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Highly Controlled Optical Transport of Cold Atoms Into A Hollow-Core Fiber

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0% found this document useful (0 votes)
5 views16 pages

Highly Controlled Optical Transport of Cold Atoms Into A Hollow-Core Fiber

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林軒宇
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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arXiv:1805.06333v1 [physics.

atom-ph] 16 May 2018

Highly controlled optical transport of cold atoms


into a hollow-core fiber

Maria Langbecker, Ronja Wirtz, Fabian Knoch, Mohammad


Noaman, Thomas Speck, Patrick Windpassinger
Institut für Physik, Johannes Gutenberg-Universität Mainz, 55099 Mainz, Germany

E-mail: [email protected]

May 15, 2018

Abstract. We report on an efficient and highly controlled cold atom hollow-core


fiber interface, suitable for quantum simulation, information, and sensing. The main
focus of this manuscript is a detailed study on transporting cold atoms into the fiber
using an optical conveyor belt. We discuss how we can precisely control the spatial,
thermal, and temporal distribution of the atoms by, e.g., varying the speed at which
the atoms are transported or adjusting the depth of the transport potential according
to the atomic position. We characterize the transport of atoms to the fiber tip for
these different parameters. In particular, we show that by adapting the transport
potential we can lower the temperature of the transported atoms by a factor of 6,
while reducing the transport efficiency only by a factor 2. For atoms transported
inside the fiber, we can obtain a transport efficiency into the fiber of more than 40%
and we study the influence of the different transport parameters on the time-dependent
optical depth signal. When comparing our measurements to the results of a classical
transport simulation, we find a good qualitative agreement.

1. Introduction

Cold atoms are an ideal system for quantum simulation, computation, and sensing due to
the high degree of control over their external as well as internal parameters. In the most
common case, these atomic properties are manipulated by coupling the atoms to a light
field. Thus, for a precise control, a well-defined atom-light interface is necessary. One
possibility for an efficient atom-light interface are cold atoms inside a hollow-core fiber.
Here, both light and atoms can overlap tightly throughout the length of the fiber and
hence the interaction region can be several orders of magnitude larger than in free space.
This also increases the optical depth Dopt , which is a figure of merit for the effective
light-matter interaction strength. Achievements with cold atoms in hollow-core fibers
Highly controlled optical transport of cold atoms into a hollow-core fiber 2

so far include ground-state electro-magnetically induced transparency [1, 2, 3], used


for example for an all-optical switch [1] and for light storage [3], exciting and probing
Rydberg atoms [4], precision spectroscopy [5], and atom interferometry [6].
One key prerequisite for these applications is the controlled preparation of the atomic
sample inside the hollow-core fiber. Different techniques have been demonstrated to
load cold or ultracold atoms inside a hollow-core fiber, including the use of a single-
beam red-detuned dipole trap as a guide [7, 8], a hollow beam blue-detuned dipole
trap, free fall under gravity, a magnetic funnel [9], a dark funnel in combination with
a red-detuned dipole trap beam [10] or combinations of the above [6, 11]. The most
controllable way to transport atoms into a hollow-core fiber is to use a moving optical
lattice, a so-called optical conveyor belt, first demonstrated by Okaba et al. [5]. A
major advantage of this technique is that the atoms can be precisely transported and
held at a specific position. This can for example enable a systematic survey of the
inner part of the hollow-core fiber. Optical conveyor belts have previously been used to
transport single particles [12, 13] and Bose-Einstein-condensates [14], for the study of
coherence properties during the transport [15] and to transport cold atoms outside an
optical nanofiber [16]. For long-distance transport in free space, Bessel beams [14] or
movable lenses [17] have been used to overcome limitations of the transport potential
given by the Rayleigh range.
While transporting the atoms into the hollow-core fiber, a typical problem is heating of
the atoms [4, 5, 6, 10], for example due to their acceleration or due to the funnel shape of
the transport potential, which increases towards the fibertip. However, low temperatures
inside the fiber are advantageous, as they result e.g. in a longer free expansion time and
in less heating-induced losses of atoms. To cool the atoms during the transport, so far
Raman-sideband cooling [5] or continuous cooling in the magneto-optical trap until the
atoms enter the fiber [10] have been employed.
In this manuscript, we introduce a method of controlling the atomic temperature by
adapting the potential depth of the optical conveyor belt according to the position of the
atoms. We transport the cold atoms over a distance of several millimeters towards and
into our hollow-core fiber and characterize the influence of both frequency (acceleration)
and amplitude (trap depth) ramps. By optimizing these transport settings, we show
that we can realize a wide range of temperatures and corresponding particle numbers,
which we compare to the results of a classical transport simulation. Further, we analyze
the influence of the fiber on the transport process by studying measurements for atoms
transported outside and inside the hollow-core fiber.
Highly controlled optical transport of cold atoms into a hollow-core fiber 3

Figure 1. Schematic of the experimental setup. The main part shows a sketch of the
vacuum system and the important beam paths, coupled through the hollow-core fiber.
The inset shows a sketch of the optical lattice potential (lattice constant not to scale),
which increases from the MOT position to the fiber tip and stays at constant depth
inside the hollow-core fiber.

