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首页> 外文期刊>Nature Communications >Non-additivity of molecule-surface van der Waals potentials from force measurements
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Non-additivity of molecule-surface van der Waals potentials from force measurements

机译:力测量得出的分子表面范德华势的非可加性

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Van der Waals (vdW) forces act ubiquitously in condensed matter. Despite being weak on an atomic level, they substantially influence molecular and biological systems due to their long range and system-size scaling. The difficulty to isolate and measure vdW forces on a single-molecule level causes our present understanding to be strongly theory based. Here we show measurements of the attractive potential between differently sized organic molecules and a metal surface using an atomic force microscope. Our choice of molecules and the large molecule-surface separation cause this attraction to be purely of vdW type. The experiment allows testing the asymptotic vdW force law and its validity range. We find a superlinear growth of the vdW attraction with molecular size, originating from the increased deconfinement of electrons in the molecules. Because such non-additive vdW contributions are not accounted for in most first-principles or empirical calculations, we suggest further development in that direction.
机译:范德华力(vdW)在凝聚态中无处不在。尽管它们在原子水平上很弱,但由于它们的射程远和系统尺寸大,它们在很大程度上影响分子和生物系统。在单分子水平上分离和测量vdW力的困难使我们目前的理解强烈地基于理论。在这里,我们显示了使用原子力显微镜对不同尺寸的有机分子与金属表面之间的吸引力进行测量的结果。我们对分子的选择以及大分子与表面的分离导致这种吸引作用完全是vdW类型的。该实验允许测试渐近vdW力定律及其有效范围。我们发现vdW引力随着分子大小的超线性增长,这是由于分子中电子的去约束度增加所致。由于在大多数第一原理或经验计算中都没有考虑到此类非加性的vdW贡献,因此我们建议朝该方向进一步发展。

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