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Optical Pumping of Metastable Helium Atoms in
Polarized Electron Sources
I. Brissaud
To cite this version:
J.
Phys.
II France 5(1995)
497-506 APRIL 1995, PAGE 497Classification
Physics
Abstracts 42 65J 32.80POptical
Pumping
of
Metastable
Helium
Atoms
in
Polarized
Electron
Sources
1. Brissaud
Institut de
Physique
Nucldaire,
91406Orsay
Cedex, France(Received
I June 1994, revised 12December1994,
accepted 22December1994)
Abstract. In this paper we present a
comparison
between theOrsay
and RiceUniversity
polarized
electron sources. Differentexplanations
of the polarizationdegradation
are discussedfor the two cases. For the Rice source
radiation,
trapping
can account for the observed reductionin
polarization
because of thehigh
absorption
cross sections associated with the Di transitionSome improvements are proposed that
might
increase the electronpolarization.
1. Introduction
Ten years ago Walters et al.
ill designed
apolarized
electron sourceusing
a heliumafter-glow.
This was based on thepolarization
of helium metastable atomsby
optical
pumping.
A chemi-ionization reaction with
C02
Produced
freepolarized
electrons. At thattime,
thissource
provided
results farsuperior
to those of conventional AsGa sources(polarization
lim-ited to
50%). Following
a series ofimprovements
theflowing
afterglow
source couldprovide
amaximum
polarization
of87%
at electron currentsIe
= 0.I~tA;
but this decreased to50%
forIe
= 70
~tA
[2].In 1989 the Institut de
Physique
Nucl6aire atOrsay
chose the Riceequipment
for thepro-jected
European
Electron AcceleratorFacility
(ELFE),
but with somechanges.
The resultsnow obtained at
Orsay
[3] are very close to those obtained with the Rice source and show thesame decrease in
polarization
athigh
extracted currents. Toexplain
thiseffect,
we studiedsometime ago radiation
trapping
[4] in theOrsay
case [5]; we now extend this discussion to theRice source. More
generally
we compare thespecific
characteristics and theperformances
ofthe two sources to propose
design
improvements.
2.
Comparison
Between theOrsay
and Rice SourcesThe differences between the two sources [2~6] are shown in Table I. The main one is the choice
at
Orsay
of the electricdipole
Do
transition(between
the2P(
and25(
substates)
for theoptical
pumping
(Fig. I).
TheDoppler
width at ambienttemperature
and thesplitting
between the2P]
and2P]
states are 1.7 and 2.4GHz~
respectively.
Thus these transitions arepartially
Table I. Main
difleTences
between Rice andOTsay
so~Tces.RICE ORSAY
-4x103cms-1 1,2x104cms-1
Dj Do
Laser Single mode Mulumode,
low power (120 mW) hnewidth =2 5 GHz
Exuacuon High vacuum Falr vacuum
0200-050mb 005-010mb Rice
Orsay
+1 p3 o ~p3
o +i +1~s3
o o iFig
I.Optical
pumping
transition used at Rice andOrsay
sources with a+ and 7rlights.
overlapping.
The Rice group built asingle
mode~
low power(120
mW),
stabilized LNA laser [7]and could
optically
pump on theDi
transition withoutexciting
the2P]
state,
which can leadto
depolarization.
Theoretically
theDi
transition cangive
100%
polarization
with a a+ ora-
light
beam. AtOrsay,
optical
pumping
is undertakenusing
a commercial MicrocontroleNd-YAG laser
equipped
with a LNAcrystal
[8]. This multimode laser has 2.5 GHzlinewidth~
but is
powerful
ii Watt)
andcomparatively
inexpensive.
Pumping
on theDi
transition isvery difficult or
impossible
with this laser withoutexciting
the J = 2 state. However withsimultaneous a and1r pump beams one can pump
using
the2P(
state which is wellseparated
from the
2P(
stateIA
= 29GHz).
