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Atomic-scale insights into the interfacial instability of superlubricity in hydrogenated amorphous carbon films

机译:氢化非晶碳膜中超润滑性界面不稳定性的原子尺见解

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摘要

The origin of instability or even disappearance of the superlubricity state in hydrogenated amorphous carbon (a-C:H) film in the presence of oxygen or water molecules is still controversial. Here, we address this puzzle regarding the tribochemical activities of sliding interfaces at the nanoscale. The results reveal that gaseous oxygen molecules disable the antifriction capacity of a-C:H by surface dehydrogenation of tribo-affected hydrocarbon bonds. In comparison, oxygen incorporation into the hydrocarbon matrix induces the formation of a low-density surface shear band, owing to which the friction state depends on the oxygen content. High friction of a-C:H film in humid environment originates from the “tumor-like” heterogeneous structures as formed in the highly oxidized tribolayer. Notably, an appropriate doping of silicon can completely shield the moisture effect by forming a silica-like tribolayer. These outcomes shed substantial lights upon the roadmap for achieving robust superlubricity of carbon films in a wide range of environments.
机译:在氧气或水分子存在下氢化无定形碳(A-C:H)膜中超润滑性状态的不稳定性甚至消失的起源仍然存在争议。在这里,我们解决了纳米级滑动接口的效果的拼图。结果表明,气态氧分子通过摩擦影响的烃键的表面脱氢禁用A-C:H的抗抗率能力。相比之下,氧气掺入烃基诱导低密度表面剪切带的形成,因为摩擦态取决于氧含量。潮湿环境中A-C:H膜的高摩擦源自高度氧化的Tryolayer中形成的“肿瘤样”异质结构。值得注意的是,硅的适当掺杂可以通过形成二氧化硅样Tribolayer来完全屏蔽湿气效果。这些结果在宽敞的环境中实现了在路线图上实现了大量的灯光,以实现各种环境中的碳膜的高级润滑性。

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