电解质
计时安培法
材料科学
法拉第效率
电池(电)
电极
阳极
线性扫描伏安法
电化学
循环伏安法
无机化学
化学工程
化学
物理化学
功率(物理)
工程类
物理
量子力学
作者
Lasse Dettmann,Simon Colbin,Andrew J. Naylor
标识
DOI:10.1002/admi.202500262
摘要
Abstract In rechargeable batteries a stable electrode‐electrolyte interface is the key for achieving high coulombic efficiency, rate capability, and cycle lifetime. Numerous studies are published on how the electrolyte influences the interface and whether it leads to the formation of a stable solid‐electrolyte‐interphase (SEI) on the anode surface. However, the influence of the electrode material upon formation of the SEI has so far not been a focus. In this study, the influence of battery electrode chemistry on electrolyte decomposition is highlighted by investigating three different electrode materials in model battery systems: carbonaceous (glassy carbon), semi‐conducting (silicon), and metallic (copper). Electrochemical methods including linear sweep voltammetry and chronoamperometry in combination with hard X‐ray photoelectron spectroscopy are used to unravel how and in which order SEI components nucleate depending on surface material and potential. The impact of the alkali metal cation (lithium vs sodium) upon SEI formation is additionally investigated. The findings reveal that SEI formation is highly dependent on the electrode material, reduction potential, and choice of alkali cation, emphasizing its non‐universal nature. These insights highlight the need for a thorough understanding of SEI formation mechanisms when designing advanced electrode materials and electrolytes for next‐generation batteries.
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