Interactions between a H2 Molecule and Carbon Nanostructures: A DFT Study

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Dominik Gehringer¹  David Holec¹  MaximN. Popov²  Thomas Dengg² 

[1] Department of Materials Science, Montanuniversität Leoben, Franz-Josef-Straße 18, A-8700 Leoben, Austria;Materials Center Leoben Forschung GmbH, Roseggerstraße 12, A-8700 Leoben, Austria;

关键词: hydrogen storage;    physisorption;    density functional theory;    van der waals correction;    carbon nanostructures;    defects;   

DOI  :  10.3390/c6010016

来源: DOAJ

【 摘 要 】

On a long path of finding appropriate materials to store hydrogen, graphene and carbon nanotubes have drawn a lot of attention as potential storage materials. Their advantages lie at hand since those materials provide a large surface area (which can be used for physisorption), are cheap compared to metal hydrides, are abundant nearly everywhere, and most importantly, can increase safety to existing storage solutions. Therefore, a great variety of theoretical studies were employed to study those materials. After a benchmark study of different van-der-Waals corrections to Generalized Gradient Approximation (GGA), the present Density Functional Theory (DFT) study employs Tkatchenko−Scheffler (TS) correction to study the influence of vacancy and Stone−Wales defects in graphene on the physisorption of the hydrogen molecule. Furthermore, we investigate a large-angle (1,0) grain boundary as well as the adsorption behaviour of Penta-Octa-Penta (POP)-graphene.

【 授权许可】

Unknown