Introduction

Spin-orbit coupling (SOC), as is often referred to in condensed matter physics, couples the spin of a particle to its orbital degrees of freedom. It is believed that SOC constitutes an important ingredient for quantum simulation with ultracold atoms1,2,3,4. Research on SOC is an active area due to its ubiquitous appearance in condensed matter phenomena, such as topological insulator5,6, spin Hall effect7,8 and spintronics9. In contrast to solid-state materials, where SOC originates from the orbital motion of electrons inside a crystal’s intrinsic electric field, the coupling between atomic spin and its center of mass motion has to be engineered artificially. In recent years we have witnessed great successes of artificial atomic gauge fields10,11,12,13,14,15,16,17,18,19. A popular scheme employs Raman laser fields11 to couple two atomic ground states forming a pseudo-spin-1/2 system, leading to a SOC with equal Rashba20 and Dresselhaus21 contributions. This is routinely used nowadays for both bosonic11,14 and fermionic15,16 alkali atom species. More general forms of SOC are pursued actively in a variety of settings22,23,24,25, which together with the above well understood Raman scheme26,27,28,29,30,31 significantly expand the scopes of quantum simulation using synthetic gauge fields in ultracold atoms, fostering exciting opportunities for observing novel quantum phenomena with ultracold atoms32,33,34,35,36,37,38,39,40,41,42.

The Raman scheme, pioneered by the Spielman group11, makes use of coherent atom-light interaction. As pointed out by several authors2,4,43, spontaneous emissions, nevertheless, come into play in the presence of even far off-resonant laser fields, which give rise to heating or atom loss. The effective spontaneous emission rate (heating rate) and the effective Rabi frequency for the Raman spin flip process both scale as the ratio of laser power to detuning squared and are respectively proportional to the excited state spontaneous emission rate and fine structure splitting. Thus spontaneous emission cannot be suppressed with increased detuning. At a fixed effective Rabi frequency, heating will be stronger for K atoms than for Rb and Cs atoms, because the excited state fine structure splitting for K atom is smaller. The situations are worse for Na and Li atoms, whose even smaller fine structure splittings essentially rule out the possibility for observing many body phenomena with SOC from the Raman scheme. Alternative ideas less affected by atomic spontaneous emissions are proposed, such as using narrow-line transitions in high spin atoms44,45 or manipulating a spin-dependent tunneling without spin-flip in an optical lattice tilted by a static gradient magnetic field (GMF)43. Besides heating from atomic spontaneous emission, the SOC strength realized in the Raman scheme is difficult to be tuned continuously in an experiment because it is determined by the photon recoil momentum and the intersection angle between the two Raman laser beams. An idea based on periodically modulating the effective Rabi frequency can reduce the synthesized SOC strength46, which is successfully realized in recent experiments47.

To overcome the restrictions due to atomic spontaneous emission and to enhance tunability, one can seek out spin-dependent interactions between atoms and magnetic fields to synthesize SOC, as was proposed by Xu et al.48 using repeated GMF pulses and by Anderson et al.49 using modulating GMFs. A GMF provides a spin-dependent force, which over times leads to a spin (atomic internal state) dependent momentum (spatial/orbital degrees of freedom) impulse, hence gives rise to SOC. An analogous protocol is also proposed to generate SOC for atoms in an optical lattice50. These ideas can be applied to all spinful atoms48,49. A modulating GMF is recently used to produce a state dependent optical lattice for ultracold fermionic atoms51. The procedure for obtaining an effective Hamiltonian from such a periodically driven quantum system is developed in ref. 52. A non-uniform magnetic field is also widely used to couple electronic spin and orbital degrees of freedom in the condensed matter systems53,54,55.

