准固态Li-SPAN电池的内置兼容电极-电解质界面。

IF 16.9
Tao Zhang, Zhengyuan Shen, Xinhui Pan, Man Zhang, Tong Lian, Keqing Shi, Ji Qian, Li Li, Feng Wu, Renjie Chen
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引用次数: 0

摘要

锂硫电池因其高能量密度和低成本而被认为是下一代储能系统的理想选择。硫化聚丙烯腈(SPAN)作为正极材料因其固-固转化机理而受到广泛关注,但锂金属阳极问题一直制约着Li-SPAN电池的性能。开发具有良好电极-电解质相容性的锂硫电池固态电解质是迫切需要的。在此,我们通过原位聚合界面构建展示了双界面优化策略,该策略协同增强了固体聚合物电解质(SPE)与锂金属阳极和SPAN阴极之间的界面相容性。预埋在SPE中的引发剂在界面处引发了1,3-二恶烷(DOL)的原位聚合,从而大大降低了电极/电解质界面阻抗。此外,由于在SPAN上形成了富无机且致密的阴极电解质界面相,释放的氟乙烯碳酸酯(FEC)进入poly-DOL界面可以进一步降低阻抗,增强循环过程中的界面稳定性,同时阻止多硫化物的溶解。因此,Li-SPAN电池可以在0.5℃下运行200多次,容量保持率为90%。我们相信这一策略为高能固态锂硫电池的发展提供了前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-Built Compatible Electrode-Electrolyte Interphases for Quasi-Solid-State Li-SPAN Batteries.

Lithium-sulfur batteries have been regarded as a promising candidate for next-generation energy storage systems owing to their high energy density and low cost. Sulfurized polyacrylonitrile (SPAN) as a cathode material has received wide interest due to the solid-solid conversion mechanism, while the Li-SPAN cell performance has been limited by the notorious issue of lithium metal anode. Developing solid-state electrolytes for lithium-sulfur batteries with favorable electrode-electrolyte compatibility is urgently desired. Herein, we demonstrate a dual-interface optimization strategy through in-situ polymerization interface construction, which synergistically enhances interfacial compatibility between the solid polymer electrolyte (SPE) and both the lithium metal anode and SPAN cathode. The initiator pre-buried in the SPE triggers the in-situ polymerization of 1,3-dioxolane (DOL) at the interface, thereby greatly reducing the electrode/electrolyte interfacial impedance. Additionally, the released fluoroethylene carbonate (FEC) into the poly-DOL interface could further reduce the impedance and enhance the interface stability during cycling, simultaneously preventing the dissolution of polysulfides, owing to the inorganic-rich and dense cathode electrolyte interphase formed on SPAN. As a result, the Li-SPAN cell could operate more than 200 cycles at 0.5C with a capacity retention of 90%. We believe that this strategy provides prospects for the development of high-energy solid-state lithium-sulfur batteries.

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