Insight into the Electrode Mechanism in Lithium-Sulfur Batteries with Ordered Microporous Carbon Confined Sulfur as the Cathode

被引:389
作者
Li, Zhen [1 ]
Yuan, Lixia [1 ]
Yi, Ziqi [1 ]
Sun, Yongming [1 ]
Liu, Yang [1 ]
Jiang, Yan [1 ]
Shen, Yue [1 ]
Xin, Ying [2 ]
Zhang, Zhaoliang [2 ]
Huang, Yunhui [1 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Adv Battery Mat & Syst MOE, Sch Mat Sci & Engn, Wuhan 430074, Hubei, Peoples R China
[2] Univ Jinan, Shandong Prov Key Lab Fluorine Chem & Chem Mat, Sch Chem & Chem Engn, Jinan 250022, Shandong, Peoples R China
关键词
ENHANCED CYCLABILITY; PERFORMANCE; POLYSULFIDE; COMPOSITES; GROWTH;
D O I
10.1002/aenm.201301473
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In lithium-sulfur batteries, small S2-4 molecules show very different electrochemical responses from the traditional S-8 material. Their exact lithiation/ delitiation mechanism is not clear and how to select proper electrolytes for the S2-4 cathodes is also ambiguous. Here, S2-4 and S-8/S2-4 composites with highly ordered microporous carbon as a confining matrix are fabricated and the electrode mechanism of the S2-4 cathode is investigated by comparing the electrochemical performances of the S2-4 and S2-4/S-8 electrodes in various electrolytes combined with theoretical calculation. Experimental results show that the electrolyte and microstructure of carbon matrix play important roles in the electrochemical performance. If the micropores of carbon are small enough to prevent the penetration of the solvent molecules, the lithiation/ delithiation for S2-4 occurs as a solid-solid process. The irreversible chemically reactions between the polysulfudes and carbonates, and the dissolution of the poly-sulfides into the ethers can be effectively avoided due to the steric hindrance. The confined S2-4 show high adaptability to the electrolytes. The sulfur cathode based on this strategy exhibits excellent rate capability and cycling stability.
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页数:8
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