电解质
化学
碳酸乙烯酯
无机化学
阳极
电化学
碳酸丙烯酯
X射线光电子能谱
化学工程
电极
工程类
物理化学
作者
Ahmet Oguz Tezel,Daniel Streich,Aurélie Guéguen,Maria Hahlin,Svein Sunde,Kristina Edström,Petr Novák,Ann Mari Svensson
标识
DOI:10.1149/1945-7111/abb567
摘要
Addition of small amounts of tris(hexafluoroisopropyl)borate (THFIPB) has previously been shown to improve the capacity of graphite anodes in a wide temperature window during long-term cycling in electrolytes based on LiPF6 in ethylene carbonate (EC) and diethylene carbonate (DMC) solvents. Here, we demonstrate that the addition of THFIPB accelerates the LiPF6 hydrolysis, and consumes residual water. The SEI formation and composition was studied by operando electrochemical mass spectrometry (OEMS), X-ray photoelectron spectroscopy (XPS), and ex situ diffuse reflectance spectroscopy (DRIFT). Differences in the surface products are observed for the THFIPB containing electrolyte already upon exposure of graphite anodes to the electrolyte. Both the mechanism and the kinetics of the EC reduction reaction are affected, as evidenced by the shift in the C2H4 evolution peak to higher potentials as compared to the reference electrolyte. Addition of THFIPB leads to formation of a SEI layer enriched in inorganic components; salt reduction products at high potentials, and inorganic carbonate at lower potentials. The SEI formed is more conductive but slightly less passivating. The SEI formed in the reference electrolyte is dominated by organic compounds, also at high potentials, facilitated by the trace amounts of water inevitably found in the electrolyte.
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