Electrolyte design for robust gradient solid-electrolyte interfaces to enable high-performance silicon anodes for pouch batteries

电解质 法拉第效率 阳极 材料科学 碳酸乙烯酯 碳酸二乙酯 化学工程 溶剂 无机化学 电极 化学 有机化学 工程类 物理化学
作者
Shenggong He,Shimin Huang,Xinzhou Liu,Xianggang Zeng,Hedong Chen,Lingzhi Zhao,Hadia Noor,Xianhua Hou
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:489: 150620-150620 被引量:14
标识
DOI:10.1016/j.cej.2024.150620
摘要

Silicon (Si) anodes has emerged as an ideal anode for the next generation of lithium-ion batteries owing to its high specific capacity. Nevertheless, Si particles undergo large volume expansion during cycling, inducing the continuous fragmentation/re-formation of the solid-electrolyte interphase (SEI) layer, which leads to rapid capacity decay and low Coulombic efficiency in EC-based carbonate electrolytes. Herein, a weakly solvating electrolyte with boric acid tris(hexafluoroisopropyl) ester (BTHE), 2,2,2-trifluoroethyl methyl carbonate (FDEC), and fluoroethylene carbonate (FEC) is developed to build a stable SEI. BTHE is introduced as a functional additive, which is induce anion and fluorinated solvent to form a gradient rigid–soft coupling SEI layer. In contrast to other anion-derived interfaces, weakly solvating electrolyte has been proven to construct a highly robust and stable –CF3-rich-organic outer layer and LiF-rich inner layer SEI on the Si anodes, resulting in approximately 99.9 % ultra-high Coulombic efficiency and ultra-high areal capacity (∼8.1 mAh cm−2). Beyond proof of concept, a 2.68 Ah Si||LiNi0.8Mn0.1Co0.1O2 pouch cell has an impressive 84.3 % capacity retention after 1000 cycles and could work normally at temperatures ranging from −30 °C to 100 °C based on this electrolyte, representing a pioneering report in pouch cells incorporating Si anodes.
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