Hasa Ivana, Haregewoin Atetegeb M, Zhang Liang, Tsai Wan-Yu, Guo Jinghua, Veith Gabriel M, Ross Philip N, Kostecki Robert
Energy Storage & Distributed Resources Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, California 94720, United States.
Advanced Light Source, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, California 94720, United States.
ACS Appl Mater Interfaces. 2020 Sep 9;12(36):40879-40890. doi: 10.1021/acsami.0c09384. Epub 2020 Aug 26.
This work focuses on the mechanisms of interfacial processes at the surface of amorphous silicon thin-film electrodes in organic carbonate electrolytes to unveil the origins of the inherent nonpassivating behavior of silicon anodes in Li-ion batteries. Attenuated total reflection Fourier-transform infrared spectroscopy, X-ray absorption spectroscopy, and infrared near-field scanning optical microscopy were used to investigate the formation, evolution, and chemical composition of the surface layer formed on Si upon cycling. We found that the chemical composition and thickness of the solid/electrolyte interphase (SEI) layer continuously change during the charging/discharging cycles. This SEI layer "breathing" effect is directly related to the formation of lithium ethylene dicarbonate (LiEDC) and LiPF salt decomposition products during silicon lithiation and their subsequent disappearance upon delithiation. The detected appearance and disappearance of LiEDC and LiPF decomposition compounds in the SEI layer are directly linked with the observed interfacial instability and poor passivating behavior of the silicon anode.
这项工作聚焦于非晶硅薄膜电极在有机碳酸盐电解质表面的界面过程机制,以揭示锂离子电池中硅阳极固有非钝化行为的根源。采用衰减全反射傅里叶变换红外光谱、X射线吸收光谱和红外近场扫描光学显微镜来研究循环过程中硅表面形成的表面层的形成、演化及化学成分。我们发现,在充电/放电循环过程中,固体/电解质界面(SEI)层的化学成分和厚度会持续变化。这种SEI层的“呼吸”效应与硅锂化过程中碳酸亚乙酯锂(LiEDC)和LiPF盐分解产物的形成直接相关,且在脱锂时它们会随后消失。在SEI层中检测到的LiEDC和LiPF分解化合物的出现和消失与观察到的硅阳极界面不稳定性和钝化性能差直接相关。