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In-situ EC-AFM and ex-situ XPS characterization to investigate the mechanism of SEI formation in highly concentrated aqueous electrolyte for Li-ion batteries

机译:原位EC-AFM和异位XPS表征研究高浓度锂离子电池电解液中SEI的形成机理

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The structure and chemical composition of solid electrolyte interphase (SEI) play a critical role in the performance of Li-ion batteries. However, the complexity of SEI layer and lack of relevant and efficient characterization techniques limit understanding of SEI formation mechanism and associated properties. Moreover, compared with organic electrolyte-based SEI, few studies have focused on aqueous electrolyte-based solid-electrolyte interphase (A-SEI). Herein, we present in-situ AFM images to demonstrate the morphological evolution of SEI in the presence of 21M lithium bis(trifluoromethane sulfonyl) imide (LiTFSI) aqueous electrolyte. Moreover, a combination of electrochemical-controlled atomic force microscopy (EC-AFM) and ex-situ X-ray photoelectron spectroscopy (XPS) is utilized to unveil the mechanism of SEI formation and identify its components. The results reveal that A-SEI layer is unevenly distributed and the inner and outer layers are mainly composed of Li2CO3 and LiF, respectively. The Young's modulus of 4-6 nm thick SEI layer is found to be 30 +/- 10 GPa. The current study provides novel insights into the formation of A-SEI by using in-situ AFM and provides a baseline for the future development of aqueous electrolytes for Li-ion batteries.
机译:固体电解质中间相(SEI)的结构和化学成分在锂离子电池的性能中起着至关重要的作用。但是,SEI层的复杂性以及缺乏相关有效的表征技术限制了对SEI形成机理和相关属性的理解。此外,与基于有机电解质的SEI相比,很少有研究集中在基于水性电解质的固体电解质中间相(A-SEI)上。在这里,我们提出原位原子力显微镜图像,以证明在21M双(三氟甲烷磺酰基)酰亚胺锂(LiTFSI)水性电解质存在下SEI的形态演变。此外,结合了电化学控制原子力显微镜(EC-AFM)和异位X射线光电子能谱(XPS)揭示了SEI的形成机理并鉴定了其成分。结果表明,A-SEI层分布不均匀,内外层主要由Li2CO3和LiF组成。发现4-6nm厚的SEI层的杨氏模量为30 +/- 10GPa。当前的研究为通过使用原位原子力显微镜形成A-SEI提供了新的见解,并为锂离子电池水性电解质的未来发展提供了基线。

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