The effectiveabsorption
cross-sections,
corrected to takeinto account the laser width [9]~ are
approximately
6 timeshigher
for theDi
transition thanfor the
Do
transition: I-e- the final statedensity
leads to a factor3,
and an additional factor 2N°4 OPTICAL PUMPING
/METASTABLES
499Another difference between the Rice and
Orsay
systems
is the helium bulk flowvelocity
in the
afterglow,
which is a factor of twolarger
in theOrsay
source. Thus the metastabledecay
lengths
[10],
andconsequently
the metastabledensity
and the extracted electron current,are
larger
atOrsay
for the same pressure. But metastable atoms in the25(
state (+~5%
concentration
depending
on the Laval nozzletuning)
also survive passage down the flowtube(the
lifetime islonger
than theflight time)
and cangenerate
unpolarized
electrons. At Rice carewas exercised to reduce the
background
gas pressure in the extractionsystem.
This eliminateselectrons due to ionization and excitation of the
background
gas.3. Rate
Equation
Radiation3lrapping
The rate
equations
are different from theOrsay
case [5]. Ifn+,
n°,
n~,N+,
N°,
N~ are thedensities of
25(
and2P(
atoms~
respectively,
in the substates m=
+l~ 0, -1,
at apoint
T andtime
t,
the sixequations
that describe these densities are:dn~ n~ N~
N°
n~~
Tp
~
3T ~ 3T Tr
dy~0 y~0
fit+
fit-~0
$
Tp~
3T~3T
Tr~"~
= ~~ +~~
~~(l)
dt 3T 3T Tr dN~N-~
Tdfil0
y~-fil0
~
Tp T
dfil+
~0
fit+~
Tp T
where T is the lifetime of the
2P/
stateIT
=10~~
s)
and Tr is the relaxation time of metastables.The relaxation time Tr describes
phenomenologically
the loss of metastables to the wallsill]
and is calculated
[10~12]
by
Tr =aR~P/(DP)
with DP = 470tor.cm~s~~
and a =0.27,
R and P
being
the radius and the helium pressure in the source,respectively.
Acomplete
discussion of the measurement and calculation of Tr at Rice is
presented by
Keliher[10].
Thequantity
Tp is the sc-calledpumping
time definedby
=
)~
~),
whereIT
is the totalTp V0
laser power distributed over area
S;
hvo
is the energyquantum
for afrequency
vo "c/Ao,
withlo
= 1.083 ~tm. We denote
by
lo
thewavelength
involved in the transition from the metastable
"ground
state~'25(
to the excited state2P(.
The level-to-levelabsorption
cross section aa isdeduced from the classical state-to-state
absorption
cross section [9] forunpolarized
light
j2
is the
Doppler
distribution around vo(13]j
so aa =-Flu
vo).
The laser width correction27rT
is not
justified
in the Rice case because itsfrequency
width isnegligible.
Note theintensity
I =
IT
IS
is thesignificant
parameter
rather thanIT-Equations
ii
describe the metastablepopulations
in a framefollowing
the gas flow. Thesepopulations
are a function of timeonly.
The deduced metastablepolarization
~+
~-~°~
n+ + n° +
n-~~~
is not
dependent
on Tr, butonly
on Tp. This means that thepolarization
never reaches asteady
state
it
~oo),
but if thelight
is intenseenough
andfor
thepumping
areagreat
enough,
Pal canbe
large.
Thisdescription
isslightly
different for a sealedcell~
where adischarge
repopulates
themetastable sublevels which are
destroyed
at the cell wall[14].
In this case~repopulation
wouldintroduce additional terms
n/3Tr
in the rateequations.
But calculationsusing
theequation
system
ii)
show that thepolarization
is not verydependent
on these terms. To check thevalidity
of themodel,
we calculated thepolarization
as a function of laser power~ which wasmeasured at Rice [2] for a low metastable
density
in
<10~
cm~~)
for which radiationtrapping
is
negligible.
Figure
2 demonstrates that the results agree very well with theexperimental
data.Radiation
trapping
is thereabsorption
ofunpolarized
radiation emittedby
thedecay
ofex-cited states
during
theoptical pumping
process.Figure
3 shows all the emission andabsorption
transitions. To take
reabsorption
into account~ we add to the rateequations
ii)
specific
termsfollowing
theprocedure
proposed by
Anderson et al.[15]
Forexample~
the additional term tothe third
equation
in(I)
has theshape.
)~
d~/dv[P~m(9)F(v
vo))
xexp[-(Y
II
~j
al
(9)(n~
N~
)] 80 o 60 40 20 0 1 mW 1Fig.
