插层(化学)
阴极
离子
溶剂
钠
无机化学
材料科学
化学
化学工程
有机化学
工程类
物理化学
作者
Philipp Adelhelm,Yanan Sun,Gustav Åvall,Shu‐Han Wu,Guillermo A. Ferrero,Hui Wang,Katherine Mazzio,Matteo Bianchini,Volodymyr Baran,Sebastian Risse
出处
期刊:Research Square - Research Square
日期:2024-06-25
被引量:2
标识
DOI:10.21203/rs.3.rs-4564500/v1
摘要
Abstract Solvent co-intercalation, i.e. the combined intercalation of ions and solvent molecules into electrode materials, is an additional but much less explored lever for modifying the properties of electrodes in metal-ion batteries (metal= Li, Na, Mg, …). So far, the knowledge on solvent co-intercalation is relatively scarce and largely limited to graphite anodes, for which in Na-ion batteries, the co-intercalation of glyme molecules is found to be very fast and highly reversible over many cycles. The use of co-intercalation in metal-ion batteries, however, still lacks a scientific breakthrough with respect to cathode active materials (CAMs). Here, we show for a series of Na-layered sulfide CAMs (NaxMS2, M = Ti, V, Cr, and mixtures) by experimental methods and theory, under which conditions solvent co-intercalation occurs and how this process impacts the phase behavior, electrode breathing, redox potential, and cycle life compared to “Na+-only” intercalation. Overall, co-intercalation provides an alternative way for designing CAMs.
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