Transitionless quantum driving for spin systems

Benjamín Loewe, Rafael Hipolito, Paul M. Goldbart

Wen-Wu Liu, Chun‐Ling Zhang, Ling Zhang

Chun‐Ling Zhang, Wen-Wu Liu

Zhenyu Xu, Wen‐Long You, Yuli Dong +2 more

Transitionless quantum driving, also known as counterdiabatic driving, is a unique shortcut technique to adiabaticity, enabling a fast-forward evolution to the same target quantum states as those in the adiabatic case. However, as nothing is free, the fast evolution is obtained at the cost of stronger driving fields. Here, given the system initially gets prepared in equilibrium states, we construct relations between the dynamical evolution speed and the cost rate of transitionless quantum driving in two scenarios: one that preserves the transitionless evolution for a single energy eigenstate (individual driving), and the other that maintains all energy eigenstates evolving transitionlessly (collective driving). Remarkably, we find that individual driving may cost as much as collective driving, in contrast to the common belief that individual driving is more economical than collective driving in multilevel systems. We then present a potentially practical proposal to demonstrate the above phenomena in a three-level Landau-Zener model using the electronic spin system of a single nitrogen-vacancy center in diamond.

Kazutaka Takahashi

We apply the method of transitionless quantum driving for time-dependent quantum systems to spin systems. For a given Hamiltonian, the driving Hamiltonian is constructed so that the adiabatic states of the original system obey the Schrödinger equation. For several typical systems such as the XY spin chain and the Lipkin-Meshkov-Glick model, the driving Hamiltonian is constructed explicitly. We discuss possible interesting situations when the driving Hamiltonian becomes time independent and when the driving Hamiltonian is equivalent to the original one. For many-body systems, a crucial problem occurs at the quantum phase transition point where the energy gap between the ground and first excited states becomes zero. We discuss how the defect can be circumvented in the present method.

Kristel F. L. Michielsen