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Gas-Phase Lubrication of ta-C by Glycerol and Hydrogen Peroxide. Experimental and Computer Modeling

机译:甘油和过氧化氢的ta-C气相润滑。实验与计算机建模

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摘要

Tetrahedrally coordinated hydrogen-free amorphous diamond-like carbon coating (denoted as ta-C) presents ultralow friction under boundary lubrication conditions at 80 °C in presence of OH-containing molecules. To understand the mechanism of ultralow friction, we performed gas-phase lubrication experiments followed by time-of-flight secondary ion mass spectrometry (ToF-SIMS) analyses and this using two simple molecules: deuterated glycerol and hydrogen peroxide. The experiments were complemented by computer simulations using the ReaxFF reactive force field. These simulations suggest a ta-C surface rich in sp^2 carbon with some reactive sp^1 carbon atoms, in agreement with previous energy filtered transmission electron microscopy (EFTEM) results. Sliding simulations show that the carbon surface atoms react with glycerol and hydrogen peroxide to form OH-termination. Moreover, the hydroxylation is then followed by the chemical dissociation of some of the glycerol molecules leading to the formation of water. This is in agreement with the secondary ion mass spectrometry (SIMS) analyses and mass spectrometer results obtained with gas-phase lubrication experiments with the same molecules. Both experimental and computer simulations strongly suggest that the hydroxylation of the carbon surface is at the origin of ultralow friction together with the formation of water-rich film in the sliding interface.
机译:四面配位的无氢无定形类金刚石碳涂层(表示为ta-C)在边界润滑条件下,在80°C且存在含OH的分子的情况下表现出超低摩擦。为了了解超低摩擦的机理,我们进行了气相润滑实验,然后进行了飞行时间二次离子质谱(ToF-SIMS)分析,并使用两个简单分子进行了分析:氘代甘油和过氧化氢。使用ReaxFF反作用力场的计算机模拟对实验进行了补充。这些模拟表明,富含sp ^ 2碳和一些反应性sp ^ 1碳原子的ta-C表面与先前的能量过滤透射电子显微镜(EFTEM)结果一致。滑动模拟显示碳表面原子与甘油和过氧化氢反应形成OH端基。而且,羟基化之后是一些甘油分子的化学离解,从而导致水的形成。这与通过相同分子的气相润滑实验获得的二次离子质谱(SIMS)分析和质谱仪结果一致。实验和计算机模拟都强烈表明,碳表面的羟基化是超低摩擦的起源,同时在滑动界面上形成了富水膜。

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