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链长和相态对自组装单分子层粘附/摩擦行为的综合影响。

Combined effect of chain length and phase state on adhesion/friction behavior of self-assembled monolayers.

作者信息

Lee Dae Ho, Oh Taebyoung, Cho Kilwon

机构信息

Department of Chemical Engineering, School of Environmental Science and Engineering, Polymer Research Institute, Pohang University of Science and Technology, Pohang 790-784, South Korea.

出版信息

J Phys Chem B. 2005 Jun 9;109(22):11301-6. doi: 10.1021/jp051232t.

Abstract

The combined effects of phase state and chain length on the adhesion and friction behavior of self-assembled monolayers (SAMs) are demonstrated using atomic force microscopy (AFM). The phase state of n-alkyltrichlorosilane monolayers of varying chain length (C-8, C-12, and C-18) was controlled by adjusting the preparation temperature. The adhesion forces and friction coefficients were observed to increase dramatically around the phase-transition temperature of each monolayer. The phase state effect was more prominent for the longer chain SAMs, which is attributed to the larger deformation volume associated with disordered monolayers. The adhesion/friction diagram for chain length effect with a wide range of phase states is successfully presented. This study reveals that the chain length effect on adhesion/friction can be correctly evaluated by examining the phase-state dependence of adhesion/friction behind the chain length effect.

摘要

利用原子力显微镜(AFM)证明了相态和链长对自组装单分子层(SAMs)粘附和摩擦行为的综合影响。通过调节制备温度来控制不同链长(C-8、C-12和C-18)的正烷基三氯硅烷单分子层的相态。观察到在每个单分子层的相变温度附近,粘附力和摩擦系数急剧增加。对于较长链的SAMs,相态效应更为显著,这归因于与无序单分子层相关的更大变形量。成功绘制了具有广泛相态的链长效应的粘附/摩擦图。这项研究表明,通过研究链长效应背后的粘附/摩擦的相态依赖性,可以正确评估链长对粘附/摩擦的影响。

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