This article reports our observation of a tunable SOC with equal Rashba and Dresselhaus contributions in a spin-1 87Rb atomic Bose-Einstein condensate (BEC) synthesized by modulating a one dimensional (1D) GMF48,49. In the absence of other non-commuting interaction terms, The SOC with strengh kso we report corresponds to a spin-dependent momentum shift mFkso to the single-particle dispersion curves for spin component mF, which gives rise to the three crossing dispersion curves for the three spin components of spin-1 atoms. The synthesized SOC is confirmed through the following two observations: first, we measure the excitation of the collective dipole mode of a condensate in a harmonic trap after abruptly turning on the SOC; and second, we achieve the adiabatic loading of condensed atoms into the minimum energy state at shifted momentum when SOC is gradually turned on by slowly ramping up the amplitude of the modulating GMF.

Results

Our experiments synthesize an effective 1D SOC by applying a time-periodically modulating 1D GMF with zero average48,49, as illustrated in Fig. 1. The GMF provides a spin-dependent force for a spin F atom (with mass m). Here, μB is the Bohr magneton, gF is the Lande g-factor and Fx,y,z denotes the x-, y- and z-component of spin vector F. Although the net impulse over one period is zero, the accumulated distance an atom moves depends on its spin state, which implies the atom acquires a spin dependent group velocity. Thus atomic spin and its center-of-mass motion (orbital) is coupled by GMF pulses. The origin for the synthesized 1D SOC can be understood more straightforwardly when we consider the extreme case where each period contains a pair of two opposite GMF pulses of impulse ±kso capping the ends of free evolution over time T. These two pulses enact a unitary transformation, which displaces the canonical momentum by a spin-dependent quantity, i.e., where , as shown in Fig. 1(b). Hence, the effective Hamiltonian results from a spin dependent momentum shift to the free particle Hamiltonian . For the sinusoidal modulating GMF used in our experiments, the atomic dynamics is governed by . Based on the Floquet theory, the effective time-independent Hamiltonian Heff is given by (more details in supplementary material)

Figure 1
figure 1

A schematic illustration of SOC synthesized from a periodic GMF.

(a) A periodically modulated GMF with zero average imparts opposite forces (black arrows or gray dashed arrows at different times) to the (red disk and arrow) and (blue disk and arrow) states of the F = 1 hyperfine manifold. (b) Each modulation period is composed of a pair of short opposite GMF pulses (blue triangles), which provide impulses ±kso with free evolution sandwiched in between, translating canonical momentum kz → kz − ksoFz, leading to the SOC as shown in the blue rectangular box48. The continuous driving limit of a sinusoidal modulation with zero average is adopted in our experiment for its better technical stability49. (c) The experimental setup involves bias (gray) and gradient (blue) magnetic coils. A BEC (red football) is placed at the center of the gradient coils and aligned along the bias field.

where , c1 = 1/2 and c2 = 3/8. q is the quadratic Zeeman shift (QZS) of the bias field used for selecting the 1D GMF from a 3D quadrupole magnetic field (see supplementary material). The c1 and c2 terms on the rhs of Eq. (1) describe the synthesized SOC and the effective QZS, respectively. The latter together with q can be further tuned to zero or negative by an off-resonant dressing microwave field56. The above physical picture remains approximately valid in the presence of an external harmonic trap if the modulation frequency ωmod = 2π/T is far greater than the trap frequency.

Our experiments are performed in a single chamber BEC setup as described elsewhere57. We create a 87Rb BEC of 1.2 × 105 atoms in state in a crossed dipole trap with trapping frequencies , as illustrated in Fig. 1(c). The 1D GMF is implemented by a combination of a 3D quadrupole magnetic field and a 5.7 Gauss bias field , whose linear and quadratic Zeeman shifts are (2π) 4 MHz and (2π) 2.34 kHz, respectively (see supplementary material). The modulation frequency ωmod for the GMF is (2π) 1.0 kHz unless stated otherwise. To generate a SOC strength kso = 1 kL = 8.0554 μm−1, where kL = 2πL is the one photon recoil momentum at a laser wavelength λL = 780 nm, the required peak magnetic field gradient . The centers of the gradient field coils and the optical trap are aligned within 50 μm to minimize short-term magnetic field fluctuation during modulation (see supplementary material).

