Abstract
A self-healing polymer (SHP) with abundant hydrogen bonds, appropriate viscoelasticity, and stretchability is a promising binder to improve cycle performance of Si microparticle anodes in lithium (Li) ion batteries. Besides high capacity and long cycle life, efficient rate performance is strongly desirable for practical Si anode implementation. Here, polyethylene glycol (PEG) groups are incorporated into the SHP, facilitating Li ionic conduction within the binder. The concept of the SHP-PEG binder involves improving the interface between Si microparticles and electrolytes after cycling based on the combination of self-healing ability and fast Li ionic conduction. Through the systematic study of mixing PEG Mw and ratio, the polymeric binder combining SHP and PEG with Mw 750 in an optimal ratio of 60:40 (mol%) achieves a high discharging capacity of ≈2600 mA h g−1, reasonable rate performance especially when >1C and maintains 80% of their initial capacity even after ≈150 cycles at 0.5C. The described concept for the polymeric binder, embedding both self-healing ability and high Li ionic conductivity, should be equally useful for next generation batteries utilizing high capacity materials which suffer from huge volume change during cycling.
Original language | English (US) |
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Article number | 1703138 |
Journal | Advanced Energy Materials |
Volume | 8 |
Issue number | 14 |
DOIs | |
State | Published - May 15 2018 |
Funding
The authors acknowledge funding support from the Assistant Secretary for Energy, Office of Vehicle Technologies of the U.S. Department of Energy through the Battery 500 Consortium. T.M. acknowledges support by Sony Corporation
Keywords
- ionic conductivity
- lithium-ion batteries
- microparticles
- self-healing
- silicon
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- General Materials Science