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Register a new userCoherent control in the ground and optically excited state of an ensemble of erbium dopants
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Ensembles of erbium dopants can realize quantum memories and frequency converters that operate in the minimal-loss wavelength band of fiber optical communication. Their operation requires the initialization, coherent control and readout of the electronic spin state. In this work, we use a split-ring microwave resonator to demonstrate such control in both the ground and optically excited state. The presented techniques can also be applied to other combinations of dopant and host, and may facilitate the development of new quantum memory protocols and sensing schemes.
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The stability and outstanding coherence of dopants and other atom-like defects in tailored host crystals make them a leading platform for the implementation of distributed quantum information processing and sensing in quantum networks. Albeit the required efficient light-matter coupling can be achieved via the integration into nanoscale resonators, in this approach the proximity of interfaces is detrimental to the coherence of even the least-sensitive emitters. Here, we establish an alternative: By integrating a 19 micrometer thin erbium-doped crystal into a cryogenic Fabry-Perot resonator with a quality factor of nine million, we can demonstrate 59(6)-fold enhancement of the emission rate, corresponding to a two-level Purcell factor of 530(50), while preserving lifetime-limited optical coherence up to 0.54(1) ms. With its emission at the minimal-loss wavelength of optical fibers and its outcoupling efficiency of 46(8) %, our system enables coherent and efficient nodes for long-distance quantum networks.
Attosecond pulses can ionize atoms in a coherent process. Since the emerging fragments are entangled, however, each preserves only a fraction of the initial coherence, thus limiting the chance of guiding the ion subsequent evolution. In this work, we use emph{ab initio} simulations of pump-probe ionization of helium above the $2s/2p$ threshold to demonstrate how this loss of coherence can be controlled. Thanks to the participation of $2ell nell$ states, coherence between the ionic $2s$ and $2p$ states, which are degenerate in the non-relativistic limit, results in a stationary, delay-dependent electric dipole. From the picosecond real-time beating of the dipole, caused by the fine-structure splitting of the $n=2$ manifold, it is possible to reconstruct all original ion coherences, including between antiparallel-spin states, which are sensitive probe of relativistic effects in attosecond photoemission.
Quantum chemistry is one of the important applications of quantum information technology. Especially, an estimation of the energy gap between a ground state and excited state of a target Hamiltonian corresponding to a molecule is essential. In the previous approach, an energy of the ground state and that of the excited state are estimated separately, and the energy gap can be calculated from the subtraction between them. Here, we propose a direct estimation of the energy gap between the ground state and excited state of the target Hamiltonian with quantum annealing. The key idea is to combine a Ramsey type measurement with the quantum annealing. This provides an oscillating signal with a frequency of the energy gap, and a Fourier transform of the signal let us know the energy gap. Based on typical parameters of superconducting qubits, we numerically investigate the performance of our scheme when we estimate an energy gap between the ground state and first excited state of the Hamiltonian. We show robustness against non-adiabatic transitions between the ground state and first-excited state. Our results pave a new way to estimate the energy gap of the Hamiltonian for quantum chemistry.
A bacterial photosynthetic light harvesting complex PLHC absorbs a photon and transfers this energy almost perfectly at room temperature RT to a Reaction Center RC, where charge separation occurs. While there are a number of possible light absorbers involved in this process, our focus is the B850 and B875 complexes. We propose that the dominant feature of the ground states in the B850 ring and the B875 open chain are pseudo one dimensional metals due to each bacteriochlorophyll a BChl containing a coordinated magnesium ion Mg2+. The Mg ion structure undergoes a static Peierls distortion that results in symmetry breaking that changes the even spacing of the Mg/BChl molecules comprising the chains to the experimentally observed Mg/BChl dimers. The results are charge density waves CDW, one for each type of the two complexes that result in an energy gap in the single particle electronic spectrum and coherent phonon s spanning the entire rings. The ground state CDWs seem to have two functions the first is to form a stable optical platform and the second is to suppress radical formation and energy dissipation of the coherent excited state by creating single particle energy gaps. After excitation by a photon, the B850 exciton delocalizes on the ring a second photon can form a two-level exciton polariton that could be an alternative explanation for the splitting of the B850 exciton band. The coherent polariton formed could actively participate in uphill electronic energy transfer EET. Additionally we suggest other possible energy storage mechanisms and entanglement possibilities. We suggest experimental studies to clarify these proposals.
Light transport in a dense and disordered cold atomic ensemble, where the cooperation of atomic dipoles essentially modifies their coupling with the radiation modes, offers an alternative approach to light-matter interfacing protocols. Here, we show how the cooperativity and quasi-static dipole interaction affect the process of light propagation under the conditions of electromagnetically-induced transparency (EIT). We perform comparative analysis of the self-consistent approach with ab-initio microscopic calculations and emphasize the role of the interatomic interaction in the dipoles dynamics. Our results show that in such a dense and strongly disordered system the EIT-based light storage protocol stays relatively insensitive to configuration variations and can be obtained with essentially less atoms than it is normally needed for dilute configurations.
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