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Carboxylic acid anchoring groups for the construction of self-assembled monolayers on organic device electrodes

机译:羧酸锚固基团,用于在有机器件电极上构建自组装单层膜

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We have investigated the surface adsorption of carboxylic acid derivatives on both an aluminium cathode and an indium-tin oxide anode, commonly used in light emitting devices. For this purpose, a series of benzoic acids with systematically varying dipole moments were used to form self-assembled monolayers on these electrodes. The work function shifts induced by the adsorbed molecules were measured by the Kelvin probe method, while the surface densities of the adsorbed molecules were inferred from Langmuir isotherm measurements. It appeared that the work function shifts correlate linearly with the molecular dipole moment measured in the gas phase. Furthermore, the dipole moment which is formed upon adsorption depends crucially on the surface acido-basicity of the electrode. The difference of the adsorption dipoles on indium-tin oxide and aluminium is as high as 3.5 D indicating a very different binding mechanism in the two cases.
机译:我们已经研究了羧酸衍生物在铝阴极和铟锡氧化物阳极上的表面吸附,这些阴极通常用于发光器件中。为此,使用一系列具有系统变化的偶极矩的苯甲酸在这些电极上形成自组装单分子层。通过开尔文探针法测量由吸附的分子引起的功函数位移,而从Langmuir等温线测量推导吸附的分子的表面密度。似乎功函数位移与气相中测得的分子偶极矩线性相关。此外,由吸附形成的偶极矩主要取决于电极的表面酸碱度。铟锡氧化物和铝上吸附偶极子的差异高达3.5 D,表明这两种情况下的结合机理非常不同。

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