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A noninteracting quantum-dot array side coupled to a quantum wire is studied. Transport through the quantum wire is investigated by using a noninteracting Anderson tunneling Hamiltonian. The conductance at zero temperature develops an oscillating band with resonances and antiresonances due to constructive and destructive interference in the ballistic channel, respectively. Moreover, we have found an odd-even parity in the system, whose conductance vanishes for an odd number of quantum dots while it becomes 2e 2 /h for an even number. We established an explicit relation between this odd-even parity and the positions of the resonances and antiresonances of the conductivity with the spectrum of the isolated quantum-dot array.

In this article we study electronic transport through a triple quantum dot molecule attached in parallel to leads in presence of a magnetic flux. We have obtained analytical expressions of the linear conductance and density of states for the molecule in equilibrium at zero temperature.As a consequence of quantum interference, the conductance exhibits one Breit-Wigner and two

The electronic transport through a parallel double quantum-dot molecule attached asymmetrically to leads is studied under a magnetic field. We model the system by means of a non interacting twoimpurity Anderson Hamiltonian. We find that the conductance shows Fano and Dicke effects that can be controlled by the magnetic flux.

The electronic transport of a noninteracting quantum ring side-coupled to a quantum wire is studied via a single-band tunneling tight-binding Hamiltonian. We found that the system develops an oscillating band with antiresonances and resonances arising from the hybridization of the quasibound levels of the ring and the coupling to the quantum wire. The positions of the antiresonances correspond exactly to the electronic spectrum of the isolated ring. Moreover, for a uniform quantum ring the conductance and the persistent current density were found to exhibit a particular odd-even parity related with the ring-order. The effects of an in-plane electric field was also studied. This field shifts the electronic spectrum and damps the amplitude of the persistent current density. These features may be used to control externally the energy spectra and the amplitude of the persistent current.

The existence of bound states in the continuum was predicted at the dawn of quantum mechanics by von Neumann and Wigner. In this work we discuss the mechanism of formation of these exotic states and the feasibility to observe them experimentally in symmetrical heterostructures composed by segments of graphene ribbons with different widths forming a graphene quantum dot. We identify the existence of bound states in the continuum in these graphene quantum dot systems by means of local density of states and electronic conductance calculations.

We study the thermoelectric properties of rectangular graphene rings connected symmetrically or asymmetrically to the leads. A side-gate voltage applied across the ring allows for the precise control of the electric current flowing through the system. The transmission coefficient of the rings manifest Breit-Wigner line shapes and/or Fano line shapes, depending on the connection configuration, the width of nanoribbons forming the ring and the side-gate voltage. We find that the thermopower and the figure of merit are greatly enhanced when the chemical potential is tuned close to resonances. Such enhancement is even more pronounced in the vicinity of Fano-like antiresonances which can be induced by a side-gate voltage independently of the geometry. This opens a possibility to use the proposed device as a tunable thermoelectric generator.

In this work we address the effects on the conductance of graphene nanoribbons (GNRs) of organic molecules adsorbed at the ribbon edge. We studied the case of armchair and zigzag GNRs with quasi-one-dimensional side-attached molecules, such as linear poly-aromatic hydrocarbons and poly(para-phenylene). These nanostructures are described using a single-band tight-binding Hamiltonian and their electronic conductance and density of states are calculated within the Green's function formalism based on real-space renormalization techniques. We found that the conductance exhibits an even-odd parity effect as a function of the length of the attached molecules. Furthermore, the corresponding energy spectrum of the molecules can be obtained as a series of Fano antiresonances in the conductance of the system. The latter result suggests that GNRs can be used as a spectrograph sensor device.