Molecular design of electrolyte additives for high-voltage fast-charging lithium metal batteries

被引:0
|
作者
Ou, Yu [1 ]
Hou, Wenhui [1 ]
Zhu, Da [2 ]
Li, Changjian [1 ]
Zhou, Pan [1 ]
Song, Xuan [1 ]
Xia, Yingchun [1 ]
Lu, Yang [1 ]
Yan, Shuaishuai [1 ]
Zhou, Hangyu [1 ,3 ]
Cao, Qingbin [1 ]
Zhou, Haiyu [1 ]
Liu, Hao [1 ]
Ma, Xiao [1 ]
Liu, Zhi [1 ]
Xu, Hong [2 ]
Liu, Kai [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
[3] China Acad Safety Sci & Technol, Beijing 100012, Peoples R China
基金
美国国家科学基金会; 北京市自然科学基金;
关键词
ION BATTERIES; ANODE;
D O I
10.1039/d4ee04282d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The incorporation of lithium metal as an anode material in lithium metal batteries (LMBs) offers a transformative pathway to surpass the energy density limits of conventional lithium-ion batteries (LIBs). However, the integration of lithium metal with traditional carbonate-based electrolytes is plagued by challenges, such as the instability of the solid electrolyte interphase (SEI) and the cathode-electrolyte interphase (CEI) at high voltages and high rates. To address these issues, we designed and tested a novel bifunctional additive, vinyl sulfonyl fluoride (VSF), that demonstrates the ability to stabilize both the SEI and CEI under fast-charging and high-voltage conditions. Through a combination of density functional theory (DFT), molecular dynamics (MD) simulations, and electrochemical evaluations, we show that VSF promotes the formation of thin, uniform, and inorganic-rich interfacial layers, which enhance lithium-ion transport and mitigate the degradation typically observed in high-energy LMBs. Full-cell and pouch-cell cycling experiments reveal that VSF significantly improves cycling stability and rate performance, particularly under extreme conditions. The findings highlight VSF as a promising additive for advancing the commercialization of high-performance LMBs.
引用
收藏
页码:1464 / 1476
页数:13
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