Kashtanov Stepan, Zhuang Guorong V, Augustsson Andreas, Nordgren Joseph, Luo Y, Ross Philip N, Guo Jinghua
Advanced Light Source Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
J Phys Chem B. 2007 Oct 11;111(40):11658-61. doi: 10.1021/jp072141u. Epub 2007 Sep 18.
The electronic structure of pol(ethylene oxide) (PEO) in a thin (<1 mu) film sample was experimentally probed by X-ray emission spectroscopy. Both nonresonant and resonant X-ray emission spectra were simulated by using density functional theory (DFT) applied to four different models representing different conformations in the polymer. Calculated spectra were compared with experimental results for the PEO film. It was found that the best fit was obtained with the polymer conformation in PEO electrolytes from which the salt (LiMF6, M = P, As, or Sb) had been removed. This conformation is different from the crystalline bulk polymer and implies that film casting, commonly used to form electrolytes for Li polymer batteries, induces the same conformation in the polymer not depending upon the presence of salt.
通过X射线发射光谱对厚度小于1微米的聚环氧乙烷(PEO)薄膜样品的电子结构进行了实验探测。利用密度泛函理论(DFT)对代表聚合物中不同构象的四种不同模型进行模拟,得到了非共振和共振X射线发射光谱。将计算得到的光谱与PEO薄膜的实验结果进行了比较。结果发现,对于去除了盐(LiMF6,M = P、As或Sb)的PEO电解质中的聚合物构象,拟合效果最佳。这种构象不同于结晶态本体聚合物,这意味着常用于制备锂聚合物电池电解质的流延成膜法会使聚合物形成相同的构象,而与盐的存在无关。