A robust interphase via in-situ pre-reconfiguring lithium anode surface for long-term lithium-oxygen batteries

被引:24
作者
Xu, Pan [1 ]
Lin, Xiaodong [1 ]
Sun, Zongqiang [1 ]
Li, Kaixuan [1 ]
Dou, Wenjie [1 ]
Hou, Qing [1 ]
Zhou, Zhiyou [1 ]
Yan, Jiawei [1 ]
Zheng, Mingsen [1 ]
Yuan, Ruming [1 ]
Dong, Quanfeng [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat iChEM, Engn Res Ctr Electrochem Technol,Minist Educ,State, Xiamen 361005, Fujian, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2022年 / 72卷
基金
中国国家自然科学基金;
关键词
Solid-electrolyte interphase; Guanylthiourea; Sulfur-modified Li surface; Li metal; Li-O; 2; batteries; SINGLET OXYGEN; LI-O-2; BATTERIES; METAL ANODE; ELECTROLYTE; GENERATION; SHUTTLE; DESIGN; LI2O2; ION;
D O I
10.1016/j.jechem.2022.04.025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Lithium-oxygen (Li-O2) battery is considered as one of the most promising alternatives because of its ultrahigh theoretical energy density. However, their cycling stability is severely restricted by the uncontrollable dendrite growth and serious oxygen corrosion issue on Li surface. Herein, a sulfur-modified Li surface can be successfully constructed via chemical reaction of guanylthiourea (GTU) molecule on Li, which can induce the selectively fast decomposition of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) to form a smooth and stable inorganics-rich solid-electrolyte interphase (IR-SEI) during the subsequent electrochemical process. Such an IR-SEI cannot only offer a highly reversible and stable Li plating/stripping chemistry with dendrite-free property (10 mA cm-2-10 mAh cm-2, > 0.5 years; 3 mA cm-23 mAh cm-2, > 1 year) but also endows the Li metal an anti-oxygen corrosion function, thereby significantly improving the cycling stability of Li-O2 batteries. This work provides a new idea for constructing functional solid-electrolyte interphase (SEI) to achieve highly stable Li metal anode. (c) 2022 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press.
引用
收藏
页码:186 / 194
页数:9
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