for the experiment. We use a series of optics to pre-
pare the polarisations before splitting the circular po-
larised light with a 50:50 beam splitter into the in-
terferometer. It is here we obtain the σ
+/−
terms as
displayed in figure 1. Before entering the vapour cell
one of the beams is attenuated with a neutral density
filter (ND filter), making it into our weak probe beam.
Two solenoids surround the vapour cell within
three layers of µ-metal shielding. These are driven by
an arbitrary signal generator. The first (modulation)
solenoid is driven with a square wave correspond-
ing to approximately 1nT of between 250-300KHz,
which is used as the reference for the signal recovery
lock-in amplifier. The second solenoid is also con-
nected to the arbitrary signal generator and is driven
with a sine wave with frequencies between 2-8Hz.
The human heart has a frequency range of 1-1.67Hz,
with higher frequency components.
The raw signal is collected via a photodiode and
then connected to the input of the signal recovery
lock-in amplifier. The lock-in amplifier allows very
small signals to be extracted from the large amounts
of noise, using this system we have gained sensitiv-
ities in the range of a fetal heart beat. An example
of test data taken using a simulated heartbeat is dis-
played in figure 5.
Figure 5: A sceen dump of data take on the experiment.
The centre trace is the raw input signal, a simulated QRS,
the lower trace is the raw data from the photodiode and the
upper trace is the 20 trace avarage.
3 CONCLUSIONS
With current data we can measure magnetic fields of
the order of a fetal heart beat. The experiment is
still at a very early stage of development, therefore
the current data acquisition method is not suitable for
clinical applications. However even at this stage the
experiment has shown a great deal of promise as a
potential MCG device. We expect, with some calibra-
tion, to obtain at least femtotelsa sensitivities (Fleis-
chhauer and Scully, 1994), with the possibility of us-
ing more optical fibres and replacing the modulation
solenoid with an alternative scheme such as an acous-
tic or electro-optic modulator (AOM/EOM). These
improvements will move this research closer to being
a competitive device for performing clinical MCG tri-
als.
ACKNOWLEDGEMENTS
This work is funded by an EPSRC DTA.
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