No Arabic abstract
We demonstrate that two remote qubits can be entangled through an optically active intermediary even if the coupling strengths between mediator and qubits are different. This is true for a broad class of interactions. We consider two contrasting scenarios. First, we extend the analysis of a previously studied gate operation which relies on pulsed, dynamical control of the optical state and which may be performed quickly. We show that remote spins can be entangled in this case even when the intermediary coupling strengths are unequal. Second, we propose an alternative adiabatic control procedure, and find that the system requirements become even less restrictive in this case. The scheme could be tested immediately in a range of systems including molecules, quantum dots, or defects in crystals.
Nuclear spins of noble gases can maintain coherence for hours at ambient conditions owing to their extraordinary isolation by the enclosing, complete electronic shells. This isolation, however, impedes the ability to manipulate and control them by optical means or by physical coupling to other spin gases. Here we experimentally achieve strong coherent coupling between noble-gas spins and the optically-accessible spins of alkali-metal vapor. Stochastic spin-exchange collisions, underlying the coupling, accumulate to a coherent periodic exchange of spin excitations between the two gases. We obtain a coupling rate 10 times higher than the decay rate, observe the resultant avoided crossing in the spectral response of the spins, and demonstrate the external control over the coupling by magnetic fields. These results open a route for efficient and rapid interfacing with noble-gas spins for applications in quantum sensing and information.
We propose a protocol for entanglement swapping which involves tripartite systems. The generation of remote entanglement induced by the Bell measurement can be easily certified by additional local measurements. We illustrate the protocol in the case of continuous variable systems where the certification is effective for an appropriate class of three-mode Gaussian states. We then apply the protocol to optomechanical systems, showing how mechanical entanglement between two remote micromechanical resonators can be generated and certified via local optical measurements.
The radiation pressure of two detuned laser beams can create a stable trap for a suspended cavity mirror; here it is shown that such a configuration entangles the output light fields via interaction with the mirror. Intra-cavity, the opto-mechanical system can become entangled also. The degree of entanglement is quantified spectrally using the logarithmic negativity. Entanglement survives in the experimentally accessible regime of gram-scale masses subject to thermal noise at room temperature.
A recently proposed purification method, in which the Zeno-like measurements of a subsystem can bring about a distillation of another subsystem in interaction with the former, is utilized to yield entangled states between distant systems. It is shown that the measurements of a two-level system locally interacting with other two spatially separated not coupled subsystems, can distill entangled states from the latter irrespectively of the initial states of the two subsystems.
Spin-bearing molecules are promising building blocks for quantum technologies as they can be chemically tuned, assembled into scalable arrays, and readily incorporated into diverse device architectures. In molecular systems, optically addressing ground-state spins would enable a wide range of applications in quantum information science, as has been demonstrated for solid-state defects. However, this important functionality has remained elusive for molecules. Here, we demonstrate such optical addressability in a series of synthesized organometallic, chromium(IV) molecules. These compounds display a ground-state spin that can be initialized and read out using light, and coherently manipulated with microwaves. In addition, through atomistic modification of the molecular structure, we tune the spin and optical properties of these compounds, paving the way for designer quantum systems synthesized from the bottom-up.