Dipole oscillations

To confirm the effect of the synthesized SOC from the modulating GMF, we first excite the collective dipole mode of a single spin component atomic condensate in a harmonic trap by abruptly turning on the modulating GMF. By rewriting the effective Hamiltonian (1) as and interchanging the roles of the conjugate variable pair kz and z, it’s easy to find that this effective Hamiltonian is equivalent to that of a particle moving in a displaced harmonic trap. Here, we neglected the extra QZS which only causes an overall energy shift. A particle displaced from the center of a harmonic trap will oscillate back and forth periodically, which is indeed what we observe. Both the position and momentum of the condensate oscillate at the trap frequency ωz. Solving the Heisenberg equations of motion given by Heff, we obtain the averaged momentum , where for the component. The oscillation is around c1ksomF with a peak to peak amplitude . As shown in Fig. 2(a), in our experiments we abruptly turn on the modulating GMF, at a corresponding SOC strength of kso = 7.5 μm−1 and persist for variable hold time. After integer multiple periods of the modulation, the crossed dipole trap is turned off in less than 10 μs. Condensed atoms are expanded for about 24 ms, during which different Zeeman components are Stern-Gerlach separated by an inhomogeneous magnetic field along x-direction. For all three spin components, atomic center-of-mass momenta are derived from their shifted positions along z-direction with respect to their locations when SOC is absent. As shown in Fig. 2(c), the observed results are in good agreement with our theoretical predictions.

Figure 2
figure 2

Collective dipole oscillation of a single spin component condensate observed after abruptly turning on kso = 7.5 μm−1 with ωmod = (2π) 1.0 kHz.

(a) The time sequence of our experiments: abruptly turning on a constant amplitude modulation GMF corresponding to kso = 7.5 μm−1, followed by 24 ms of time of flight (TOF) before Stern-Gerlach imaging. (b) Absorption images of (top row), (middle row) and (bottom row) components after different hold time (duration of the modulating GMF). The dashed lines are for kz = 0, or without SOC. (c) Atomic momentum for (red squares), (black rhombuses) and (blue disks) spin components as a function of hold time. The rhs vertical labels are in units of kL and solid lines denote theoretical predictions.

SOC shifted minimum energy state

As a second confirmation, we observe that the atom’s minimum energy state is adiabatically adjusted to a finite none-zero momentum kz = c1ksomF for the state when the modulation amplitude is slowly ramped up as shown in Fig. 3(a). In the presence of SOC, the minimum of the single-particle dispersion for the spin state is located at c1ksomF. According to the adiabatic theorem, if the ramp of kso is slow enough, atoms will follow the ramp and stay at the shifted minimum. In this set of experiments, atoms are prepared at the initial spin state of   by applying a π/2 pulse to the state (0, 0, 1)T. The modulation amplitude is then ramped up to a final value within 200 ms. After turning off the optical trap, we measure the momentum for each spin component. We find good agreement with theoretical predictions as shown in Fig. 3(c). To confirm the adiabaticity, kso is ramped up from 0 to 4.9 μm−1 in 100 ms and then back to 0 in another 100 ms. We find atomic center-of-mass momentum returns to 0 without noticeable heating. We also check the dependence of c1 on the modulation frequency ωmod and find that c1 essentially remains a constant as long as .

Figure 3
figure 3

Atoms adiabatically follow the energy minimum shifted to finite momentum with increased SOC strength.

