arXiv subjects

Elena Kuznetsova

Publications and source records attributed to Elena Kuznetsova.

14 recordsLinked to original sources

arXiv2023

Engineering chiral spin interactions with Rydberg atoms

We propose to simulate the anisotropic and chiral Dzyaloshinskii-Moriya (DM) interaction with Rydberg atom arrays. The DM Hamiltonian is engineered in a one-dimensional optical lattice or trap array with effective long-range Rydberg spins, interacting indirectly via a mobile mediator Rydberg atom. A host of XXZ and DM Hamiltonians can be simulated with out-of-phase sign periodic coupling strengths; for initial states in a stationary condensate, the DM interaction vanishes. This theory allows for determination of the DM interaction (DMI) vector components from first principles. The inherent anisotropy of the Rydberg-Rydberg interactions, facilitates the DMI coupling to be tuned so as to be comparable to the XXZ interaction. Our results make plausible the formation of non-trivial topological spin textures with Rydberg atom arrays.

physics.atom-ph↗

arXiv2018

Effective spin-spin interactions in bilayers of Rydberg atoms and polar molecules

We show that indirect spin-spin interactions between effective spin-1/2 systems can be realized in two parallel 1D optical lattices loaded with polar molecules and/or Rydberg atoms. The effective spin can be encoded into low-energy rotational states of polar molecules or long-lived states of Rydberg atoms, tightly trapped in a deep optical lattice. The spin-spin interactions can be mediated by Rydberg atoms, placed in a parallel shallow optical lattice, interacting with the effective spins by charge-dipole (for polar molecules) or dipole-dipole (for Rydberg atoms) interaction. Indirect XX, Ising and XXZ interactions with interaction coefficients $J^{\bot}$ and $J^{zz}$ sign varying with interspin distance can be realized, in particular, the $J_{1}-J_{2}$ XXZ model with frustrated ferro-(antiferro-)magnetic nearest (next-nearest) neighbor interactions.

quant-ph↗

arXiv2016

Rydberg atom mediated non-destructive readout of collective rotational states in polar molecule arrays

We analyze in detail the possibility to use charge-dipole interaction between a single polar molecule or a 1D molecular array and a single Rydberg atom to read out rotational populations. The change in the Rydberg electron energy is conditioned on the rotational state of the polar molecules, allowing for realization of a CNOT quantum gate between the molecules and the atom. Subsequent readout of the atomic fluorescence results in a non-destructive measurement of the rotational state. We study the interaction between a 1D array of polar molecules and an array or a cloud of atoms in a Rydberg superatom (blockaded) state and calculate the resolved energy shifts of Rb(60s) with KRb and RbYb molecules, with N=1, 3, 5 molecules. We show that collective molecular rotational states can be read out using the conditioned Rydberg energy shifts.

quant-ph↗

arXiv2015

Adiabatic rapid passage two-photon excitation of a Rydberg atom

We considered the two-photon adiabatic rapid passage excitation of a single atom from the ground to a Rydberg state. Three schemes were analyzed: both pump and Stokes fields chirped and pulsed, only the pump field is chirped, and only the pump field is pulsed and chirped while the Stokes field is continuous wave (CW). In all three cases high transfer efficiencies $>99\%$ were achieved for the experimentally realizable Rabi frequencies and the pulse durations of the fields.

quant-ph↗

arXiv2015

Chirped pulse excitation of two-atom Rydberg states

We analyze excitation of two ground state atoms to a double Rydberg state by a two-photon chirped optical pulse in the regime of adiabatic rapid passage. For intermediate Rydberg-Rydberg interaction strengths, relevant for atoms separated by $\sim$ten $μ$m, adiabatic excitation can be achieved at experimentally feasible Rabi frequencies and chirp rates of the pulses, resulting in high transfer efficiencies. We also study the adiabatic transfer between ground and Rydberg states as a means to realize a controlled phase gate between atomic qubits.

quant-ph↗

arXiv2013

Enhanced index of refraction in four-wave mixing media

Refractive index enhancement accompanied by vanishing absorption in a four-level atomic system interacting with two control and two probe fields in a regime of four-wave mixing (FWM) has been predicted and studied in the present work. We analyzed the maximal index enhancement in the four-level FWM system and gave index estimates for a real atomic gas of $^{40}$K, taking into account its multilevel structure and collisional and Doppler broadenings at large atomic densities. We also discussed how vanishing absorption with no nearby amplification can be realized in a two species system, consisting of a four-level FWM and a two-level system, where the latter provides additional absorption for one of the probe fields. We numerically estimated the index change in a system composed of $^{40}$K and $^{39}$K gases.

quant-ph↗

arXiv2013

Single atom trapping and control inside a nanosize photonic crystal cavity

We analyze a possibility to trap, control and load a single atom inside a nanosize cavity formed in a photonic crystal. We consider a 1D nanobeam crystal having two nearly degenerate localized modes with mode maxima at the central air gap, forming a cavity with a mode volume <λ^{3}. For this system we found that an atom can be trapped by a mode detuned from an atomic transition and controled by the second resonant mode. We show that atomic motion can be cooled using cavity-enhanced rf Sisyphus cooling. We also discuss how an atom can be loaded inside the nanosize crystal air gap from short-wavelength optical tweezers.

quant-ph↗

arXiv2012

Cluster state generation using van der Waals and dipole-dipole interactions in optical lattices

