Abstract
The importance of the solid electrolyte interphase (SEI) layer for enhanced Li-ion storage has been well established, but primary understanding of the chemical components and structure of SEI layer on MXene-based electrodes remains incomplete. Here, we characterized the morphology and components of SEI layer on Ti3C2Tx and Ti3C2Tx/Fe2O3 electrode materials through combination of X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy and transmission electron microscopy (TEM). The results show the SEI layer formed on pillar-structured Ti3C2Tx/Fe2O3 is dense and intact after long cycling, while the SEI layer on Ti3C2Tx electrode is noncontinuous. The pillar-structured Ti3C2Tx/Fe2O3 exhibits significantly enhanced capacity of 449.6 mAh g−1 at 300 mA g−1 after 100 cycles compared with Ti3C2Tx (140.2 mAh g−1) owing to the intact SEI layer with friendly chemical components. This work elaborates a recognition for SEI layer in MXene-based electrode, which provides a useful strategy for further SEI engineering.
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