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A Microscopically Heterogeneous Colloid Electrolyte for Extremely Fast-Charging and Long-Calendar-Life Silicon-Based Lithium-Ion Batteries.
Zhang, Weifeng; Zou, Wenwu; Jiang, Guoxing; Qi, Shengguang; Peng, Siyuan; Song, Huiyu; Cui, Zhiming; Liang, Zhenxing; Du, Li.
Afiliação
  • Zhang W; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Zou W; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Jiang G; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Qi S; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Peng S; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Song H; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Cui Z; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Liang Z; South China University of Technology, School of Chemistry and Chemical Engineering, CHINA.
  • Du L; South China University of Technology, 381 Wushan Road Tianhe District, Guangzhou, CHINA.
Angew Chem Int Ed Engl ; : e202410046, 2024 Jul 20.
Article em En | MEDLINE | ID: mdl-39032152
ABSTRACT
Fast-charging capability and calendar life are critical metrics in rechargeable batteries, especially in silicon-based batteries that are susceptible to sluggish Li+ desolvation kinetics and HF-induced corrosion. No existing electrolyte simultaneously tackles both these pivotal challenges. Here we report a microscopically heterogeneous covalent organic nanosheet (CON) colloid electrolyte for extremely fast-charging and long-calendar-life Si-based lithium-ion batteries. Theoretical calculations and operando Raman spectroscopy reveal the fundamental mechanism of the multiscale noncovalent interaction, which involves the mesoscopic CON attenuating the microscopic Li+-solvent coordination, thereby expediting the Li+ desolvation kinetics. This electrolyte design enables extremely fast-charging capabilities of the full cell, both at 8C (83.1% state of charge) and 10C (81.3% state of charge). Remarkably, the colloid electrolyte demonstrates record-breaking cycling performance at 10C (capacity retention of 92.39% after 400 cycles). Moreover, benefiting from the robust adsorption capability of mesoporous CON towards HF and water, a notable improvement is observed in the calendar life of the full cell. This study highlights the role of microscopically heterogeneous colloid electrolytes in enhancing the fast-charging capability and calendar life of Si-based Li-ion batteries. Our work offers fresh perspectives on electrolyte design with multiscale interactions, providing insightful guidance for the development of alkali-ion/metal batteries operating under harsh environments.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article