Dynamically lithium-compensated polymer artificial SEI to assist highly stable lithium-rich manganese-based anode-free lithium metal batteries

被引:0
|
作者
Ming-Ji Peng [1 ,2 ]
Jin-Qiu Zhou [3 ]
Ting-Ting Han [4 ]
Yang Zhou [1 ]
Jie Liu [3 ]
Na Xu [5 ]
Zhen-Kang Wang [1 ,2 ]
Wen-Bin Lin [6 ]
Cheng-Lin Yan [1 ,2 ]
机构
[1] Key Laboratory of Core Technology of High Specific Energy Battery and Key Materials for Petroleum and Chemical Industry,College of Energy,Soochow University
[2] Light Industry Institute of Electrochemical Power Sources
[3] School of Chemistry and Chemical Engineering,Nantong University
[4] State Key Laboratory of Space Power-Sources Technology,Shanghai Institute of Space Power-Sources
[5] Centre énergie,Matériaux et Télécommunications,Institut National de la Recherche Scientifique
[6] Zhangjiagang Industrial Technologies,Soochow University
关键词
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中图分类号
O646 [电化学、电解、磁化学]; TM912 [蓄电池];
学科分类号
0808 ; 081704 ;
摘要
Owing to the unique structure,anode-free lithium metal batteries(AFLMBs) have higher energy density and lower production cost than traditional lithium metal batteries(LMBs) or lithium-ion batteries(LIBs),However,AFLMBs suffer from an inherently finite Li reservoir and exhibit poor cycle stability,low Coulombic efficiency(CE) and severe dendrite growth.In this work,polydiallyl lithium disulfide(PDS-Li) was successfully synthesized and coated on Cu current collector by electrochemical polymerization.The PDS-Li acts as an additional lithium resource to compensate for the irreversible loss of lithium during cycling.In addition,the special structure and lithiophilicity of PDS-Li contribute to lower nucleation overpotential and uniform lithium deposition.When coupled with Li-rich manganese-based(LRM)cathode of Li1.2Mn0.54Ni0.13Co0.13O2,the anode-free full cell exhibits significantly improved cycle stability over 100 cycles and capacity retention of 63.3% and 57% after 80 and 100 cycles,respectively.We believe that PDS-Li can be used to ensure stable cycling performance and high-energy-density in AFLMBs.
引用
收藏
页码:2527 / 2535
页数:9
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