Vovusha Hakkim, Amorim Rodrigo G, Scheicher Ralph H, Sanyal Biplab
Division of Materials Theory, Department of Physics and Astronomy, Uppsala University Box 516 SE-751 20 Uppsala Sweden
RSC Adv. 2018 Feb 8;8(12):6527-6531. doi: 10.1039/c7ra11664k. eCollection 2018 Feb 6.
The interfaces in 2D hybrids of graphene and h-BN provide interesting possibilities of adsorbing and manipulating atomic and molecular entities. In this paper, with the aid of density functional theory, we demonstrate the adsorption characteristics of DNA nucleobases at different interfaces of 2D hybrid nanoflakes of graphene and h-BN. The interfaces provide stronger binding to the nucleobases in comparison to pure graphene and h-BN nanoflakes. It is also revealed that the individual dipole moments of the nucleobases and nanoflakes dictate the orientation of the nucleobases at the interfaces of the hybrid structures. The results of our study point towards a possible route to selectively control the orientation of individual molecules in biosensors.
石墨烯与六方氮化硼二维杂化材料中的界面为吸附和操控原子及分子实体提供了有趣的可能性。在本文中,借助密度泛函理论,我们展示了DNA核碱基在石墨烯与六方氮化硼二维杂化纳米片不同界面处的吸附特性。相较于纯石墨烯和六方氮化硼纳米片,这些界面与核碱基的结合更强。研究还表明,核碱基和纳米片的单个偶极矩决定了核碱基在杂化结构界面处的取向。我们的研究结果为在生物传感器中选择性控制单个分子的取向指明了一条可能的途径。