2. Materials and Methods

2.1. Experimental Setup

Our complete experimental setup has been described in detail in [4]. Figure 1 shows the
details important for the transport procedure. We load a magneto-optical trap (MOT)
of Rubidium 87 atoms at a distance of |zµ | = 5.9 mm from the tip of our hollow-core
fiber. The fiber used in this work is a hollow-core photonic crystal Kagomé type fiber
[18] with a length of 10 cm, a core diameter of 60 µm and a mode field diameter of
about 42 µm. At the MOT position, the cold atoms are loaded into a red-detuned
optical lattice, which is created by two counter-propagating hollow-core-fiber-coupled
trap beams at 805 nm. In addition to standard absorption imaging on a CCD camera
outside the fiber, we have the possibility to detect the atomic absorption along the fiber
axis using a resonant hollow-core-fiber-coupled probe beam.

2.2. Highly controlled transport

While loading the atoms into the optical lattice, the relative frequency detuning ∆ν
between the two dipole trap beams is set to zero. By increasing ∆ν, we create an
optical conveyor belt to transport the atoms towards and into the fiber. The properties
of this transport depend on the exact shape of the frequency ramp ∆ν(t). In principle,
arbitrary frequency ramps are possible in our setup as we can control the two dipole
beam trap frequencies separately with two acousto-optical modulators which are driven
by individual outputs of a programmable arbitrary waveform generator (FlexDDS by
WieserLabs). We typically accelerate the atoms by ramping the frequency detuning
of one of the beams linearly to a maximum value of a few hundred kilohertz. Before
probing, we decelerate them by ramping the frequency detuning again down to zero.
Highly controlled optical transport of cold atoms into a hollow-core fiber 4

Given the frequency detuning ∆ν(t), we can determine the velocity of the moving lattice
with wavelength λ, which corresponds to the transport velocity of the atoms, by
λ
v(t) = ∆ν(t), (1)
2
then integrate or differentiate this equation to find position and acceleration of the
atoms. For the example of a linearly increasing frequency detuning, the final position
of the atoms and the maximum acceleration during the ramp are given by
λ∆νmax ∆t λ ∆νmax
z(∆t) = z0 + and amax = (2)
4 2 ∆t
respectively, where z0 is the initial atomic position, ∆νmax the maximum applied
frequency detuning and ∆t the duration of the ramp. By choosing the appropriate
frequency ramp, we can thus precisely control the atomic position, velocity and
acceleration.

2.3. Adapting the potential depth

Atoms in the optical lattice experience the trapping potential [19]


2r 2
!
2
U(r, z, t) = Udip exp − 2 cos (π∆φ(t) − kz(t)), (3)
ω (z(t))
1/2
where ω (z(t)) = ω0 (1 + z(t)2 /zR2 ) is the waist of the Gaussian beam at position z(t),
with zR = πω02/λ being the Rayleigh range and ω0 being the minimal beam waist at the
fiber tip. The time-dependent phase shift ∆φ(t) depends on the frequency ramp ∆ν(t)
as
Z
∆φ(t) = ∆ν(t)dt, (4)

which in the easiest case of constant detuning ∆ν reduces to ∆φ(t) = ∆νt. The potential
depth is given by
!
2 2ΓD2 ΓD1
Udip (z) = 2πc 3
+ 3 I(z), (5)
ωD2 ∆D2 ωD1 ∆D1
where ωD1/D2 is the transition frequency from ground to excited state, ΓD1/D2 is the
decay rate from the excited state and ∆D1/D2 the detuning of the dipole trap beam
from the transition frequency for the Rubidium D1 and D2 lines, respectively. The
position-dependent maximum intensity of the dipole trap beams is given by
2P
I(z) = , (6)
πω(z(t))2
where P is the power in each of the dipole trap beams.

