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Lee, Sang-Young
Energy Soft-Materials Lab.
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dc.citation.endPage 12112 -
dc.citation.number 24 -
dc.citation.startPage 12103 -
dc.citation.title JOURNAL OF MATERIALS CHEMISTRY A -
dc.citation.volume 5 -
dc.contributor.author Yoo, JongTae -
dc.contributor.author Ju, Young-Wan -
dc.contributor.author Jang, Ye-Ri -
dc.contributor.author Gwon, Ohhun -
dc.contributor.author Park, Sodam -
dc.contributor.author Kim, Ju-Myung -
dc.contributor.author Lee, Chang Kee -
dc.contributor.author Lee, Sun-Young -
dc.contributor.author Yeon, Sun-Hwa -
dc.contributor.author Kim, Guntae -
dc.contributor.author Lee, Sang-Young -
dc.date.accessioned 2023-12-21T22:10:41Z -
dc.date.available 2023-12-21T22:10:41Z -
dc.date.created 2017-07-10 -
dc.date.issued 2017-06 -
dc.description.abstract A longstanding challenge facing energy conversion/storage materials is their low electrical conductivity, which often results in unwanted sluggish electrochemical reactions. Here, we demonstrate a new class of one-pot surface engineering strategy based on metallic single-walled carbon nanotube (mSWCNT)-enriched, ivy-like conductive nanonets (mSC nanonets). The mSC nanonets are formed on the surface of electrode materials through a poly(9,9-di-n-octylfluorenyl-2,7-diyl) (PFO)-assisted sonication/filtration process. PFO is known as a dispersant for SWCNTs that shows a higher affinity for semiconducting SWCNTs (sSWCNTs) than for mSWCNTs. Driven by this preferential affinity of PFO, sSWCNTs are separated from mSWCNTs in the form of sSWCNT/PFO hybrids, and the resulting enriched mSWCNTs are uniformly deposited on electrode materials in the form of ivy-like nanonets. Various electrode materials, including lithium-ion battery cathodes/anodes and perovskite catalysts, are chosen to explore the feasibility of the proposed concept. Due to their ivy-like conductive network, the mSC nanonets increase the electronic conductivity of the electrode materials without hindering their ionic transport, eventually enabling significant improvements in their redox reaction rates, charge/discharge cyclability, and bifunctional electrocatalytic activities. These exceptional physicochemical advantages of the mSC nanonets, in conjunction with the simplicity/versatility of the one-pot surface engineering process, offer a new and facile route to develop advanced electrode materials with faster electrochemical reaction kinetics. -
dc.identifier.bibliographicCitation JOURNAL OF MATERIALS CHEMISTRY A, v.5, no.24, pp.12103 - 12112 -
dc.identifier.doi 10.1039/c6ta10675g -
dc.identifier.issn 2050-7488 -
dc.identifier.scopusid 2-s2.0-85021646759 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/22398 -
dc.identifier.url http://pubs.rsc.org/en/Content/ArticleLanding/2017/TA/C6TA10675G#!divAbstract -
dc.identifier.wosid 000403664800017 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title One-pot surface engineering of battery electrode materials with metallic SWCNT-enriched, ivy-like conductive nanonets -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Energy & Fuels; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Energy & Fuels; Materials Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus WALLED CARBON NANOTUBES -
dc.subject.keywordPlus RECHARGEABLE LITHIUM BATTERIES -
dc.subject.keywordPlus OXYGEN REDUCTION -
dc.subject.keywordPlus ION BATTERIES -
dc.subject.keywordPlus SINGLE-WALL -
dc.subject.keywordPlus AIR BATTERIES -
dc.subject.keywordPlus ARRAYS -
dc.subject.keywordPlus TEMPERATURE -
dc.subject.keywordPlus MECHANISMS -
dc.subject.keywordPlus GRAPHENE -

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