No Arabic abstract
The coherence time constitutes one of the most critical parameters that determines whether or not interference is observed in an experiment. For photons, it is traditionally determined by the effective spectral bandwidth of the photon. Here we report on multi-photon interference experiments in which the multi-photon coherence time, defined by the width of the interference signal, depends on the number of interfering photons and on the measurement scheme chosen to detect the particles. A theoretical analysis reveals that all multi-photon interference with more than two particles features this dependence, which can be attributed to higher-order effects in the mutual indistinguishability of the particles. As a striking consequence, a single, well-defined many-particle quantum state can exhibit qualitatively different degrees of interference, depending on the chosen observable. Therefore, optimal sensitivity in many-particle quantum interferometry can only be achieved by choosing a suitable detection scheme.
We propose a new method of resonant enhancement of optical Kerr nonlinearity using multi-level atomic coherence. The enhancement is accompanied by suppression of the other linear and nonlinear susceptibility terms of the medium. We show that the effect results in a modification of the nonlinear Faraday rotation of light propagating in an Rb87 vapor cell by changing the ellipticity of the light.
Integrated single-photon detectors open new possibilities for monitoring inside quantum photonic circuits. We present a concept for the in-line measurement of spatially-encoded multi-photon quantum states, while keeping the transmitted ones undisturbed. We theoretically establish that by recording photon correlations from optimally positioned detectors on top of coupled waveguides with detuned propagation constants, one can perform robust reconstruction of the density matrix describing the amplitude, phase, coherence and quantum entanglement. We report proof-of-principle experiments using classical light, which emulates single-photon regime. Our method opens a pathway towards practical and fast in-line quantum measurements for diverse applications in quantum photonics.
We investigated the depth dependence of coherence times of nitrogen-vacancy (NV) centers through precisely depth controlling by a moderately oxidative at 580{deg}C in air. By successive nanoscale etching, NV centers could be brought close to the diamond surface step by step, which enable us to trace the evolution of the number of NV centers remained in the chip and to study the depth dependence of coherence times of NV centers with the diamond etching. Our results showed that the coherence times of NV centers declined rapidly with the depth reduction in their last about 22 nm before they finally disappeared, revealing a critical depth for the influence of rapid fluctuating surface spin bath. By monitoring the coherence time variation with depth, we could make a shallow NV center with long coherence time for detecting external spins with high sensitivity.
We study the effect of the exciton fine-structure splitting on the polarisation-entanglement of photon pairs produced by the biexciton cascade in a single quantum dot. The entanglement is found to persist despite separations between the intermediate energy levels of up to 4 micro-eV. Measurements demonstrate that entanglement of the photon pair is robust to the dephasing of the intermediate exciton state responsible for the first order coherence time of either single photon. We present a theoretical framework taking into account the effects of spin-scattering, background light and dephasing. We distinguish between the first-order coherence time, and a parameter which we measure for the first time and define as the cross-coherence time.
Spins of negatively charged nitrogen-vacancy (NV$^-$) defects in diamond are among the most promising candidates for solid-state qubits. The fabrication of quantum devices containing these spin-carrying defects requires position-controlled introduction of NV$^-$ defects having excellent properties such as spectral stability, long spin coherence time, and stable negative charge state. Nitrogen ion implantation and annealing enable the positioning of NV$^-$ spin qubits with high precision, but to date, the coherence times of qubits produced this way are short, presumably because of the presence of residual radiation damage. In the present work, we demonstrate that a high temperature annealing at 1000$^circ$C allows 2 millisecond coherence times to be achieved at room temperature. These results were obtained for implantation-produced NV$^-$ defects in a high-purity, 99.99% $^{12}$C enriched single crystal chemical vapor deposited diamond. We discuss these remarkably long coherence times in the context of the thermal behavior of residual defect spins. [Published in Physical Review B {bf{88}}, 075206 (2013)]