Dicke State Generation and Extreme Spin Squeezing via Rapid Adiabatic Passage.

Considering the unique energy level structure of the one-axis twisting Hamiltonian in combination with standard rotations, we propose the implementation of a rapid adiabatic passage scheme on the Dicke state basis. The method permits to drive Dicke states of the many-atom system into entangled states with maximum quantum Fisher information. The designed states allow us to overcome the classical limit of phase sensitivity in quantum metrology and sensing. We show how to generate superpositions of Dicke states, which maximize metrological gain for a Ramsey interferometric measurement. The proposed scheme is remarkably robust to variations of the driving field and has favorable time scaling, especially for a small to moderate (∼1000) number of atoms, where the total time does not depend on the number of atoms.

Circularly polarized light-induced potentials and the demise of excited states.

In the presence of strong electric fields, the excited states of single-electron molecules and molecules with large transient dipoles become unstable because of anti-alignment, the rotation of the molecular axis perpendicular to the field vector, where bond hardening is not possible. We show how to overcome this problem by using circularly polarized electromagnetic fields. Using a full quantum description of the electronic, vibrational, and rotational degrees of freedom, we characterize the excited electronic state dressed by the field and analyze its dependence on the bond length and angle and the stability of its vibro-rotational eigenstates. Although the dynamics is metastable, most of the population remains trapped in this excited state for hundreds of femtoseconds, allowing quantum control. Contrary to what happens with linearly polarized fields, the photodissociation occurs along the initial molecular axis, not perpendicular to it.

Enhancement of entanglement concentration using catalysts.

Auxiliary pure quantum entangled states shared between two parties can act as catalysts in bipartite entanglement transformations. The participation of a catalyst state in the transformation can enhance its success probability. We consider transformations involving entanglement concentration of a finite number of copies of arbitrary two-qubit pure states into a single copy of a maximally entangled two-qubit pure state using bipartite local quantum operations and classical communication aided by a catalyst state. We show the enhancement of success probabilities of the catalyst-assisted procedure compared to the case where no catalysts are used. The optimal two-qubit catalyst and the maximum probability of the transformation using such catalysts can be obtained analytically. The enhancement of concentration success probability using catalysts of higher dimensions is demonstrated numerically. Finally, catalyst aided strategies for obtaining multiple maximally entangled two-qubit states are discussed.

Control defeasance by anti-alignment in the excited state.

We predict anti-alignment dynamics in the excited state of H2+ or related homonuclear dimers in the presence of a strong field. This effect is a general indirect outcome of the strong transition dipole and large polarizabilities typically used to control or to induce alignment in the ground state. In the excited state, however, the polarizabilities have the opposite sign compared to those in the ground state, generating a torque that aligns the molecule perpendicular to the field, deeming any laser-control strategy impossible.

Grid-Based Ehrenfest Model To Study Electron-Nuclear Processes.

The two-dimensional electron-nuclear Schrödinger equation using soft-core Coulomb potentials has been a cornerstone for modeling and predicting the behavior of one-active-electron diatomic molecules, particularly for processes where both bound and continuum states are important. The model, however, is computationally expensive to extend to more electron or nuclear coordinates. Here we propose use of the Ehrenfest approach to treat the nuclear motion, while the electronic motion is still solved by quantum propagation on a grid. In this work, we present results for a one-dimensional treatment of H2+, where the quantum and semiclassical dynamics can be directly compared, showing remarkably good agreement for a variety of situations. The advantage of the Ehrenfest approach is that it can be easily extended to treat as many nuclear degrees of freedom as needed.

Anomalous Rabi Oscillations in Multilevel Quantum Systems.

We show that the excitation probability of a state within a manifold of levels undergoes Rabi oscillations with the frequency determined by the energy difference between the states and not by the pulse area, for sufficiently strong pulses. The population and coherence remains in the two-level subsystem formed by the initial and target state even at Rabi frequencies exceeding the energy difference. The observed dynamics can be useful in nonlinear spectroscopy and quantum state preparation.

Two-qubit atomic gates: spatio-temporal control of Rydberg interaction.

By controlling the temporal and spatial features of light, we propose a novel protocol to prepare two-qubit entangling gates on atoms trapped at close distance, which could potentially speed up the operation of the gate from the sub-micro to the nanosecond scale. The protocol is robust to variations in the pulse areas and the position of the atoms, by virtue of the coherent properties of a dark state, which is used to drive the population through Rydberg states. From the time-domain perspective, the protocol generalizes the one proposed by Jaksch and coworkers [Jaksch et al., Phys. Rev. Lett., 2000, 85, 2208], with three pulses that operate symmetrically in time, but with different pulse areas. From the spatial-domain perspective, it uses structured light. We analyze the map of the gate fidelity, which forms rotated and distorted lattices in the solution space. Finally, we study the effect of an additional qubit to the gate performance and propose generalizations that operate with multi-pulse sequences.

Temperature Sensitivity of 14N-V and 15N-V Ground-State Manifolds.

