Development of high-energy non-aqueous lithium-sulfur batteries via redox-active interlayer strategy

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作者
Byong-June Lee
Chen Zhao
Jeong-Hoon Yu
Tong-Hyun Kang
Hyean-Yeol Park
Joonhee Kang
Yongju Jung
Xiang Liu
Tianyi Li
Wenqian Xu
Xiao-Bing Zuo
Gui-Liang Xu
Khalil Amine
Jong-Sung Yu
机构
[1] Daegu Gyeongbuk Institute of Science & Technology (DGIST),Department of Energy Science and Engineering
[2] Argonne National Laboratory,Chemical Sciences and Engineering Division
[3] Pusan National University,Department of Nanoenergy Engineering
[4] Korea University of Technology and Education (KOREATECH),Department of Chemical Engineering
[5] Argonne National Laboratory,X
[6] Stanford University,ray Science Division
[7] Mohammed VI Polytechnic University (UM6P),Materials Science and Engineering
[8] Energy Science and Engineering Research Center,Materials Science, Energy and Nano
[9] DGIST,engineering Department
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摘要
Lithium-sulfur batteries have theoretical specific energy higher than state-of-the-art lithium-ion batteries. However, from a practical perspective, these batteries exhibit poor cycle life and low energy content owing to the polysulfides shuttling during cycling. To tackle these issues, researchers proposed the use of redox-inactive protective layers between the sulfur-containing cathode and lithium metal anode. However, these interlayers provide additional weight to the cell, thus, decreasing the practical specific energy. Here, we report the development and testing of redox-active interlayers consisting of sulfur-impregnated polar ordered mesoporous silica. Differently from redox-inactive interlayers, these redox-active interlayers enable the electrochemical reactivation of the soluble polysulfides, protect the lithium metal electrode from detrimental reactions via silica-polysulfide polar-polar interactions and increase the cell capacity. Indeed, when tested in a non-aqueous Li-S coin cell configuration, the use of the interlayer enables an initial discharge capacity of about 8.5 mAh cm−2 (for a total sulfur mass loading of 10 mg cm−2) and a discharge capacity retention of about 64 % after 700 cycles at 335 mA g−1 and 25 °C.
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