2.2 Bose-Einstein condensates for atom interferometry
2.2.3 Atomic interaction effects
The effect of atomic interactions on the phase evolution in an atom interferometer is commonly regarded as a major obstacle for achieving good sensitivities in interferometers based on Bose-Einstein condensates. In the following, we will estimate the mean field shifts based on the Thomas-Fermi density distributions described in the previous section. For a quantitative analysis of the relative phase evolution of the two states in the interferometer, we follow the
2.2 Bose-Einstein condensates for atom interferometry 39 0 5 10 15 20 25 30 0 100 200 300 400 500 600 700 Time of flight (ms) FWHM along x ( µ m) 0 5 10 15 20 25 30 0 100 200 300 400 500 600 700 800 Time of flight (ms) FWHM along y ( µ m) (a) (b)
Figure 2.1:Time-of-flight central cloud widths (a) perpendicular to and (b) along the weak trapping direction. The red lines represent a thermal cloud ofT=1µK, the blue long-dashed line a condensate in the Thomas-Fermi limit and the black short-dashed line a condensate with no interactions. The cloud width are calculated for an atom numberN=106and trapping frequenciesω
x=ωz=209.2 Hz and
ωy=18.3 Hz.
approach in[86]and write the two-state wave function as
Φ(r,t) =ca(t)φa(r) +cb(t)φb(r). (2.16) The number of atoms in each state is given byNa=|ca(t)|2andNb=|cb(t)|2, and the overall wave function is normalised to the total atom number, �|Φ(r,t)|2d3r =Na+Nb=N. It follows thatφa(r)andφb(r)are normalised to one. The equations of motion forca(t)and
cb(t)are obtained from the Gross-Pitaevskii equation (2.2): i˙ca=ωaca+ (UaaNa+UabNb)ca≡αaca
i˙cb=ωbcb+ (UbbNb+UabNa)cb≡αbcb.
(2.17) Here,Ui j = għhi j
�
|φi(r)|2|φj(r)|2d3r is related to the scattering length ai j between statesi and j viagi j =4πħh2ai j/m. The energies of the two states in the absence of interactions are
ħhωa andħhωb. The phase evolution of stateiis described byαi, and the relative phase evolves
at a rate
α≡αa−αb=ωa−ωb+ (Uaa−Uab)Na−(Ubb−Uab)Nb. (2.18) The interaction-induced reduction of interferometric sensitivity is due to uncertainties in the numbers Na and Nb. We are particularly interested in the uncertainty in number and the dephasingduring the free evolution in the interferometer, i.e. after the first beam splitter. For a non-entangled ensemble of atoms, the limit of how well we can know the number after the first beam splitter is given by the quantum projection noise, which sets a lower bound for the uncertainty in relative atom number,σNa−Nb =
�N. Assuming a 50
/50 split on the beam splitter, we setNa= (N±�N)/2 andNb= (N∓�N)/2. The relative phase evolves as
α=ωa−ωb+ (Uaa−Uab)
N±�N
2 −(Ubb−Uab)
N∓�N
2 . (2.19)
The important quantity is the uncertainty in the phase evolution due to relative number fluctuations. The uncertainty in the phase evolution rateαis given by
σα=
Uaa+Ubb−2Uab 2
�N
40 Chapter 2. Bose-condensed sources for precision measurements
Figure 2.2: Calculated dephas- ing rateσα as a function of ex- pansion time. The maximum dephasing rate is 3.5 Hz for a trapped condensate. More than 99% of the atomic interaction en- ergy is converted to kinetic en- ergy during the first 10 ms of free expansion. The dephasing rates are obtained for condensate of N=106atoms and trapping
frequencies ωx=ωz=209.2 Hz andωy=18.3 Hz. 0 5 10 15 20 25 30 10−3 10−2 10−1 100 101 Time of flight (ms) Dephasing rate σ α / 2 π (Hz)
σα is the dephasing rate during the free evolution in the interferometer. We shall calculate σα for the time-of-flight Thomas-Fermi density profiles introduced in the previous section. For
simplicity, we will consider the case where the two states are spatially separated; this condition is fulfilled for interferometers with atomic clouds of sufficiently narrow spatial width (BECs) and a large enough momentum transfer during the beam splitting. For spatially separated states, we can neglect the interstate interaction termUabin equation (2.20). We shall assume a condensate withN =106 87Rb atoms and the trapping parameters of the QUIC trap described in section 2.4. The differences in the scattering lengths of different internal states in87Rb differ by�10%. For reasons of simplicity, we usea=100a0, independent of the internal atomic
state. From equation (2.8), we calculateUaa=Ubband the dephasing rateσα. The results are
graphed in figure 2.2. The maximum dephasing rate isσα=2π×3.5 Hz; it decreases by more than two orders of magnitude within the first 10 ms of free expansion. To achieve quantum projection noise limited operation with 106 atoms,3 the (mean) dephasing rateσ
α must be
kept below 2π×5×10−4/T. Here,T is the free evolution time in the interferometer. For an
interferometer withT=100 ms, this means a dephasing rate below 5 mHz which is achieved after 18 ms of free expansion in our setup.