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Dual-doped mesoporous carbon/SWCNT nanoshells for Li-ion battery electrode materials

Author(s)
Ye-Ri
Advisor
Lee, Sang-Young
Issued Date
2017-02
URI
https://scholarworks.unist.ac.kr/handle/201301/72102 http://unist.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002332947
Abstract
There is no doubt that rechargeable lithium-ion batteries (LIBs) have been developed as an electrical power source in a wide variety of energy storage systems including portable electronics, electric vehicles (EVs) and plug-in hybrid electric vehicle (PHEVs). Continuous advanced demands for higher energy density energy storage systems strongly push us to develop breakthroughs for improved cathode materials of LIBs. Recently, over-lithiated layered metal oxides (xLi2MnO3•(1-x)LiMO2, [M=Ni, Co, Mn], OLOs) materials, which are widely used in cathode materials of LIBs for high discharge capacity (over 250 mAh/g), are struggling with fast capacity fading and Mn dissolution on the unstable lithium-rich layered metal oxides surface. The poor electrical conductivity of lithium-rich layered metal oxides and Mn dissolution-triggered by-products are known to induce serious capacity fading during charge/discharge cycling. As a newly-synthesized polymeric ionic liquid (PIL)-driven material/single-walled carbon nanotube (SWCNT) nano-architecture strategy to develop an ion/electron-conductive nanoshells far beyond traditional surface modification, we have demonstrated single-walled carbon nanotube (SWCNT)-embedded and dual atom (nitrogen (N) and sulfur (S))-doped mesoporous carbon shells (referred to as “SMC” shell) on the LNMO (LiNi0.5Mn1.5O4) as well as OLO (0.49Li2MnO3·0.51LiNi0.37Co0.24Mn0.39O2) surface. The SMC-coated electrode materials are fabricated via simple mixing of pristine active materials in the SWCNT/PIL mixture solution and the subsequent one-pot carbonization process of the coated PIL on active materials surface. The PIL synthesized herein consists of poly(1-vinyl-3-ethylimidazolium) cations and dodecyl sulfate counter anions, of which chemical structures are purposeful designed to achieve multifunctional roles as: i) precursor of conformal/continuous carbon shell, ii) dual (N and S)-doping source, iii) porogen, and iv) SWCNT dispersant. Driven by such chemical/structural originality, the SMC effectively reduces unwanted interfacial side reactions between the cathode materials and liquid electrolyte while charge/discharge process. As a consequence, the SMC-coated cathode materials provided unprecedented improvements in the high-performance (rate capability, cycling performance and thermal stability) of lithium-ion batteries. The SMC-coated cathode materials hold a great deal of promise as a facile and versatile platform surface modification technology for high-performance batteries and also open a new opportunity for next-generation multifunctional molecularly-designed, ion/electron-conductive nanoshells on electrode materials that are in strong pursuit of progress in electrochemical performance.
Publisher
Ulsan National Institute of Science and Technology (UNIST)
Degree
Master
Major
Department of Energy Engineering

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