阳极
锂(药物)
电解质
容量损失
材料科学
氧化还原
电化学
离子
锂离子电池
电极
纳米技术
储能
化学工程
电池(电)
化学
有机化学
物理化学
冶金
物理
工程类
内分泌学
功率(物理)
医学
量子力学
作者
Juyoung Jang,Inyeong Kang,Jinkwan Choi,Hyangsoo Jeong,Kyung‐Woo Yi,Jihyun Hong,Minah Lee
标识
DOI:10.1002/anie.202002411
摘要
Abstract Prelithiation is of great interest to Li‐ion battery manufacturers as a strategy for compensating for the loss of active Li during initial cycling of a battery, which would otherwise degrade its available energy density. Solution‐based chemical prelithiation using a reductive chemical promises unparalleled reaction homogeneity and simplicity. However, the chemicals applied so far cannot dope active Li in Si‐based high‐capacity anodes but merely form solid–electrolyte interphases, leading to only partial mitigation of the cycle irreversibility. Herein, we show that a molecularly engineered Li–arene complex with a sufficiently low redox potential drives active Li accommodation in Si‐based anodes to provide an ideal Li content in a full cell. Fine control over the prelithiation degree and spatial uniformity of active Li throughout the electrodes are achieved by managing time and temperature during immersion, promising both fidelity and low cost of the process for large‐scale integration.
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