Low-dose cryogenic TEM and EELS reveal SEI nanostructures in silicon anodes, indicating design strategies for improved stability.
Silicon anodes suffer from unstable solid electrolyte interphases (SEI) that drive capacity fade. Here, using low-dose cryogenic TEM and EELS under suppressed bulk Li–Si alloying (0.1 V vs Li/Li+ cutoff, 10 cycles), we resolve the atomic-scale SEI nanostructures induced by fluoroethylene carbonate (FEC), ethylene sulfite (ES), and lithium difluorophosphate (LiPO2F2). FEC forms a dense ∼20 nm LiF-rich nanocrystal scaffold, ES produces a 10–20 nm heterogeneous mosaic of LiF/Li2SO4 within an organic-rich matrix, and LiPO2F2 yields an ultrathin (∼10 nm) inorganic-dominated but brittle layer. Despite being the thickest, the FEC-derived SEI delivers the best long-term cycling stability. Mechanistically, optimal performance arises from a balanced architecture that combines strong electronic insulation, efficient Li+ transport across grain boundaries, and mechanical coherence rather than minimized thickness alone. These findings identify composition and nanostructural continuity as key regulators of interfacial stability in silicon anodes.
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Zhang et al. (2026) studied this question.
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