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A LiF-Rich Solid Electrolyte Interphase in a Routine Carbonate Electrolyte by Tuning the Interfacial Chemistry Behavior of LiPF6 for Stable Li Metal Anodes
被引:18
作者:
Zhang, Jing
[1
]
Yue, Xinyang
[2
]
Wu, Zeyu
[1
]
Chen, Yuanmao
[2
]
Bai, Yu
[1
]
Sun, Kening
[1
]
Wang, Zhenhua
[1
]
Liang, Zheng
[2
]
机构:
[1] Beijing Inst Technol, Sch Chem Engn & Environm, Being Key Lab Chem Power Source & Green Catalysis, Beijing 100081, Peoples R China
[2] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
基金:
中国国家自然科学基金;
关键词:
lithium metal anode;
LiF;
solid electrolyteinterphase;
LiPF6;
electrochemical decomposition;
LITHIUM-METAL;
HIGH-ENERGY;
BATTERIES;
MECHANISMS;
D O I:
10.1021/acs.nanolett.3c03340
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Lithium (Li) dendrite growth in a routine carbonate electrolyte (RCE) is the main culprit hindering the practical application of Li metal anodes. Herein, we realize the regulation of the LiPF6 decomposition pathway in RCE containing 1.0 M LiPF6 by introducing a "self-polymerizing" additive, ethyl isothiocyanate (EITC), resulting in a robust LiF-rich solid electrolyte interphase (SEI). The effect of 1 vol % EITC on the electrode/electrolyte interfacial chemistry slows the formation of the byproduct LixPOFy. Such a LiF-rich SEI with EITC polymer winding exhibits a high Young's modulus and a uniform Li-ion flux, which suppresses dendrite growth and interface fluctuation. The EITC-based Li metal cell using a Li4Ti5O12 cathode delivers a capacity retention of 81.4% over 1000 cycles at 10 C, outperforming its counterpart. The cycling stability of 1 Ah pouch cells was further evaluated under EITC. We believe that this work provides a new method for tuning the interfacial chemistry of Li metal through electrolyte additives.
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页码:9609 / 9617
页数:9
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