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Submitted on 1 Jan 1990
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Wavelength comparison and Rydberg constant
determination
J.C. Garreau, M. Allegrini, L. Julien, F. Biraben
To cite this version:
High
resolution
spectroscopy
of the
hydrogen
atom
III.
Wavelength comparison
and
Rydberg
constant
determination
J.C. Garreau(*),
M.Allegrini(**),
L. Julien and F. BirabenLaboratoire de
Spectroscopie
Hertzienne del’ENS(***),
Université Pierre et Marie Curie, 4place
Jussieu, Tour 12, E0175252 Paris Cedex 05, France.
(Received
2February
1990, revised 15 June 1990, accepted 27 June1990)
Résumé. - Cet article est le dernier d’une série de trois donnant une
description
détaillée de notremesure récente de la constante de
Rydberg.
Nous y décrivonssoigneusement
la méthode de mesuredes
longueurs
d’onde. Leslongueurs
d’onde des trois transitions A deuxphotons
2S-8D, 2S-10D et2S-12D dans
l’hydrogène
et le deutérium sontcomparées à
celle d’un laser He-Ne stabilisé sur l’iode,laser
qui
est actuellement la meilleure référence dans le domaineoptique.
Cettecomparaison
estfaite à l’aide d’un étalon
Fabry-Perot
degrande
stabilité. Lesdéphasages à
la réflexion sontpris
encompte en
changeant
lalongueur
de cette cavité("méthode
des miroirsvirtuels").
Pour mesurer ledéphasage
de Fresnel nous étudions la différence defréquence
entre lepremier
mode transverse etle mode fondamental de cette cavité. A
partir
des sixlongueurs
d’onde mesurées, nous déduisons unenouvelle valeur de la constante de
Rydberg
R~ = 109737,315709(18)
cm-1,
laplus
précise à
l’heureactuelle. A
partir
desdéplacements isotopiques
entrel’hydrogène
et le deutérium nous déduisonsaussi une valeur pour le rapport de masse entre le proton et l’électron:
mp/me
= 1836.15259(24).
Abstract. 2014 This
paper is the last of a series
giving
a detaileddescription
of our recent determi-nation of theRydberg
constant. Here wecarefully
describe thewavelength
comparison
procedure.
Thewavelengths
of the threetwo-photon
transitions 2S-8D, 2S-10D, and 2S-12D inhydrogen
and deuterium arecompared
to that of anI2-stabilized
He-Ne laser which is the present best referencein the
optical
domain. Thekey
of thiscomparison
is ahigh stability Fabry-Perot
cavity
etalon. The reflectivephase
shifts are taken into accountby
changing
thelength
of thiscavity
("virtual
mirrorsmethod").
In order to measure the Fresnelphase
shift westudy
thefrequency
difference between the first transverse mode and the fundamental mode of thecavity.
From the six measuredwavelengths
wededuce a new value for the
Rydberg
constant, R~ =109737.315709(18)
cm-1,
currently
the mostprecise
one. The H-Disotopic
shifts have been also measured and a value for theproton-to-electron
mass ratio is deduced:
mp/me
=1836.15259(24).
ClassificationPhysics Abstracts
35.10 - 06.20J - 32.80K
1. Introduction.
This paper is the last of a series of three
(referred
as papersI, II
andIII), giving
acomplete
description
of our recent determination of theRydberg
constant[1] .
Our method is to measurethe
wavelengths
of the 2S-nDDoppler-free
twophoton
transitions in an atomic beam ofhydrogen
or deuterium n =
8, 10, 12.
Inpaper 1
[2],
we have described theprinciple
of ourexperiment
and theexperimental procedure
used to observe lines as narrow as 600 kHz. In paper II[3],
we havecarefully analyzed
thelineshape
of thetwo-photon
transitions. As a result we know the atomicfrequency positions
withrespect
to a very stable referencecavity (FPR).
We descnbe now the measurement of the
Rydberg
constant. In section 2 wepresent
thewave-length
measurements, and in section 3 we descnbe the détermination of theRydberg
constant.2.
Wavelength
measurement.2.1 STANDARD LASER - The transition
wavelength
is measuredby
interferometrictechniques
based on the
comparison
of ourdye
laserwavelength
withthè
one of anl2 2013
stabilized He-Nelaser at 633 nm. This He-Ne laser is the best reference in the
optical
domain since itsfrequency
has been measured withrespect
to the cesium clock[4].
