6 research outputs found
Theory of Polar Corrections to Donor Binding
We calculate the optical phonon correction to the binding energy of electrons
to donors in cubic materials. Previous theories calculated the Rydberg energy
reduced by the effective mass and the static dielectric function. They omitted
an important energy term from the long-range polarization of the ionized donor,
which vanishes for the neutral donor. They also omitted the donor-phonon
interaction. Including these terms yields a new formula for the donor binding
energy
Estados excitados de impurezas y propiedades colectivas en heteroestructuras semiconductoras
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Donor impurity in vertically-coupled quantum-dots under hydrostatic pressure and applied electric field
In this work we make a predictive study on the binding energy of the ground state for hydrogenic donor impurity in vertically-coupled quantum-dot structure, considering the combined effects of hydrostatic pressure and in growth-direction applied electric field. The approach uses a variational method within the effective mass approximation. The low dimensional structure consists of three cylindrical shaped GaAs quantum-dots, grown in the z-direction and separated by Ga1-xAlxAs barriers. In order to include the pressure dependent Γ – X crossover in the barrier material a phenomenological model is followed. The main findings can be summarized as follows: 1) for symmetrical and asymmetrical dimensions of the structures, the binding energy as a function of the impurity position along the growth direction of the heterostructure has a similar behavior to that shown by the non-correlated electron wave function with maxima for the impurity in the well regions and minima for the impurity in the barrier regions, 2) for increasing radius of the system, the binding energy decreases and for R large enough reaches the limit of the binding energy in a coupled quantum well heterostructure, 3) the binding energy increases for higher Aluminum concentration in the barrier regions, 4) depending of the impurity position and of the structural dimensions of the system (well width and barrier thickness) – and because changing the height of the potential barrier makes possible to induce changes in the degree of symmetry of the carrier-wave function –, the electric field and hydrostatic pressure can cause the impurity binding energy increases or decreases, and finally 5) the line-shape of the binding energy curves are mainly given by the line-shape of the Coulomb interaction.
Donor-impurity related binding energy and photoinization cross-section in quantum dots: electric and magnetic fields and hydrostatic pressure effects
We have studied the behavior of the binding energy and photoionization cross-section of a donor-impurity in cylindrical-shape GaAs-Ga0.7Al0.3As quantum dots, under the effects of hydrostatic pressure and in-growth direction applied electric and magnetic fields. We have used the variational method under the effective mass and parabolic band approximations. Parallel and perpendicular polarizations of the incident radiation and several values of the quantum dot geometry have also been considered. Our results show that the photoionization cross-section growths as the hydrostatic pressure is increased. For parallel polarization of the incident radiation, the photoionization cross-section decreases when the impurity is shifted from the center of the dot. In the case of perpendicular polarization of the incident radiation, the photoionization cross-section increases when the impurity is shifted in the radial direction of the dot. For on-axis impurities the transitions between the ground state of the impurity and the ground state of the quantum dot are forbidden. In the low pressure regime (less than 13.5 kbar) the impurity binding energy growths linearly with pressure, and in the high pressure regime (higher than 13.5 kbar) the binding energy growths up to a maximum and then decreases. Additionally, we have found that the applied electric and magnetic fields may favor the increase or decrease in binding energy, depending on the impurity position