Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability

The practical implementation of Li–S technology has been hindered by short cycle life and poor rate capability owing to deleterious effects resulting from the varied solubilities of different Li polysulfide redox products. Here, we report the preparation and utilization of composites with a sulfur-r...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ACS applied materials & interfaces 2016-06, Vol.8 (21), p.13437-13448
Hauptverfasser: Dirlam, Philip T, Park, Jungjin, Simmonds, Adam G, Domanik, Kenneth, Arrington, Clay B, Schaefer, Jennifer L, Oleshko, Vladimir P, Kleine, Tristan S, Char, Kookheon, Glass, Richard S, Soles, Christopher L, Kim, Chunjoong, Pinna, Nicola, Sung, Yung-Eun, Pyun, Jeffrey
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 13448
container_issue 21
container_start_page 13437
container_title ACS applied materials & interfaces
container_volume 8
creator Dirlam, Philip T
Park, Jungjin
Simmonds, Adam G
Domanik, Kenneth
Arrington, Clay B
Schaefer, Jennifer L
Oleshko, Vladimir P
Kleine, Tristan S
Char, Kookheon
Glass, Richard S
Soles, Christopher L
Kim, Chunjoong
Pinna, Nicola
Sung, Yung-Eun
Pyun, Jeffrey
description The practical implementation of Li–S technology has been hindered by short cycle life and poor rate capability owing to deleterious effects resulting from the varied solubilities of different Li polysulfide redox products. Here, we report the preparation and utilization of composites with a sulfur-rich matrix and molybdenum disulfide (MoS2) particulate inclusions as Li–S cathode materials with the capability to mitigate the dissolution of the Li polysulfide redox products via the MoS2 inclusions acting as “polysulfide anchors”. In situ composite formation was completed via a facile, one-pot method with commercially available starting materials. The composites were afforded by first dispersing MoS2 directly in liquid elemental sulfur (S8) with sequential polymerization of the sulfur phase via thermal ring opening polymerization or copolymerization via inverse vulcanization. For the practical utility of this system to be highlighted, it was demonstrated that the composite formation methodology was amenable to larger scale processes with composites easily prepared in 100 g batches. Cathodes fabricated with the high sulfur content composites as the active material afforded Li–S cells that exhibited extended cycle lifetimes of up to 1000 cycles with low capacity decay (0.07% per cycle) and demonstrated exceptional rate capability with the delivery of reversible capacity up to 500 mAh/g at 5 C.
doi_str_mv 10.1021/acsami.6b03200
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1793566077</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1793566077</sourcerecordid><originalsourceid>FETCH-LOGICAL-a330t-e33f96169b5d8b5b9b8322c8880fbc5a28491b7193cfb263c5c8ed46573a56943</originalsourceid><addsrcrecordid>eNp1kMtKxDAUhoMo3rcuJUsROubSpO1Sx8sII4Kj65KkqUbSZkxShtn5Dr6hT2J0RneuzuHw_R-cH4AjjEYYEXwmVBCdGXGJKEFoA-ziKs-zkjCy-bfn-Q7YC-EVIZ4gtg12SIELzHO-CxZXVne6j8LC2WDbwUPRN_DO2aVsdD908NKEdDeNhmPXzV0wUQfYOg-n5vP9YwYvRIzam3RcmPgCp65_huOlsjoBrf6xTczzS_YgYlKIuZDGmrg8AFutsEEfruc-eLq-ehxPsun9ze34fJoJSlHMNKVtxTGvJGtKyWQlS0qIKssStVIxQcq8wrLAFVWtJJwqpkrd5JwVVDBe5XQfnKy8c-_eBh1i3ZmgtLWi124INS4qyjhHRZHQ0QpV3oXgdVvPvemEX9YY1d9l16uy63XZKXC8dg-y080f_ttuAk5XQArWr27wfXr1P9sXfE6KXQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1793566077</pqid></control><display><type>article</type><title>Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability</title><source>ACS Publications</source><creator>Dirlam, Philip T ; Park, Jungjin ; Simmonds, Adam G ; Domanik, Kenneth ; Arrington, Clay B ; Schaefer, Jennifer L ; Oleshko, Vladimir P ; Kleine, Tristan S ; Char, Kookheon ; Glass, Richard S ; Soles, Christopher L ; Kim, Chunjoong ; Pinna, Nicola ; Sung, Yung-Eun ; Pyun, Jeffrey</creator><creatorcontrib>Dirlam, Philip T ; Park, Jungjin ; Simmonds, Adam G ; Domanik, Kenneth ; Arrington, Clay B ; Schaefer, Jennifer L ; Oleshko, Vladimir P ; Kleine, Tristan S ; Char, Kookheon ; Glass, Richard S ; Soles, Christopher L ; Kim, Chunjoong ; Pinna, Nicola ; Sung, Yung-Eun ; Pyun, Jeffrey</creatorcontrib><description>The practical implementation of Li–S technology has been hindered by short cycle life and poor rate capability owing to deleterious effects resulting from the varied solubilities of different Li polysulfide redox products. Here, we report the preparation and utilization of composites with a sulfur-rich matrix and molybdenum disulfide (MoS2) particulate inclusions as Li–S cathode materials with the capability to mitigate the dissolution of the Li polysulfide redox products via the MoS2 inclusions acting as “polysulfide anchors”. In situ composite