Our experiments began with nearly pure ≈1.8×105 atom 87Rb BECs in the ∣F=1,mF=−1⟩ state confined in a crossed optical dipole trap. The trap consisted of a pair of 1064nm laser beams propagating along x^−y^ (1/e2 radii of wx^+y^≈120μm and wz^≈50μm) and −x^−y^ (1/e2 radii of wx^−y^≈wz^≈65μm).
We prepared equal mixtures of ∣F=1,mF=−1⟩ and ∣1,0⟩ using an initially off resonant rf magnetic field Brf(t)x^. We adiabatically ramped δ to δ≈0 in 15ms, decreased the rf coupling strength Ωrf to about 150Hz≪ℏωq in 6ms, and suddenly turned off Ωrf, projecting the BEC into an equal superposition of ∣mF=−1⟩ and ∣mF=0⟩. We subsequently ramped δ to its desired value in 6ms and then linearly increased the intensity of the Raman lasers from zero to the final coupling Ω in 70ms.
2 Magnetic fields
Three pairs of Helmholtz coils, orthogonally aligned along x^+y^, x^−y^ and z^, provided bias fields (Bx+y,Bx−y,and Bz). By monitoring the ∣F=1,mF=−1⟩ and ∣1,0⟩ populations in a nominally resonant rf dressed state, prepared as above, we observed a short-time (below ≈10 minutes) RMS field stability gμBBRMS/h≲80Hz. The field drifted slowly on longer time scales (but changed abruptly when unwary colleagues entered through our laboratory’s ferromagnetic doors). We compensated for the drift by tracking the rf and Raman resonance conditions.
Due to the small energy scales involved in the experiment, it was crucial to minimize magnetic field gradients. We detected stray gradients by monitoring the spatial distribution of ∣mF=−1⟩-∣mF=0⟩ spin mixtures after TOF. Small magnetic field gradients caused this otherwise miscible mixture to phase separate along the direction of the gradient. We canceled the gradients in the x^−y^ plane with two pairs of anti-Helmholtz coils, aligned along x^+y^ and x^−y^, to gμBB′/h≲0.7Hz/μm.
References
3 SO coupled Hamiltonian
Our system consisted of a F=1 BEC with a bias magnetic field along y^ at the intersection of two Raman laser beams propagating along x^+y^ and −x^+y^ with angular frequencies ωL and ωL+ΔωL, respectively. The rank-1 tensor light shift of these beams produced an effective Zeeman magnetic field along the z direction with Hamiltonian H^R=ΩRσˇ3,zcos(2kLx^+ΔωLt), where σˇ3,x,y,z are the 3×3 Pauli matrices and we define 1ˇ3 as the 3×3 identity matrix. If we take y^ as the natural quantization axis (by expressing the Pauli matrices in a rotated basis σˇ3,y→σˇ3,z, σˇ3,x→σˇ3,y, and σˇ3,z→σˇ3,x) and make the rotating wave approximation, the Hamiltonian for spin states {∣mF=+1⟩,∣0⟩,∣−1⟩} in the frame rotating at ΔωL is
As we justify below, ∣mF=+1⟩ can be neglected for large enough ℏωq, which gives the effective two-level Hamiltonian
for the pseudo-spin ∣↑⟩=∣mF=0⟩ and ∣↓⟩=∣−1⟩ where Ω=ΩR/2. After a local pseudo-spin rotation by θ(x^)=2kLx^ about the pseudo-spin z^ axis followed by a global pseudo-spin rotation σˇz→σˇy, σˇy→σˇx, and σˇx→σˇz, the 2×2 Hamiltonian takes the SO coupled form
The SO term linear in k^x results from the non-commutation of the spatially-dependent rotation about the pseudo-spin z axis and the kinetic energy.
4 Effective two-level system
For atoms in ∣mF=−1⟩ and ∣mF=0⟩ with velocities ℏ\mathpzckx/m≈0 and Raman-coupled near resonance, δ≈0, the ∣mF=+1⟩ state is detuned from resonance owing to the ℏωq=3.8EL quadratic Zeeman shift. For δ/4EL≪1 and Ω<4EL, Δ(Ω,δ)≈δ[1−(Ω/4EL)2]1/2.
5 Effect of the neglected state
In our experiment, we focused on the two level system formed by the ∣mF=−1⟩ and ∣mF=0⟩ states. We verified the validity of this assumption by adiabatically eliminating the ∣mF=+1⟩ state from the full three level problem. To second order in Ω, this procedure modifies the detuning δ and SO coupling strength α in Eq. 1 by
In these expressions, we have retained only largest term in a 1/ωq expansion. In our experiment, where ℏωq=3.8EL, δ is substantially changed at our largest coupling Ω=7EL. To maintain the desired detuning δ in the simple 2-level model (i.e., Δ≈δ+δ(2)=0 in Fig. 1c), we changed gμBB0 by as much as 3EL to compensate for δ(2). We did not correct for the always small change to α.
Although both terms are small at the Ω=0.2EL transition from miscible to immiscible, slow drifts in B0 prompted us to locate Δ=0 empirically from the equal population condition, NT↑′=NT↓′. As a result, δ in Eq. 1 implicitly includes the perturbative correction δ(2).
