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双配位诱导的聚偏氟乙烯/LiGaLaZrO/丁二腈复合固体电解质用于增强全固态锂电池的倍率性能

Dual-Coordination-Induced Poly(vinylidene fluoride)/LiGaLaZrO/Succinonitrile Composite Solid Electrolytes Toward Enhanced Rate Performance in All-Solid-State Lithium Batteries.

作者信息

Cao Shiyu, Chen Fei, Shen Qiang, Zhang Lianmeng

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China.

International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China.

出版信息

ACS Appl Mater Interfaces. 2023 Aug 9;15(31):37422-37432. doi: 10.1021/acsami.3c06179. Epub 2023 Jul 27.

Abstract

Pursuing high energy and power density in all-solid-state lithium batteries (ASSLBs) has been the focus of attention. However, due to their inferior ion transport, their rate performance is limited compared to traditional lithium-ion batteries. Herein, a dual-coordination mechanism is first proposed to construct a high-performance poly(vinylidene fluoride)/LiGaLaZrO/succinonitrile (PVDF/LLZO/SN) composite solid electrolyte. The dual-coordination interactions of SN with both LLZO and Li in lithium salts allow SN to act like a branched chain of PVDF, realizing an increase in the free volume of the composite electrolyte. Meanwhile, SN molecules are immobilized within the electrolyte membrane by coordinating with LLZO, ensuring good interfacial stability. Profiting from the dual-coordination mechanism, the PVDF/LLZO/SN composite solid electrolyte combines enhanced electrochemical performance and interfacial compatibility. When applied to ASSLBs, the composite solid electrolyte enables the battery to operate at rates up to 6 C. The LiFePO/Li batteries operated at 4 C can still deliver a high capacity retention rate of 96.4% after 50 cycles. Notably, these batteries also exhibit good long-cycle stability. After 500 cycles at 0.5 C, the discharge capacity was maintained at 145.9 mAh g.

摘要

追求全固态锂电池(ASSLBs)的高能量和功率密度一直是人们关注的焦点。然而,由于其离子传输性能较差,与传统锂离子电池相比,其倍率性能受到限制。在此,首次提出一种双配位机制来构建高性能的聚偏氟乙烯/锂镓镧锆氧化物/丁二腈(PVDF/LLZO/SN)复合固体电解质。丁二腈(SN)与锂盐中的LLZO和Li的双配位相互作用使SN能够像聚偏氟乙烯的支链一样发挥作用,实现复合电解质自由体积的增加。同时,SN分子通过与LLZO配位而固定在电解质膜内,确保了良好的界面稳定性。得益于双配位机制,PVDF/LLZO/SN复合固体电解质兼具增强的电化学性能和界面兼容性。当应用于全固态锂电池时,这种复合固体电解质能使电池在高达6 C的倍率下运行。在4 C下运行的磷酸铁锂/锂(LiFePO/Li)电池在50次循环后仍能保持96.4%的高容量保持率。值得注意的是,这些电池还表现出良好的长循环稳定性。在0.5 C下进行500次循环后,放电容量保持在145.9 mAh g。

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