Solid polymer electrolytes of ionic liquids via a bicontinuous ion transport channel for lithium metal batteries

Solid polymer electrolytes (SPEs) are a key component of solid-state lithium metal batteries. For attaining high ionic conductivity and high mechanical strength simultaneously, nanostructured SPEs are designed to have functionally separated ion transporting channels and solid-phase walls. Here, we r...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-01, Vol.11 (4), p.1676-1683
Hauptverfasser: Cho, Won-Jang, Cho, Seok-Kyu, Lee, Jun Hyuk, Yoon, Jeong Hoon, Kwon, Sangwoo, Park, Chanui, Lee, Won Bo, Yoo, Pil J., Lee, Minjae, Park, Sungkyun, Kang, Tai Hui, Yi, Gi-Ra
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Solid polymer electrolytes (SPEs) are a key component of solid-state lithium metal batteries. For attaining high ionic conductivity and high mechanical strength simultaneously, nanostructured SPEs are designed to have functionally separated ion transporting channels and solid-phase walls. Here, we report ion-conductive bicontinuous solid polymer electrolytes (Bi-SPEs) from thermodynamically stable bicontinuous microemulsions of ionic liquids and diacrylates in the presence of amphiphilic ionic liquids and lithium salt. From stable bicontinuous microemulsions with 10–30 wt% amphiphilic ionic liquids, free-standing Bi-SPE films were successfully obtained by photopolymerization and then implemented in lithium metal batteries. At 10 wt% of amphiphilic ionic liquids, the ionic conductivity increased up to 1.4 mS cm −1 keeping the mechanical strength at 0.8 MPa. A LiFePO 4 -paired lithium metal cell exhibits a stable discharge capacity of 121.9 mA h g −1 with 90.3% capacity retention (CE = 99.9%) over 300 cycles at 0.5 C and 30 °C.
ISSN:2050-7488
2050-7496
DOI:10.1039/D2TA08139C