Here ωmod = (2π) 1.0 kHz. (a) The time sequence of our experiments: adiabatically ramping up GMF modulation amplitude to a given kso, followed by TOF before Stern-Gerlach imaging. (b) Absorption images of (top row), (middle row), (bottom row) components for different kso. The dashed lines are for kz = 0, or for without SOC. With the increase of SOC strength, the observed shapes for the atomic condensate cloud become increasingly distorted, indicating enhanced excitations of higher spatial modes. We believe this is due to the increased violation of the adiabatic condition when ramping the SOC strength to higher strength. Additionally, parametric heating from magnetic field gradient modulation also contributes. (c) Atomic center-of-mass momentum for (red squares), (black rhombuses) and (blue disks) spin component as a function of kso, compared with theoretical predictions (solid lines).

Discussion

The results of Fig. 3 demonstrate tunability of the SOC we synthesize. For our protocol based on temporally modulating GMFs, a point of detrimental importance concerns heating which causes relaxation and atom loss from condensates.

As mentioned before, one of the major heating mechanisms for the Raman scheme is photon scattering from the Raman laser. For different alkaline metal atoms, the situation varies significantly. A list of all alkaline metal atom data are shown in Table 1. For cesium and rubidium, the heating rate is very low, the Raman scheme works very well. For potassium, the heating will cause significant problem at the temperature scale of many quantum many body phenomenon. For sodium and lithium, the huge heating rate will quickly destroy the BEC or degenerate Fermi gas.

Table 1 The heating rate for atoms inside a harmonic trap due to spontaneous emission is estimated to be , where ωR is the resonant photon recoil frequency and kB is the Boltzmann constant.

As atomic spontaneous emission is absent in our experiments, the most likely heating mechanism comes from parametric processes associated with the temporal modulation. To minimize parametric heating, we modulate the GMF far away from the characteristic frequencies of our system. The typical trapping frequency is about (2π) 100 Hz and the mean field interaction energy is around (2π) 200 Hz. When modulated at ωmod = (2π) 1.0 kHz, heating is found to be moderate and acceptable for the reported experiments, based on the observed condensate life time. To measure the life time, we adiabatically increase the SOC strength to prepare atoms into an equilibrium state from a initial spin state and measure the fractions of remaining atoms as functions of time. The worst case occurs for condensates in the component, whose life time is found to be around 310 ms for kso = 4.9 μm−1 corresponding to a recoil energy of 1.3 kHz, as shown in Fig. 4(a). The life time of our system is comparable to the reported values for the Raman scheme with Rb atoms11. It can be further improved by increasing the modulation frequency. Figure 4(b) displays the dependence of the atomic cloud size after 24 ms of TOF expansion on modulation frequency at a fixed kso = 4.9 μm−1. The cloud radius is found to decrease with increasing modulation frequency, which confirms the expected heating suppression with increased modulation frequency. Thus enhanced performances of the GMF scheme is expected if our experiments can be carried out with atomic chip based setups, which routinely provide higher GMFs and faster modulations58,59.

Figure 4
figure 4

(a) The fraction of remaining atoms (due to heating loss from the trap) as a function of the time (after the modulating GMF is turned off) for component at kso = 4.9 μm−1. Dots denote measurement points, while the solid line is an exponential fit. The optical trap frequencies are respectively and ωmod = (2π) 1.0 kHz. The insert Stern-Gerlach images show the three spin components displaced along the vertical direction as a result of spin dependent momentum impulses from SOC; (b) The condensate size R (fitted radius) after 24 ms TOF expansion (black square) for component at kso = 4.9 μm−1 as a function of modulation frequency ωmod. The dashed line denotes the same size without SOC or at kso = 0 μm−1. Hold time is 100 ms. The optical trap frequencies are respectively .

As demonstrated in our experiments, the SOC synthesized from GMF enacts spin-dependent momentum shifts to the single-particle dispersion curves, leading to curve crossings between different spin states. Inspired by the idea of ref. 50, we find that these crossings can be tuned into avoided crossings when spin flip mechanism is introduced as elaborated in more detail in the supplementary material.