We measure electron- and nuclear-spin transition frequencies in the ground state of nitrogen-vacancy (N-V) centers in diamond for two nitrogen isotopes (14N-V and 15N-V) over temperatures ranging from 77 to 400 K. Measurements are performed using Ramsey interferometry and direct optical readout of the nuclear and electron spins. We extract coupling parameters Q (for 14N-V), D, A‖, A⊥, and γe/γn, and their temperature dependences for both isotopes. The temperature dependences of the nuclear-spin transitions within the ms=0 spin manifold near room temperature are found to be 0.52(1) ppm/K for 14N-V(|mI = -1⟩ ↔ |mI = +1⟩) and -1.1(1) ppm/K for 15N-V(|mI = -1/2⟩ ↔ |mI = +1/2⟩). An isotopic shift in the zero-field splitting parameter D between 14N-V and 15N-V is measured to be ~ 120 kHz. Residual transverse magnetic fields are observed to shift the nuclear-spin transition frequencies, especially for 15N-V. We have precisely determined the set of parameters relevant for the development of nuclear-spin-based diamond quantum sensors with greatly reduced sensitivity to environmental factors.

Electro-magnetically controlled acoustic metamaterials with adaptive properties.

A design of actively controlled metamaterial is proposed and discussed. The metamaterial consists of layers of electrically charged nano or micro particles exposed to external magnetic field. The particles are also attached to compliant layers in a way that the designed structure exhibits two resonances: mechanical spring-mass resonance and electro-magnetic cyclotron resonance. It is shown that if the cyclotron frequency is greater than the mechanical resonance frequency, the designed structure could be highly attenuative (40-60 dB) for vibration and sound waves in very broad frequency range even for wavelength much greater than the thickness of the metamaterial. The approach opens up wide range of opportunities for design of adaptively controlled acoustic metamaterials by controlling magnetic field and/or electrical charges.

Demonstration of diamond nuclear spin gyroscope.

We demonstrate the operation of a rotation sensor based on the nitrogen-14 (14N) nuclear spins intrinsic to nitrogen-vacancy (NV) color centers in diamond. The sensor uses optical polarization and readout of the nuclei and a radio-frequency double-quantum pulse protocol that monitors 14N nuclear spin precession. This measurement protocol suppresses the sensitivity to temperature variations in the 14N quadrupole splitting, and it does not require microwave pulses resonant with the NV electron spin transitions. The device was tested on a rotation platform and demonstrated a sensitivity of 4.7°/s (13 mHz/Hz), with a bias stability of 0.4 °/s (1.1 mHz).

Chirped-pulse adiabatic control in coherent anti-Stokes Raman scattering for imaging of biological structure and dynamics.

Two novel control methods based on adiabatic passage are proposed to be implemented in coherent anti-Stokes Raman scattering (CARS) microscopy for noninvasive imaging of biological structure and dynamics. The first method provides optimal pulse-area control of the resonant vibrational transitions by using a pair of equally linear-chirped pulses. The second method, named the 'roof' method, utilizes the chirp sign variation at the central time and gives robust adiabatic excitation of the resonant vibrational mode. Both methods are robust with respect to suppression of the off-resonant transitions. The methods allow one to achieve chemical sensitivity with high resolution and can be used to obtain CARS spectra of biological molecules with efficiently suppressed background.

Vibrationally state-selective spin-orbit transfer with strong nonresonant pulses.

By dynamic Stark shift using strong nonresonant pulses, we show that it is in principle possible to prepare arbitrary superposition states of mixed multiplicity. By a proper choice of parameters, the transfer of population is shown to follow the Rabi formula, where the initial and target states are now vibrational states of two light-induced molecular potentials of different multiplicity. Starting from nonstationary wave packets, the spin transfer can proceed via parallel transfer using a single pulse or by sequential transfer using a pulse sequence. A simple model is proposed to analyze the properties of both schemes and the feasibility of their experimental implementation for spin-orbit transitions in Rb2.

Phase-controlled collapse and revival of entanglement of two interacting qubits.

We demonstrate the strong dependence of the entanglement dynamics of two distinguishable qubits in a trap on the relative phase of the pulses used for excitation. We show that the population and entanglement exhibits collapses and full revivals when the initial distribution of phonons is a coherent state.

Optical control of the singlet-triplet transition in Rb2.

By controlling nonresonant dynamic Stark shifts it is possible to effectively decouple the intramolecular couplings of simple molecules. We have illustrated this effect in the 1 (1)Sigma(u)-->1 (3)Pi(u) transition in Rb(2). The laser scheme implies two important control knobs: the laser frequency, which must be chosen to avoid both single and multiphoton resonances and to select different electronic environments for the singlet and triplet states, and the pulse intensity, which must amplify the asymmetry in the dynamic polarizabilities that allows the decoupling, avoiding undesired strong-pulse effects. The mechanism of the scheme implies not only brute-force energy shifts but also light-induced reshaping of the potentials to avoid the undesired crossings. Quantitative aspects of the method are analyzed by using molecular models of increasing complexity for Rb(2).

Quantum phase control of entanglement.

A method of phase control of entanglement in two-qubit systems is proposed. We show that by changing a relative phase of the pulses that drive the transitions in a two-qubit system with closed-loop couplings, one can control entanglement at will. The method relies on adiabatic dynamics via time-delayed pulse sequences and can be implemented with both resonant and nonresonant transitions.

Implementing quantum gates on oriented optical isomers.

Optical enantiomers are proposed to encode molecular two-qubit information processing. Using sequences of pairs of nonresonant optimally polarized pulses, different schemes to implement quantum gates, and to prepare entangled states, are described. We discuss the role of the entanglement phase and the robustness of the pulse sequences which depend on the area theorem. Finally, possible scenarios to generalize the schemes to n-qubit systems are suggested.