Abstract
The increasing demand for short charging time on electric vehicles has motivated realization of fast chargeable lithium-ion batteries (LIBs). However, shortening the charging time of LIBs is limited by Li+ intercalation process consisting of liquid-phase diffusion, de-solvation, SEI crossing, and solid-phase diffusion. Herein, we propose a new strategy to accelerate the de-solvation step through a control of interaction between polymeric binder and solvent-Li+ complexes. For this purpose, three alkali metal ions (Li+, Na+, and K+) substituted carboxymethyl cellulose (Li-, Na-, and K-CMC) are prepared to examine the effects of metal ions on their performances. The lowest activation energy of de-solvation and the highest chemical diffusion coefficient were observed for Li-CMC. Specifically, Li-CMC cell with a capacity of 3 mAh cm−2 could be charged to >95% in 10 min, while a value above >85% was observed after 150 cycles. Thus, the presented approach holds great promise for the realization of fast charging.
| Original language | English |
|---|---|
| Article number | e12509 |
| Journal | Energy and Environmental Materials |
| Volume | 7 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2024 |
Bibliographical note
Publisher Copyright:© 2022 The Authors. Energy & Environmental Materials published by John Wiley & Sons Australia, Ltd on behalf of Zhengzhou University.
Keywords
- de-solvation
- digital twins
- fast charging
- graphite anodes
- polymeric binders