In conclusion, we experimentally demonstrate a tunable SOC synthesized by a modulating GMF for a spin-1 87Rb BEC. We tune the SOC strength by changing the momentum impulse from the GMF. The observed coherence time is reasonably long compared to the Raman scheme for rubidium and expected to be much better than the Raman scheme for sodium and lithium, pointing to promising experimental opportunities. The scheme we realized relies on spin-dependent Zeeman interactions, thus is naturally extendable to high-spin atomic states, like the spin-1 case we demonstrate here. It adds to the recent report of spin-1 SOC60 concatenated from two pseudo-spin-1/2 subsystems with Raman laser couplings. Our experiment opens up a new avenue in the synthesizing SOC with atom species not suitable with the Raman scheme and presents an important addition to quantum simulation with tunable SOC couple strength.

Methods

Condensate production

Atomic 87Rb Bose-Einstein condensates are produced employing laser cooling followed by evaporative cooling in a single vacuum chamber, which consists of a 32 mm × 32 mm wide and 300 mm long quartz cell, a Rb reservoir and vacuum pumps. The quartz cell is ideally suited for magnetic field modulation as it prevents eddy current, which could cause short term fluctuations to the bias field. To optimize the applications of fast and strong GMF modulation by small gradient coils and to allow for three dimensional (3D) optical access, MOT collected from background atoms are magnetically transported 10 cm to a location 8 mm away from the inside wall of the glass cell. They are first RF evaporative cooled in a hybrid trap consisting of a magnetic quadruple trap and a crossed optical dipole trap for 5 seconds. The crossed dipole trap derives from two 1064 nm laser beams (with 1/e2 Gaussian diameter 120 μm) propagating along x- and z- directions, respectively. The magnetic quadrupole field gradient is then ramped down to transfer atoms to the crossed dipole trap. Condensation occurs after a final evaporation by ramping down the power of the crossed dipole trap in 3 seconds. At the end of the final evaporation the crossed dipole trap frequencies are . A condensate in state with 1.2 × 105 atoms is produced every 40 seconds. To minimize heating from the near-resonant driving of the modulating GMF, we further ramp down ωz to 2π × 31.8 Hz in 500 ms after BEC production, which reduces ωx and ωy respectively to 2π × 74.6 Hz and 2π × 67.5 Hz.

Magnetic field control

Three pairs of Helmholtz coils are used to control the homogeneous bias magnetic field. While transferring atoms from the hybrid trap into the crossed dipole trap, a 0.7 Gauss bias field along z-direction is simultaneously turned on in order to maintain atoms in state. In the last 1.5 seconds of evaporative cooling, we ramp up the bias field to 5.7 Gauss and hold on to this value. The Larmor frequency of the bias field is calibrated by RF driven Rabi oscillations between Zeeman sublevels. The residual magnetic field gradient is compensated to below 2 mGauss/cm by a pair of anti-Helmholtz coils along z-direction.

A pair of small anti-Helmholtz coils is used to modulate the GMF with a modulation amplitude up to 100 Gauss/cm at a frequency of (2π) 1.0 kHz. The radius for the gradient coils is 15 mm. The two coils are separated at an inner distance of 36 mm. Each coil consists of 12 turns of winding and produces an inductance of about 10 μH. The gradient coil size is much larger than the 120 μm beam waist of our dipole trap, which produces a homogeneous gradient field inside the crossed dipole trap. The coils are small enough to ensure fast and strong GMF modulation. The current for the gradient coils is regulated by a home made fast (10 μs rise time) and precise (100 ppm) linear bipolar current controller, whose phase compensation is carefully analysed and tuned for stable running with the inductive load. The gradient coil is mounted on a 3D low magnetic translation stage for precise alignment of the gradient coils. The center of the gradient field is aligned within 50 μm with the BEC, which is found to be crucial for minimizing short term bias field fluctuations during GMF modulation.

Additional Information

How to cite this article: Luo, X. et al. Tunable atomic spin-orbit coupling synthesized with a modulating gradient magnetic field. Sci. Rep. 6, 18983; doi: 10.1038/srep18983 (2016).