硅
材料科学
阳极
电解质
相间
双层
重量分析
电化学
薄脆饼
化学工程
氧化硅
纳米技术
氧化物
膜
化学
电极
冶金
物理化学
工程类
有机化学
生物
生物化学
遗传学
氮化硅
作者
Caleb Stetson,Manuel Schnabel,Zhifei Li,Steven P. Harvey,Chun‐Sheng Jiang,Andrew G. Norman,Steven C. DeCaluwe,Mowafak Al‐Jassim,Anthony K. Burrell
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-10-30
卷期号:5 (12): 3657-3662
被引量:28
标识
DOI:10.1021/acsenergylett.0c02081
摘要
Silicon has been investigated in recent years as an alloying anode material to enhance gravimetric energy density in lithium-ion batteries. While recent developments have suggested that silicon oxides exhibit improved cycling stability over pure Si, the origin of the improved cycling performance is still poorly understood. The initial solid electrolyte interphase (SEI) formation mechanisms on Si wafers with both native oxide and chemically etched thermal oxide coatings are investigated structurally, chemically, and morphologically in the nanoscale. After one electrochemical cycle, microscopy reveals that SEI formed on native SiOx features the typical SEI bilayer structure with a carbon-rich outer SEI layer and an inorganic-rich inner SEI layer. In contrast, the SEI formed on chemically etched thermal oxide shows an inversion in the structure. This work observes distinct initial SEI formation mechanisms on the HF-etched SiO2 surface, which may be partially responsible for improved cycle life observed in SiOx-based anode materials.
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