Figure 2 shows the behaviour of the trap depth Udip (z) between the MOT position
and the fiber tip (main figure, solid line). The inset shows a zoom close to the MOT
Highly controlled optical transport of cold atoms into a hollow-core fiber 5

Potential depth [mK]


-1

Lattice potential [mK]


0
-2

-0.2
-3

-0.4
-4 0 1 2 3 4 5
Distance [lattice constant]

-5
-5.9 -5 -4 -3 -2 -1 0
Distance from fiber tip [mm]

Figure 2. Potential depth (cf. (5)) as function of distance from fiber tip for the case
without laser intensity ramp down (solid line) and for the case of laser intensity ramp
down with n = 1 (cf. (7), dashed line). The inset shows the optical lattice created by
the two counter-propagating dipole trap beams (cf. (3)).

position to illustrate the lattice trapping potential U(r = 0, z, t = 0). For z < 0, the
beam waist of the dipole trap beams, which have their focal point at the fiber tip,
increases and thus intensity I(z) and potential depth Udip (z) decrease. We define the
two limiting points as U0 = Udip (z = zµ ) for the potential depth at the MOT position
and Umax = Udip (z = 0) for the maximum potential depth at the fiber tip. Inside the
fiber for z > 0, the trap depth will stay constant at Umax , when neglecting the coupling
efficiencies of the dipole trap beams into the fundamental mode of the hollow-core fiber.
These are typically above 90% for our setup. For our typical experimental parameters,
we find Umax ≈ 5 mK and U0 ≈ 400 µK.
To load the atoms into the optical lattice, U0 needs to be much larger than typical
temperatures in the MOT of tens of µK, which imposes requirements on the trapping
parameters. For example, for a far-detuned dipole trap at 1064 nm, achieving the same
trap depth would require extremely high-power trapping beams of more than 10 W per
beam (cf. (5)). To keep the laser powers moderate, we therefore choose to work with a
near-detuned dipole trap at 805 nm. This, however, limits the lifetime of atoms in the
dipole trap as will be discussed later.

Apart from this natural change in potential depth given by the Gaussian beam
propagation, we can additionally modify the potential depth by changing the power
P of our dipole trap laser beams. We change the laser power in such a way that we
adapt the potential depth to the position of the atoms, which inherently depends on
time for a given frequency ramp (cf. (2)). The time-dependent potential including the
amplitude ramp-down of the dipole trap beams has the form
 !2   !2 −1
z(t) z(t)
Udip (z, t) = nU0 1 + A  1 +  , (7)
zR zR
Highly controlled optical transport of cold atoms into a hollow-core fiber 6

with
zµ2 + (1 − n)zR2
A= (8)
nzµ2
as a correction factor to maintain the overall shape of the potential. Here, n controls
the final potential depth as Umax = nU0 . For example, if choosing n = 1, the trap depth
is being kept constant for all distances from the fiber tip and thus for the duration of
the entire frequency ramp (see figure 2, main figure, dashed line).
In addition to this overall change in the dipole trap powers, we further can include
individual corrections for each of the two dipole trap beam powers, e.g. to compensate
for fiber coupling losses at high frequency detunings or for different initial power levels
of the two dipole trap beams.

2.4. Data acquisition and analysis

Outside the fiber, we characterize the atoms before and after the transport using
standard absorption imaging on a CCD camera perpendicular to the fiber axis. By
fitting a Gaussian density profile to the atomic cloud, we determine the number of
atoms and the position of the atomic sample. We measure the radial temperature of
the atomic cloud using the standard time-of-flight expansion method.
For probing along the fiber axis and inside the hollow-core fiber, we use a circularly
polarized probe beam resonant to the 87 Rb transition 5S1/2 (F = 2) → 5P3/2 (F ′ = 3)
with an intensity much below the saturation intensity. This probe beam is coupled
through the hollow-core fiber and then into a single-mode-fiber-coupled photomultiplier
tube. With this second fiber-coupling, we select the part of the probe beam that has
been guided in the fundamental mode of the hollow-core fiber. To ensure that we only
measure atoms transported inside the hollow-core fiber, we apply a resonant push beam
outside the fiber just before probing, which is perpendicular to the fiber axis.
From the frequency-dependent absorption profile of the probe beam, h we determine
i the
2
optical depth Dopt by a fit to the transmission T = exp −Dopt / 1 + 4 (∆/Γ) , where
∆ is the detuning of the probe beam and Γ the natural linewidth of the excited state.
These spectroscopy measurements are performed in a time-resolved pulsed probing
scheme, where the dipole trap is switched off for the duration of the probe pulses,
as explained in detail in [4]. To estimate the atomic temperature inside the fiber, we use
a release-and-recapture fit, similar to e.g. [9]. We assume that during the dipole trap off
2
time toff = 2 µs the atomic cloud expands to rat = r02 + vat
2 2
toff , where r02 = ω02(kB T )/Udip
2
and vat = 2(kB T )/m, with T assumed to be constant throughout the probing process.
We calculate the number of atoms recaptured by the dipole trap using the overlap
integral of the probe beam intensity distribution exp ( − 2r 2 /ω02) with the atomic density
distribution n(r) = n0 exp (−r 2 /rat2
) inside the fiber with core radius Rc . After N of
Highly controlled optical transport of cold atoms into a hollow-core fiber 7

