Variable search for orientation, uniformly optimal search for identity.

This work was supported by the Economic and Social Research Council (ES/S016120/1 to Amelia R. Hunt, Principal Investigator, Alasdair D. F. Clarke Co-investigator). Additional support came from the James S. McDonnell Foundation (Scholar award to Amelia R. Hunt). The authors wish to extend their gratitude for the contribution of Jessica Christie, who collected and prepared the icon stimuli and collected the data for the first experiment. They also wish to thank Jacqueline von Seth for helping with piloting the experiments and additional data collection. Open Access funding provided by University of Leicester:Peer reviewe

Monitoring Entanglement Evolution and Collective Quantum Dynamics

We generalize a recently developed scheme for monitoring coherent quantum dynamics with good time-resolution and low backaction [Reuther et al., Phys. Rev. Lett. 102, 033602 (2009)] to the case of more complex quantum dynamics of one or several qubits. The underlying idea is to measure with lock-in techniques the response of the quantum system to a high-frequency ac field. We demonstrate that this scheme also allows one to observe quantum dynamics with many frequency scales, such as that of a qubit undergoing Landau-Zener transitions. Moreover, we propose how to measure the entanglement between two qubits as well as the collective dynamics of qubit arrays.Comment: 11 pages, 5 figure

Crystallographically oriented magnetic ZnFe2O4 nanoparticles synthesized by Fe implantation into ZnO

In this paper, a correlation between structural and magnetic properties of Fe implanted ZnO is presented. High fluence Fe^+ implantation into ZnO leads to the formation of superparamagnetic alpha-Fe nanoparticles. High vacuum annealing at 823 K results in the growth of alpha-Fe particles, but the annealing at 1073 K oxidized the majority of the Fe nanoparticles. After a long term annealing at 1073 K, crystallographically oriented ZnFe2O4 nanoparticles were formed inside ZnO with the orientation relationship of ZnFe2O4(111)[110]//ZnO(0001)[1120]. These ZnFe2O4 nanoparticles show a hysteretic behavior upon magnetization reversal at 5 K.Comment: 21 pages, 7 figures, accepted by J. Phys. D: Appl. Phy

Ground-state properties of the spin-1/2 antiferromagnetic Heisenberg model on the triangular lattice: A variational study based on entangled-plaquette states

We study, on the basis of the general entangled-plaquette variational ansatz, the ground-state properties of the spin-1/2 antiferromagnetic Heisenberg model on the triangular lattice. Our numerical estimates are in good agreement with available exact results and comparable, for large system sizes, to those computed via the best alternative numerical approaches, or by means of variational schemes based on specific (i.e., incorporating problem dependent terms) trial wave functions. The extrapolation to the thermodynamic limit of our results for lattices comprising up to N=324 spins yields an upper bound of the ground-state energy per site (in units of the exchange coupling) of $-0.5458(2)$ [$-0.4074(1)$ for the XX model], while the estimated infinite-lattice order parameter is $0.3178(5)$ (i.e., approximately 64% of the classical value).Comment: 8 pages, 3 tables, 2 figure

Investigation of molecular dimers by ensemble and single molecule spectroscopy

We have investigated molecular dimers with different electronic coupling strengths by bulk and single molecule spectroscopy. In one of the dimers the two monomers (perylene-monoimide) are directly connected via a single bond while in the other one they are separated by the benzil motif. The close proximity of the monomers in the first case gives rise to excitonic band splitting which is clearly observable in the bulk absorption spectra. For the benzil structure the electronic interactions are governed by Förster-type energy hopping between the monomers. Fluorescence intensity trajectories at the single molecule level show one-step and two-step bleaching behaviour which appears to be very similar for both dimers. However, emission spectra recorded simultaneously with the trajectories indicate spectral changes which allow to distinguish between weakly and strongly coupled dimers. In the latter case the spectral shape changes significantly when excitonic coupling has been lifted because of photochemical transformation of one of the monomers