Diamondoid All-Carbon Porous Aromatic Framework Host for Lithium–Sulfur Batteries

IF 12.1 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2025-04-24 DOI:10.1002/smll.202500388
Viksit Kumar, Bharathkumar H. Javaregowda, George Devasia, Aswini Narayanan, Sailaja Krishnamurty, Kothandam Krishnamoorthy, Sukumaran Santhosh Babu
{"title":"Diamondoid All-Carbon Porous Aromatic Framework Host for Lithium–Sulfur Batteries","authors":"Viksit Kumar,&nbsp;Bharathkumar H. Javaregowda,&nbsp;George Devasia,&nbsp;Aswini Narayanan,&nbsp;Sailaja Krishnamurty,&nbsp;Kothandam Krishnamoorthy,&nbsp;Sukumaran Santhosh Babu","doi":"10.1002/smll.202500388","DOIUrl":null,"url":null,"abstract":"<p>Lithium-sulfur batteries (LSBs) hold incredible potential as next-generation energy storage systems. However, practical applications of LSBs are significantly hindered by several critical challenges. For the first time, scalable all-carbon porous 3D polymers (3DPs) that do not contain heteroatoms or functional groups and do not require post-functionalization are investigated as hosts in lithium–sulfur batteries, demonstrating enhanced cycling stability and overall battery performance. The pyrene-containing 3DP exhibits 75% capacity retention after 600 cycles at 1 C and 52% capacity retention after 1300 cycles at 0.2 C, better than phenyl comprising 3DP. Furthermore, even at higher sulfur loading (4.1 mg cm<sup>−2</sup>) with an electrolyte/sulfur ratio of 5 µL mg<sup>−1</sup>, pyrene 3DP displayed a high capacity of 600 mA h g<sup>−1</sup> and stable performance over 250 cycles with negligible capacity fade. The defined pore structure of 3DPs prevents the migration of polysulfides through physical confinement and the large π-clouds of 3DPs interact with the negative charge-bearing polysulfides generated in charge–discharge cycles through anion-π interaction. In this way, The design ensures that the host 3DPs interact with neutral sulfur and anionic polysulfides, resulting in an excellent performance.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 23","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202500388","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Lithium-sulfur batteries (LSBs) hold incredible potential as next-generation energy storage systems. However, practical applications of LSBs are significantly hindered by several critical challenges. For the first time, scalable all-carbon porous 3D polymers (3DPs) that do not contain heteroatoms or functional groups and do not require post-functionalization are investigated as hosts in lithium–sulfur batteries, demonstrating enhanced cycling stability and overall battery performance. The pyrene-containing 3DP exhibits 75% capacity retention after 600 cycles at 1 C and 52% capacity retention after 1300 cycles at 0.2 C, better than phenyl comprising 3DP. Furthermore, even at higher sulfur loading (4.1 mg cm−2) with an electrolyte/sulfur ratio of 5 µL mg−1, pyrene 3DP displayed a high capacity of 600 mA h g−1 and stable performance over 250 cycles with negligible capacity fade. The defined pore structure of 3DPs prevents the migration of polysulfides through physical confinement and the large π-clouds of 3DPs interact with the negative charge-bearing polysulfides generated in charge–discharge cycles through anion-π interaction. In this way, The design ensures that the host 3DPs interact with neutral sulfur and anionic polysulfides, resulting in an excellent performance.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
锂硫电池用金刚石全碳多孔芳族框架主体
锂硫电池(lsb)作为下一代储能系统具有不可思议的潜力。然而,LSBs的实际应用受到几个关键挑战的严重阻碍。研究人员首次研究了不含杂原子或官能团、不需要后功能化的可扩展全碳多孔3D聚合物(3DPs)作为锂硫电池的载体,证明了其增强的循环稳定性和整体电池性能。含芘的3DP在1℃下循环600次后容量保持率为75%,在0.2℃下循环1300次后容量保持率为52%,优于含苯基的3DP。此外,即使在较高的硫负载(4.1 mg cm−2),电解质/硫比为5 μ L mg−1时,芘3DP也显示出600 mA h g−1的高容量,并且在250次循环中性能稳定,容量衰减可以忽略不计。3DPs的孔隙结构通过物理约束阻止了多硫化物的迁移,其大π云通过阴离子-π相互作用与充放电循环中产生的带负电荷的多硫化物相互作用。通过这种方式,该设计确保了宿主3d打印机与中性硫和阴离子多硫化物相互作用,从而获得了优异的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
期刊最新文献
Additive Engineering for Ambient Blade-Coated CsPbBr3 Films Enabling High-Performance Self-Powered X-Ray Detection Correction to “Near-Infrared Emission Carbon Dots Derived from Bromo-Substituted Perylene Derivatives with Simultaneously High Type I/II ROS Generation for Effective Bacterial Elimination and Tumor Ablation” Push-Pull Interplay of Soft/Hard Magnetic Spin Junctions for High Performance Ammonium Ion Pseudo-Capacitors H-Aggregated Squaraine Probe NIR-II/MRI Double Reversal Imaging for Liver Cancer Precise Surgical Navigation Tunable Room Temperature Phosphorescence From Pillar-Layer Metal–Organic Frameworks by Ligand Halogen-Functionalization
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1