such release-recapture cycles, the optical depth is given by


! !!!N
Nat σ± S23 2ω02 R2 2R2
Dopt (N) = 1 − exp − 2c exp − 2c , (9)
πω02 2
2rat + ω02 rat ω0
where σ± is the resonant cross section and S23 the hyperfine transition strength [20].
We determine the initial atom number Nat for N = 1 and rat = r0 .

2.5. Theoretical simulations

To model the atomic transport, we assume all Rubidium atoms to be frictionless


(very low temperatures) and independent, i.e. we neglect particle-particle interactions
(low atom density). Thus, the single particle dynamics is solely governed by the
dipole trap potential (cf. (3)), for which we solve Newton’s equations of motion
numerically by employing the implicit Adams integrator provided in the Python package
SciPy [21].
To prepare the initial state, we position 1500 particles at x = y = 0 mm, while
z-positions are drawn from a Gaussian distribution according to the experimental
parameters. In a second step, every particle’s z-position is shifted such that it coincides
with its closest potential energy minimum. To initialize a starting temperature, the
particle velocities are drawn from a Gaussian distribution with zero mean and width
σvx = σvy = σvz = (kB Tinit /m)1/2 . Since all particles are positioned in potential energy
minima, part of their average kinetic energy is converted into potential energy. Assuming
a quadratic form around the potential minima and employing the equipartition theorem,
the particle ensemble’s equilibrated temperature is given by ≈ 1/2 Tinit . After a short
equilibration period of 20 ms we randomly select 1280 particles that did not escape the
dipole trap, which are then used as the initial ensemble for the transport simulations.
This number of particles is given by the available number of computational kernels.

To identify particles that have escaped the dipole trap, we monitor the total energy Ei (t)
of every particle individually. For Ei (t) > 0 the particle escapes the trap and is no longer
considered when computing ensemble averages. The loss of particles due to lifetime is
taken into account at the final transport position. Finally, to estimate uncertainties of
the quantities of interest, e.g., temperature and fraction of trapped particles, we split
the full ensemble into 20 subensembles and compute the standard error.

3. Results and Discussion

In this section, we present a thorough characterization of our transport method and


discuss the influence of the different transport parameters such as frequency and
amplitude ramps on temperature and transport efficiency. First, we will concentrate on
atoms transported to the fiber tip just outside the fiber (Section 3.1) to characterize the
Highly controlled optical transport of cold atoms into a hollow-core fiber 8
(a) (b) Frequency ramp (c) Position

Frequency detuning [kHz]


250 -1

Transport position [mm]


200 -2
t1 = 0 ms
150 -3

100 -4

50 -5
t2 = 30 ms
0 -6
0 50 100 0 50 100
Time [ms] Time [ms]

t3 = 70 ms (d) Velocity (e) Acceleration

Transport acceleration [m/s2]


0.1 5

Transport velocity [m/s]


0
t4 = 110 ms 0.05

-5

-5.9 mm -1.5 mm 0 mm 0 -10


0 50 100 0 50 100
(initial MOT position) (final position) (fiber tip)
Time [ms] Time [ms]

Figure 3. (a) Absorption images of an exemplary transport process. (c)-(e) Frequency


detuning as well as atomic center of mass position, transport velocity and acceleration
as a function of time. (Data points: Experimental data, solid lines: theoretical model
(cf. section 2.2). Error bars represent statistical errors.)

transport itself, before investigating the influences of the hollow-core fiber by comparing
the properties of atoms transported inside the fiber (Section 3.2).

3.1. Results outside the fiber

To set the stage, we first demonstrate the transport process with a simple example.
Figure 3 (a) shows absorption images of an exemplary transport process for different
time steps within the transport time. We determine the center-of-mass position z(t)
of the atomic cloud for each time step, which we differentiate to calculate velocity and
acceleration during the transport. In this example, we use a linear frequency ramp
∆ν(t) of 0 to 200 kHz in 100 ms to accelerate the atoms and a linear frequency ramp of
200 to 0 kHz in 10 ms for deceleration, as shown in figure 3 (b). Figure 3 (c)-(e) show
both theoretical and experimental values for the position, velocity and acceleration of
the atoms during this transport procedure. The agreement between experimental data
and theoretical model confirms our high degree of control over the position of the atomic
sample.

