Enhanced reduction of graphene oxide by means of charging and electric fields applied to hydroxyl groups

We present a first-principles study of the effects of charging and perpendicular electric fields on hydroxyl groups, both of which mediate the reduction of graphene oxide through the formation of H2O and H 2O2. Starting with an investigation of the interaction between the hydroxyl groups and graphene, we determine the equilibrium binding geometry, binding energy, and the diffusion path with a minimum energy barrier and show that those equilibrium properties are strongly affected by external agents. While co-adsorbed H and O form bound OH, co-adsorbed H and OH in close proximity form H2O with almost no energy barrier. When negatively charged or subjected to a perpendicular electric field, the energy barrier between two OH co-adsorbed in close proximity is weakened or totally suppressed, forming an oxygen atom strongly bound at the bridge site, together with a water molecule. The water molecule by itself is very weakly bound to graphene and is prone to desorb from the surface, leading to the reduction of graphene oxide. It is therefore demonstrated that the reduction of graphene oxide is promoted to a large extent by negative charging or an applied perpendicular electric field, through the formation of weakly bound water molecules from hydroxyl groups. © 2013 IOP Publishing Ltd

Effects of charging and electric field on graphene functionalized with titanium

Titanium atoms are adsorbed to graphene with a significant binding energy and render diverse functionalities to it. Carrying out first-principles calculations, we investigated the effects of charging and static electric field on the physical and chemical properties of graphene covered by Ti adatoms. When uniformly Ti covered graphene is charged positively, its antiferromagnetic ground state changes to ferromagnetic metal and attains a permanent magnetic moment. Static electric field applied perpendicularly causes charge transfer between Ti and graphene, and can induce metal-insulator transition. While each Ti adatom adsorbed to graphene atom can hold four hydrogen molecules with a weak binding, these molecules can be released by charging or applying electric field perpendicularly. Hence, it is demonstrated that charging and applied static electric field induce quasi-continuous and side specific modifications in the charge distribution and potential energy of adatoms absorbed to single-layer nanostructures, resulting in fundamentally crucial effects on their physical and chemical properties. © 2013 IOP Publishing Ltd

Effects of charging and electric field on graphene oxide

We present a first-principles study of various effects of charging and electric field on the oxidation/deoxidation of graphene oxide consisting of only epoxy groups. We first determined the proper basis set, which hinders the spurious spilling of electrons of graphene oxide when negatively charged or exerted by perpendicular electric field, and treated with periodic boundary conditions. We then showed that the electric field perpendicularly applied to graphene surface provide side-specific functionalization. We found that the bonds between oxygen and graphene are weakened under applied electric field. For specific values of excess charge or electric field, an oxygen atom that is normally adsorbed to the bridge site in equilibrium moves to the top site. By directly charging and/or by applying electric field, one can monitor this migration as well as desorption of the oxygen adatom. In spite of the negative formation energy, an energy barrier prevents individually adsorbed oxygen atoms from forming oxygen molecules. This energy barrier is dramatically weakened upon negative charging or exertion of an electric field. Our results explain why the reduction of graphene oxide can be facilitated by these external effects. © 2013 American Chemical Society

Tunable dynamics of a flake on graphene: Libration frequency

In this paper we investigated the interaction between a graphene nanoflake anchored to the 2D graphene monolayer. This interaction is attractive but weak and is capable of setting a well defined registry in equilibrium. Rotational and linear displacements from equilibrium registry generate restoring forces, which can be controlled by external agents. Similar flakes can be self-assembled and can also execute simple harmonic motion as if a physical pendulum. Oscillation of a nanoflake about their equilibrium registries resulting in a characteristic libration frequency is predicted. This frequency depends on the size and geometry of the flake. Moreover, the libration frequency, as well as the electronic and magnetic properties of the flake+monolayer systems, can be tuned by a foreign molecule anchored to the flake, by electric charging and applied parallel and perpendicular electric and magnetic fields. When the sliding of the flake is combined with rotation, the friction force can be reduced dramatically. It is surprising that weak interaction can offer such features at nanoscale, which may offer potential applications. Our predictions are obtained by first-principles calculations based on density functional theory. © 2017 American Physical Society