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arXiv:1506.00517 · Scientific Reports

Logical operations with single x-ray photons via dynamically-controlled nuclear resonances

Jonas Gunst, Christoph H. Keitel, Adriana Pálffy

Published Apr 27, 2016• 27 citations
arXivHTMLPDF

Abstract

Photonic qubits lie at the heart of quantum information technology, often encoding information in their polarization state. So far, only low-frequency optical and infrared photons have been employed as flying qubits, as the resources that are at present easiest to control. With their essentially different way of interacting with matter, x-ray qubits would bear however relevant advantages: they are extremely robust, penetrate deep through materials, and can be focused down to few-nm waveguides, allowing unprecedented miniaturization. Also, x-rays are resonant to nuclear transitions, which are very well isolated from the environment and present long coherence times. Here, we show theoretically that x-ray polarization qubits can be dynamically controlled by nuclear Mössbauer resonances. The control knob is played by nuclear hyperfine magnetic fields, that allow via fast rotations precise processing of single x-ray quanta polarization. With such rotations, single-qubit and binary logical operations such as a destructive C-NOT gate can be implemented.

DOI
10.1038/srep25136

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Photonic qubits lie at the heart of quantum information technology, often encoding information in their polarization state. So far, only low-frequency optical and infrared photons have been employed as flying qubits, as the resources that are at present easiest to control. With their essentially different way of interacting with matter, x-ray qubits would bear however relevant advantages: they are extremely robust, penetrate deep through materials, and can be focused down to few-nm waveguides, allowing unprecedented miniaturization. Also, x-rays are resonant to nuclear transitions, which are very well isolated from the environment and present long coherence times. Here, we show theoretically that x-ray polarization qubits can be dynamically controlled by nuclear Mössbauer resonances. The control knob is played by nuclear hyperfine magnetic fields, that allow via fast rotations precise processing of single x-ray quanta polarization. With such rotations, single-qubit and binary logical operations such as a destructive C-NOT gate can be implemented.
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Spins in condensed matter, especially well-isolated nuclear spins, offer attractive quantum degrees of freedom for computing, sensing, and networking because of their long coherence times. The possibility of electric-field control is an important feature for practical scalable quantum technologies, but, typically, nuclear spins couple only weakly to electric fields in conventional semiconductor hosts, limiting operation efficiency. Here we show that a choice of a highly polarizable oxide host can overcome this bottleneck. In Mn2+ doped ZnO, electric-field modulation of the spin Hamiltonian is amplified by hyperfine-coupled electron spins, and offers efficient electric-field manipulation of an I = 5/2 nuclear spin qudit, in a manner analogous to the hyperfine enhancement of conventional nuclear magnetic resonance. We demonstrate both resonant and non-resonant coherent manipulation using a single uniaxial electric field applied along the crystalline c-axis, the polarization axis of ZnO. This approach allows universal single-qudit gate operations with efficiencies comparable to or exceeding those of conventional magnetic-field driving. These results support the deployment of doped oxides as active host materials for electrically controllable spin qubits, highlighting the importance of materials design in developing scalable quantum technologies.
Means to coherently control single x-ray photons in resonant scattering of light off nuclei by electric or magnetic fields are investigated theoretically. In order to derive the time response in nuclear forward scattering, we adapt the Maxwell–Bloch equations known from quantum optics to describe the resonant light pulse propagation through a nuclear medium. Two types of time-dependent perturbations of nuclear forward scattering are considered for coherent control of the resonantly scattered x-ray quanta. Firstly, the simultaneous coherent propagation of two pulses through the nuclear sample is addressed. We find that the signal of a weak pulse can be enhanced or suppressed by a stronger pulse simultaneously propagating through the sample in counter-propagating geometry. Secondly, the effect of a time-dependent hyperfine splitting is investigated and we put forward a scheme that allows parts of the spectrum to be shifted forward in time. This is the inverse effect of coherent photon storage and may become a valuable technique if single x-ray photon wavepackets are to become the information carriers in future photonic circuits.
Generating strong interactions between single quanta of light and matter is central to quantum information science, and a key component of quantum computers and long-distance quantum networks. In quantum information processing, these interactions are required to create elementary logic operations (quantum gates) between stationary matter quantum bits (qubits) and photonic qubits that can be transmitted over long distances. Efficient quantum gates between photonic and matter qubits are a crucial enabler for a broad range of applications that include robust quantum networks, nondestructive quantum measurements, and strong photon-photon interactions. So far these qubit-photon gates have been achieved using single atoms and at microwave frequencies in circuit QED systems. Their implementation with solidstate quantum emitters, however, has remained a difficult challenge. We demonstrate that the qubit state of a photon can be controlled by a single solid-state qubit composed of a quantum dot (QD) strongly coupled to an optical nanocavity. We show that the QD acts as a coherently controllable qubit system that conditionally flips the polarization of a photon reflected from the cavity mode on picosecond timescales. This operation implements a controlled NOT (cNOT) logic gate between the QD and the incident photon, which is a universal quantum operation that can serve as a general light-matter interface for remote entanglements and quantum computations. Our results represent an important step towards an all solid-state implementation of quantum networks and quantum computers, and provide a versatile approach for controlling and probing interactions between a photon and a single quantum emitter on ultra-fast timescales.
Heralded entanglement between macroscopical samples is an important resource for present quantum technology protocols, allowing quantum communication over large distances. In such protocols, optical photons are typically used as information and entanglement carriers between macroscopic quantum memories placed in remote locations. Here we investigate theoretically a new implementation which employs more robust x-ray quanta to generate heralded entanglement between two crystal-hosted macroscopical nuclear ensembles. Mössbauer nuclei in the two crystals interact collectively with an x-ray spontaneous parametric down conversion photon that generates heralded macroscopical entanglement with coherence times of approximately 100 ns at room temperature. The quantum phase between the entangled crystals can be conveniently manipulated by magnetic field rotations at the samples. The inherent long nuclear coherence times allow also for mechanical manipulations of the samples, for instance to check the stability of entanglement in the x-ray setup. Our results pave the way for first quantum communication protocols that use x-ray qubits.
We introduce a technique to store and manipulate single x-ray photons, which relies on dynamically controlled absorption via nuclear hyperfine magnetic splitting. This scheme is inherently suitable for storage, on-demand generation, and dynamical manipulation of single x-ray photons, for instance, the manipulation of the temporal shape, temporal splitting, the interference between x-ray photons, and the control of the polarization. Our approach provides more opportunities in x-ray quantum information.