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首页> 外文期刊>Applied Surface Science >Determination of sp~2 and sp~3 phase fractions on the surface of diamond films from C1s, valence band X-ray photoelectron spectra and CKVV X-ray-excited Auger spectra
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Determination of sp~2 and sp~3 phase fractions on the surface of diamond films from C1s, valence band X-ray photoelectron spectra and CKVV X-ray-excited Auger spectra

机译:C1S,价带X射线光电子谱和CKVV X射线激发螺旋谱法测定SP〜2和SP〜3相位馏分在金刚石薄膜表面上的测定

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摘要

The practice of applying the methods for determining the relative contents of carbon atoms in sp(2) and sp(3) hybridization states from the profiles of C1s X-ray photoelectron and carbon KVV (CKVV) Auger spectra is analyzed. Difficulties in using C1s and CKVV spectra for determining the sp(2)/sp(3) ratios are discussed. A method is proposed for evaluating the fractions of sp(2) and sp(3) phases based on the fitting of the valence band X-ray photoelectron spectra by superposition of valence band spectra of samples with carbon atoms in pure sp(2) and sp(3) states. Relative fractions of sp(2) and sp(3) phases on the virgin surfaces of two ultrananocrystalline diamond films, and on their surfaces subjected to friction, were determined using C1s spectra, CKVV Auger spectra, and valence band spectra. All three methods gave the results that are consistent for virgin film surfaces with accuracy of 2%, and for the surfaces of films subjected to friction, 15%. In contrast to the ultrananocrystalline films, three XPSbased methods applied to a microcrystalline diamond film yielded significantly different sp(2)/sp(3) ratios. The reasons for this discrepancy are shown to lie in different analysis depths of these methods, and in different morphology of the film surfaces.
机译:分析了从C1S X射线光电子和碳KVV(CKVV)螺旋谱的曲线中SP(2)和SP(3)杂交状态下碳原子的相对含量的方法的实践。讨论了使用C1S和CKVV光谱来确定用于确定SP(2)/ SP(3)比率的困难。提出了一种方法,用于评估SP(2)和SP(3)相的级别基于价带X射线光电子谱的拟合通过纯SP(2)中的碳原子的碳原子叠加SP(3)州。使用C1S光谱,CKVV螺旋螺旋光谱和价带光谱测定SP(2)和SP(3)阶段的SP(2)和SP(3)相的相对级分,以及经受摩擦的摩擦的表面。所有三种方法都提供了对原始薄膜表面一致的结果,精度为2%,并且对于经受摩擦的薄膜表面,15%。与超混晶膜相反,施加到微晶金刚石膜的三种XPSBASED方法产生显着不同的SP(2)/ SP(3)比率。该差异的原因显示在这些方法的不同分析深度中,以及薄膜表面的不同形貌。

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