2. Electronpolarization
as a function of laser power. Experimental data [2] andpolarization
calculated without radiation
trapping
by
rateequations
(I)
The parameters are IT = 80 mW,R
N°4 OPTICAL
PUMPING/METASTABLES
501 +1 +1 o p3 o i -i~j'
(,'
+I +1 025(
0 E mission AbsorptionFig.
3 Emission andabsorption
transitions involved in electricdipole
transition25(
2P(
forunpolarized
radiations. A= mf m~ is the
magnetic
quantum number transfer in these transitionsFor A
= mf m~ = 0 the transition is forbidden.
x
(~j
a)(9)(n°
N~)j
(3)
where 9 is the
angle
between f/
and the direction of themagnetic
field.The first factor is the electric
dipole
deexcitationprobability
of the N~ atoms in2Pi
stateat the
point
T'. This radiation is attenuatedalong
thepath
f/
by
the transition a ~ b(second
factor).
The last factorgives
the radiationabsorption
by
the transition c ~ d at thepoint
f. Theabsorption
cross sectional
corresponds
to theabsorption
of emitted radiationcharacterised
by
the transition Am=
(mf
m~)
= k and absorbedby
the transition Am =(m
f
m~)
= I Thesequantities
are deduced from the matrix elements of thedipole
operator
0
as <
i[f~(9)
Vi
f
> [~~f~
(9) being
the field of the incident wave[7].
Appendix gives
thenine values of
al
(9) (available
only
for theDi
transition in heliumpumping)
and the additionalterm
(3)
aftersimplification
(same
example
of the thirdEq.
(1)).
The NAG code from the CERN
library
is used to solve theequation
system
(1+ 3).
Theinput
parameters
are:al
laser powerIT
" 80 mW
b)
irradiation area S = 40cm~.
4. Results and Discussion
The rate
equations
give
the metastable densities as a function of time. We have calculatedthe metastable
polarization
using
aflight
timecorresponding
to alength
ofapproximately
6 cm. Note that the
experimental
uncertainties(1/4
plate,
optics,
chemi-ionizationeificiency~
spin
singlet
25[
metastable presence~ etc. are not includedalthough they
limit the attainablepolarization
to below 100%. These corrections are estimated to beapproximately
10%[2].
Asthe maximum
polarization
at Rice is87%,
this value is chosen as the normalization factor ofThe most serious
assumption
of theprevious
calculation(Eq. (4))
was that n~ and NJdensities are
independent
of theposition
f whereasthey
have anapproximately
parabolic
radialprofile [12,17].
Animprovement
to the calculationspreviously
presented
is to assume that thedensities have a
cos(1rT/2R) spatial
distribution. Thisassumption
is more realistic becausethe radiation emitted at T = R has a
higher probability
to escape than at the center (T =0).
Unfortunately,
by
including density
variation~
thecomputer
times becomeunreasonably long.
Certainly
a moresophisticated
procedure
must bedeveloped,
assuggested
by Happer
andRedsun
[18].
Nevertheless~
for arough
understanding
of theexperimental
data of the Ricegroup the
previous
calculations are sufficient. In the future wehope
to obtain more accuratemetastable
polarization
data and toimprove
thecomparison
withsophisticated
calculations.In the present work the cosine function distribution is used
only
to calculate thepolariza-tion values versus the metastable
density
(Fig.
4)
because the results with and without thedensity
correction are very close: athigh density
(n
>10~°
cm~3)
this correction increasesthe
polarization
by
10%approximately.
Experimental
datapreviously
published
[2] are shownon the same
figure.
Thecorresponding
metastable concentrations were determinedby
absorp-tion of the
light
emittedby
a heliumlamp
[10] and are inaccurate.Nevertheless,
one sees anagreement
despite
the crudeness of thereabsorption
model. The conclusion is that radiationtrapping
isresponsible
for thepolarization
decrease athigh
metastable concentrations orhigh
electron currents.
Fortunately
the Rice results can beimproved by
changing
theexperimental
set-up and
procedure:
laser~
geometry,
etc.Figure
4 also shows the metastablepolarization
forthe
Orsay
source. In this case thetrapping
becomessignificant
only
at metastable densitieshigher
than those used at Rice because the effectiveabsorption
cross-section is lower for theDo
transition than for theDi
transition. This proves the value ofoptical
pumping
using
theDo
transition.The
polarization
is calculated as a function of the total laser power(Fig.