6 Origin of the effective interaction term
The additional c↑↓′ term in the interaction Hamiltonian for dressed spins directly results from transforming into the basis of dressed spins, which are
where ℏKx/m is the group velocity, Kx=q−q↑ for ∣↑′⟩ and Kx=q−q↓ for ∣↓′⟩, and ϵ=Ω/8EL≪1. Thus, in second quantized notation, the dressed field operators transform according to
where q↑≈−1−4ϵ2kL≈−kL and q↓≈1−4ϵ2kL≈kL. Inserting the transformed operators into
gives the interaction Hamiltonian for dressed spins which can be understood order-by-order (both c2/c0 and ϵ are treated as small parameters). In this analysis, the terms proportional to c2 are unchanged to order c2/c0, and we only need to evaluate the transformation of the spin-independent term (proportional to c0). At O(ϵ) and O(ϵ3) all the terms in the expansion include high spatial frequency e±2ikLx or e±4ikLx prefactors. For density distributions that vary slowly on the λ/2 length scale these average to zero. The O(ϵ2) term, however, has terms without these modulations, and is
giving rise to c↑↓′=c0Ω2/(8EL2).
7 Mean field phase diagram
We compute the mean-field phase diagram for a ground state BEC composed of a mixture of dressed spins in an infinite homogeneous system. This applies to our atoms in a harmonic trap in the limit of R≫ξs, where R is the system size, ξs=ℏ2/2m∣c2+c↑↓′∣n is the spin healing length and n is the density. We first minimize the interaction energy H^I at fixed N↑′,↓′, with an effective interaction c↑↓′ as a function of Ω. The two dressed spins are either phase-mixed, both fully occupying the system’s volume V, or phase-separated with a fixed total volume constraint V=V↑′+V↓′. For the phase-separated case, minimizing the free energy gives the volumes V↑′ and V↓′, determined by N↑′,↓′ and V. The interaction energy of a phase-mixed state is smaller than that of a phase-separated state for the miscibility condition c0+c2+c↑↓′/2<c0(c0+c2), corresponding to Ω<Ωc. This condition is independent of N↑′,↓′: for any N↑′,↓′ the system is miscible at Ω<Ωc. Then, at a given Ω, we minimize the sum of the interaction energy and the single-particle energy from the Raman detuning, (N↑′−N↓′)δ/2, allowing N↑′,↓′ to vary. For the miscible case (Ω<Ωc), the BEC is a mixture with fraction N↓′/(N↑′+N↓′)∈(0,1) only in the range of detuning δ∈(δ0−Wδ,δ0+Wδ), where δ0=c2n/2, Wδ=∣δ0∣(1−Ω/Ωc)1/2 and n=(N↑′+N↓′)/V. For the immiscible case (Ω>Ωc), Wδ=(c2/8c0)c2n is negligibly small compared to c2n.
Figure 2b shows the mean field phase diagram as a function of (Ω,δ), where δ/EL is displayed with a quasi-logarithmic scaling, sgn(δ/EL)[log10(∣δ/EL∣+∣δmin/EL∣)−log10∣δmin/EL∣], in order to display δ within the range of interest. This scaling function smoothly evolves from logarithmic for ∣δ∣≫δmin, ≈sgn(δ/EL)log10∣δ/EL∣, to linear for ∣δ∣≪δmin, ≈δ, where δmin/EL=0.001EL=1.5Hz.
In our measurement of the dressed spin fraction f↓′ (see Fig. 3a), δ=0 is determined from the NT↑′=NT↓′ condition. We identify this condition as δ=δ0 and apply it for all hold time th. Because ∣δ0∣≈3Hz is below our ≈80Hz RMS field noise, we are unable to distinguish δ0 from 0.
8 Recombining TOF images of dressed spins
To probe the dressed spin states (Eq. 6), each of which is a spin and momentum superposition, we adiabatically mapped them into bare spins, ∣↑,\mathpzckx=q↑+kL⟩ and ∣↓,\mathpzckx=q↓−kL⟩, respectively. Then, in each image outside a ≈90μm radius disk containing the condensate for each spin distribution, we fit nT↑′,T↓′(x,y) to a gaussian modeling the thermal background and subtracted that fit from nT↑′,T↓′(x,y) to obtain the condensate 2D density n↑′,↓′(x,y). Thus, for each dressed spin we readily obtained the temperature, total number NT↑′,T↓′, and condensate densities n↑′,↓′(x,y).
To analyze the miscibility from the TOF images where a Stern-Gerlach gradient separated individual spin states, we recentered the distributions to obtain n↑′(x,y) and n↓′(x,y). This took into account the displacement due to the Stern-Gerlach gradient and the nonzero velocities ℏ\mathpzckx/m of each spin state (after the adiabatic mapping). The two origins were determined by the following: we loaded the dressed states at a desired coupling Ω but with detuning δ chosen to put all atoms in either ∣↓′⟩ or ∣↑′⟩. Since q↑,↓=∓(1−Ω2/32EL2)kL (see Fig. 1c), these velocities ℏ\mathpzckx/m=ℏ(q↑+kL)/m,ℏ(q↓−kL)/m depend slightly on Ω, and our technique to determine the distributions’ origin accounts for this effect.
9 Calibration of Raman Coupling
Both Raman lasers were derived from the same Ti:Sapphire laser at λ≈804.1 nm, and were offset from each other by a pair of AOMs driven by two phase locked frequency synthesizers near 80MHz. We calibrated the Raman coupling strength Ω by fitting the three-level Rabi oscillations between the mF=−1,0,and+1 states driven by the Raman coupling to the expected behavior.