Synergistic Poly(Ionic Liquid)-CMC binder with ionic liquid electrolytes for high-performance, polysulfide-free lithium-sulfur batteries

Lithium–sulfur (Li-S) batteries are among the most promising next-generation energy storage technologies due to their high theoretical energy density and the abundance of sulfur. However, their practical implementation is limited by active material loss, unstable electrode interfaces, intermediate polysulfide dissolution, and low sulfur utilization. In this study, we present a hybrid binder composed of a lithium-ion-conductive poly(ionic liquid) (PIL), poly(diallyldimethylammonium) bis(trifluoromethanesulfonyl)imide (PDADMA-TFSI), and carboxymethyl cellulose (CMC) engineered to operate synergistically with ionic liquid (IL) electrolytes based on trimethylisobutylphosphonium bis(fluorosulfonyl)imide [P 111i4 ][FSI] and N-trimethyl-N-propylammonium bis(fluorosulfonyl)imide [N 1113 ][FSI]. This PIL-CMC binder significantly improves interfacial stability and enables efficient sulfur utilization in polysulfide-free cycling. Among all combinations tested, 50 mol% LiTFSI in [N 1113 ][FSI] exhibited the best electrochemical performance, sustaining capacities above 1100 mA h g −1 for over 100 cycles at 50 °C. A reduced total binder content formulation (5 wt% PIL and 5 wt% CMC) maintained comparable performance, suggesting potential for further optimization. Electrochemical analysis revealed low voltage polarization and high Coulombic efficiency of up to 99.5 %, while UV–vis and Raman spectroscopy confirmed the absence of dissolved polysulfides. Overall, this work demonstrates a robust and scalable strategy for realizing additive-free, thermally stable Li-S cathodes, emphasizing the importance of binder–electrolyte integration in the design of high-performance Li-S batteries. • Poly(ionic liquid)–CMC binder enhances sulfur utilization and cycling stability. • Mixed binder promotes ionic conductivity and mechanical integrity synergy. • Ionic liquid electrolytes suppress polysulfide dissolution for stable cycling. • Ammonium-based IL electrolyte improves lithium-ion transport and SEI stability. • Cells retain capacities >1100 mAh g −1 over 100 cycles at 50 °C.

Authors

Institutions

Publication Details

Journal
Journal of Power Sources
Published
2025-09-05
DOI
https://doi.org/10.1016/j.jpowsour.2025.238278
Citations
1
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.73
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synergistic Poly(Ionic Liquid)-CMC binder with ionic liquid electrolytes for high-performance, polysulfide-free lithium-sulfur batteries

Paul M. Bayley, Robert Kerr, Frederick Nti, Patrick C. Howlett et al.
1 citations
Journal of Power Sources
Advanced Battery Materials and Technologies
0.73
article

Synergistic Poly(Ionic Liquid)-CMC binder with ionic liquid electrolytes for high-performance, polysulfide-free lithium-sulfur batteries

Paul M. Bayley, Robert Kerr, Frederick Nti, Patrick C. Howlett, Ajit Kumar, Sam Rowlands, Maria Forsyth
article en
1 citations

Abstract

Lithium–sulfur (Li-S) batteries are among the most promising next-generation energy storage technologies due to their high theoretical energy density and the abundance of sulfur. However, their practical implementation is limited by active material loss, unstable electrode interfaces, intermediate polysulfide dissolution, and low sulfur utilization. In this study, we present a hybrid binder composed of a lithium-ion-conductive poly(ionic liquid) (PIL), poly(diallyldimethylammonium) bis(trifluoromethanesulfonyl)imide (PDADMA-TFSI), and carboxymethyl cellulose (CMC) engineered to operate synergistically with ionic liquid (IL) electrolytes based on trimethylisobutylphosphonium bis(fluorosulfonyl)imide [P 111i4 ][FSI] and N-trimethyl-N-propylammonium bis(fluorosulfonyl)imide [N 1113 ][FSI]. This PIL-CMC binder significantly improves interfacial stability and enables efficient sulfur utilization in polysulfide-free cycling. Among all combinations tested, 50 mol% LiTFSI in [N 1113 ][FSI] exhibited the best electrochemical performance, sustaining capacities above 1100 mA h g −1 for over 100 cycles at 50 °C. A reduced total binder content formulation (5 wt% PIL and 5 wt% CMC) maintained comparable performance, suggesting potential for further optimization. Electrochemical analysis revealed low voltage polarization and high Coulombic efficiency of up to 99.5 %, while UV–vis and Raman spectroscopy confirmed the absence of dissolved polysulfides. Overall, this work demonstrates a robust and scalable strategy for realizing additive-free, thermally stable Li-S cathodes, emphasizing the importance of binder–electrolyte integration in the design of high-performance Li-S batteries. • Poly(ionic liquid)–CMC binder enhances sulfur utilization and cycling stability. • Mixed binder promotes ionic conductivity and mechanical integrity synergy. • Ionic liquid electrolytes suppress polysulfide dissolution for stable cycling. • Ammonium-based IL electrolyte improves lithium-ion transport and SEI stability. • Cells retain capacities >1100 mAh g −1 over 100 cycles at 50 °C.

Journal of Power SourcesVol. 658
Deakin University (AU)
Openalex Percentile: Top 24%
Advanced Battery Materials and Technologies
0.73
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.