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arXiv:1703.03269

Designing spin and orbital exchange Hamiltonians with ultrashort electric field transients

Martin Eckstein, Johan H. Mentink, Philipp Werner

Published Mar 9, 2017• 21 citations
arXivHTMLPDF

Abstract

We demonstrate how electric fields with arbitrary time profile can be used to control the time-dependent parameters of spin and orbital exchange Hamiltonians. Analytic expressions for the exchange constants are derived from a time-dependent Schrieffer-Wolff transformation, and the validity of the resulting effective Hamiltonian is verified for the case of a quarter-filled two-orbital Hubbard model, by comparing to the results of a full nonequilibrium dynamical mean-field theory simulation. The ability to manipulate Hamiltonians with arbitrary time-dependent fields, beyond the paradigm of Floquet engineering, opens the possibility to control intertwined spin and orbital order using laser or THz pulses which are tailored to minimize electronic excitations.

DOI
10.48550/arxiv.1703.03269

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cond-mat.mes-hallCross-listedarXiv:2606.14487•Jun 15, 2026
We demonstrate how electric fields with arbitrary time profile can be used to control the time-dependent parameters of spin and orbital exchange Hamiltonians. Analytic expressions for the exchange constants are derived from a time-dependent Schrieffer-Wolff transformation, and the validity of the resulting effective Hamiltonian is verified for the case of a quarter-filled two-orbital Hubbard model, by comparing to the results of a full nonequilibrium dynamical mean-field theory simulation. The ability to manipulate Hamiltonians with arbitrary time-dependent fields, beyond the paradigm of Floquet engineering, opens the possibility to control intertwined spin and orbital order using laser or THz pulses which are tailored to minimize electronic excitations.
In order to have a better understanding of ultrafast electrical control of exchange interactions in multi-orbital systems, we study a two-orbital Hubbard model at half filling under the action of a time-periodic electric field. Using suitable projection operators and a generalized time-dependent canonical transformation, we derive an effective Hamiltonian which describes two different regimes. First, for a wide range of non-resonant frequencies, we find a change of the bilinear Heisenberg exchange J_{\textrm{ex}} J ex that is analogous to the single-orbital case. Moreover we demonstrate that also the additional biquadratic exchange interaction B_{\textrm{ex}} B ex can be enhanced, reduced and even change sign depending on the electric field. Second, for special driving frequencies, we demonstrate a novel spin-charge coupling phenomenon enabling coherent transfer between spin and charge degrees of freedom of doubly ionized states. These results are confirmed by an exact time-evolution of the full two-orbital Mott-Hubbard Hamiltonian.
We have studied theoretically the possibility of ultra-fast manipulation of a single electron spin in 2D semiconductor quantum dots, by means of high-frequency time-dependent electric fields. The electron spin degree of freedom is excited through spin-orbit coupling, and the procedure may be enhanced by the presence of a static magnetic field. We use quantum optimal control theory to tailor the temporal profile of the electric field in order to achieve the most effective manipulation. The scheme predicts significant control over spin operations in times of the order of picoseconds -- an ultrafast time scale that permits to avoid the effects of decoherence if this scheme is to be used as a tool for quantum information processing.
We use quantum optimal control theory algorithms to design external electric fields that drive the coupled spin and orbital dynamics of an electron in a double quantum dot, subject to the spin-orbit coupling and Zeeman magnetic fields. We obtain time profiles of multifrequency electric field pulses which increase the rate of spin-flip transitions by several orders of magnitude in comparison with monochromatic fields, where the spin Rabi oscillations were predicted to be very slow. This precise (with fidelity higher than $1\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}4}$) and fast (at the time scale of the order of 0.1 ns, comparable with the Zeeman spin rotation and the interdot tunneling time) simultaneous control of the spin and position is achieved while keeping the electron in the four lowest tunneling- and Zeeman-split levels through the duration of the pulse. The proposed algorithms suggest effective applications in spintronics and quantum information devices.
We consider driving multiorbital Mott insulators using laser radiation. We derive general expressions for periodically driven spin-orbital models using time-dependent perturbation theory in the strong interaction limit. We show that the effective exchange interactions of the Floquet spin-orbital Hamiltonian are highly tunable via variations of the frequency, amplitude, and polarization of the laser. We also take the effect of a finite bandwidth of excitations into account and study possible heating effects. We further apply our formalism to orthorhombic titanates YTiO_{3} and LaTiO_{3} based on first-principles calculations, and we find that the spin exchange interactions in these compounds can be engineered to a large extent by tuning the frequency and electric-field amplitude of the laser.
Nonequilibrium control of electronically ordered hidden phases may lead to the development of ultrafast switches and memory devices. In this study, we demonstrate tunable hidden orders in the half-filled photodoped two-orbital extended Hubbard model. Using steady-state nonequilibrium dynamical mean-field theory, we clarify the coexistence and interplay of nonthermal charge, spin, and orbital order. The hidden state at low effective temperature and sufficiently high photodoping is reminiscent of Kugel-Khomskii order in the two-orbital Hubbard model at 14\frac{1}{4}41​ and 34\frac{3}{4}43​ filling, but it emerges out of a nonequilibrium charge-ordered state and exhibits a different magnetic structure. A low-energy effective Hamiltonian is used to analyze the exchange processes that stabilize the nonthermal order.
Tuning spin-orbit coupling is essential in controlling both spin and charge in confined semiconductor nanostructures, yet it is rarely a truly controllable parameter. Here, we show control over the spin-orbit Hamiltonian in quantum dots and the resulting quantum states by tailoring the confinement potential with atomic-scale precision. Using scanning tunnelling microscopy and spectroscopy, we pattern individual Cs ions into designer quantum dot structures on the surface of indium antimonide, in which electrons from a two-dimensional electron gas are confined with chosen in-plane electric-field gradients. We then quantify the atomic level structure, both spatially resolving the orbital character of the electronic states and their magnetic-field evolution. We demonstrate that the level structure, including the induced zero-field splitting, can be tailored by the designed geometry of the local electric fields. These effects can be described using a Hamiltonian that allows consistent treatment of the confinement-induced spin-orbit coupling beyond the conventional Bychkov-Rashba description. This Hamiltonian is derived from a multiband k.p model and takes the energy dependence of the relevant physical parameters into account. Such precise control of spin-orbit coupling in semiconductor quantum dots is relevant to quantum and spintronic technologies.