Ion channel-gated covalent organic framework membrane for sustainable lithium–sulfur batteries

Lithium-sulfur (Li-S) batteries hold promise as a compelling alternative to current state-of-the-art Li-ion batteries due to their high theoretical capacity, low cost and the natural abundance of sulfur. However, the practical realization of Li-S batteries has been plagued by the longstanding trade-off issue between polysulfide shuttle suppression and Li⁺ transport. Here, we report an ion channel-gated covalent organic framework (COF) as an ionic diode membrane strategy to address this conflicting requirement. By tuning the chemical structure of tethered anions, the resulting COF features 1D anionic channels with optimized charge delocalization and pore size. The bulky anions enhance Li⁺ dissociation and conduction while effectively repelling polysulfides dissolved from S cathodes. Additionally, the COF ionic diode mitigates self-discharge and inhibits parasitic reactions. Consequently, Li-S cells assembled with the COF ionic diode improve charge/discharge capacities and cycle life under constrained operating conditions.

Authors

Institutions

Publication Details

Journal
National Science Review
Published
2025-05-16
DOI
https://doi.org/10.1093/nsr/nwaf193
Citations
14
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
10.23

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ion channel-gated covalent organic framework membrane for sustainable lithium–sulfur batteries

Sang‐Young Lee, Jong‐Beom Baek, Zhongping Li, Kun Ryu et al.
14 citations
National Science Review
Advanced Battery Materials and Technologies
10.23
article

Ion channel-gated covalent organic framework membrane for sustainable lithium–sulfur batteries

Sang‐Young Lee, Jong‐Beom Baek, Zhongping Li, Kun Ryu, Kyeongseok Oh, Dong‐Hwa Seo, Jeong‐Min Seo, Sodam Park, Xiaoming Liu, Changqing Li, Jae‐Seung Kim, Hyunseok Moon, Yuxin Hou
article en
14 citations

Abstract

Lithium-sulfur (Li-S) batteries hold promise as a compelling alternative to current state-of-the-art Li-ion batteries due to their high theoretical capacity, low cost and the natural abundance of sulfur. However, the practical realization of Li-S batteries has been plagued by the longstanding trade-off issue between polysulfide shuttle suppression and Li⁺ transport. Here, we report an ion channel-gated covalent organic framework (COF) as an ionic diode membrane strategy to address this conflicting requirement. By tuning the chemical structure of tethered anions, the resulting COF features 1D anionic channels with optimized charge delocalization and pore size. The bulky anions enhance Li⁺ dissociation and conduction while effectively repelling polysulfides dissolved from S cathodes. Additionally, the COF ionic diode mitigates self-discharge and inhibits parasitic reactions. Consequently, Li-S cells assembled with the COF ionic diode improve charge/discharge capacities and cycle life under constrained operating conditions.

National Science ReviewVol. 12(7)
Korea Advanced Institute of Science and Technology (KR), Yonsei University (KR), Jilin University (CN), University of Chicago (US), Division of Materials Science and Engineering (AU), Ulsan National Institute of Science and Technology (KR)
National Research Foundation, Yonsei University, Korea Institute for Advancement of Technology, Korea Institute of Science and Technology, Korea Institute of Science and Technology Information, National Research Foundation of Korea, National Research Council of Science and Technology
Openalex Percentile: Top 2%
Advanced Battery Materials and Technologies
10.23
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.