Large-scale atomistic density functional theory calculations of phosphorus-doped silicon quantum bits
- Author(s): Greenman, L;
- Whitley, HD;
- Whaley, KB
- et al.
Published Web Locationhttps://doi.org/10.1103/PhysRevB.88.165102
We present density functional theory calculations of phosphorus dopants in bulk silicon and of several properties relating to their use as spin qubits for quantum computation. Rather than a mixed pseudopotential or a Heitler-London approach, we have used an explicit treatment for the phosphorus donor and examined the detailed electronic structure of the system as a function of the isotropic doping fraction, including lattice relaxation due to the presence of the impurity. Doping electron densities (ρdoped- ρbulk) and spin densities (ρ↑- ρ↓) are examined in order to study the properties of the dopant electron as a function of the isotropic doping fraction. Doping potentials (Vdoped-Vbulk) are also calculated for use in calculations of the scattering cross sections of the phosphorus dopants, which are important in the understanding of electrically detected magnetic resonance experiments. We find that the electron density around the dopant leads to nonspherical features in the doping potentials, such as trigonal lobes in the (001) plane at energy scales of +12 eV near the nucleus and of -700 meV extending away from the dopants. These features are generally neglected in effective mass theory and will affect the coupling between the donor electron and the phosphorus nucleus. Our density functional calculations reveal detail in the densities and potentials of the dopants which are not evident in calculations that do not include explicit treatment of the phosphorus donor atom and relaxation of the crystal lattice. These details can also be used to parametrize tight-binding models for simulation of large-scale devices. © 2013 American Physical Society.