In fact we have two12-
stabilized He-Ne lasers which arecontinuously compared
andrunning
with an12
cold-finger
temperature
of 16° Cand a modulation
peak-to
peak amplitude
of 5 MHz. In order to check these referencelasers,
we have made a
frequency comparison
with a standard He-Ne laser of the Institut National deMétrologie (INM).
Thiscomparison
was made everyday
at thebeginning
and at the end of theexperiment
Thefrequency
différence value between the INM laser(stabilized
on the dhyperfine
component
of the127 I2
11 -5R(127) transition)
and ours one(stabilized
on the fcomponent)
was 26.195
(5)
MHz(mean
of the data obtainedduring
about amonth). 1àking
into account thevalue for this différence
(26.224
MHz[5]
),
we deduce that our laser was +29 kHz shifted withrespect
to the INM one. The INM laser has beenpreviously
compared
with the one of the Bureau International des Poids et Mesures(laser
BIPM2).
Withrespect
to this laser the INM laser was-23 kHz shifted
[6] .
Finally
our12-stabilized
laser is +6 kHz shifted withrespect
to the BIPMone. We have assumed that the
frequency
of the BIPM laser(stabilized
on the icomponent)
is asmeasured
by
D.A.Jennings
et aL[4]
with a 1.6 x10-10
relativeuncertainty:
1àking
into account the value for thei-f
splitting (138.892
MHz[5]
),
we deduce thefrequency
value for
the f
component
of ourIz-stabilized
He-Ne laser:We have used this value for the
wavelength
measurements and for theRydberg
constant determi-nation.2.2 INTERFERENCE APPARATUS The
key element
for the interferometriccomparison
is anon-degenerate
Fabry-Perot
etalon(FPE)
kept
under a vacuum lower than10 - 6
mbar. In these condi-tions the error due to the index variation between thecompared wavelengths
is reduced to about10-15.
Thisoptical cavity
is built with two silver coatedmirrors,
one fiat and the otherspherical
(R
= 60cm),
inoptical
contact to a zerodur rod. Its finesse is - 60 at 633 nm and - 100 at 778Fig.
1. -Experimental
set-up for thewavelength comparison.
Figure
1 shows theexpérimental
set-up
for thewavelength
comparison.
Asexplained
in paper 1[2] ,
thedye
laserfrequency
is known withrespect
to a referencePabry-Perot cavity
(FPR)
which is locked to anI2-stabilized
He-Ne laser. Thedye
laserfrequency
isprecisely
scannedby
means of anacousto-optic
modulator inconjunction
with acomputer-controlled frequency
synthesizer.
Withthis
apparatus
we haveprecisely
measured thefrequency
différence
f2p
between thetwo-photon
transitionfrequency
and theAiry
peaks
of the referencecavity
[3] .
Figure
2 shows the relativeposition
of the atomicsignal
withrespect
to theAiry peaks
of the referencecavity
FPR and of theFabry-Perot
etalon FPE. For thewavelength comparison
we have to measure thefrequency
difference
AR
between theiodine f
component
and the closestpeak
of the FPE. For that purposean
auxiliary
He-Ne laser is mode-matched and locked to the FPEcavity.
The beatfrequency
be-tween the
auxiliary
and the standard He-Ne laser is measuredby
afrequency
counter. We havealso to measure the
frequency
differenceAIR
between thetwo-photon signal
and the closestpeak
NIR
of the FPEcavity.
We haveAIR
=f2p
+fFP, where
ffp
is thefrequency
difference betweena
given Airy peak
of the referencecavity
FPR and one of the etaloncavity
FPE(Fig.
2).
In orderto measure the
frequency ,
fFp,
thedye
laser is scanned to the résonance with the etaloncavity
FPE,
and mode-matched to thiscavity.
Itsfrequency
is locked to the etaloncavity through
thecomputer.
Thedye
laserfrequency
is modulated(about
1 MHzpeak-to-peak
at 1.2kHz)
and the modulation of the transmitted beam is detectedby
a lock-inamplifier.
After conversionby
an
analog-digital
converter, thesignal
is readby
thecomputer,
which drives theacousto-optic
modulator in order to cancel the
output
of the lock-inamplifier.
