Physical systems representing qubits typically have one or more accessible quantum states in addition to the two states that encode the qubit. We demonstrate that active involvement of such auxiliary states can be beneficial in constructing entangling two-qubit operations. We investigate the general case of two multi-state quantum systems coupled via a quantum resonator. The approach is illustrated with the examples of three systems: self-assembled InAs/GaAs quantum dots, NV-centers in diamond, and superconducting transmon qubits. Fidelities of the gate operations are calculated based on numerical simulations of each system.
We propose a fast, scalable all-optical design for arbitrary two-qubit operations for defect qubits in diamond (NV centers) and in silicon carbide, which are promising candidates for room temperature quantum computing. The interaction between qubits is carried out by microcavity photons. The approach uses constructive interference from higher energy excited states activated by optical control. In this approach the cavity mode remains off-resonance with the directly accessible optical transitions used for initialization and readout. All quantum operations are controlled by near-resonant narrow-bandwidth optical pulses. We perform full quantum numerical modeling of the proposed gates and show that high-fidelity operations can be obtained with realistic parameters.
We give the results of density functional calculations for graphene with a widely varying fluorine adsorptions. We give a systematic analysis of the adsorption energies, lattice constants, bulk modulus, bandgap openings, and magnetic properties. We find that a number of different adsorption geometries and a range of physical properties can occur for each adsorbate coverage. The systems are found to range from metallic to semiconducting with widely vary band gaps, and a number of interesting magnetic phases are found. We expect that many of these structures may occur in real materials systems. Further that a listing of the properties found here may help in determining what fluorinated graphenes are produced experimentally.
We propose a mechanism to control the interaction between adsorbates on graphene. The interaction between a pair of adsorbates---the change in adsorption energy of one adsorbate in the presence of another---is dominated by the interaction mediated by graphenes pi-electrons and has two distinct regimes. Ab initio density functional, numerical tight-binding, and analytical calculations are used to develop the theory. We demonstrate that the interaction can be tuned in a wide range by adjusting the adsorbate-graphene bonding or the chemical potential.
