Small-Molecule Sulfur Iodine Cathodes for Fast-Kinetic Lithium–Sulfur Batteries

Lithium–sulfur batteries (LSBs) hold great promise for next-generation energy storage due to their high theoretical energy density. However, their practical application is hindered by sluggish sulfur redox kinetics and the severe shuttle effect. In this work, a small-molecule sulfur–iodine (S–I) composite is physically confined within a porous carbon host, which not only enhances the electronic conductivity but also accelerates sulfur reaction kinetics and improves cycling stability by effectively suppressing polysulfide shuttling. Concurrently, the present work delivers a high specific capacity of 814 mAh g–1 with 80 wt % active material loading and demonstrate stable cycling over 250 cycles. Notably, even at an ultrahigh loading of 90 wt %, a substantial capacity of 530 mAh g–1 is retained. These results highlight the crucial role of porous carbon-confined small-molecule S–I cathodes in enhancing sulfur redox kinetics and cycling stability, offering a viable strategy for high-performance LSBs.

Authors

Institutions

Publication Details

Journal
ACS Applied Energy Materials
Published
2026-04-22
DOI
https://doi.org/10.1021/acsaem.6c00530
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Small-Molecule Sulfur Iodine Cathodes for Fast-Kinetic Lithium–Sulfur Batteries

C Y Zhang, Fu‐Sheng Ke, Ming Zhou, Weihong Lai et al.
ACS Applied Energy Materials
Advanced Battery Materials and Technologies
article

Small-Molecule Sulfur Iodine Cathodes for Fast-Kinetic Lithium–Sulfur Batteries

C Y Zhang, Fu‐Sheng Ke, Ming Zhou, Weihong Lai, Yun‐Xiao Wang, Bing-Hong Huang, Guanghe Guo
article en

Abstract

Lithium–sulfur batteries (LSBs) hold great promise for next-generation energy storage due to their high theoretical energy density. However, their practical application is hindered by sluggish sulfur redox kinetics and the severe shuttle effect. In this work, a small-molecule sulfur–iodine (S–I) composite is physically confined within a porous carbon host, which not only enhances the electronic conductivity but also accelerates sulfur reaction kinetics and improves cycling stability by effectively suppressing polysulfide shuttling. Concurrently, the present work delivers a high specific capacity of 814 mAh g–1 with 80 wt % active material loading and demonstrate stable cycling over 250 cycles. Notably, even at an ultrahigh loading of 90 wt %, a substantial capacity of 530 mAh g–1 is retained. These results highlight the crucial role of porous carbon-confined small-molecule S–I cathodes in enhancing sulfur redox kinetics and cycling stability, offering a viable strategy for high-performance LSBs.

ACS Applied Energy MaterialsVol. 9(9)
University of Shanghai for Science and Technology (CN), Fudan University (CN), Wuhan University (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, Large-Scale Instrument and Equipment Sharing Foundation of Wuhan University
Affordable and clean energy
Openalex Percentile: Top 23%
Advanced Battery Materials and Technologies
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.