期刊论文详细信息
JOURNAL OF ALLOYS AND COMPOUNDS 卷:845
An extremely high rate Li-S battery with hybrid electrolyte
Article
Xu, Yang-Hai1,2  Zhang, Quan-Feng1  Fan, Bo1  Xue, Bai1  Chen, Hui-Jian1  Zhang, Xiang-Hua1  Luo, Zhong-Kuan3  Wang, Fang3  Le Coq, David4  Calvez, Laurent4  Ma, Hong-Li4  Fan, Ping1 
[1] Shenzhen Univ, Coll Phys & Energy, Inst Thin Film Phys & Applicat, Shenzhen Key Lab Adv Thin Films & Applicat, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
[3] Shenzhen Univ, Coll Chem & Environm Engn, 3688 Nanhai Ave, Shenzhen 518060, Peoples R China
[4] Univ Rennes, CNRS, ISCR, UMR 6226, FR-3504 Rennes, France
关键词: Li10SnP2S12;    Sulfide solid electrolyte;    Hybrid electrolyte;    Li-S battery;    Lithium dendrites;    Safety;   
DOI  :  10.1016/j.jallcom.2020.156261
来源: Elsevier
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【 摘 要 】

Polysulfide shuttling and lithium dendrites are two major issues which hinder the development of high-performance Li-S batteries. An ideal solution is to employ hybrid electrolyte consisting of sulfide solid electrolyte (SSE) and liquid electrolyte (LE), where SSE functions as a barrier for suppressing polysulfide shuttling and lithium dendrite growth while LE works as fast Li+ transport media. In this work, Li10SnP2S12 membranes, with a ceramic-like dense structure, provide a rigid barrier for preventing polysulfide shuttling and lithium dendrite growth. Meanwhile, its high ionic conductivity of 3.33 x 10(-3) S/cm (25 degrees C), accompanied with good wetting and Li+ transport abilities of LE, renders the hybrid electrolyte system an excellent Li+ dynamic property. Consequently, the Li-S batteries fabricated with this SSE-based hybrid electrolyte system can operate at an extremely high charge/discharge rate. At a rate of 5C (7.10 mA/cm(2)), the batteries show an initial discharge capacity of 659.4 mAh/g, maintain at 471.4 mAh/g and 413.3 mAh/g after 50 and 100 cycles,showing a capacity retention of 71.53% and 62.67%, respectively. It is also proposed that a competitive mechanism exists between the electrochemical reaction and side reaction during cycling, where the electrochemical reaction dominates at high rates. (C) 2020 Elsevier B.V. All rights reserved.

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