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Microdomain sulfur-impregnated CeO2-coated CNT particles for high-performance Li-S batteries
•Formation of microdomain sulfur in CeO2 nanoparticle-modified CNTs.•Fast charge/discharge by microdomain sulfur and hierarchical pore CNT particles.•Stable operation with a capacity reduction of 0.044%/cycle at high C-rate.•High areal capacity of 5.6 mAh/cm2 under high loading conditions. Li-S cath...
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Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-06, Vol.390, p.124548, Article 124548 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Formation of microdomain sulfur in CeO2 nanoparticle-modified CNTs.•Fast charge/discharge by microdomain sulfur and hierarchical pore CNT particles.•Stable operation with a capacity reduction of 0.044%/cycle at high C-rate.•High areal capacity of 5.6 mAh/cm2 under high loading conditions.
Li-S cathode loaded with microdomain sulfur is preferred because of its high utilization of sulfur during charging and discharging. Encapsulating sulfur in porous carbon has often been used to form microdomain sulfur, but is limited by the charge/ion diffusion resistance in the pores. Here we demonstrate the formation of microdomain sulfur in the open pore CNT assembly. We obtain microdomain sulfur on CNTs coated with CeO2 nanoparticles, explained by local spontaneous dewetting. Our microdomain sulfur-deposited CNT-based electrodes perform fast kinetics of sulfur transformation and high utilization of sulfur, especially at high C-rate and high current density conditions. Li-S battery cells with our electrodes achieve excellent long-term stability under high C-rate (capacity reduction of 0.044% per cycle up to 300 cycles at 2C), and high capacity even with high sulfur loading (an areal capacity of 5.6 mAh/cm2). Our approach presents facile and low-cost route to designing high performance Li-S batteries. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2020.124548 |