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Register a new userSoliton Trap in Strained Graphene Nanoribbons
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The wavefunction of a massless fermion consists of two chiralities, left-handed and right-handed, which are eigenstates of the chiral operator. The theory of weak interactions of elementally particle physics is not symmetric about the two chiralities, and such a symmetry breaking theory is referred to as a chiral gauge theory. The chiral gauge theory can be applied to the massless Dirac particles of graphene. In this paper we show within the framework of the chiral gauge theory for graphene that a topological soliton exists near the boundary of a graphene nanoribbon in the presence of a strain. This soliton is a zero-energy state connecting two chiralities and is an elementally excitation transporting a pseudospin. The soliton should be observable by means of a scanning tunneling microscopy experiment.
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We report the experimental observation of conductance quantization in graphene nanoribbons, where 1D transport subbands are formed due to the lateral quantum confinement. We show that this quantization in graphene nanoribbons can be observed at temperatures as high as 80 K and channel lengths as long as 1.7 $mu$m. The observed quantization is in agreement with that predicted by theoretical calculations.
A theoretical study of the transport properties of zigzag and armchair graphene nanoribbons with a magnetic barrier on top is presented. The magnetic barrier modifies the energy spectrum of the nanoribbons locally, which results in an energy shift of the conductance steps towards higher energies. The magnetic barrier also induces Fabry-Perot type oscillations, provided the edges of the barrier are sufficiently sharp. The lowest propagating state present in zigzag and metallic armchair nanoribbons prevent confinement of the charge carriers by the magnetic barrier. Disordered edges in nanoribbons tend to localize the lowest propagating state, which get delocalized in the magnetic barrier region. Thus, in sharp contrast to the case of two-dimensional graphene, the charge carriers in graphene nanoribbons cannot be confined by magnetic barriers. We also present a novel method based on the Greens function technique for the calculation of the magnetosubband structure, Bloch states and magnetoconductance of the graphene nanoribbons in a perpendicular magnetic field. Utilization of this method greatly facilitates the conductance calculations, because, in contrast to excising methods, the present method does not require self-consistent calculations for the surface Greens function.
The paper presents a theoretical description of the effects of strain induced by out-of-plane deformations on charge distributions and transport on graphene. A review of a continuum model for electrons using the Dirac formalism is complemented with elasticity theory to represent strain fields. The resulting model is cast in terms of scalar and pseudo-magnetic fields that control electron dynamics. Two distinct geometries, a bubble, and a fold are chosen to represent the most commonly observed deformations in experimental settings. It is shown that local charge accumulation regions appear in deformed areas, with a peculiar charge distribution that favors the occupation of one sublattice only. This unique phenomenon that allows distinguishing each carbon atom in the unit cell, is the manifestation of a sublattice symmetry broken phase. For specific parameters, resonant states appear in localized charged regions, as shown by the emergence of discrete levels in band structure calculations. These findings are presented in terms of intuitive pictures that exploit analogies with confinement produced by square barriers. In addition, electron currents through strained regions are spatially separated into their valley components, making possible the manipulation of electrons with different valley indices. The degree of valley filtering (or polarization) for a specific system can be controlled by properly designing the strained area. The comparison between efficiencies of filters built with this type of geometries identifies extended deformations as better valley filters. A proposal for their experimental implementations as a component of devices and a discussion for potential observation of novel physics in strained structures are presented at the end of the article.
Strain fold-like deformations on armchair graphene nanoribbons (AGNRs) can be properly engineered in experimental setups, and could lead to a new controlling tool for gaps and transport properties. Here, we analyze the electronic properties of folded AGNRs relating the electronic responses and the mechanical deformation. An important and universal parameter for the gap engineering is the ribbon percent width variation, i.e., the difference between the deformed and undeformed ribbon widths. AGNRs bandgap can be tuned mechanically in a well defined bounded range of energy values, eventually leading to a metallic system. This characteristic provides a new controllable degree of freedom that allows manipulation of electronic currents. We show that the numerical results are analytically predicted by solving the Dirac equation for the strained system.
We theoretically study the strain effect on the Casimir interactions in graphene based systems. We found that the interactions between two strained graphene sheets are strongly dependent on the direction of stretching. The influence of the strain on the dispersion interactions is still strong in the presence of dielectric substrates but is relatively weak when the substrate is metallic. Our studies would suggest new ways to design next generation devices.
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