We present a scalable method for generation of a cluster state for measurement-based quantum computing using van der Waals or dipole-dipole interactions between neutral atoms or polar molecules in an optical lattice. Nearest neighbor entanglement is accomplished by performing a phase gate using interaction of atoms in Rydberg states or molecules in large dipole moment states. All nearest neighbors are sequentially entangled in a finite number of operations, independent of the number of qubits, producing a 1D cluster state. A universal 2D cluster state can be generated in several ms in a two-dimensional optical lattice by producing a series of 1D cluster states in one lattice direction, followed by application of the entangling operations in another lattice direction. We discuss the viability of the scheme with Rb Rydberg atoms.

quant-ph↗

arXiv2011

Rydberg atom mediated polar molecule interactions: a tool for molecular-state conditional quantum gates and individual addressability

We study the possibility to use interaction between a polar molecule in the ground electronic and vibrational state and a Rydberg atom to construct two-qubit gates between molecular qubits and to coherently control molecular states. A polar molecule within the electron orbit in a Rydberg atom can either shift the Rydberg state, or form Rydberg molecule. Both the atomic shift and the Rydberg molecule states depend on the initial internal state of the polar molecule, resulting in molecular state dependent van der Waals or dipole-dipole interaction between Rydberg atoms. Rydberg atoms mediated interaction between polar molecules can be enhanced up to $10^{3}$ times. We describe how the coupling between a polar molecule and a Rydberg atom can be applied to coherent control of molecular states, specifically, to individual addressing of molecules in an optical lattice and non-destructive readout of molecular qubits.

quant-ph↗

arXiv2009

Phase gate and readout with an atom/molecule hybrid platform

We suggest a combined atomic/molecular system for quantum computation, which takes advantage of highly developed techniques to control atoms and recent experimental progress in manipulation of ultracold molecules. We show that two atoms of different species in a given site, {\it e.g.}, in an optical lattice, could be used for qubit encoding, initialization and readout, with one atom carrying the qubit, the other enabling a gate. In particular, we describe how a two-qubit phase gate can be realized by transferring a pair of atoms into the ground rovibrational state of a polar molecule with a large dipole moment, and allowing two molecules to interact via their dipole-dipole interaction. We also discuss how the reverse process of coherently transferring a molecule into a pair of atoms could be used as a readout tool for molecular quantum computers.

quant-ph↗

arXiv2008

Efficient formation of ground state ultracold molecules via STIRAP from the continuum at a Feshbach resonance

We develop a complete theoretical description of photoassociative Stimulated Raman Adiabatic Passage (STIRAP) near a Feshbach resonance in a thermal atomic gas. We show that it is possible to use low intensity laser pulses to directly excite the continuum at a Feshbach resonance and transfer nearly the entire atomic population to the lowest rovibrational level in the molecular ground state. In case of a broad resonance, commonly found in several diatomic alkali molecules, our model predicts a transfer efficiency $η$ up to 97% for a given atom pair, and up to 70% when averaged over an atomic ensemble. The laser intensities and pulse durations needed for optimal transfer are $10^2-10^3$ W/cm$^2$ and several $μ$s. Such efficiency compares to or surpasses currently available techniques for creating stable diatomic molecules, and the versatility of this approach simplifies its potential use for many molecular species.

quant-ph↗

arXiv2008

Formation of deeply bound molecules via chainwise adiabatic passage

We suggest and analyze a novel technique for efficient and robust creation of dense ultracold molecular ensembles in their ground rovibrational state. In our approach a molecule is brought to the ground state through a series of intermediate vibrational states via a {\em multistate chainwise Stimulated Raman Adiabatic Passage} (c-STIRAP) technique. We study the influence of the intermediate states decay on the transfer process and suggest an approach that minimizes the population of these states, resulting in a maximal transfer efficiency. As an example, we analyze the formation of $^{87}$Rb$_{2}$ starting from an initial Feshbach molecular state and taking into account major decay mechanisms due to inelastic atom-molecule and molecule-molecule collisions. Numerical analysis suggests a transfer efficiency $>$ 90%, even in the presence of strong collisional relaxation as are present in a high density atomic gas.

quant-ph↗

arXiv2007

Schemes for robust quantum computation with polar molecules: analysis of experimental feasibility

We analyse recently proposed physical implementations of a quantum computer based on polar molecules. A set of general requirements for a molecular system is presented, which would provide an optimal combination of quantum gate times, coherence times, number of operations, high gate accuracy and experimental feasibility. We proceed with a detailed analysis of a scheme utilizing switchable dipole-dipole interactions between polar molecules. Switchable dipole-dipole interaction is an efficient tool for realization of two-qubit quantum gates, necessary to construct a universal set of gates. We consider three possible realizations of a phase gate using specific molecules, such as CO, NF, alkali dimers and alkaline-earth monohalides. We suggest suitable electronic states and ransitions and investigate requirements for the pulses driving them. Finally, we analyse possible sources of decoherence.

quant-ph↗

arXiv2006

Generation of coherent terahertz pulses in Ruby at room temperature

We have shown that a coherently driven solid state medium can potentially produce strong controllable short pulses of THz radiation. The high efficiency of the technique is based on excitation of maximal THz coherence by applying resonant optical pulses to the medium. The excited coherence in the medium is connected to macroscopic polarization coupled to THz radiation. We have performed detailed simulations by solving the coupled density matrix and Maxwell equations. By using a simple $V$-type energy scheme for ruby, we have demonstrated that the energy of generated THz pulses ranges from hundreds of pico-Joules to nano-Joules at room temperature and micro-Joules at liquid helium temperature, with pulse durations from picoseconds to tens of nanoseconds. We have also suggested a coherent ruby source that lases on two optical wavelengths and simultaneously generates THz radiation. We discussed also possibilities of extension of the technique to different solid-state materials.

quant-ph↗