formation was completed via a facile, one-pot method with commercially available starting materials. The composites were afforded by first dispersing MoS2 directly in liquid elemental sulfur (S8) with sequential polymerization of the sulfur phase via thermal ring opening polymerization or copolymerization via inverse vulcanization. For the practical utility of this system to be highlighted, it was demonstrated that the composite formation methodology was amenable to larger scale processes with composites easily prepared in 100 g batches. Cathodes fabricated with the high sulfur content composites as the active material afforded Li–S cells that exhibited extended cycle lifetimes of up to 1000 cycles with low capacity decay (0.07% per cycle) and demonstrated exceptional rate capability with the delivery of reversible capacity up to 500 mAh/g at 5 C.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.6b03200</identifier><identifier>PMID: 27171646</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>ACS applied materials &amp; interfaces, 2016-06, Vol.8 (21), p.13437-13448</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-e33f96169b5d8b5b9b8322c8880fbc5a28491b7193cfb263c5c8ed46573a56943</citedby><cites>FETCH-LOGICAL-a330t-e33f96169b5d8b5b9b8322c8880fbc5a28491b7193cfb263c5c8ed46573a56943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.6b03200$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.6b03200$$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/27171646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dirlam, Philip T</creatorcontrib><creatorcontrib>Park, Jungjin</creatorcontrib><creatorcontrib>Simmonds, Adam G</creatorcontrib><creatorcontrib>Domanik, Kenneth</creatorcontrib><creatorcontrib>Arrington, Clay B</creatorcontrib><creatorcontrib>Schaefer, Jennifer L</creatorcontrib><creatorcontrib>Oleshko, Vladimir P</creatorcontrib><creatorcontrib>Kleine, Tristan S</creatorcontrib><creatorcontrib>Char, Kookheon</creatorcontrib><creatorcontrib>Glass, Richard S</creatorcontrib><creatorcontrib>Soles, Christopher L</creatorcontrib><creatorcontrib>Kim, Chunjoong</creatorcontrib><creatorcontrib>Pinna, Nicola</creatorcontrib><creatorcontrib>Sung, Yung-Eun</creatorcontrib><creatorcontrib>Pyun, Jeffrey</creatorcontrib><title>Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability</title><title>ACS applied materials &amp; interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>The practical implementation of Li–S technology has been hindered by short cycle life and poor rate capability owing to deleterious effects resulting from the varied solubilities of different Li polysulfide redox products. Here, we report the preparation and utilization of composites with a sulfur-rich matrix and molybdenum disulfide (MoS2) particulate inclusions as Li–S cathode materials with the capability to mitigate the dissolution of the Li polysulfide redox products via the MoS2 inclusions acting as “polysulfide anchors”. In situ composite formation was completed via a facile, one-pot method with commercially available starting materials. The composites were afforded by first dispersing MoS2 directly in liquid elemental sulfur (S8) with sequential polymerization of the sulfur phase via thermal ring opening polymerization or copolymerization via inverse vulcanization. For the practical utility of this system to be highlighted, it was demonstrated that the composite formation methodology was amenable to larger scale processes with composites easily prepared in 100 g batches. Cathodes fabricated with the high sulfur content composites as the active material afforded Li–S cells that exhibited extended cycle lifetimes of up to 1000 cycles with low capacity decay (0.07% per cycle) and demonstrated exceptional rate capability with the delivery of reversible capacity up to 500 mAh/g at 5 C.</description><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKxDAUhoMo3rcuJUsROubSpO1Sx8sII4Kj65KkqUbSZkxShtn5Dr6hT2J0RneuzuHw_R-cH4AjjEYYEXwmVBCdGXGJKEFoA-ziKs-zkjCy-bfn-Q7YC-EVIZ4gtg12SIELzHO-CxZXVne6j8LC2WDbwUPRN_DO2aVsdD908NKEdDeNhmPXzV0wUQfYOg-n5vP9YwYvRIzam3RcmPgCp65_huOlsjoBrf6xTczzS_YgYlKIuZDGmrg8AFutsEEfruc-eLq-ehxPsun9ze34fJoJSlHMNKVtxTGvJGtKyWQlS0qIKssStVIxQcq8wrLAFVWtJJwqpkrd5JwVVDBe5XQfnKy8c-_eBh1i3ZmgtLWi124INS4qyjhHRZHQ0QpV3oXgdVvPvemEX9YY1d9l16uy63XZKXC8dg-y080f_ttuAk5XQArWr27wfXr1P9sXfE6KXQ</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Dirlam, Philip T</creator><creator>Park, Jungjin</creator><creator>Simmonds, Adam G</creator><creator>Domanik, Kenneth</creator><creator>Arrington, Clay B</creator><creator>Schaefer, Jennifer L</creator><creator>Oleshko, Vladimir P</creator><creator>Kleine, Tristan S</creator><creator>Char, Kookheon</creator><creator>Glass, Richard S</creator><creator>Soles, Christopher