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用于室温固态锂电池的聚环氧乙烷基电解质/超高镍阴极界面处的定制锂溶剂化鞘层

Customized Li Solvation Sheath at the Poly(ethylene oxide)-Based Electrolyte/Ultrahigh-Nickel Cathode Interface toward Room-Temperature Solid-State Lithium Batteries.

作者信息

Dai Yuqing, Tan Jiaxu, Hou Zihan, You Bianzheng, Luo Gui, Deng Duo, Peng Wenjie, Wang Zhixing, Guo Huajun, Li Xinhai, Yan Guochun, Duan Hui, Wang Ying, Wu Feixiang, Wang Jiexi

机构信息

Engineering Research Center of the Ministry of Education for Advanced Battery Materials, Hunan Provincial Key Laboratory of Nonferrous Value-Added Metallurgy, School of Metallurgy and Environment, Central South University, Changsha 410083, China.

BASF ShanShan Battery Material Co., LTD, Changsha 410205, China.

出版信息

ACS Nano. 2024 Aug 20;18(33):22518-22532. doi: 10.1021/acsnano.4c07997. Epub 2024 Aug 7.

Abstract

The matching of poly(ethylene oxide) (PEO)-based electrolytes with ultrahigh-nickel cathode materials is crucial for designing new-generation high-energy-density solid-state lithium metal batteries (SLMBs), but it is limited by serious interfacial side reactions between PEO and ultrahigh-nickel materials. Here, a high-concentration electrolyte (HCE) interface with a customized Li solvation sheath is constructed between the cathode and the electrolyte. It induces the formation of an anion-regulated robust cathode/electrolyte interface (CEI), reduces the unstable free-state solvent, and finally achieves the compatibility of PEO-based electrolytes with ultrahigh-nickel cathode materials. Meanwhile, the corrosion of the Al current collector caused by lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) ions is prevented by lithium difluoro(oxalato)borate (LiDFOB) ions. The synergistic effect of the double lithium salt is achieved by a well-tailored ratio of TFSI and DFOB in the first solvation sheath of Li. Compared with reported PEO-based SLMBs matched with ultrahigh-nickel (Ni ≥ 90%) cathodes, the SLMB in this work delivers a high discharge specific capacity of 216.4 mAh g (0.1C) even at room temperature. This work points out a direction to optimize the cathode/electrolyte interface.

摘要

聚环氧乙烷(PEO)基电解质与超高镍正极材料的匹配对于设计新一代高能量密度固态锂金属电池(SLMB)至关重要,但它受到PEO与超高镍材料之间严重的界面副反应的限制。在此,在正极和电解质之间构建了具有定制锂溶剂化鞘层的高浓度电解质(HCE)界面。它诱导形成阴离子调控的稳健正极/电解质界面(CEI),减少不稳定的自由态溶剂,最终实现PEO基电解质与超高镍正极材料的相容性。同时,二氟草酸硼酸锂(LiDFOB)离子可防止双(三氟甲磺酰)亚胺锂(LiTFSI)离子对铝集流体的腐蚀。通过在锂的第一溶剂化鞘层中精心调整TFSI和DFOB的比例,实现了双锂盐的协同效应。与报道的与超高镍(Ni≥90%)正极匹配的PEO基SLMB相比,这项工作中的SLMB即使在室温下也具有216.4 mAh g(0.1C)的高放电比容量。这项工作为优化正极/电解质界面指明了方向。

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