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Hydration force in the atomic force microscope: A computational study.

机译:原子力显微镜中的水合力:一项计算研究。

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摘要

Using a hard sphere model and numerical calculations, the effect of the hydration force between a conical tip and a flat surface in the atomic force microscope (AFM) is examined. The numerical results show that the hydration force remains oscillatory, even down to a tip apex of a single water molecule, but its lateral extent is limited to a size of a few water molecules. In general, the contribution of the hydration force is relatively small, but, given the small imaging force ( approximately 0.1 nN) typically used for biological specimens, a layer of water molecules is likely to remain "bound" to the specimen surface. This water layer, between the tip and specimen, could act as a "lubricant" to reduce lateral force, and thus could be one of the reasons for the remarkably high resolution achieved with contact-mode AFM. To disrupt this layer, and to have a true tip-sample contact, a probe force of several nanonewtons would be required. The numerical results also show that the ultimate apex of the tip will determine the magnitude of the hydration force, but that the averaged hydration pressure is independent of the radius of curvature. This latter conclusion suggests that there should be no penalty for the use of sharper tips if hydration force is the dominant interaction between the tip and the specimen, which might be realizable under certain conditions. Furthermore, the calculated hydration energy near the specimen surface compares well with experimentally determined values with an atomic force microscope, providing further support to the validity of these calculations.
机译:使用硬球模型和数值计算,在原子力显微镜(AFM)中检查了锥形尖端和平坦表面之间的水合力的影响。数值结果表明,水化力保持振荡,甚至下降到单个水分子的顶端,但其横向范围仅限于几个水分子的大小。通常,水合力的贡献相对较小,但是,鉴于通常用于生物样本的成像力较小(约0.1 nN),水分子层很可能会保持与样本表面的“结合”。尖端和样本之间的水层可以充当“润滑剂”以减小横向力,因此可能是采用接触模式AFM获得极高分辨率的原因之一。为了破坏该层并具有真正的尖端-样品接触,将需要几纳牛顿的探测力。数值结果还表明,尖端的最终顶点将确定水合力的大小,但平均水合压力与曲率半径无关。后一个结论表明,如果水合力是尖端与样品之间的主要相互作用,则在使用尖锐尖端时不应受到任何惩罚,这在某些条件下是可以实现的。此外,计算出的样品表面附近的水合能与原子力显微镜实验确定的值相比较,为这些计算的有效性提供了进一步的支持。

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