1,821 research outputs found

    Exchange coupling between silicon donors: the crucial role of the central cell and mass anisotropy

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    Donors in silicon are now demonstrated as one of the leading candidates for implementing qubits and quantum information processing. Single qubit operations, measurements and long coherence times are firmly established, but progress on controlling two qubit interactions has been slower. One reason for this is that the inter donor exchange coupling has been predicted to oscillate with separation, making it hard to estimate in device designs. We present a multivalley effective mass theory of a donor pair in silicon, including both a central cell potential and the effective mass anisotropy intrinsic in the Si conduction band. We are able to accurately describe the single donor properties of valley-orbit coupling and the spatial extent of donor wave functions, highlighting the importance of fitting measured values of hyperfine coupling and the orbital energy of the 1s1s levels. Ours is a simple framework that can be applied flexibly to a range of experimental scenarios, but it is nonetheless able to provide fast and reliable predictions. We use it to estimate the exchange coupling between two donor electrons and we find a smoothing of its expected oscillations, and predict a monotonic dependence on separation if two donors are spaced precisely along the [100] direction.Comment: Published version. Corrected b and B values from previous versio

    Surface code architecture for donors and dots in silicon with imprecise and nonuniform qubit couplings

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    A scaled quantum computer with donor spins in silicon would benefit from a viable semiconductor framework and a strong inherent decoupling of the qubits from the noisy environment. Coupling neighbouring spins via the natural exchange interaction according to current designs requires gate control structures with extremely small length scales. We present a silicon architecture where bismuth donors with long coherence times are coupled to electrons that can shuttle between adjacent quantum dots, thus relaxing the pitch requirements and allowing space between donors for classical control devices. An adiabatic SWAP operation within each donor/dot pair solves the scalability issues intrinsic to exchange-based two-qubit gates, as it does not rely on sub-nanometer precision in donor placement and is robust against noise in the control fields. We use this SWAP together with well established global microwave Rabi pulses and parallel electron shuttling to construct a surface code that needs minimal, feasible local control.Comment: Published version - more detailed discussions, robustness to dephasing pointed out additionall

    Livestock and livelihoods in the IGAD region: A policy and institutional analysis

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    Including livestock in the CAADP compacts: A framework for analysis for CAADP country teams

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    The livestock sector in the CAADP compacts: Evidence from IGAD countries. Review paper

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    G_2 gauge theory at finite temperature

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    The gauge group being centreless, G2G_2 gauge theory is a good laboratory for studying the role of the centre of the group for colour confinement in Yang-Mills gauge theories. In this paper, we investigate G2G_2 pure gauge theory at finite temperature on the lattice. By studying the finite size scaling of the plaquette, the Polyakov loop and their susceptibilities, we show that a deconfinement phase transition takes place. The analysis of the pseudocritical exponents give strong evidence of the deconfinement transition being first order. Implications of our findings for scenarios of colour confinement are discussed.Comment: 17 pages, 8 figure

    Praziquantel: its use in control of schistosomiasis in sub-Saharan Africa and current research needs

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    Treatment with praziquantel (PZQ) has become virtually the sole basis of schistosomiasis control in sub-Saharan Africa and elsewhere, and the drug is reviewed here in the context of the increasing rate that it is being used for this purpose. Attention is drawn to our relative lack of knowledge about the mechanisms of action of PZQ at the molecular level, the need for more work to be done on schistosome isolates that have been collected recently from endemic areas rather than those maintained in laboratory conditions for long periods, and our reliance for experimental work mainly on Schistosoma mansoni, little work having been done on S. haematobium. There is no evidence that resistance to PZQ has been induced in African schistosomes as a result of its large-scale use on that continent to date, but there is also no assurance that PZQ and/or schistosomes are in any way unique and that resistant organisms will not be selected as a result of widespread drug usage. The failure of PZQ to produce complete cures in populations given a routine treatment should therefore solicit considerable concern. With few alternatives to PZQ currently available and/or on the horizon, methods to monitor drug-susceptibility in African schistosomes need to be devised and used to help ensure that this drug remains effective for as long a time as possibl
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