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Strength by atomic force microscopy (AFM): Molecular dynamics of water layer squeezing on magnesium oxide

机译:原子力显微镜(AFM)的强度:氧化镁上水层挤压的分子动力学

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摘要

Localised strength testing of materials is often carried out in an atomic force microscope (AFM), as foreseen by Kelly in his book Strong Solids (Clarendon Press, Oxford, 1966). During AFM indentation experiments, contamination can strongly influence the observed strength and theoretical interpretation of the results is a major problem. Here, we use molecular dynamics computer modelling to describe the contact of NaCl and MgO crystal probes onto surfaces, comparable to an AFM experiment. Clean NaCl gave elastic, brittle behaviour in contact simulations at 300 K, whereas MgO was more plastic, leading to increased toughness. This paper also considers the strength of an oxide substrate contaminated by water molecules and tested by indentation with a pyramidal probe of oxide crystal. Recent theory on the effect of liquid contaminant layers on surface strength has been mainly focussed on Lennard Jones (LJ) molecules with some studies on alcohols and water, described by molecular dynamics, which allows the molecules to be squeezed out as the crystal lattice is deformed. In this work, we have focused on water by studying the forces between a magnesium oxide (MgO) atomic force microscope (AFM) probe and an MgO slab. Force versus separation has been plotted as the AFM probe was moved towards and away from the substrate. Simulation results showed that the water layers could be removed in steps, giving up to four force peaks. The last monolayer of water could not be squeezed out, even at pressures where MgO deformed plastically. Interestingly, with water present, strength was reduced, but more in tensile than compressive measurements. In conclusion, water contaminating the oxide surface in AFM strength testing is structured. Water layer squeezing removal can be predicted by molecular modelling, which may be verified by AFM experiments to show that water can influence the strength of perfect crystals at the nanometre scale.
机译:材料的局部强度测试通常是在原子力显微镜(AFM)中进行的,正如凯利(Kelly)在他的《坚固固体》(克拉伦登出版社,牛津,1966年)中所预见的那样。在原子力显微镜压痕实验中,污染会严重影响观察到的强度,结果的理论解释是一个主要问题。在这里,我们使用分子动力学计算机建模来描述NaCl和MgO晶体探针在表面上的接触,这与AFM实验相当。清洁的NaCl在300 K的接触模拟中具有弹性,脆性,而MgO更具塑性,从而提高了韧性。本文还考虑了被水分子污染并通过用金字塔形的氧化物晶体探针压痕测试的氧化物基质的强度。关于液体污染物层对表面强度影响的最新理论主要集中在Lennard Jones(LJ)分子上,并通过分子动力学描述了对醇和水的一些研究,该研究使分子在晶格变形时被挤出。 。在这项工作中,我们通过研究氧化镁(MgO)原子力显微镜(AFM)探针和MgO平板之间的力将重点放在水上。随着AFM探针移向和移离基材,绘制了力与分离的关系图。仿真结果表明,可以逐步去除水层,最多给出四个力峰。即使在MgO塑性变形的压力下,也无法挤出最后的单层水。有趣的是,在存在水的情况下,强度降低了,但是拉伸强度比压缩强度更大。总而言之,构成了在AFM强度测试中污染氧化物表面的水。水层挤压的去除可以通过分子建模来预测,这可以通过原子力显微镜实验验证,以表明水可以影响纳米级完美晶体的强度。

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  • 来源
    《Philosophical Magazine》 |2010年第32期|p.4117-4128|共12页
  • 作者单位

    a Chemical Engineering, University of Birmingham, Edgbaston, B15 2TT, UK b STFC, Daresbury Laboratory, Warrington, UK;

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