石墨烯
拉曼光谱
插层(化学)
材料科学
石墨
晶格常数
分子物理学
电荷密度
从头算量子化学方法
衍射
凝聚态物理
分析化学(期刊)
纳米技术
化学
复合材料
无机化学
分子
光学
物理
量子力学
有机化学
色谱法
作者
Julio C. Chacón-Torres,Ludger Wirtz,Thomas Pichler
出处
期刊:ACS Nano
[American Chemical Society]
日期:2013-09-18
卷期号:7 (10): 9249-9259
被引量:97
摘要
We present detailed multi frequency resonant Raman measurements of potassium graphite intercalation compounds (GICs). From a well controlled and consecutive in-situ intercalation and high temperature de-intercalation approach the response of each stage up to stage VI is identified. The positions of the G and 2D lines as a function of staging depend on the charge transfer from K to the graphite layers and on the lattice expansion. Ab-initio calculations of the density and the electronic band-structure demonstrate that most (but not all) of the transferred charge remains on the graphene sheets adjacent to the intercalant layers. This leads to an electronic decoupling of these "outer" layers from the ones sandwiched between carbon layers and consequently to a decoupling of the corresponding Raman spectra. Thus higher stage GICs offer the possibility to measure the vibrations of single, double, and multi-layer graphene under conditions of biaxial strain. This strain can additionally be correlated to the in-plane lattice constants of GICs determined by x-ray diffraction. The outcome of this study demonstrates that Raman spectroscopy is a very powerful tool to identify local internal strain in pristine and weakly charged single and few-layer graphene and their composites, yielding even absolute lattice constants.
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