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Nano storage-boxes constructed by the vertical growth of MoS2 on graphene for high-performance Li-S batteries

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dc.title Nano storage-boxes constructed by the vertical growth of MoS2 on graphene for high-performance Li-S batteries en
dc.contributor.author Cui, Bowen
dc.contributor.author Cai, Xiaomin
dc.contributor.author Wang, Wenqiang
dc.contributor.author Sáha, Petr
dc.contributor.author Wang, Gengchao
dc.relation.ispartof Journal of Energy Chemistry
dc.identifier.issn 2095-4956 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2022
utb.relation.volume 66
dc.citation.spage 91
dc.citation.epage 99
dc.type article
dc.language.iso en
dc.publisher Elsevier B.V.
dc.identifier.doi 10.1016/j.jechem.2021.06.035
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S2095495621003909
dc.subject edge-richMoS(2) en
dc.subject nano boxes en
dc.subject catalytic conversion en
dc.subject lithium-sulfur batteries en
dc.description.abstract In order to accelerate the reaction kinetics of lithium-sulfur batteries, the introduction of electro catalysis and proper structural control of the sulfur cathode is urgently needed. MoS2 nano sheets was selectively grown vertically (V-MoS2) on the microwave-reduced graphene (rGO) sheets through chemical coupling to construct a self-supporting sulfur cathode with a nano storage-box structure (V-MoS2 as the wall and rGO as the bottom). RGO, which has a high conductivity of 37 S cm−1, greatly accelerates the transfer of electrons from the active sites on the edge of the layer to the solution. The introduction of carbon tubes can connect the abundant pores in the foam and act as a long-range conductive path. The 2D-orthogonal-2D structure maximally exposes the edge active sites of MoS2, and together with graphene form a nano reactor of sulfur, intermediate lithium polysulfides and discharge product Li2S(2). The effective combination of the microstructure confinement of the nano storage-boxes and the efficient synchronous catalytic mechanism of V-MoS2 greatly improves the electrochemical performance of the lithium-sulfur batteries. As a result, the assembled lithium-sulfur battery displays a high initial discharge capacity of 1379 mAh g−1, good cycle stability (86% capacity retention after 500 cycles at 0.1C) and superior rate performance. © 2021 Science Press en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1010506
utb.identifier.obdid 43883555
utb.identifier.scopus 2-s2.0-85112360398
utb.identifier.wok 000701749300012
utb.source j-scopus
dc.date.accessioned 2021-08-24T07:27:45Z
dc.date.available 2021-08-24T07:27:45Z
dc.description.sponsorship National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21875065, 51673064]; International Science & Technology Cooperation Program of China [2016YFE0131200]
dc.description.sponsorship National Natural Science Foundation of China, NSFC: 21875065, 51673064; International Science and Technology Cooperation Programme, ISTCP: 2016YFE0131200
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Sáha, Petr
utb.fulltext.sponsorship We greatly appreciate the financial supports of the National Natural Science Foundation of China (21875065, 51673064), and the International Science & Technology Cooperation Program of China (2016YFE0131200).
utb.wos.affiliation [Cui, Bowen; Cai, Xiaomin; Wang, Wenqiang; Wang, Gengchao] East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, Sch Mat Sci & Engn, Shanghai Key Lab Adv Polymer Mat, Shanghai 200237, Peoples R China; [Saha, Petr] Tomas Bata Univ, Univ Inst, Ctr Polymer Syst, Tr T Bati 5678, Zlin 76001, Czech Republic
utb.scopus.affiliation Shanghai Key Laboratory of Advanced Polymeric Materials, Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China; Centre of Polymer Systems, University Institute, Tomas Bata University, Tř. T. Bati 5678, Zlin, Zlín 76001, Czech Republic
utb.fulltext.projects 21875065
utb.fulltext.projects 51673064
utb.fulltext.projects 2016YFE0131200
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