5 for two metastabledensities
(7
x10~
and10~°
cm~~).
This calculation shows that saturation is almost reached atIT
" 80
mW~
as was confirmedby
the Rice measurements.Increasing
the laser powerimproves
oi~~~l
~--~-jj,
'~",,
a oRsAy ~~ ,~
50 RICE 10~ 10'° ~ 10" n[cm-Fig.
4. Polarization calculatedversus the metastable
density
for theOrsay
and llice sources. Thecosine
profile
is included(al
or not(b).
Theexperimental
data are presented with error bars. Theempty
points
correspond
to the metastabledensity
measuredby
laser atOrsay.
The other ones(full
N°4 OPTICAL
PUMPING/METASTABLES
503 ioo Poll%) ~ a so 50 loo 150Total laser power lmw)
Fig.
5. Polarization calculated versus the total laser power for metastabledensity
of 10~°cm~3
(al
and 7 x 10~cm~3
(b).
The curve(cl
is thepolarization
calculated without radiationtrapping
correction.
the
polarization
only
slightly.
We have assumed that the laserlight
beam ishomogeneous
overthe
pumping
volume. Infact,
measurements of thelight
distribution atpoint
T show a Gaussiandistribution. This could lead to the unsaturatiou of some metastables. This effect must be
negligible
with the Riceset-up
where two baffles concentrate the metastable beam and increasethe
polarization
by
10% [19].
On the other hand it mustplay
alarge
role atOrsay.
Figure
5also shows the
polarization
ueTsw the laser power, calculated without thetrapping
corrections.Then the
polarization
is87%
except
at low power(IT
less than 50mW)
when thepumping
time Tp becomes
large.
To reduce the radiation
trapping
it seemsinteresting
to reduce the dimension of theoptical
pumping
chamber. In this way the metastabledensity~
I-e- the electroncurrent,
decreases(the
decay length
is shorter[10,
12]).
Therefore anoptimization
process isrequired.
5. Conclusion
From our
calculations,
it appears that thepolarization
degradation
of the Rice source ismostly
due to radiation
trapping,
as it wassuspected
by
Walters et al.[20~21].
The curves inFigure
4show
clearly
that this effect is moreimportant
at Rice than atOrsay
because theabsorption
cross-sections are
higher
for theDi
transition: the factor 6 between these cross sectionsexplains
approximately
the shift between the curves. Sincespin
polarization
is conserved inchemi-ionization reactions
(checked
atRice)
and the extractiongeometry
is identical in the twosources, one
expects
electronpolarization
superior
atOrsay
than at Rice for the samehigh
electron currents. In
fact,
theexperimental
values of thesepolarizations
[2,
3] are close. Thisdisagreement
ispresently
studied[22].
To increase the
polarization
at Rice it would be fruitful to useoptical
pumping by
Do
tran-sition under the
present
conditions. Afterthat,
some minorimprovements
in theexperimental
conditions could be tested to increase the
polarization:
I)
an increase of the laser power per unitarea~
it)
animprovement
of the electron extractionefficiency
so as to work at lower metastabledensities: in this way, a
higher
polarization
should be reached for the same current, andiii)
aclassical
technique,
I-e- decrease the effectiveabsorption
cross sectionsby
detuning
the laserfrequency
to thewings
of the atomic resonance line[23].
Acknowledgments
The author would like to thank G.K. Walters for
communicating
the Riceexperimental
dataand for many comments and
encouragements.
Heclearly
showed thephysical
differencesbe-tween the
discharge
cell and theflowing
afterglow
and the consequences. Fruitful"interconti-nental" discussions with G-W- Rutherford were a
great
pleasure.
Ouracknowledgements
aredue to W. L.
Anderson,
G.Lampel
and B.Cagnac
forhelpful
conversations. We also thankA. Talbot and N.
Revoyre
for the nicetyping
of this paper and for theirpatience.
Appendix
The same
assumptions
as thosepreviously
proposed by
Anderson et al.[15]
are used tosimplify
equations
(3):
I)
thepumping
chamber is ainfinitely
long
cylinder
of radiusR(R
= 5cm)
withnon-reflective
walls,
it)
the densities n~ and N~ are taken to beindependent
ofposition
7,iii)
the laserlight
ishomogeneous.
