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在Triton X-100/水体系的六方溶致液晶相中制备的金表面烷硫醇自组装单分子层。

Self-assembled monolayers of alkanethiols on gold prepared in a hexagonal lyotropic liquid crystalline phase of Triton X-100/water system.

作者信息

Ganesh V, Lakshminarayanan V

机构信息

Raman Research Institute, C.V. Raman Avenue, Sadashivanagar, Bangalore-560080, India.

出版信息

Langmuir. 2006 Feb 14;22(4):1561-70. doi: 10.1021/la0519296.

Abstract

In this paper, we have reported a new method of preparing self-assembled monolayers (SAMs) of decanethiol and hexadecanethiol on gold surface by using a lyotropic liquid crystalline phase as an adsorbing medium. The stability and blocking ability of these SAMs were characterized using grazing angle Fourier transform infrared (FTIR) spectroscopy and electrochemical techniques such as cyclic voltammetry and electrochemical impedance spectroscopy. The lyotropic liquid crystalline medium possesses a hexagonal structure consisting of a nonionic surfactant Triton X-100, water, and the corresponding thiol, which provides a highly hydrophobic environment to solubilize the alkanethiols and later to facilitate their delivery to the gold surface. We find that the SAMs formed from the hexagonal liquid crystalline phase are highly compact and have excellent electrochemical blocking ability towards the redox probes compared to conventional SAMs prepared from commonly used organic solvents such as ethanol. From the impedance studies, we have determined the capacitance of the monolayer-coated electrodes and the surface coverage of the SAM, which has been found to be >99.98% on gold surface. We have also estimated the extent of ionic permeability through the film and measured the rate constants for the redox reactions on the SAM-modified electrodes. Our results show that the rate constants of Fe(CN)6 and Ru(NH3)6 redox couples are very much lower in the case of monolayers prepared in liquid crystalline phase compared to the SAM formed in 1 mM thiol in ethanol solution, suggesting a better blocking ability of the SAMs in the former case. From the grazing angle FTIR spectroscopic studies and capacitance measurements, we have ruled out any coadsorption of surfactant molecules on the Au surface. These results suggest that SAMs of very low defect density and extremely low ionic permeability can be obtained when a hexagonal lyotropic liquid crystalline phase is used as an adsorbing medium.

摘要

在本文中,我们报道了一种以溶致液晶相作为吸附介质,在金表面制备癸硫醇和十六烷硫醇自组装单分子层(SAMs)的新方法。使用掠角傅里叶变换红外(FTIR)光谱以及循环伏安法和电化学阻抗谱等电化学技术对这些SAMs的稳定性和阻挡能力进行了表征。溶致液晶介质具有由非离子表面活性剂吐温X-100、水和相应的硫醇组成的六方结构,它提供了一个高度疏水的环境来溶解链烷硫醇,并随后促进它们传递到金表面。我们发现,与由乙醇等常用有机溶剂制备的传统SAMs相比,由六方液晶相形成的SAMs高度致密,对氧化还原探针具有优异的电化学阻挡能力。通过阻抗研究,我们确定了单层包覆电极的电容和SAM的表面覆盖率,发现在金表面其表面覆盖率>99.98%。我们还估计了离子透过膜的程度,并测量了SAM修饰电极上氧化还原反应的速率常数。我们的结果表明,与在乙醇溶液中1 mM硫醇中形成的SAM相比,在液晶相中制备的单层中Fe(CN)6Ru(NH3)6氧化还原对的速率常数要低得多,这表明在前一种情况下SAMs具有更好的阻挡能力。通过掠角FTIR光谱研究和电容测量,我们排除了表面活性剂分子在金表面的任何共吸附。这些结果表明,当使用六方溶致液晶相作为吸附介质时,可以获得缺陷密度非常低且离子渗透性极低的SAMs。

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