Bose 2.2 User Manual Page 46

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From the exit of the ZS, the atoms travel only a short distance until they reach the
center of the trapping chamber, where they are captured in a magneto-optical trap (MOT).
While standard three-dimensional MOTs [129, Ch.9.4] are widely used in experiments
with alkali atoms [132, 133], a large inelastic two-body loss coefficient for excited state
collisions severly limits the maximum number of chromium atoms that can be accumulated
in such trap [123, 134]. Fortunately, the large magnetic dipole moment of chromium allows
for an alternative loading mechanism: the
C
ontinuous
L
oading of a
I
offe-
P
ritchard
(CLIP) magnetic trap [135, 136], illustrated in Fig. 3.2(a). The magnetic quadrupole
field, produced by the pair of cloverleaf coils, is used for operating a two-dimensional
MOT in radial direction plus a molasses on the
z
-axis, using the
7
S
3
7
P
4
cooling
transition. With a branching ratio 1
:
250
,
000 the atoms decay from the excited state
7
P
4
to the
5
D
4
meta-stable state. There they are decoupled from the MOT cycle, but
remain magnetically trapped. Owing to the small branching ratio, the atoms are cooled
approximately to Doppler temperature (
T
D
= 124
K
) in the MOT cycle, before they
arrive in the meta-stable state. After around six seconds of loading time, the population
in the
5
D
4
state saturates at
N
2
·
10
8
. We then switch off the MOT light and excite
the atoms from the
5
D
4
to the
7
P
3
state by a 20
ms
light pulse from the repump-laser at
λ
= 663
.
2
nm
. From there the atoms decay back to the
7
S
3
ground-state, as shown in
Fig. 3.2(b).
As a next step, we compress the atomic cloud in the magnetic trap (MT) by maximally
ramping up the current through the cloverleaf coils. The sample heats up to
T
1
mK
,
and we then perform Doppler cooling by flashing the axial MOT beams onto the dense
sample [137]. Without loosing atoms, we gain two orders of magnitude in phase-space
density (PSD) [138]. After this process, the PSD is
ρ
10
7
which provides good starting
conditions for the RF-induced evaporation cooling
26
[128, 139–141].
In most experiments using alkali elements, evaporative cooling in a magnetic trap is
used to reach the ultra-low critical temperature for Bose-Einstein condensation [1–3, 128].
However, it turned out that this is not possible in chromium: due to the anisotropic
dipole-dipole interaction, the magnetic quantum number
m
J
is not a conserved quantity
in a two-body scattering process, which leads to a heating of the chromium sample by
the so-called dipolar relaxation [126, 142–144]. As the atoms are initially trapped in the
magnetic sublevel of highest Zeeman energy
27
(
m
J
= +3) spin-changing collisions are
accompanied with a release of energy leading to the heating of the sample. By adjusting
daily the magnetic offset field during the RF evaporation to the minimum possible positive
26
The RF-induced evaporation technique is based on the selective removal of the hottest atoms from the
sample which, after a rethermalization time, will possess a lower temperature than before.
27
Only the so-called ’low-field seeking’ states are magnetically trappable as local minima of magnetic
fields can be produced, while the creation of local maxima is impossible as a consequence of Maxwell’s
equations [145].
46
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