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Few-layer MoS2 nanosheets incorporated into hierarchical porous carbon for lithium-ion batteries

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dc.title Few-layer MoS2 nanosheets incorporated into hierarchical porous carbon for lithium-ion batteries en
dc.contributor.author Wang, Haiyan
dc.contributor.author Ren, Dayong
dc.contributor.author Zhu, Zhengju
dc.contributor.author Sáha, Petr
dc.contributor.author Jiang, Hao
dc.contributor.author Li, Chunzhong
dc.relation.ispartof Chemical Engineering Journal
dc.identifier.issn 1385-8947 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2016
utb.relation.volume 288
dc.citation.spage 179
dc.citation.epage 184
dc.type article
dc.language.iso en
dc.publisher Elsevier
dc.identifier.doi 10.1016/j.cej.2015.11.105
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S1385894715016575
dc.subject Biomass en
dc.subject Few-layer MoS2 en
dc.subject Hierarchical porous carbon en
dc.subject Lithium ion batteries en
dc.description.abstract In order to overcome the serious stacking and poor conductivity of graphene-like MoS2 nanosheets, we have developed the synthesis of few-layer MoS2 nanosheets incorporated into biomass-derived hierarchical porous carbon frameworks (labeled as MoS2/C hybrids) utilizing the strong water-absorbing power of auricularia from its inherent rich porous structure. The as-obtained MoS2/C hybrids, when applied as lithium-ion batteries anode materials, show an improved specific capacity of 707.4 mA h g-1 compared with the commercial MoS2 nanosheets (580.2 mA h g-1) and the corresponding hierarchical porous carbon (215.5 mA h g-1). More meaningfully, they possess an impressive cycle life, almost without capacity fading even after 500 cycles at 1600 mA g-1. The intriguing performance is mainly attributed to the well-dispersion of few-layer MoS2 nanosheets into hierarchical porous carbon. We believe this work will provide a new insight on the design and synthesis of novel carbon-based electrode materials for potential applications in lithium-ion batteries and other clean energy devices. © 2015 Elsevier B.V. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1005779
utb.identifier.obdid 43874957
utb.identifier.scopus 2-s2.0-84949895035
utb.identifier.wok 000370085900018
utb.identifier.coden CMEJA
utb.source j-scopus
dc.date.accessioned 2016-04-12T11:50:45Z
dc.date.available 2016-04-12T11:50:45Z
dc.description.sponsorship 21236003, NSFC, National Natural Science Foundation of China; 21522602, NSFC, National Natural Science Foundation of China
dc.description.sponsorship National Natural Science Foundation of China [21236003, 21522602]; Shanghai Rising-Star Program [15QA1401200]; International Science and Technology Cooperation Program of China [2015DFA51220]; 111 Project [B14018]; Fundamental Research Funds for the Central Universities
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Sáha, Petr
utb.fulltext.affiliation Haiyan Wang a, Dayong Ren a, Zhengju Zhu a, Petr Saha b, Hao Jiang a*, Chunzhong Li a* a Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China b Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Trida T. Bati 5678, 760 01 Zlin, Czech Republic * Corresponding authors. E-mail addresses: jianghao@ecust.edu.cn (H. Jiang), czli@ecust.edu.cn (C. Li).
utb.fulltext.dates Received 10 October 2015 Received in revised form 29 November 2015 Accepted 30 November 2015 Available online 11 December 2015
utb.fulltext.faculty University Institute
utb.fulltext.ou Centre of Polymer Systems
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