No Arabic abstract
NMR spin echo measurements of C-13 in C60, Y-89 in Y2O3, and Si-29 in silicon are shown to defy conventional expectations when more that one pi pulse is used. Multiple pi-pulse echo trains may either freeze our or accelerate the decay of the signal, depending on the pi-pulse phase. Average Hamiltonian theory, combined with exact quantum calculations, reveals an intrinsic cause for these coherent phenomena: the dipolar coupling has a many-body effect during any real, finite pulse.
This submission has been withdrawn by arXiv administrators because it is a duplicate of 0705.0667.
In spectroscopy, it is conventional to treat pulses much stronger than the linewidth as delta-functions. In NMR, this assumption leads to the prediction that pi pulses do not refocus the dipolar coupling. However, NMR spin echo measurements in dipolar solids defy these conventional expectations when more than one pi pulse is used. Observed effects include a long tail in the CPMG echo train for short delays between pi pulses, an even-odd asymmetry in the echo amplitudes for long delays, an unusual fingerprint pattern for intermediate delays, and a strong sensitivity to pi-pulse phase. Experiments that set limits on possible extrinsic causes for the phenomena are reported. We find that the action of the systems internal Hamiltonian during any real pulse is sufficient to cause the effects. Exact numerical calculations, combined with average Hamiltonian theory, identify novel terms that are sensitive to parameters such as pulse phase, dipolar coupling, and system size. Visualization of the entire density matrix shows a unique flow of quantum coherence from non-observable to observable channels when applying repeated pi pulses.
We present experimental observations and a study of quantum dynamics of strongly interacting electronic spins, at room temperature in the solid state. In a diamond substrate, a single nitrogen vacancy (NV) center coherently interacts with two adjacent S = 1/2 dark electron spins. We quantify NV-electron and electron-electron couplings via detailed spectroscopy, with good agreement to a model of strongly interacting spins. The electron-electron coupling enables an observation of coherent flip-flop dynamics between electronic spins in the solid state, which occur conditionally on the state of the NV. Finally, as a demonstration of coherent control, we selectively couple and transfer polarization between the NV and the pair of electron spins. These results demonstrate a key step towards full quantum control of electronic spin registers in room temperature solids.
Matter-wave interferometry with solids is highly susceptible to minute fluctuations of environmental fields, including gravitational effects from distant sources. Hence, experiments require a degree of shielding that is extraordinarily challenging to achieve in realistic terrestrial or even space-based set-ups. Here, we design protocols that exploit the spatial correlations that are inherent in perturbations due to distant sources to reduce significantly their impact on the visibility of interference patterns. We show that interference patterns that are robust to such type of noise can be encoded in the joint probability distribution of two or more interferometers, provided that these are initialized in suitable states. We develop a general framework that makes use of N+1 interferometers that may differ in their masses to correct for environmental potential fields up to order N in their multipole expansion. Remarkably, our approach works for fields that fluctuate stochastically in any time scale and does not require the presence of quantum correlations among the different interferometers. Finally, we also show that the same ideas can be extended to the protection of entanglement between pairs of interferometers.
The most direct approach for characterizing the quantum dynamics of a strongly-interacting system is to measure the time-evolution of its full many-body state. Despite the conceptual simplicity of this approach, it quickly becomes intractable as the system size grows. An alternate framework is to think of the many-body dynamics as generating noise, which can be measured by the decoherence of a probe qubit. Our work centers on the following question: What can the decoherence dynamics of such a probe tell us about the many-body system? In particular, we utilize optically addressable probe spins to experimentally characterize both static and dynamical properties of strongly-interacting magnetic dipoles. Our experimental platform consists of two types of spin defects in diamond: nitrogen-vacancy (NV) color centers (probe spins) and substitutional nitrogen impurities (many-body system). We demonstrate that signatures of the many-body systems dimensionality, dynamics, and disorder are naturally encoded in the functional form of the NVs decoherence profile. Leveraging these insights, we directly characterize the two-dimensional nature of a nitrogen delta-doped diamond sample. In addition, we explore two distinct facets of the many-body dynamics: First, we address a persistent debate about the microscopic nature of spin dynamics in strongly-interacting dipolar systems. Second, we demonstrate direct control over the spectral properties of the many-body system, including its correlation time. Our work opens the door to new directions in both quantum sensing and simulation.