阴极
电解质
光电发射光谱学
锂(药物)
带材弯曲
分析化学(期刊)
材料科学
薄膜
化学工程
吸附
电极
图层(电子)
化学
X射线光电子能谱
物理化学
纳米技术
光电子学
有机化学
内分泌学
工程类
医学
作者
Thomas Späth,Mathias Fingerle,Natalia Schulz,Wolfram Jaegermann,René Hausbrand
标识
DOI:10.1021/acs.jpcc.6b05881
摘要
The formation of electrode–electrolyte interfaces is of key importance for the stability and performance of lithium-ion batteries. To increase efficiency and lifetime, a detailed understanding of the processes at these interfaces is necessary. Both chemical reactions resulting in the formation of interface layers as well as double layer formation, i.e., band bending, influence the batteries’ properties. In this contribution, we investigate the interface formation between a thin film LiCoO 2 cathode material and a solvent adsorbate. Using a surface-science approach, dimethyl sulfoxide (DMSO, (CH 3 ) 2 SO) was used as molecular probe and adsorbed stepwise onto LiCoO 2 at low temperature. After each step, the interface was analyzed by synchrotron-based soft X-ray photoemission spectroscopy (SXPS). We established the energy level alignment of the LiCoO 2 −DMSO interface, showing a band bending downward in the cathode material attributed to Li-ion transport into the adsorbate phase. Lithium transport results in the formation of a reaction layer containing Li 2 CO 3 and Li 2 O, constituting a solid electrolyte interphase layer (SEI).
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