Qubit coherence control in a nuclear spin bath

Coherent dynamics of localized spins in semiconductors is limited by spectral diffusion arising from dipolar fluctuation of lattice nuclear spins. Here we extend the semiclassical theory of spectral diffusion for nuclear spins I=1/2 to the high nuclear spins relevant to the III-V materials and show that applying successive qubit pi-rotations at a rate approximately proportional to the nuclear spin quantum number squared (I^2) provides an efficient method for coherence enhancement. Hence robust coherent manipulation in the large spin environments characteristic of the III-V compounds is possible without resorting to nuclear spin polarization, provided that the pi-pulses can be generated at intervals scaling as I^{-2}

Quantum theory for electron spin decoherence induced by nuclear spin dynamics in semiconductor quantum computer architectures: Spectral diffusion of localized electron spins in the nuclear solid-state environment

We consider the decoherence of a single localized electron spin due to its coupling to the lattice nuclear spin bath in a semiconductor quantum computer architecture. In the presence of an external magnetic field and at low temperatures, the dominant decoherence mechanism is the spectral diffusion of the electron spin resonance frequency due to the temporally fluctuating random magnetic field associated with the dipolar interaction induced flip-flops of nuclear spin pairs. The electron spin dephasing due to this random magnetic field depends intricately on the quantum dynamics of the nuclear spin bath, making the coupled decoherence problem difficult to solve. We provide a formally exact solution of this non-Markovian quantum decoherence problem which numerically calculates accurate spin decoherence at short times, which is of particular relevance in solid-state spin quantum computer architectures. A quantum cluster expansion method is developed, motivated, and tested for the problem of localized electron spin decoherence due to dipolar fluctuations of lattice nuclear spins. The method is presented with enough generality for possible application to other types of spin decoherence problems. We present numerical results which are in quantitative agreement with electron spin echo measurements in phosphorus doped silicon. We also present spin echo decay results for quantum dots in GaAs which differ qualitatively from that of the phosphorus doped silicon system. Our theoretical results provide the ultimate limit on the spin coherence (at least, as characterized by Hahn spin echo measurements) of localized electrons in semiconductors in the low temperature and the moderate to high magnetic field regime of interest in scalable semiconductor quantum computer architectures.Comment: 23 pages, 15 figure

Wavefunction considerations for the central spin decoherence problem in a nuclear spin bath

Decoherence of a localized electron spin in a solid state material (the ``central spin'' problem) at low temperature is believed to be dominated by interactions with nuclear spins in the lattice. This decoherence is partially suppressed through the application of a large magnetic field that splits the energy levels of the electron spin and prevents depolarization. However, dephasing decoherence resulting from a dynamical nuclear spin bath cannot be removed in this way. Fluctuations of the nuclear field lead to uncertainty of the electron's precessional frequency in a process known as spectral diffusion. This article considers the effect of the electron's wavefunction shape upon spectral diffusion and provides wavefunction dependent decoherence time formulas for free induction decay as well as spin echoes and concatenated dynamical decoupling schemes for enhancing coherence. We also discuss dephasing of a qubit encoded in singlet-triplet states of a double quantum dot. A central theoretical result of this work is the development of a continuum approximation for the spectral diffusion problem which we have applied to GaAs and InAs materials specifically

Electron spin coherence in metallofullerenes: Y, Sc and La@C82

Endohedral fullerenes encapsulating a spin-active atom or ion within a carbon cage offer a route to self-assembled arrays such as spin chains. In the case of metallofullerenes the charge transfer between the atom and the fullerene cage has been thought to limit the electron spin phase coherence time (T2) to the order of a few microseconds. We study electron spin relaxation in several species of metallofullerene as a function of temperature and solvent environment, yielding a maximum T2 in deuterated o-terphenyl greater than 200 microseconds for Y, Sc and La@C82. The mechanisms governing relaxation (T1, T2) arise from metal-cage vibrational modes, spin-orbit coupling and the nuclear spin environment. The T2 times are over 2 orders of magnitude longer than previously reported and consequently make metallofullerenes of interest in areas such as spin-labelling, spintronics and quantum computing.Comment: 5 pages, 4 figure

Environmental effects on electron spin relaxation in N@C60

We examine environmental effects of surrounding nuclear spins on the electron spin relaxation of the N@C60 molecule (which consists of a nitrogen atom at the centre of a fullerene cage). Using dilute solutions of N@C60 in regular and deuterated toluene, we observe and model the effect of translational diffusion of nuclear spins of the solvent molecules on the N@C60 electron spin relaxation times. We also study spin relaxation in frozen solutions of N@C60 in CS2, to which small quantities of a glassing agent, S2Cl2 are added. At low temperatures, spin relaxation is caused by spectral diffusion of surrounding nuclear 35Cl and 37Cl spins in the S2Cl2, but nevertheless, at 20 K, T2 times as long as 0.23 ms are observed.Comment: 7 pages, 6 figure

Self-ordered nanoporous lattice formed by chlorine atoms on Au(111)

A self-ordered nanoporous lattice formed by individual chlorine atoms on the Au(111) surface has been studied with low-temperature scanning tunneling microscopy, low-energy electron diffraction, and density functional theory calculations. We have found out that room-temperature adsorption of 0.09–0.30 monolayers of chlorine on Au(111) followed by cooling below 110 K results in the spontaneous formation of a nanoporous quasihexagonal structure with a periodicity of 25–38 Å depending on the initial chlorine coverage. The driving force of the superstructure formation is attributed to the substrate-mediated elastic interaction

Temperature dependence of the EPR linewidth of Yb3+ - ions in Y0.99Yb0.01Ba2Cu3OX compounds: Evidence for an anomaly near TC

Electron paramagnetic resonance experiments on doped Yb3+ ions in YBaCuO compounds with different oxygen contents have been made. We have observed the strong temperature dependence of the EPR linewidth in the all investigated samples caused by the Raman processes of spin-lattice relaxation. The spin-lattice relaxation rate anomaly revealed near TC in the superconducting species can be assigned to the phonon density spectrum changesComment: 10 pages, 4 figures Renewed versio