National Centre for Scientific Research "Demokritos", Institute of Nanoscience and Nanotechnology INN, 15310 Athens, Greece.
Molecules. 2022 Jan 31;27(3):956. doi: 10.3390/molecules27030956.
We use molecular dynamics to compute the free energy of carbon nanoparticles crossing a hydrophobic-hydrophilic interface. The simulations are performed on a biphasic system consisting of immiscible solvents (i.e., cyclohexane and water). We solvate a carbon nanoparticle into the cyclohexane layer and use a pull force to drive the nanoparticle into water, passing over the interface. Next, we accumulate a series of umbrella sampling simulations along the path of the nanoparticle and compute the solvation free energy with respect to the two solvents. We apply the method on three carbon nanoparticles (i.e., a carbon nanocone, a nanotube, and a graphene nanosheet). In addition, we record the water-accessible surface area of the nanoparticles during the umbrella simulations. Although we detect complete wetting of the external surface of the nanoparticles, the internal surface of the nanotube becomes partially wet, whereas that of the nanocone remains dry. This is due to the nanoconfinement of the particular nanoparticles, which shields the hydrophobic interactions encountered inside the pores. We show that cyclohexane molecules remain attached on the concave surface of the nanotube or the nanocone without being disturbed by the water molecules entering the cavity.
我们使用分子动力学来计算碳纳米粒子穿过疏水-亲水界面的自由能。模拟是在由不混溶溶剂(即环己烷和水)组成的双相系统上进行的。我们将碳纳米粒子溶解在环己烷层中,并使用拉力将纳米粒子驱入水中,越过界面。接下来,我们沿着纳米粒子的路径积累一系列伞状采样模拟,并相对于两种溶剂计算溶剂化自由能。我们将该方法应用于三个碳纳米粒子(即碳纳米角锥、纳米管和石墨烯纳米片)。此外,我们在伞状模拟过程中记录了纳米粒子的水可及表面积。尽管我们检测到纳米粒子的外表面完全被润湿,但纳米管的内表面部分润湿,而角锥的内表面仍然干燥。这是由于特定纳米粒子的纳米限制,它屏蔽了孔内遇到的疏水性相互作用。我们表明,环己烷分子附着在纳米管或角锥的凹面,而不会被进入腔的水分子干扰。