L</creator><creator>Kim, Chunjoong</creator><creator>Pinna, Nicola</creator><creator>Sung, Yung-Eun</creator><creator>Pyun, Jeffrey</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160601</creationdate><title>Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability</title><author>Dirlam, Philip T ; Park, Jungjin ; Simmonds, Adam G ; Domanik, Kenneth ; Arrington, Clay B ; Schaefer, Jennifer L ; Oleshko, Vladimir P ; Kleine, Tristan S ; Char, Kookheon ; Glass, Richard S ; Soles, Christopher L ; Kim, Chunjoong ; Pinna, Nicola ; Sung, Yung-Eun ; Pyun, Jeffrey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a330t-e33f96169b5d8b5b9b8322c8880fbc5a28491b7193cfb263c5c8ed46573a56943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dirlam, Philip T</creatorcontrib><creatorcontrib>Park, Jungjin</creatorcontrib><creatorcontrib>Simmonds, Adam G</creatorcontrib><creatorcontrib>Domanik, Kenneth</creatorcontrib><creatorcontrib>Arrington, Clay B</creatorcontrib><creatorcontrib>Schaefer, Jennifer L</creatorcontrib><creatorcontrib>Oleshko, Vladimir P</creatorcontrib><creatorcontrib>Kleine, Tristan S</creatorcontrib><creatorcontrib>Char, Kookheon</creatorcontrib><creatorcontrib>Glass, Richard S</creatorcontrib><creatorcontrib>Soles, Christopher L</creatorcontrib><creatorcontrib>Kim, Chunjoong</creatorcontrib><creatorcontrib>Pinna, Nicola</creatorcontrib><creatorcontrib>Sung, Yung-Eun</creatorcontrib><creatorcontrib>Pyun, Jeffrey</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>ACS applied materials &amp; interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dirlam, Philip T</au><au>Park, Jungjin</au><au>Simmonds, Adam G</au><au>Domanik, Kenneth</au><au>Arrington, Clay B</au><au>Schaefer, Jennifer L</au><au>Oleshko, Vladimir P</au><au>Kleine, Tristan S</au><au>Char, Kookheon</au><au>Glass, Richard S</au><au>Soles, Christopher L</au><au>Kim, Chunjoong</au><au>Pinna, Nicola</au><au>Sung, Yung-Eun</au><au>Pyun, Jeffrey</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability</atitle><jtitle>ACS applied materials &amp; interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>8</volume><issue>21</issue><spage>13437</spage><epage>13448</epage><pages>13437-13448</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>The practical implementation of Li–S technology has been hindered by short cycle life and poor rate capability owing to deleterious effects resulting from the varied solubilities of different Li polysulfide redox products. Here, we report the preparation and utilization of composites with a sulfur-rich matrix and molybdenum disulfide (MoS2) particulate inclusions as Li–S cathode materials with the capability to mitigate the dissolution of the Li polysulfide redox products via the MoS2 inclusions acting as “polysulfide anchors”. In situ composite formation was completed via a facile, one-pot method with commercially available starting materials. The composites were afforded by first dispersing MoS2 directly in liquid elemental sulfur (S8) with sequential polymerization of the sulfur phase via thermal ring opening polymerization or copolymerization via inverse vulcanization. For the practical utility of this system to be highlighted, it was demonstrated that the composite formation methodology was amenable to larger scale processes with composites easily prepared in 100 g batches. Cathodes fabricated with the high sulfur content composites as the active material afforded Li–S cells that exhibited extended cycle lifetimes of up to 1000 cycles with low capacity decay (0.07% per cycle) and demonstrated exceptional rate capability with the delivery of reversible capacity up to 500 mAh/g at 5 C.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27171646</pmid><doi>10.1021/acsami.6b03200</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1944-8244
ispartof ACS applied materials & interfaces, 2016-06, Vol.8 (21), p.13437-13448
issn 1944-8244
1944-8252
language eng
recordid cdi_proquest_miscellaneous_1793566077
source ACS Publications
title Elemental Sulfur and Molybdenum Disulfide Composites for Li–S Batteries with Long Cycle Life and High-Rate Capability
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T19%3A26%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Elemental%20Sulfur%20and%20Molybdenum%20Disulfide%20Composites%20for%20Li%E2%80%93S%20Batteries%20with%20Long%20Cycle%20Life%20and%20High-Rate%20Capability&rft.jtitle=ACS%20applied%20materials%20&%20interfaces&rft.au=Dirlam,%20Philip%20T&rft.date=2016-06-01&rft.volume=8&rft.issue=21&rft.spage=13437&rft.epage=13448&rft.pages=13437-13448&rft.issn=1944-8244&rft.eissn=1944-8252&rft_id=info:doi/10.1021/acsami.6b03200&rft_dat=%3Cproquest_cross%3E1793566077%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1793566077&rft_id=info:pmid/27171646&rfr_iscdi=true