3.1.1. Effect of frequency ramps on particle number For characterizing the transport
process, we use different types of acceleration and deceleration ramps and discuss their
influence on the transport efficiency without actively adapting the trapping potential. As
a figure of merit, we use the number of transported atoms relative to the initial particle
number loaded into the optical lattice at the MOT position. We detect the transported
atoms directly after the end of the transport process without additional holding time or
time of flight. Figure 4 (a) shows three different frequency ramps for accelerating the
Highly controlled optical transport of cold atoms into a hollow-core fiber 9
(a) 1200
(b) 0.8 (c) 0.8

compared to initial particle number


1000 kHz in (1+9+1) ms
Frequency detuning [kHz]

1000

Transport efficiency,

Transport efficiency,
0.6 0.6

lifetime-corrected
800 1000 kHz in (20+1) ms

600 0.4 0.4

400

200 kHz in (100+1) ms 0.2 0.2


200

0
0 20 40 60 80 100 0 0
1000 kHz constant 1000 kHz linear 200 kHz linear 1000 kHz constant 1000 kHz linear 200 kHz linear
Time [ms]

Figure 4. Transport efficiency for different frequency ramps. (a) Frequency detuning
as function of time for different frequency ramps. (b) Transport efficiency compared
to initial particle number. (c) Transport efficiency corrected for atom-loss due to finite
lifetime in the dipole trap. (Error bars represent statistical errors.)

Table 1. Velocity and acceleration for different frequency ramps (cf. section 2.2).

Frequency ramp (Max.) Velocity (Max.) Acceleration Deceleration


1000 kHz constant 0.4 m/s 400 m/s2 400 m/s2
1000 kHz linear 0.4 m/s 20 m/s2 400 m/s2
200 kHz linear 0.08 m/s 0.8 m/s2 80 m/s2

atoms. Two ramps have a linear increase in frequency detuning, which corresponds to a
constant acceleration of the transported atoms as in the example shown in figure 3. The
fastest ramp has a 1 ms frequency ramp-up and then a constant frequency detuning,
which corresponds to a constant velocity of the transported atoms. We choose the
timings for the different ramps according to the maximum frequency detuning in such a
way that the atoms are always transported to the same final position 1.8 mm in front of
the fiber tip. The velocity and acceleration for the different ramps (cf. section 2.2) are
given in table 1. As we decelerate the atoms within 1 ms for all ramps, the magnitude
of the deceleration is much larger than of the acceleration. However, even for the fastest
ramp we are still far below the maximum acceleration amax = U0 k/m = 2.8 × 105 m/s2 ,
for which the atoms are still transported in their potential wells [13]. Since we detect
immediately after the transport, the transport efficiency is mainly influenced by the
acceleration ramp.
We observe that the fastest ramp with 1000 kHz constant detuning has the highest
transport efficiency (Figure 4 (b)). The efficiency decreases as the ramp time increases,
that is for linear ramps and lower maximum detunings. This effect is due to the finite
lifetime of atoms held in the dipole trap, which is for example limited by scattering of the
dipole trap beams, resonant light from the dipole trap tapered amplifiers [22] and the
background vacuum pressure. To correct our transport efficiencies for the finite lifetime
in the trap, we compare the number of transported atoms with the atom number at the
initial position after the same holding time (see figure 4 (c)). Here, we observe that all
Highly controlled optical transport of cold atoms into a hollow-core fiber 10

studied frequency ramps show a similar lifetime-corrected transport efficiency, with the
slowest ramp showing the highest value. That means that within our experimentally
possible range of frequency detunings, the lifetime has the largest effect on the transport
efficiency. Thus, for the highest absolute final atom number, constant detuning ramps
at high detunings are the best choice for our experimental parameters due to their fast
ramping speed. They are for example better suited for transporting atoms further into
the fiber. However, for higher detunings we observe a tail of atoms trailing behind the
transported atoms, which corresponds to atoms lost from the transport process. They
may be the reason for the lower lifetime-corrected transport efficiency for the two high
detuning ramps. Thus, for experiments not limited by lifetime, slower ramps might be
preferable. We further note that all our transport ramps are fundamentally limited by a
transport efficiency of about 70%, even when taking the lifetime correction into account.
Limiting factors could be amplitude and phase noise on our dipole trap beams, as these
have been shown to have an impact on long-distance transport [14].

