Ion Selective Covalent Organic Framework Enabling Enhanced Electrochemical Performance of Lithium–Sulfur Batteries
Ion selective separators with the capability of conducting lithium ion and blocking polysulfides are critical and highly desired for high-performance lithium–sulfur (Li–S) batteries. Herein, we fabricate an ion selective film of covalent organic framework (denoted as TpPa-SO3Li) onto the commercial...
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Veröffentlicht in: | Nano letters 2021-04, Vol.21 (7), p.2997-3006 |
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creator | Cao, Yu Wu, Hong Li, Gang Liu, Cheng Cao, Li Zhang, Yiming Bao, Wei Wang, Huili Yao, Yuan Liu, Shuo Pan, Fusheng Jiang, Zhongyi Sun, Jie |
description | Ion selective separators with the capability of conducting lithium ion and blocking polysulfides are critical and highly desired for high-performance lithium–sulfur (Li–S) batteries. Herein, we fabricate an ion selective film of covalent organic framework (denoted as TpPa-SO3Li) onto the commercial Celgard separator. The aligned nanochannels and continuous negatively charged sites in the TpPa-SO3Li layer can effectively facilitate the lithium ion conduction and meanwhile significantly suppress the diffusion of polysulfides via the electrostatic interaction. Consequently, the TpPa-SO3Li layer exhibits excellent ion selectivity with an extremely high lithium ion transference number of 0.88. When using this novel functional layer, the Li–S batteries with a high sulfur loading of 5.4 mg cm–2 can acquire a high initial capacity of 822.9 mA h g–1 and high retention rate of 78% after 100 cycles at 0.2 C. This work provides new insights into developing high-performance Li–S batteries via ion selective separator strategy. |
doi_str_mv | 10.1021/acs.nanolett.1c00163 |
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Herein, we fabricate an ion selective film of covalent organic framework (denoted as TpPa-SO3Li) onto the commercial Celgard separator. The aligned nanochannels and continuous negatively charged sites in the TpPa-SO3Li layer can effectively facilitate the lithium ion conduction and meanwhile significantly suppress the diffusion of polysulfides via the electrostatic interaction. Consequently, the TpPa-SO3Li layer exhibits excellent ion selectivity with an extremely high lithium ion transference number of 0.88. When using this novel functional layer, the Li–S batteries with a high sulfur loading of 5.4 mg cm–2 can acquire a high initial capacity of 822.9 mA h g–1 and high retention rate of 78% after 100 cycles at 0.2 C. This work provides new insights into developing high-performance Li–S batteries via ion selective separator strategy.</description><identifier>ISSN: 1530-6984</identifier><identifier>EISSN: 1530-6992</identifier><identifier>DOI: 10.1021/acs.nanolett.1c00163</identifier><identifier>PMID: 33764070</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Nano letters, 2021-04, Vol.21 (7), p.2997-3006</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a414t-470ff9d8cbef7dc8a99937913d0a917c686520d1518de87c4e80c786a6d71aac3</citedby><cites>FETCH-LOGICAL-a414t-470ff9d8cbef7dc8a99937913d0a917c686520d1518de87c4e80c786a6d71aac3</cites><orcidid>0000-0002-4941-1295 ; 0000-0002-6020-9872 ; 0000-0001-6600-4459 ; 0000-0002-2492-4094</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.nanolett.1c00163$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.nanolett.1c00163$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33764070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Yu</creatorcontrib><creatorcontrib>Wu, Hong</creatorcontrib><creatorcontrib>Li, Gang</creatorcontrib><creatorcontrib>Liu, Cheng</creatorcontrib><creatorcontrib>Cao, Li</creatorcontrib><creatorcontrib>Zhang, Yiming</creatorcontrib><creatorcontrib>Bao, Wei</creatorcontrib><creatorcontrib>Wang, Huili</creatorcontrib><creatorcontrib>Yao, Yuan</creatorcontrib><creatorcontrib>Liu, Shuo</creatorcontrib><creatorcontrib>Pan, Fusheng</creatorcontrib><creatorcontrib>Jiang, Zhongyi</creatorcontrib><creatorcontrib>Sun, Jie</creatorcontrib><title>Ion Selective Covalent Organic Framework Enabling Enhanced Electrochemical Performance of Lithium–Sulfur Batteries</title><title>Nano letters</title><addtitle>Nano Lett</addtitle><description>Ion selective separators with the capability of conducting lithium ion and blocking polysulfides are critical and highly desired for high-performance lithium–sulfur (Li–S) batteries. Herein, we fabricate an ion selective film of covalent organic framework (denoted as TpPa-SO3Li) onto the commercial Celgard separator. The aligned nanochannels and continuous negatively charged sites in the TpPa-SO3Li layer can effectively facilitate the lithium ion conduction and meanwhile significantly suppress the diffusion of polysulfides via the electrostatic interaction. Consequently, the TpPa-SO3Li layer exhibits excellent ion selectivity with an extremely high lithium ion transference number of 0.88. When using this novel functional layer, the Li–S batteries with a high sulfur loading of 5.4 mg cm–2 can acquire a high initial capacity of 822.9 mA h g–1 and high retention rate of 78% after 100 cycles at 0.2 C. 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title | Ion Selective Covalent Organic Framework Enabling Enhanced Electrochemical Performance of Lithium–Sulfur Batteries |
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