We design faster-than-adiabatic state transfers (switching of quantum numbers) in time-dependent coupled-oscillator Hamiltonians. The manipulation to drive the process is found using a two-dimensional invariant recently proposed in S. Simsek and F. Mintert, Quantum 5 (2021) 409, and involves both rotation and transient scaling of the principal axes of the potential in a Cartesian representation. Importantly, this invariant is degenerate except for the subspace spanned by its ground state. Such degeneracy, in general, allows for infidelities of the final states with respect to ideal target eigenstates. However, the value of a single control parameter can be chosen so that the state switching is perfect for arbitrary (not necessarily known) initial eigenstates. Additional 2D linear invariants are used to find easily the parameter values needed and to provide generic expressions for the final states and final energies. In particular we find time-dependent transformations of a two-dimensional harmonic trap for a particle (such as an ion or neutral atom) so that the final trap is rotated with respect to the initial one, and eigenstates of the initial trap are converted into rotated replicas at final time, in some chosen time and rotation angle.
We design faster-than-adiabatic state transfers (switching of quantum numbers) in time-dependent coupled-oscillator Hamiltonians. The manipulation to drive the process is found using a two-dimensional invariant recently proposed in S. Simsek and F. Mintert, Quantum 5 (2021) 409, and involves both rotation and transient scaling of the principal axes of the potential in a Cartesian representation. Importantly, this invariant is degenerate except for the subspace spanned by its ground state. Such degeneracy, in general, allows for infidelities of the final states with respect to ideal target eigenstates. However, the value of a single control parameter can be chosen so that the state switching is perfect for arbitrary (not necessarily known) initial eigenstates. Additional 2D linear invariants are used to find easily the parameter values needed and to provide generic expressions for the final states and final energies. In particular we find time-dependent transformations of a two-dimensional harmonic trap for a particle (such as an ion or neutral atom) so that the final trap is rotated with respect to the initial one, and eigenstates of the initial trap are converted into rotated replicas at final time, in some chosen time and rotation angle.
Different methods have been recently put forward and implemented experimentally to inverse engineer the time-dependent Hamiltonian of a quantum system and accelerate slow adiabatic processes via nonadiabatic shortcuts. In the ``transitionless quantum driving'' proposed by Berry, shortcut Hamiltonians are designed so that the system follows exactly, in an arbitrarily short time, the approximate adiabatic path defined by a reference Hamiltonian. A different approach is based on first designing a Lewis-Riesenfeld invariant to carry the eigenstates of a Hamiltonian from specified initial to final configurations, again in an arbitrary time, and then constructing from the invariant the transient Hamiltonian that connects these boundary configurations. We show that the two approaches, apparently quite different in form and so far in results, are, in fact, strongly related and potentially equivalent, so that the inverse-engineering operations in one of them can be reinterpreted and understood in terms of the concepts and operations of the other one. We study, as explicit examples, expansions of time-dependent harmonic traps and the state preparation of two-level systems.
Controlling the motional state of a particle in a multidimensional space is key for fundamental science and quantum technologies. Applying a recently found two-dimensional invariant combined with linear invariants, we propose protocols to drive a particle in two dimensions so that the final harmonic trap is translated and rotated with respect to the initial one. These protocols realize a one-to-one mapping between initial and final eigenstates at some predetermined time and avoid any final excitations.
By definition, quantum adiabatic process means a slow process which allows the state to follow the instantaneous eigenstates of time-dependent Hamiltonian. For some reasons, for example, to avoid the decoherence effects, or to implement large-scale quantum information processing, we may want to speed up the adiabatic process, that is, to achieve the adiabatic-like control but in very short time. In this talk, we present new methods to speeded-up expansion and transport of cold atoms in a harmonic trap. Such shortcuts to adiabaticity provide the fast expansion or transport, in which the final atomic state is the same as in the adiabatic process, but in arbitrarily short time, keeping the same populations of vibrational levels in the initial and final trap. These methods can also be generalized to Bose-Einstein Condensates. Moreover, we present shortcuts to adiabatic passage from one internal atomic state to another in twoor three-level atoms. In detail, we can apply Berry’s transitionless quantum driving method and invariant-based inverse engineering method to accelerate the Rapid Adiabatic Passage (RAP) and Stimulated Raman Adiabatic Passage (STIRAP) in twoand three-level atomic systems, respectively. We also examine and compare the stability of different schemes concerning different types of noise and system errors. Finally, we show that the technique of shortcuts to adiabaticity in two-level system can be applied in fast and robust spin flip in a quantum dot, to avoid the decoherent effects.
Sending multiple messages on qubits encoded in different vibrational modes of cold atoms or ions along a transmission waveguide requires us to merge first and then separate the modes at input and output ends. Similarly, different qubits can be stored in the modes of a trap and be separated later. We design the fast splitting of a harmonic trap into an asymmetric double well so that the initial ground vibrational state becomes the ground state of one of two final wells, and the initial first excited state becomes the ground state of the other well. This might be done adiabatically by slowly deforming the trap. We speed up the process by inverse engineering a double-function trap using dynamical invariants. The separation (demultiplexing) followed by an inversion of the asymmetric bias and then by the reverse process (multiplexing) provides a population inversion protocol based solely on trap reshaping.
We propose an alternative scheme for constructing a shortcut to implement the quantum state transfer between two three-level atoms founded on the invariant-based inverse engineering in a cavity quantum electronic dynamics (QED) system. Quantum information can be quickly transferred between atoms by taking advantage of the cavity field as a medium. Through our design of the time-dependent laser pulse and atom–cavity coupling, we send atoms through the cavity within a short time interval, which involves the two processes of the invariant dynamics between each atom and the cavity field simultaneously. We redesign a reasonable Gaussian-type wave form in the atom–cavity coupling for a realistic experimental operation. Numerical simulation shows that the target state can be quickly populated with a high fidelity which is robust against both the parameter fluctuations and the dissipation.
Quantum adiabatic processes—that keep constant the populations in the instantaneous eigenbasis of a time-dependent Hamiltonian—are very useful to prepare and manipulate states, but take typically a long time. This is often problematic because decoherence and noise may spoil the desired final state, or because some applications require many repetitions. "Shortcuts to adiabaticity" are alternative fast processes which reproduce the same final populations, or even the same final state, as the adiabatic process in a finite, shorter time. Since adiabatic processes are ubiquitous, the shortcuts span a broad range of applications in atomic, molecular, and optical physics, such as fast transport of ions or neutral atoms, internal population control, and state preparation (for nuclear magnetic resonance or quantum information), cold atom expansions and other manipulations, cooling cycles, wavepacket splitting, and many-body state engineering or correlations microscopy. Shortcuts are also relevant to clarify fundamental questions such as a precise quantification of the third principle of thermodynamics and quantum speed limits. We review different theoretical techniques proposed to engineer the shortcuts, the experimental results, and the prospects.