电解质
金属锂
复合数
材料科学
锂(药物)
化学工程
图层(电子)
快离子导体
金属
纳米技术
电极
无机化学
化学
复合材料
冶金
工程类
内分泌学
物理化学
医学
作者
Trang Thi Vu,Hyeong Jun Cheon,Minhong Woo,Fazal ur Rehman,Hyesoo Choi,Jihwan Kim,Jeong Woo Yun,Nayan Ranjan Singha,Yoong Ahm Kim,Mincheol Chang
标识
DOI:10.1021/acssuschemeng.5c01503
摘要
Composite solid electrolytes, which comprise the flexibility of polymers with mechanical stiffness of inorganic solid electrolytes, are appealing for solid-state battery applications. However, they face challenges in simultaneously suppressing Li dendrite growth from the anode while maintaining high oxidative stability under high voltage. Here, a straightforward and scalable method is proposed by separately incorporating propylene carbonate and lithium hydroxide into a garnet-based polymer membrane; the double-layer composite polymer electrolyte with multifunctional effects is then subsequently formed through mechanically pressing them together. Propylene carbonate enhances the electrolyte’s stability against oxidation during high-voltage charging, contributing to improved battery’s energy density. Meanwhile, the reaction between the lithium hydroxide and lithium salt adjusts the SEI components on the anode side by forming a LiF-rich SEI layer, which improves the battery’s cycling stability. Benefiting from this ingenious design, the LiNi0.6Co0.2Mn0.2O2||Li cells demonstrate remarkable cycling performance for over 70 cycles, retaining 60.6% of their initial capacity at 0.1 C. Furthermore, the Li||Li symmetric cells achieved an outstanding plating and stripping reversibility of approximately 1500 h at 0.2 mA cm–2 with a small overpotential of 28 mV. This design is expected to facilitate the commercialization of electrolytes for high-voltage Li metal batteries.
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