Periodically driven systems have emerged as a useful technique to engineer the properties of quantum systems, and are in the process of being developed into a standard toolbox for quantum simulation. An outstanding challenge that leaves this toolbox incomplete is the manipulation of the states dressed by strong periodic drives. The state-of-the-art in Floquet control is the adiabatic change of parameters. Yet, this requires long protocols conflicting with the limited coherence times in experiments. To achieve fast control of nonequilibrium quantum matter, we generalize the notion of variational counterdiabatic driving away from equilibrium focusing on Floquet systems. We derive a nonperturbative variational principle to find local approximations to the adiabatic gauge potential for the effective Floquet Hamiltonian. It enables transitionless driving of Floquet eigenstates far away from the adiabatic regime. We discuss applications to two-level, Floquet band, and interacting periodically driven models. The developed technique allows us to capture nonperturbative photon resonances and obtain high-fidelity protocols that respect experimental limitations like the locality of the accessible control terms.
Periodically driven systems have emerged as a useful technique to engineer the properties of quantum systems, and are in the process of being developed into a standard toolbox for quantum simulation. An outstanding challenge that leaves this toolbox incomplete is the manipulation of the states dressed by strong periodic drives. The state-of-the-art in Floquet control is the adiabatic change of parameters. Yet, this requires long protocols conflicting with the limited coherence times in experiments. To achieve fast control of nonequilibrium quantum matter, we generalize the notion of variational counterdiabatic driving away from equilibrium focusing on Floquet systems. We derive a nonperturbative variational principle to find local approximations to the adiabatic gauge potential for the effective Floquet Hamiltonian. It enables transitionless driving of Floquet eigenstates far away from the adiabatic regime. We discuss applications to two-level, Floquet band, and interacting periodically driven models. The developed technique allows us to capture nonperturbative photon resonances and obtain high-fidelity protocols that respect experimental limitations like the locality of the accessible control terms.
Periodically driven quantum systems have emerged as one of the most versatile tools for quantum simulation, enabling the engineering of effective Hamiltonians, topological phases, and inherently nonequilibrium phenomena such as discrete time crystals. Yet fundamental challenges persist: from a spectral ambiguity that precludes a unique Floquet ground state to an inability to manipulate Floquet eigenstates beyond the adiabatic regime. This thesis demonstrates that counterdiabatic driving—a technique from adiabatic quantum control—provides a unifying framework to address these challenges. We first show that the periodic lab-frame Hamiltonian generates counterdiabatic driving for the Floquet eigenstates, revealing Floquet theory as an inverse counterdiabatic driving problem. Exploiting this equivalence, we develop geometric Floquet theory: a reformulation based on the parallel-transport gauge, which uniquely decomposes Floquet dynamics into a geometric contribution, encoded in Berry phases, and a dynamical contribution, generated by the average-energy operator. The average-energy operator provides an unambiguous sorting of the quasienergy spectrum, identifies a unique Floquet ground state at all drive frequencies, and serves as a sensitive diagnostic for heating and symmetry-breaking transitions. Inherently nonequilibrium phenomena—the 𝜋-quasienergy splitting of discrete time crystals and the anomalous edge modes of Floquet topological insulators—are traced to geometric phases. On the practical side, we exploit the intrinsic robustness of prethermal discrete time crystals for a highly frequency-selective DTC-based AC magnetic field sensing scheme and demonstrate it experimentally on a nuclear spin quantum simulator. We then generalize counterdiabatic driving to periodically driven systems. In particular, we derive a non-perturbative variational principle for the Floquet adiabatic gauge potential; this yields local, experimentally feasible control protocols for transitionless manipulation of Floquet states. We demonstrate this formalism on Floquet state preparation in an ultracold atom quantum simulator and many-body state transfer across a quantum phase transition, with significant improvements over unassisted protocols in both cases.
Counterdiabatic (CD) driving presents a way of generating adiabatic dynamics at an arbitrary pace, where excitations due to nonadiabaticity are exactly compensated by adding an auxiliary driving term to the Hamiltonian. While this CD term is theoretically known and given by the adiabatic gauge potential, obtaining and implementing this potential in many-body systems is a formidable task, requiring knowledge of the spectral properties of the instantaneous Hamiltonians and control of highly nonlocal multibody interactions. We show how an approximate gauge potential can be systematically built up as a series of nested commutators, remaining well defined in the thermodynamic limit. Furthermore, the resulting CD driving protocols can be realized up to arbitrary order without leaving the available control space using tools from periodically driven (Floquet) systems. This is illustrated on few- and many-body quantum systems, where the resulting Floquet protocols significantly suppress dissipation and provide a drastic increase in fidelity.
