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A detailed analysis of the C 1s photoemission of n-alkanethiolate films on noble metal substrates

机译:贵金属基体上正链烷硫醇盐薄膜的C 1s光发射的详细分析

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High-resolution C 1s X-ray photoemission spectra for the series of n-alkanethiolate (AT) self-assembled monolayers (SAMs) with different lengths of the alkyl chain have been acquired and analyzed in terms of initial and final state effects and fine structure of the C 1s emission. Independent of the alkyl chain length, the binding energy position of this emission was found to be higher by approximate to0.35 eV for AT SAMs on Ag substrate as compared to Au, which was attributed to the differences in the final state screening mediated by the intermolecular charge transfer. It was assumed that the extent of this effect is a function of the detailed molecular arrangement in the alkyl matrix and demonstrated that the difference in the C 1s peak position disappears as soon as this arrangement is distorted by the incorporation of sulfone moiety in the alkyl chain. In addition, a change of the C 1s peak shape from a symmetric to asymmetric line with increasing alkyl chain length has been observed. This development could be described assuming the existence of a fine structure in the C 1s emission, with two low-intensity components at the higher and lower BE sides of the main emission peak. An assignment of these components has been considered. (C) 2003 Elsevier Science B.V. All rights reserved. [References: 42]
机译:获得了具有不同烷基链长度的一系列正链烷硫醇(AT)自组装单分子层(SAM)的高分辨率C 1s X射线光发射光谱,并根据初始和最终状态效应以及精细结构进行了分析C 1s发射的独立于烷基链长度,发现该发射的结合能位置比Au高出Ag底物上的AT SAMs约0.35 eV,这归因于由A介导的最终状态筛选的差异。分子间电荷转移。假定这种影响的程度是烷基基质中详细分子排列的函数,并证明一旦通过在烷基链中引入砜部分而使这种排列扭曲,C 1s峰位置的差异就会消失。 。另外,已经观察到随着烷基链长度的增加,C 1s峰形状从对称线改变为不对称线。可以假设C 1s发射中存在精细结构,并且在主发射峰的较高和较低BE侧有两个低强度分量来描述这种发展。已经考虑了这些组件的分配。 (C)2003 Elsevier Science B.V.保留所有权利。 [参考:42]

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