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高熵锂硫银锗矿型固体电解质助力稳定全固态电池

High-Entropy Lithium Argyrodite Solid Electrolytes Enabling Stable All-Solid-State Batteries.

作者信息

Li Shenghao, Lin Jing, Schaller Mareen, Indris Sylvio, Zhang Xin, Brezesinski Torsten, Nan Ce-Wen, Wang Shuo, Strauss Florian

机构信息

Center of Smart Materials and Devices, State Key Laboratory of Advanced Technology for Materials Synthesis and Processing &, School of Material Science and Engineering, Wuhan University of Technology, Wuhan, 430070, China.

Institute of Nanotechnology, Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344, Eggenstein-Leopoldshafen, Germany.

出版信息

Angew Chem Int Ed Engl. 2023 Dec 11;62(50):e202314155. doi: 10.1002/anie.202314155. Epub 2023 Nov 13.

Abstract

Superionic solid electrolytes (SEs) are essential for bulk-type solid-state battery (SSB) applications. Multicomponent SEs are recently attracting attention for their favorable charge-transport properties, however a thorough understanding of how configurational entropy (ΔS ) affects ionic conductivity is lacking. Here, we successfully synthesized a series of halogen-rich lithium argyrodites with the general formula Li PS Cl Br (0≤x≤1.5). Using neutron powder diffraction and P magic-angle spinning nuclear magnetic resonance spectroscopy, the S /Cl /Br occupancy on the anion sublattice was quantitatively analyzed. We show that disorder positively affects Li-ion dynamics, leading to a room-temperature ionic conductivity of 22.7 mS cm (9.6 mS cm in cold-pressed state) for Li PS Cl Br (ΔS =1.98R). To the best of our knowledge, this is the first experimental evidence that configurational entropy of the anion sublattice correlates with ion mobility. Our results indicate the possibility of improving ionic conductivity in ceramic ion conductors by tailoring the degree of compositional complexity. Moreover, the Li PS Cl Br SE allowed for stable cycling of single-crystal LiNi Co Mn O (s-NCM90) composite cathodes in SSB cells, emphasizing that dual-substituted lithium argyrodites hold great promise in enabling high-performance electrochemical energy storage.

摘要

超离子固体电解质(SEs)对于大容量固态电池(SSB)应用至关重要。多组分SEs因其良好的电荷传输特性最近受到关注,然而,目前尚缺乏对构型熵(ΔS )如何影响离子电导率的深入理解。在此,我们成功合成了一系列通式为Li PS Cl Br (0≤x≤1.5)的富卤锂银锗矿。利用中子粉末衍射和P 魔角旋转核磁共振光谱对阴离子亚晶格上的S /Cl /Br占据情况进行了定量分析。我们表明,无序对锂离子动力学有积极影响,对于Li PS Cl Br (ΔS =1.98R),其室温离子电导率达到22.7 mS cm (冷压状态下为9.6 mS cm )。据我们所知,这是阴离子亚晶格的构型熵与离子迁移率相关的首个实验证据。我们的结果表明,通过调整成分复杂程度来提高陶瓷离子导体中离子电导率的可能性。此外,Li PS Cl Br SE能够使SSB电池中的单晶LiNi Co Mn O (s-NCM90)复合阴极实现稳定循环,这强调了双取代锂银锗矿在实现高性能电化学储能方面具有巨大潜力。

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