 V vs Li/Li+ to form an SEI enriched with nitrogen-containing species. Additionally, CDI facilitates the decomposition of PF6– anions, resulting in increased LiF production, which enhances the interfacial stability. As a result, the capacity retention of Gr||LFP pouch cells improves by 18% after 1000 cycles at 45 °C at a 1 P rate compared to cells with the base electrolyte. This study highlights the significance of designing electrolyte additive molecular structures to manipulate the composition and robustness of the SEI layer, offering an approach for formulating electrolytes to achieve long-lifespan LIBs.
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