3.1.2. Effect of amplitude ramps on temperature Next, we characterize the effect of our
transport procedure and the trapping potential on the temperature of the atomic cloud.
After loading the atoms into the dipole trap, we measure a temperature of T ≈ 100 µK.
This temperature corresponds to a specific energy level in the trapping potential, which
we approximate as a two-dimensional harmonic oscillator in the radial direction (see
figure 5 (a), left-hand side). The energy density EP (E) (see figure 5 (a), right-hand
side) is then given by the Boltzmann distribution P (E) = exp (−E/kB T )/Z, where Z
is the partition function [23].
After being transported to the fiber tip, the atoms will experience an increased dipole
trap potential U1 (see figure 5 (b), left-hand side). Due to this, the trapping frequency
of the harmonic oscillator will have increased and the same energy level will have a
higher energy and corresponding higher temperature T1 . Thus, if we assume entropy
to stay constant during the transport so that the atoms still occupy the same energy
level, the mean atomic temperature will also have increased (red dashed-dotted line in
figure 5 (b)). However, for this given mean temperature, not all the atoms will remain
trapped. By using a so-called truncated Boltzmann distribution [24], we calculate the
mean temperature of the remaining atoms (black dashed line in figure 5 (b)) as
 
1 − 1 + η + 12 η 2 e−η
hT1 i2D,trunc = T1 , (10)
1 − (1 + η) e−η
where η = U1 / (kB T1 ). This value of about 510 µK is in good agreement with the value
of 530(38) µK measured experimentally for the 1000 kHz linear ramp (blue data point
in figure 5 (b)).
When we keep the potential depth constant by applying an amplitude ramp-down, the
atoms which are transported to the fiber tip will nevertheless experience a change in
Highly controlled optical transport of cold atoms into a hollow-core fiber 11
(a) (b) (c)
3.5 3.5(b) 3.5

3 3 3

2.5 2.5 2.5


E(n) [mK]

E(n) [mK]

E(n) [mK]
2 2 2

1.5 1.5 1.5

1 1 1

0.5 0.5 0.5

0 0 0
-100 0 100 energy density E P(E) -100 0 100 energy density E P(E) -100 0 100 energy density E P(E)
r [ m] r [ m] r [ m]

Figure 5. Experimental and theoretical temperatures of atoms in the dipole trap


(a) at MOT position, (b) after transport to the fiber tip without amplitude ramp-
down, (c) after transport to the fiber tip with amplitude ramp-down (n = 1). On
the left-hand side of each figure the trapping potential in radial direction is plotted
with the experimentally measured temperature (data point) as well as the theoretical
mean temperature (red dashed-dotted line) and the temperature corresponding to the
truncated Boltzmann distribution (black dashed line). On the right-hand side of each
figure, the energy density EP (E) corresponding to the theoretical mean temperature
is plotted. The dark-coloured area indicates where the Boltzmann distribution is
truncated by the trapping potential.

trapping potential profile as due to the smaller beam waist the shape of the potential
will be compressed (see figure 5 (c), left-hand side). That leads to a large part of
the Boltzmann distribution to be squeezed out of the trap (see figure 5 (c), right-
hand side), thus losing about 60% of the transported atoms. The mean temperature
calculated from the truncated Boltzmann distribution of about 110 µK is much lower
than the temperature obtained for transport without amplitude ramp-down and close
to the initial temperature. Again, the theoretical calculation is in good agreement with
the experimentally measured value of 100(7) µK.
We can thus control the atomic temperature by adapting the potential depth using
amplitude ramps of the dipole trap laser beams. This comes at the cost of losing atoms
when aiming for low final temperatures.

3.1.3. Effect of combined frequency and amplitude ramps Finally, we study the
combined effect of different frequency and amplitude ramps on the transported atoms.
We exemplarily show the results for the 1000 kHz linear frequency ramp for amplitude
ramps with different final dipole trap depths, as shown in figure 6 (a). For this, we
measure both the transport efficiency compared to the initial atom number and the final
temperature of the atomic cloud (figure 6 (b), solid data points). As discussed before,
we achieve high transport efficiencies up to 55% for high final dipole trap depths, but
at the same time the temperatures are much higher than the initial temperature. When
lowering the final trap depth, both efficiency and final temperature decrease. For a final
Highly controlled optical transport of cold atoms into a hollow-core fiber 12

