阳极
电解质
锂(药物)
石墨
溶剂化
材料科学
离子
化学工程
纳米技术
化学
物理化学
电极
有机化学
医学
工程类
内分泌学
作者
Chaonan Wang,Yuansen Xie,Yingshan Huang,Shaoyun Zhou,Huanyu Xie,Hongchang Jin,Hengxing Ji
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-03-14
卷期号:63 (21): e202402301-e202402301
被引量:82
标识
DOI:10.1002/anie.202402301
摘要
Li+ de-solvation at solid-electrolyte interphase (SEI)-electrolyte interface stands as a pivotal step that imposes limitations on the fast-charging capability and low-temperature performance of lithium-ion batteries (LIBs). Unraveling the contributions of key constituents in the SEI that facilitate Li+ de-solvation and deciphering their mechanisms, as a design principle for the interfacial structure of anode materials, is still a challenge. Herein, we conducted a systematic exploration of the influence exerted by various inorganic components (Li2CO3, LiF, Li3PO4) found in the SEI on their role in promoting the Li+ de-solvation. The findings highlight that Li3PO4-enriched SEI effectively reduces the de-solvation energy due to its ability to attenuate the Li+-solvent interaction, thereby expediting the de-solvation process. Building on this, we engineer Li3PO4 interphase on graphite (LPO-Gr) anode via a simple solid-phase coating, facilitating the Li+ de-solvation and building an inorganic-rich SEI, resulting in accelerated Li+ transport crossing the electrode interfaces and interphases. Full cells using the LPO-Gr anode can replenish its 80 % capacity in 6.5 minutes, while still retaining 70 % of the room temperature capacity even at -20 °C. Our strategy establishes connection between the de-solvation characteristics of the SEI components and the interfacial structure design of anode materials for high performance LIBs.
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