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Modelling of non-contact atomic force microspy imaging of individual molecules on oxide surfaces

机译:氧化物表面上单个分子的非接触原子力显微镜成像建模

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We have modelled NC-AFM imaging of organic molecules adsorbed on the MgO(lOO) and TiO_2(1 10) surfaces, to study whether molecules adsorbed at well determined surface sites could serve as markers for chemical resolution of surface species and possible mechanisms of adsorption and manipulation of such molecules with NC-AFM tips. We calculated images of perfect MgO and TiO_2 surfaces and considered the adsorption of the formate ion and 3 - {4- [Tris-(3,5 -di-tert-butyl-phenyl)-methyl] -phenoxy} -propionic acid (C52H72O_3) at the MgO(lOO) and TiO_2(l 10) surfaces, respectively, using several types of oxide tip models. The results demonstrate that using adsorption of even small molecules, such as formate, for identifying surface chemical species in NC-AFM images may not be practical. The interaction of hydrocarbon molecules with perfect oxide surfaces is weak and their adsorption should be aided by attaching special anchoring groups. Flat molecules can be identified by their shape, but simultaneous atomic resolution inside the molecule and on the substrate under the same imaging conditions is not feasible.
机译:我们对吸附在MgO(100)和TiO_2(1 10)表面上的有机分子进行NC-AFM成像建模,以研究吸附在确定的表面位点上的分子是否可作为表面物种化学拆分的标记以及可能的吸附机理并使用NC-AFM尖端操作此类分子。我们计算了完美的MgO和TiO_2表面的图像,并考虑了甲酸离子和3- {4- [Tris-(3,5--二叔丁基-苯基)-甲基]-苯氧基}-丙酸(C52H72O_3)的吸附使用几种类型的氧化物针尖模型分别在MgO(100)和TiO_2(l 10)表面上生成)。结果表明,即使是小分子的吸附(例如甲酸盐),也不能用于识别NC-AFM图像中的表面化学物种。碳氢化合物分子与完美氧化物表面的相互作用较弱,应通过连接特殊的锚定基团来辅助其吸附。扁平分子可以通过其形状来识别,但是在相同成像条件下同时实现分子内部和衬底上原子的原子分辨是不可行的。

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