Li Jiaxian, Lu Hangjun, Zhou Xiaoyan
College of Physics and Electronic Information Engineering, Zhejiang Normal University, Jinhua 321004, China.
Nanoscale. 2020 Jun 28;12(24):12801-12808. doi: 10.1039/d0nr01113d. Epub 2020 May 19.
We systematically investigate the effects of an axial electric field on the formation and decomposition of quasi-one-dimensional nitrogen gas hydrates within a single-walled carbon nanotube (SWNT) by using molecular dynamics (MD) simulations. We find that the nitrogen hydrate in the SWNT undergoes a series of structure phase transitions with increasing electric field. Corresponding to the structure transition, the nitrogen gas releases from the carbon nanotube in the electric field range of 1 V nm to 2 V nm. However, nitrogen molecules are trapped as guest molecules, forming a molecule wire, in the ice nanotube when the electric field is less than 1 V nm or larger than 2 V nm. Our simulations indicate that the nanotube is an excellent tiny gas tank that can be used to trap gas molecules and control their release triggered sensitively by electric signals. The key to this phenomenon is the change in orientations of water dipoles induced by the electric field, which leads to the structural change in the hydrogen-bonding network and the change in the diffusion coefficient of the water molecules. Our findings here may help understanding the mechanism of the electrorelease of gas from hydrates confined in the nanoscale space.
我们通过分子动力学(MD)模拟系统地研究了轴向电场对单壁碳纳米管(SWNT)内准一维氮气水合物形成和分解的影响。我们发现,随着电场增强,SWNT中的氮气水合物会经历一系列结构相变。对应于结构转变,在1 V/nm至2 V/nm的电场范围内,氮气从碳纳米管中释放出来。然而,当电场小于1 V/nm或大于2 V/nm时,氮分子作为客体分子被困在冰纳米管中,形成分子线。我们的模拟表明,纳米管是一个出色的微型储气罐,可用于捕获气体分子并控制其由电信号灵敏触发的释放。这一现象的关键在于电场引起的水偶极子取向变化,这导致氢键网络的结构变化以及水分子扩散系数的变化。我们在此的发现可能有助于理解纳米级空间中受限水合物气体电释放的机制。