Theintegrations
overfrequency
andangle (Eqs.
(3))
areperformed
using
Hermitian and Gaussianintegration
procedures.
Theintegration
overradius is
performed
exactly.
The
trapping
contribution has then thesimplest
shape Ti
+T2
+T3
where:N°4 OPTICAL
PUMPING/METASTABLES
505 T~ =~~/~
+j~+
~/~~
j
w~j
w~j(n+
N+)F~(~lj)
+ ~ ~+w3j
(n+
N°)F3(~1~)
+ w3j(n+
N°)F~(~1~)
(4)
with 2 1 exp(-
~~'('~"
F~(q~~) = UJ 1- ~1~4(llJ
~
and 1- exp(-~)
j/(~
fi
~"J 3 j j~~~
J and#(u~
=(1
~)
)(n+
+2n°
+ n~N+
2N°
N~ +2~1~(n+
+n°
+ n-N+
N°
N~ N+ +No
~ ~ ~ ~~
2fiT
~~°
~
~°~~'~~~~~"
~ ~~°~~'~~~~~"
" ~~~ t J withj/~
~~ = ~fi
~~~ ~~~~~~~
j ~j( il j and 1l
exp(-
j)
~/(~
J 5 jfi
4(llJ
J and2~1~(1-
~1~) ~ + ~ ~ ~(n+
+ n + n~N+
N°
N~)
2 ~~x~ are the nodes and w~ the
weighting
factors of the Hermiteintegration
method[24],
and ~~the nodes and w~ the
weighting
factors of the Gaussianintegration
method[24],
with:j3
~f 1/2 ~~'~~
The cross-sections
a(z'[Q~]]j(]~~
areal
= 2sin~
9 aa(
=a°
=cos~
9 a ~sin~
9 °+ °~(l
+ cos~9)
° ~ 2cos~
9sin~
9 °° °°(l
+ cos29)
°a+
=aj
=(I
+cos~
9)
a °~T~~~
~°~ References[1]
Gray
L-G- etal.,
Rev. Sm. Instrum. 54(1983)
271, and references therein.[2] Rutherford G.H. et al., Rev. Sci. Instrum. 61
(1990)
1460, and references therein. [3] Arianer J. etal.,
Nucl. Instr. Meth. A337(1993)
1.[4]
Happer W.,
Rev. Mod.Phys.
44(1972)
169.[5] Brissaud I. and
Jacquemin
C.,
J.Phys.
II France 5(1995)
93.[6] Aminoff C-G- et al.,
Proceedings
of the 9th InternationalSymposium,
Bonn,September
1990.[7] Lynn J-G-, Ph.D.
Thesis,
lliceUniversity
(1990).
[8] Aminoff C.G. et
al., Optics
Commun. 86(1991)
92, and references therein.[9] Mitchell A-C.G. and Zemanski
M-W-,
Resonance Radiation and Excited Atoms(Cambridge
Uni-versity
Press,
London,
1961).
[10] Keliher
P-J-,
Ph.D.Thesis,
lliceUniversity
(1974)
and references therein.ill]
Phelps A-V-,
Phys.
Rev. 99(1955)
1307.[12]
Fergusson
E-E- etal.,
Adv. At. Mol.Phys.
5(1969)
1.[13]
Corney A.,
Atomic and LaserSpectroscopy
(Clarendon
Press,
Oxford,
1979).
[14] Schearer L-D- and Padetha
Tin, Phys.
Rev. A 42(1990)
4028.[15]
Tupa
D. and Anderson L-W-,Phys.
Rev. A 36(1987)
2142;Tupa
D. et al.,Phys.
Rev. A 33(1986)
lo45.[16]
Cagnac B., private
communication.[17] Bolden R.C. et al., J.
Phys
83(1970)
45.[18]
Happer
W.~private
communication.[19] Ratliff J-M-, Ph.D.
Thesis,
RiceUniversity
(1989).
[20] Keliher P-J- etal.,
Phys.
Rev. A 1(1975)
1279.[21] Walters
G-K-,
talk given at Universitdd'orsay
(1989)
andprivate
communication.[22] Brissaud
I.,
Nucl. Instr. Meth. A354(1995)
588.[23] Redsun
S-G-,
Ph.D.Thesis,
PrincetonUniversity
(1990).
[24] Abramowitz M. and