X射线光电子能谱
电解质
石墨烯
石墨
分解
材料科学
无机化学
化学工程
离子
电化学
化学
阳极
物理化学
纳米技术
电极
有机化学
工程类
作者
Kang Xu,Unchul Lee,Sheng S. Zhang,T. Richard Jow
摘要
In an attempt to depict a dynamic picture of solid electrolyte interface (SEI) formation on a graphitic anode surface during the initial forming cycle, we employed X-ray photoelectron spectroscopy in combination with a "pre-formation" technique to establish the dependence of the surface chemistry on the forming potential of the anode. A progressive transition in the 1s electron binding energies of the major elements was observed as the lithiation proceeded. However, the surface chemical species as well as their abundances seemed to stabilize around 0.55 V and remained constant during the subsequent delithiation process, indicating that a stable SEI exists thereafter. Integrating the information revealed by different analyses, we believe that the reductive decomposition of the anion starts at ca. 1.00 V, while the effective protection of the graphene surface by SEI is available after the anode is lithiated below the potential of 0.55 V vs. Li. © 2004 The Electrochemical Society. All rights reserved.
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