Interaction of H2 with a Double-Walled Armchair Nanotube by First-Principles Calculations

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• 作者：Francesca Costanzo ; Bernd Ensing ; Roberto Scipioni ; Francesco Ancilotto ; Pier Luigi Silvestrelli
• 刊名：Journal of Physical Chemistry C
• 出版年：2014
• 出版时间：July 24, 2014
• 年：2014
• 卷：118
• 期：29
• 页码：15816-15824
• 全文大小：458K
• ISSN：1932-7455

文摘

We have studied, by first-principles methods, the interaction of molecular hydrogen with a double-walled (2,10) carbon nanotube (DWCNT). This combination of the smallest possible diameter for the inner nanotube with a significantly larger outer tube allows for substantial space between the nanotube walls, in which molecular hydrogen can adsorb. We performed classical force field molecular dynamics simulations of the infinitely extended (periodic) DWCNT with varying amounts of hydrogen, which showed that, depending on the H₂ loading, both a coaxial and a noncoaxial DWCNT configuration can be stable. We then carried out the electronic structure calculations on both the coaxial and the noncoaxial geometries of the nanotubes to accurately compute the H₂ adsorption pathways inside the DWCNT. Interestingly, the noncoaxial DWCNT (2,10) shows a barrierless reaction path to dissociate the H₂ molecule. We also investigated the case of a DWCNT of finite length, whose edges are either clean or terminated with H atoms, and we searched for the favorite adsorption sites for a H₂ molecule in the interstitial region between the inner and the outer tube. The finite DWCNT whose edges are passivated by H atoms can be suggested as a potential candidate for hydrogen storage. The H₂ molecules, in fact, may enter in the cavity between the two nanotubes without reacting with the dangling bonds of the C atoms and can be physisorbed with a binding energy of about 0.06 eV, suitable for hydrogen storage. We emphasize the important role played in the physisorbed states for all the systems studied by the van der Waals interactions, which are properly included in the present study. Compared to the interaction of H₂ with graphene and the single-walled carbon nanotube (SWCNT), the existence of another carbon layer, for the coaxial DWCNT, does not significantly lower the energy barriers for chemisorption and instead enhances the binding energy of the H₂ molecule to the inner tube up to 0.1 eV.