Ionic Liquids Anchored on Carbon Synchronize Ion-Electron Transport in Liquid- and Solid-State Sulfur Batteries

Sulfur-based batteries hold great promise for next-generation energy storage owing to their high capacity and low cost, yet their performance is limited by sluggish ion transport and insulating discharge products. Here, we construct a continuous mixed ion-electron conductor network by anchoring imidazolium-based ionic liquids onto carbon nanotubes via strong π-π interactions. The ionic liquid layers provide fast Li+ pathways along the conductive framework, enabling synchronized ion–electron transport and reducing the Li2S nucleation overpotential to 28.2 mV. This interfacial design accelerates sulfur conversion and delivers outstanding cycling stability over 1000 cycles with only 0.045% capacity decay per cycle. In addition, PEO-based solid-state cells can also exhibit high sulfur utilization (>80%) and robust durability. Ah-level pouch cells achieve 1.7 Ah and 379 Wh kg–1 demonstrating that ionic liquid-anchored carbons offer a scalable strategy toward practical, high-energy lithium–sulfur batteries.

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Publication Details

Journal
ACS Energy Letters
Published
2025-11-06
DOI
https://doi.org/10.1021/acsenergylett.5c03148
Citations
3
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
2.19
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article

Ionic Liquids Anchored on Carbon Synchronize Ion-Electron Transport in Liquid- and Solid-State Sulfur Batteries

Bohan Zhang, Chuannan Geng, Zhonghao Hu, Jiaqi Lan et al.
3 citations
ACS Energy Letters
Advanced Battery Materials and Technologies
2.19
article

Ionic Liquids Anchored on Carbon Synchronize Ion-Electron Transport in Liquid- and Solid-State Sulfur Batteries

Bohan Zhang, Chuannan Geng, Zhonghao Hu, Jiaqi Lan, Wei Zhong Lv, Jiwei Shi, Sichen Gu, Yufei Zhao, Yu-Nong Lei, Jiangshan Qi
article en
3 citations

Abstract

Sulfur-based batteries hold great promise for next-generation energy storage owing to their high capacity and low cost, yet their performance is limited by sluggish ion transport and insulating discharge products. Here, we construct a continuous mixed ion-electron conductor network by anchoring imidazolium-based ionic liquids onto carbon nanotubes via strong π-π interactions. The ionic liquid layers provide fast Li+ pathways along the conductive framework, enabling synchronized ion–electron transport and reducing the Li2S nucleation overpotential to 28.2 mV. This interfacial design accelerates sulfur conversion and delivers outstanding cycling stability over 1000 cycles with only 0.045% capacity decay per cycle. In addition, PEO-based solid-state cells can also exhibit high sulfur utilization (>80%) and robust durability. Ah-level pouch cells achieve 1.7 Ah and 379 Wh kg–1 demonstrating that ionic liquid-anchored carbons offer a scalable strategy toward practical, high-energy lithium–sulfur batteries.

ACS Energy LettersVol. 10(11)
Tianjin University (CN), University Town of Shenzhen (CN), Tsinghua–Berkeley Shenzhen Institute (CN), Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN), Shenzhen Technology University (CN), Shenzhen MSU-BIT University, Tsinghua University (CN)
Openalex Percentile: Top 11%
Advanced Battery Materials and Technologies
2.19
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