Cation Additive Enabled Rechargeable LiOH-Based Lithium-Oxygen Batteries

被引:36
作者
Bi, Xuanxuan [1 ]
Li, Matthew [1 ,2 ]
Liu, Cong [1 ]
Yuan, Yifei [1 ,3 ]
Wang, Hao [1 ]
Key, Baris [1 ]
Wang, Rongyue [4 ]
Shahbazian-Yassar, Reza [3 ]
Curtiss, Larry A. [5 ]
Lu, Jun [1 ]
Amine, Khalil [1 ,6 ]
机构
[1] Argonne Natl Lab, Chem Sci & Engn Div, 9700 South Cass Ave, Lemont, IL 60439 USA
[2] Univ Waterloo, Dept Chem Engn, Waterloo Inst Nanotechnol, Waterloo, ON N2L 3G1, Canada
[3] Univ Illinois, Dept Mech & Ind Engn, Chicago, IL 60607 USA
[4] Argonne Natl Lab, Appl Mat Div, 9700 South Cass Ave, Lemont, IL 60439 USA
[5] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
[6] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
cation additive; LiOH; lithium air batteries; lithium hydroxide; lithium-oxygen batteries; LI-O-2; METAL; SUPEROXIDE; SALTS; LAYER;
D O I
10.1002/anie.202010745
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-oxygen (Li-O-2) batteries have attracted extensive research interest due to their high energy density. Other than Li2O2 (a typical discharge product in Li-O-2 batteries), LiOH has proved to be electrochemically active as an alternative product. Here we report a simple strategy to achieve a reversible LiOH-based Li-O-2 battery by using a cation additive, sodium ions, to the lithium electrolyte. Without redox mediators in the cell, LiOH is detected as the sole discharge product and it charges at a low charge potential of 3.4 V. A solution-based reaction route is proposed, showing that the competing solvation environment of the catalyst and Li+ leads to LiOH precipitation at the cathode. It is critical to tune the cell chemistry of Li-O-2 batteries by designing a simple system to promote LiOH formation/decomposition.
引用
收藏
页码:22978 / 22982
页数:5
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