Evidence map›Paper›PMID 41772972›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Regulating Solvent-Separated Ion Pairs to Control Polysulfide Redox for Fast and Stable Room-Temperature Na-S Batteries.

Xiang-Long Huang, Xue Li, Hengjia Shao, Xinran Gao, Zhengzhao Huang, Lingfei Zhao, Long Yao, Kunjie Zhu, Fu-Sheng Ke, Hua-Kun Liu and 2 more

Abstract read
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In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Xiang-Long HuangInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Xue LiGuangdong Provincial Key Laboratory of Service Safety for New Energy Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen, P. R. China.
Hengjia ShaoInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Xinran GaoInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Zhengzhao HuangCollege of Chemistry and Molecular Sciences, Wuhan University, Wuhan, P. R. China.
Lingfei ZhaoInstitute For Superconducting and Electronic Materials, Australian Institute of Innovative Materials, Innovation Campus, University of Wollongong, Wollongong, Australia.
Long YaoInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Kunjie ZhuInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Fu-Sheng KeCollege of Chemistry and Molecular Sciences, Wuhan University, Wuhan, P. R. China.
Hua-Kun LiuInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.
Wei-Hong LaiLaboratory of Advanced Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, School of Chemistry and Materials, Fudan University, Shanghai, P. R. China.
Yun-Xiao WangInstitute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai, P. R. China.ORCID https://orcid.org/0000-0003-1704-0829

Funding

China Postdoctoral Science Foundation 2024M762093National Natural Science Foundation of China 22509130National Natural Science Foundation of China 52350710795National Natural Science Foundation of China 52501285Postdoctoral Fellowship Program of CPSF GZB20240455Science and Technology Commission of Shanghai Municipality 24ZR1454500
6 · The paper itself

Abstract

The solvent-separated ion pairs in local high-concentration electrolytes (LHCE) have a profound influence on rechargeable sulfur-based batteries yet are always ignored. Herein, tailored solvent-separated ion pairs are engineered by tuning the diluent ratio in LHCE to boost sulfur redox kinetics in room-temperature sodium-sulfur (Na-S) batteries. The tailored solvent-separated ion pairs allow the sparingly dissolved polysulfides to enhance localized solid-liquid-solid transformation on reactive interfaces, so the LHCE decorated with the solvent-separated ion pairs preserves the global quasi-solid-state mechanism of sulfur while modulating its intrinsic sulfur redox kinetics. Consequently, Na-S batteries achieve excellent cyclability (fading rate of 0.017% per cycle over 2400 cycles at 1.0C) and outstanding rate performance (564 mA h g

Indexed as

interface chemistrylocal high‐concentration electrolyteNa‐S batteriesredox kineticssolvent‐separated ion pairs

Identifiers

PMID41772972
PMCPMC13170214

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.