Periodically driven quantum systems provide a powerful route to engineer novel states of matter by controlling their effective Hamiltonians through external fields. However, most treatments are usually simplified by considering the high-frequency limit, and do not account for the processes taking place in the transient regime during the onset of the drive. In this work, we introduce a time and momentum resolved tunneling spectroscopy protocol to probe the instantaneous energy spectrum of Floquet-driven systems beyond the high-frequency regime, capturing both emergent effects and non-adiabatic phenomena without requiring explicit reconstruction of the full time-dependent Green's function. We benchmark the method on driven non-interacting fermionic models, and then generalize the approach to strongly correlated systems with the aid of time-dependent density matrix renormalization group techniques. We also provide a microscopic description to the emergence of in-gap states under resonant driving, and briefly explore its finite temperature analog.
Counterdiabatic (CD) driving accelerates adiabatic protocols by prescribing auxiliary control fields, but often fails to map them to physically available operations. We derive a general formalism for such a mapping. We formulate CD driving in a variational dressed frame, where an unconstrained auxiliary generator reshapes the effective adiabatic problem while simultaneously forcing the applied correction to stay restricted to the native laboratory controls. This yields a laboratory-frame commutator equation that can be solved without constructing instantaneous eigenstates or the adiabatic and dressed-frame unitaries. The additional dressed-frame freedom reveals solutions that are inaccessible in the conventional adiabatic frame. We illustrate this mechanism in three settings: suppression of spectator errors in a multi-qubit chain driven by a single quadrature, an analytical acceleration of adiabatic Bell-state preparation with a fixed entangling interaction, and implementation of a fast adiabatic holonomic gate in a degenerate tripod manifold with correction pulses confined to the native couplings. Our results provide a systematic nonperturbative framework for constructing implementable counterdiabatic protocols beyond the conventional adiabatic frame.
Counterdiabatic driving, which enforces adiabatic evolution in arbitrary timescales, can be realised by engineering a Floquet Hamiltonian which oscillates between the Hamiltonian and its derivative requiring no additional control terms. However, the coefficients of the Floquet Hamiltoinan require knowledge of the counterdiabatic terms, which can be difficult to derive outside of a limited set of examples. We introduce a new hybrid technique for the control of quantum systems, Counterdiabatic-influenced Floquet-engineering or CAFFEINE for short. CAFFEINE parameterises the Floquet Hamiltonian for counterdiabatic driving and utilises numerical quantum optimal control in order to obtain the desired target state. This removes the need to both obtain and implement counterdiabatic terms, however, it does require the ability to quickly oscillate each term in the Hamiltonian. If this oscillation is possible, then CAFFEINE provides a framework to implement quantum annealing protocols and general quantum state preparation. We illustrate this through optimisation of two numerical examples of preparing a Bell state with two qubits and performing annealing protocols for the one-dimensional Ising model. Beyond this, we also illustrate CAFFEINE's capabilities to learn the counterdiabatic terms, which can potentially be used as a probe of quantum chaos and the geometry of quantum dynamics.
42:365303] as a means to make fast changes in the Hamiltonian without exciting transitions. Such driving in principle allows one to realize arbitrarily fast annealing protocols or implement fast dissipationless driving, circumventing standard adiabatic limitations requiring infinitesimally slow rates. These ideas were tested and used both experimentally and theoretically in small systems, but in larger chaotic systems, it is known that exact counterdiabatic protocols do not exist. In this work, we develop a simple variational approach allowing one to find the best possible counterdiabatic protocols given physical constraints, like locality. These protocols are easy to derive and implement both experimentally and numerically. We show that, using these approximate protocols, one can drastically suppress heating and increase fidelity of quantum annealing protocols in complex many-particle systems. In the fast limit, these protocols provide an effective dual description of adiabatic dynamics, where the coupling constant plays the role of time and the counterdiabatic term plays the role of the Hamiltonian.