1
(a) (b)
0 n=0.5
Dipole trap depth [mK]

n=1
-1
n=4 0.8
-2

Transport efficiency
n=7
-3
0.6
-4

-5 w/o AR
-5.9 -5 -4 -3 -2 -1 0 0.4
n=0.5
Distance from fiber tip [mm]
n=1
(c)
n=4
0.2
/ theory

n=7
theor

0.8 w/o AR
0.6
0
exp

0.4 0 100 200 300 400 500 600


n=0.5 n=1 n=4 n=7 w/o AR Final temperature T [ K]

Figure 6. (a) Potential depth as function of distance for different amplitude ramp-
downs. The black dashed line marks the final atomic position for the applied frequency
ramp. (b) Experimental (filled markers) and theoretical (empty markers) results for
transport efficiency and temperatures for atoms transported to the fiber tip for the
1000 kHz linear frequency ramp and for different amplitude ramp-downs. (c) Ratio
of experimental and theoretical values for the transport efficiency. The black dotted
line marks the mean value for all different amplitude ramps. (Error bars represent
statistical errors and errors from the fitting procedure.)

trap depth as low as 4U0 , we still observe a transport efficiency of about 45%. However,
the final temperature is reduced by more than a factor of 3. For very low final trap
depths, the transport efficiency reduces to about 25%. Still, these ramps are a good
choice if one is interested in obtaining a very low-temperature final atomic sample, with
temperatures even below the initial temperature and more than 6 times lower than the
temperatures without amplitude ramp.

We have confirmed that also the other two frequency ramps shown in figure 4 (a) exhibit
qualitatively the same behavior as discussed above and that the qualitative overall trend
for each ramp is robust with regards to day-to-day performance fluctuations of the
experiment.
The results from the theoretical simulation (section 2.5) are plotted in figure 6 (b)
(empty data points) together with the experimental results. We note a very good
agreement regarding the qualitative behavior of the different ramps. When comparing
the experimental and theoretical values for the temperatures, we see a very good
agreement for high final dipole trap depths. However, for small dipole trap depths,
we measure a higher temperature than theoretically expected. This can be due to
fluctuations in laser powers as discussed above, which most strongly influence lower
trap depths. When comparing the experimental and theoretical values for the transport
Highly controlled optical transport of cold atoms into a hollow-core fiber 13

efficiency, we find a constant correction factor of around 0.65 for the 1000 kHz linear
ramp (see figure 6 (c)). In the same way, we determine a correction factor of around
0.75 for the 200 kHz linear ramp. This confirms our previous observation of the
limited maximum lifetime-corrected transport efficiencies (cf. figure 4 (c)), where the
efficiency for the 200 kHz linear ramp was also higher than for the 1000 kHz linear
ramp. A constant correction factor further implies that the additional experimental
loss mechanism does not depend on the number of transported atoms, which would be
consistent with loss due to laser noise as discussed above. Overall, we find that our model
gives a good understanding of the transport mechanism and predicts the results for the
individual ramps well, except for correction factors for experimental imperfections.

3.2. Results inside the fiber

When transporting the atoms inside the hollow-core fiber, our figure of merit
to characterize the transport is the time-dependent optical depth Dopt , which is
proportional to the number of transported atoms, but additionally depends e.g. on
the overlap between atomic cloud and probe beam (cf. section 2.4). Due to a micro
lensing effect of the atomic cloud [25, 26], we find that calculating the optical depth
for high atomic densities is not straight forward. The details of this investigation will
be discussed elsewhere [27]. For the measurements to be discussed in the following, we
have therefore transported the atoms far enough (6 mm) inside the fiber that we expect
these lensing effects to play a minor role due to reduced atomic densities.
Figure 7 (a) shows the behavior of the optical depth during the pulsed probing process
(cf. section 2.4) for three different final dipole trap depths for the 1000 kHz constant
frequency ramp. We observe that the initial optical depth is highest for the transport
without ramping down the potential and decreases for lower final trap depths. This
corresponds to our expectations from studying the transport efficiencies outside the
fiber. We further observe that with increasing number of probe pulses the optical
depth decreases. In principle, this behavior occurs for all amplitude ramps, but is
most prominent for high final trap depths, for which the atomic cloud has a higher
temperature. We can determine this temperature using a release-and-recapture fit (cf.
section 2.4), which is also plotted in figure 7 (a).
Figure 7 (b) shows both the transport efficiency compared to the initial atom number
and the final temperature of the atomic cloud for amplitude ramps with different final
dipole trap depths for the 1000 kHz constant frequency ramp (solid data points). Here,
the results inside the fiber are qualitatively very similar to the results we have obtained
outside the fiber. Without amplitude ramp-down, we obtain both higher transport
efficiencies and higher temperatures, while when ramping down the amplitude to lower
final trap depths, both transport efficiency and temperatures decrease. Also the overall
shape of this decrease agrees well with the measurements outside the fiber. Our
Highly controlled optical transport of cold atoms into a hollow-core fiber 14

