Dai Huidong, Gomes Luisa, Maxwell Derrick, Zamani Somayeh, Yang Kevin, Atienza Dianne, Dale Nilesh, Mukerjee Sanjeev
Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.
Department of Chemical Engineering, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.
ACS Appl Mater Interfaces. 2024 Feb 21;16(7):8639-8654. doi: 10.1021/acsami.3c15670. Epub 2024 Feb 9.
Vinylene carbonate (VC) is a widely used electrolyte additive in lithium-ion batteries for enhanced solid electrolyte interphase formation on the anode side. However, the cathode electrolyte interphase (CEI) formation with VC has received a lot less attention. This study presents a comprehensive investigation employing advanced in situ/operando-based Raman and X-ray absorption spectroscopy (XAS) to explore the effect of electrolyte composition on the CEI formation and suppression of surface reconstruction of LiNiMnCoO (NMC) cathodes. A novel chemical pathway via VC polymerization is proposed based on experimental results. In situ Raman spectra revealed a new peak at 995 cm, indicating the presence of C-O semi-carbonates resulting from the radical polymerization of VC. Operando Raman analysis unveiled the formation of NiO at 490 cm in the baseline system under ultrahigh voltage (up to 5.2 V). However, this peak was conspicuously absent in the VC electrolyte, signifying the effectiveness of VC in suppressing surface reconstruction. Further investigation was carried out utilizing in situ XAS compared X-ray absorption near edge structure spectra from cells of 3 and 20 cycles in both electrolytes at different operating voltages. The observed shift at the Ni K-edge confirmed a more substantial reduction of Ni in the baseline electrolyte compared to that in the VC electrolyte, thus indicating less CEI protection in the former. A sophisticated extended X-ray absorption fine structure analysis quantitatively confirmed the effective suppression of rock-salt formation with the VC electrolyte during the charging process, consistent with the operando Raman results. The in situ XAS results thus provided additional support for the key findings of this study, establishing the crucial role of VC polymerization in enhancing CEI stability and mitigating surface reconstruction on NMC cathodes. This work clarifies the relationship between the enhanced CEI layer and NMC degradation and inspires rational electrolyte design for long-cycling NMC cathodes.
碳酸亚乙烯酯(VC)是一种广泛应用于锂离子电池的电解质添加剂,用于增强阳极侧固体电解质界面的形成。然而,VC在阴极电解质界面(CEI)形成方面受到的关注要少得多。本研究采用先进的原位/操作拉曼光谱和X射线吸收光谱(XAS)进行了全面调查,以探讨电解质组成对LiNiMnCoO(NMC)阴极CEI形成和表面重构抑制的影响。基于实验结果,提出了一种通过VC聚合的新化学途径。原位拉曼光谱显示在995 cm处出现一个新峰,表明存在由VC自由基聚合产生的C-O半碳酸盐。操作拉曼分析揭示了在超高电压(高达5.2 V)下基线系统中490 cm处NiO的形成。然而,该峰在VC电解质中明显不存在,这表明VC在抑制表面重构方面的有效性。利用原位XAS进一步研究,比较了两种电解质在不同工作电压下3个和20个循环的电池的X射线吸收近边结构光谱。在Ni K边观察到的位移证实,与VC电解质相比,基线电解质中Ni的还原程度更大,因此表明前者的CEI保护较少。复杂的扩展X射线吸收精细结构分析定量证实了在充电过程中VC电解质有效抑制了岩盐的形成,这与操作拉曼结果一致。原位XAS结果因此为该研究的关键发现提供了额外支持,确立了VC聚合在增强CEI稳定性和减轻NMC阴极表面重构方面的关键作用。这项工作阐明了增强的CEI层与NMC降解之间的关系,并为长循环NMC阴极的合理电解质设计提供了启示。