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Interaction and UV-Stability of Various Organic Capping Agents on the Surface of Anatase Nanoparticles

机译:锐钛矿型纳米颗粒表面上各种有机封端剂的相互作用和紫外稳定性

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摘要

Anatase nanoparticles synthesized by the sol-gel method were surface-functionalized with long alkyl chain coupling agents as compatibilizers for a nonpolar environment, containing different anchor groups for surface interaction namely phosphonate (dodecyl phosphonate), carboxylate (dodecanoic acid), sulfate (sodium dodecyl sulphate), and amine (dodecyl amine). It was shown that the surface of the nanoparticles can be functionalized with the various surface groups applying similar reaction conditions. The kind of surface interaction was analyzed applying FTIR spectroscopy. The phosphonate and the carboxylate groups interact with the surface via quite strong covalent or coordinative interactions, respectively. The sulfate and amine based coupling agents on the other hand exhibit electrostatic interactions. UV stability studies of the surface bound groups revealed different degradation mechanisms for the various functionalities and moreover showed that phosphonates are the most stable among the investigated surface capping groups.
机译:通过溶胶-凝胶法合成的锐钛矿型纳米颗粒用长烷基链偶联剂作为非极性环境的增容剂进行表面官能化处理,其中包含用于表面相互作用的不同锚定基团,即膦酸酯(十二烷基膦酸酯),羧酸酯(十二烷酸),硫酸盐(十二烷基钠)硫酸盐)和胺(十二烷基胺)。结果表明,可以通过应用相似的反应条件的各种表面基团将纳米颗粒的表面官能化。使用FTIR光谱分析了表面相互作用的种类。膦酸酯基和羧酸酯基团分别通过相当强的共价或配位相互作用与表面相互作用。另一方面,基于硫酸盐和胺的偶联剂表现出静电相互作用。表面键合基团的紫外线稳定性研究揭示了各种官能团的降解机理不同,而且表明膦酸酯在所研究的表面封端基团中最稳定。

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