(a) 25 (b)
1
w/o AR
w/o AR n=1
20
n=4 n=2
n=4
n=4
n=1
n=1
15 0.8 n=7
D opt

w/o AR

Transport efficiency
10
0.6
5

0 0.4
0 200 400 600 800 1000
Number of pulses
(c)
0.2
theory
theor

0.8
0.6
//

0
exp
exp

0.4 0 200 400 600 800 1000


n=1 n=2 n=4 n=7 w/o AR Final temperature T [ K]

Figure 7. (a) Decay of the optical depth with number of probe pulses for different
amplitude ramp-downs (data points) and corresponding release-and-recapture fit
(Equation (9), solid line). (b) Experimental (filled markers) and theoretical (empty
markers) results for transport efficiency and temperatures for atoms transported 6
mm inside the fiber for the 1000 kHz constant frequency ramp for different amplitude
ramp-downs. (c) Comparison of experimental and theoretical values for the transport
efficiency. The black dotted line marks the mean value for all different amplitude
ramps. (Error bars represent errors from the fitting procedure.)

transport efficiencies range from more than 40% for an atomic ensemble at about 940 µK
to about 10% for a very cold atomic ensemble at about 70 µK. Thus, by adapting the
trap depth, we can lower our final temperatures by more than a factor of 10, while only
decreasing the transport efficiency by a factor of 4.
As for the measurements outside the fiber, we note a very good agreement between
experimental results and the results from the theoretical simulation (section 2.5, shown
in figure 7 (b) as empty data points) regarding the qualitative behavior of the different
ramps. When comparing the experimental and theoretical values for the transport
efficiency, we again find a constant correction factor (see figure 7 (c)). With a value of
about 0.5, it is lower than the correction factor measured outside the fiber. One reason
for this is that the experimental limitations for the transport as observed outside the fiber
have a stronger impact for longer transport distances. Another effect the theory does
not consider is influences from the fiber itself other than keeping the trapping potential
constant. Thus, a lower experimental transport efficiency points to an experimental
limit when loading the atoms into the fiber. We expect the main reason for this to be
imperfect coupling of the dipole trap beams into the fundamental mode of the hollow-
core fiber as discussed in section 2.3, as we have observed that this overlap strongly
influences the transfer efficiency of atoms from outside to inside the fiber. This effect
Highly controlled optical transport of cold atoms into a hollow-core fiber 15

leads to a lower effective trap depth, which can also accommodate for the experimental
values for the temperatures lying systematically below the theoretical values.

With our transport without amplitude ramp-down, we calculate a loading efficiency


from the MOT into the hollow-core fiber of about 2.7%, which is very comparable to
values reported in other groups (2.5% in [10] and 3% in [11]). We also would like to
point out that this number represents a lower limit for our loading efficiency, as we
measure atoms transported already 6 mm inside the fiber.

4. Conclusion

In conclusion, we have presented a detailed study on the transport of cold atoms


both inside and outside a hollow-core fiber using an optical conveyor belt. We have
found that by applying optimized frequency and amplitude ramps we can control a
wide range of transport efficiencies and final atomic temperatures. In particular, we
can prepare final atomic ensembles at the same temperature as before the transport.
Depending on the individual experimental requirements, we can find a compromise
between the final number of atoms and their temperature. While for atoms with a higher
mean temperature, we can achieve higher absolute transport efficiencies, colder atomic
ensembles show an extended observation time before colliding with the fiber walls,
which is advantageous for in-fiber experiments. We further find that our experimental
results agree qualitatively well with the theorectical simulation and we have a good
understanding of the correction factors between experiment and theory. Our high
degree of control over the atom-fiber interface will for example allow for experiments to
systematically survey the inner part of the hollow-core fiber. We also expect our results
to be of importance for other conveyor belt or atoms-in-fiber experiments for reducing
heating during transport.

Acknowledgments

We are very grateful to Florian Stuhlmann who set up and programmed the FlexDDS
during his bachelor’s thesis. We thank Parvez Islam and Wei Li for helpful discussions
and we further thank the GPPMM group of Fetah Benabid for design and production of
the hollow-core fibers for our experiment. We gratefully acknowledge financial support
by the DFG SPP 1929 GiRyd, the DFG via the collaborative research center TRR 146
(Project No. A7) and FP7-PEOPLE-2012-ITN-317485 (QTea).

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