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The interface electronic structure of thiol terminated molecules on cobalt and gold surfaces

机译:钴和金表面硫醇封端分子的界面电子结构

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摘要

The bonding strength and interfacial electronic properties of biphenyldimethyldithiol (HS-CH2-C6H4-C6H4-CH2-SH) adsorbed on Au(111) and polycrystalline cobalt are identified from combined photoemission and inverse photoemission. In order to develop a better understanding of the thiol functional group to metal surface interaction, the stable orientation, bonding site, bonding strength and interfacial electronic properties of methylthiol (S-CH3) adsorbed on Au(111) and Co(0001) have been determined by ab initio density functional calculations. Both experiment and theory suggest that thiol bonding to cobalt surfaces is stronger compared to gold surfaces. The transfer of charge toward the adsorbed sulfur is greater for the thiols on cobalt than on gold.
机译:从组合的光发射和逆光发射确定了联苯基二甲基二硫醇(HS-CH2-C6H4-C6H4-CH2-SH)吸附在Au(111)和多晶钴上的结合强度和界面电子性能。为了更好地理解硫醇官能团与金属表面的相互作用,已经研究了吸附在Au(111)和Co(0001)上的甲硫醇(S-CH3)的稳定取向,键合部位,键合强度和界面电子性质。由头算密度函数计算确定。实验和理论均表明,与金表面相比,硫醇与钴表面的结合更牢固。钴上的硫醇比金上的电荷向吸附的硫的转移更大。

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