Supplementary information files for "Tracing the cross‐talk phenomenon of Vinylethylene Carbonate to unveil its counterintuitive influence as an electrolyte additive on high‐voltage lithium‐Ion batteries"

<p dir="ltr">Supplementary information files for "Tracing the cross‐talk phenomenon of Vinylethylene Carbonate to unveil its counterintuitive influence as an electrolyte additive on high‐voltage lithium‐Ion batteries"</p><p dir="ltr"><br></p><p dir="ltr">The formation of effective interphases is crucial to enable high-performance lithium-ion batteries. This can be facilitated by the introduction of electrolyte additives, ensuring improved stability and transport properties. The identification of proper additives requires a comprehensive understanding of the fundamental mechanisms of interfacial reactions governing interphase formation. This study presents a detailed investigation of widely known and less conventional interphase-forming additives in high-voltage LiNi_0.6Mn_0.2Co_0.2O₂, NMC622 | | artificial graphite cells. The electrochemical characterization shows that cells containing vinylethylene carbonate (VEC) significantly outperform all other investigated electrolyte formulations. Surprisingly, gas chromatography-mass spectroscopy measurements of the electrolyte composition after cycling indicate the formation of an ineffective solid-electrolyte interphase (SEI) in the presence of VEC. A thorough analysis of the interfacial composition via operando shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS) and surface-enhanced Raman spectroscopy elucidates rather the formation of an effective cathode-electrolyte interphase (CEI). This phenomenon results from the reductive reaction of VEC on the anode, followed by the product transfer and electro-polymerization of reaction products on the cathode. Additionally, focused ion beam secondary ion mass spectrometry (FIB-SIMS) with a time of flight (ToF)-detector is used to analyze the elemental spatial distribution of Li-species and Mn in the respective SEIs.</p><p dir="ltr">© The Author(s), CC BY 4.0</p>