Blass Johanna, Albrecht Marcel, Bozna Bianca L, Wenz Gerhard, Bennewitz Roland
INM - Leibniz Institute of New Materials, Campus D2 2, Saarland University, 66123 Saarbrücken, Germany.
Nanoscale. 2015 May 7;7(17):7674-81. doi: 10.1039/c5nr00329f.
We introduce a molecular toolkit for studying the dynamics in friction and adhesion from the single molecule level to effects of multivalency. As experimental model system we use supramolecular bonds established by the inclusion of ditopic adamantane connector molecules into two surface-bound cyclodextrin molecules, attached to a tip of an atomic force microscope (AFM) and to a flat silicon surface. The rupture force of a single bond does not depend on the pulling rate, indicating that the fast complexation kinetics of adamantane and cyclodextrin are probed in thermal equilibrium. In contrast, the pull-off force for a group of supramolecular bonds depends on the unloading rate revealing a non-equilibrium situation, an effect discussed as the combined action of multivalency and cantilever inertia effects. Friction forces exhibit a stick-slip characteristic which is explained by the cooperative rupture of groups of host-guest bonds and their rebinding. No dependence of friction on the sliding velocity has been observed in the accessible range of velocities due to fast rebinding and the negligible delay of cantilever response in AFM lateral force measurements.
我们介绍了一种分子工具包,用于研究从单分子水平到多价效应的摩擦和粘附动力学。作为实验模型系统,我们使用通过将双位金刚烷连接分子包含到两个表面结合的环糊精分子中建立的超分子键,这两个环糊精分子分别连接到原子力显微镜(AFM)的尖端和平坦的硅表面。单个键的断裂力不取决于拉伸速率,这表明在热平衡状态下探测到了金刚烷和环糊精的快速络合动力学。相比之下,一组超分子键的拉脱力取决于卸载速率,揭示了一种非平衡情况,这种效应被认为是多价效应和悬臂惯性效应的综合作用。摩擦力表现出粘滑特性,这可以通过主客体键组的协同断裂及其重新结合来解释。由于快速重新结合以及AFM侧向力测量中悬臂响应的延迟可忽略不计,在可达到的速度范围内未观察到摩擦力对滑动速度的依赖性。