During
the measurement(about
2
minutes),
thecomputer
recordssimultaneously
f FP
(twice
thefrequency
of theacousto-optic
fluctuation of the
length
of thiscavity
andfFp
andAR
fluctuate. These fluctuations are correlatedand,
in order to eliminatethem,
thecomputer
calculâtes thequantity :
Fig.
Z - Relativeposition
of thetwo-photon signal
with respect to theAiry peaks
of the referencecavity
and of the etaloncavity.
This
quantity
isindependent
of thelength
fluctuations of the etaloncavity
FPE andcorresponds
to the
ffp
value obtainedwhen AR -
OR (Aor is
a fixedvalue,
close to theexperimental
one andarbitrarily fixed).
1b obtain a
precise
wavelength
measurement, it is necessary that thefrequencies
of thedye
laserand of the
auxiliary
He-Ne laser coincide with the resonancefrequencies
of the etaloncavity
FPE. lb take into account theintensity
variation due to thegain
curve of theauxiliary
He-Nelaser,
wemonitor the difference between the transmitted beam
through
the etaloncavity
and a reference beamhaving
the sameintensity.
We have tested theefficiency
of thisprocedure by locking
theauxiliary
He-Ne laser to twoadjacent
peaks
NR
andNR - 1
of the etalon FPE.By
this means weobtain a measurement of the free
spectral
range of thiscavity
(frequency
measurement)
which canbe
compared
with the mostprecise
value obtainedby
interferometry (wavelength
measuremènt).
Asexplained
in thefollowing,
we have used two etaloncavity lengths,
10 cm and 50 cm. Thecomparison
between the two freespectral
range measurements isgiven
in table I. Asystematic
discrepancy
appears in the short etalon measurements. In this case we reach the limit of thedifferential method used to eliminate the
gain
curve effect because the twoAiry peaks
of theetalon
cavity
are in thewings
of this curve. In ourwavelength
measurements we have used themean of the two results obtained when the
auxiliary
He-Ne laser is locked to theNR
andNR -
1peaks.
We estimate the error in the controlloop
of the He-Ne laserfrequency
on the short etaloncavity
to be ± 9 kHz(half
the difference between the two freespectral
rangemeasurements).
1àking
into account the virtual mirrorsprocedure,
which will beexplained
in thefollowing,
thiserror introduces an
uncertainty of 4.7 x
10-12
in the final result. Measurement with thelong cavity
etalon
always
involves anAiry peak
at thetop
of the He-Negain
curve and our differential methodcorresponding
to anuncertainty
of 1.3 x10-12
in the final result. The same kind of error canexist for the
dye
laserfrequency servo-loop.
Nevertheless these errors can beneglected
becausei)
the finesse of the etaloncavity
islarger
in the infrared domain than in the red one;ü)
there isno
dependence
of thedye
laserintensity
versus thedye
laserfrequency
(we
have verified that thesignal
at the modulationfrequency
of thedye
laserfrequency
isnegligible).
Table I. Free
spectral
range measurmentof
the etaloncavity
FPE.1
2.3 VIRTLJAL MIRRORS METHOD. - The
frequencies
of the red and infrared radiations inside the etaloncavity
FPE are determinedby
the resonant condition:where L is the
cavity length,
N is aninteger
numbers
is the reflectivephase
shift for thelight
offrequency v
and 03A6 the Fresnelphase
shift. The Fresnelphase
shiftdepends only
on thecavity
geometry.
Its measurement will be described in thefollowing.
The reflectivephase
shift 1/;
dueto the mirror
coating
iswavelength dependent
and is eliminatedby
the method of virtual mirrorsby using alternately
two rods of différentlengths (10
cm and 50cm)
for the etaloncavity.
Thismethod is
explained
in detail in reference[7] .
The basic idea is that the reflectivephase
shift
is
independent
of thecavity length.
We can write the resonant condition(1)
for thelong
and the shortcavity (labelled 1
and srespectively)
and for the red and infrared radiations(R
and IRlabels)
which arecompared.
Forexample,
we have for thelong
etalon and for the infraredfrequency:
where
bIR
is the fractional order relative to thehigher frequency Airy peak.
It is the ratio betweenthe
frequency splitting
AI
IR(see Fig. 2)
and the Creespectral
range c .
From theequations (2)
2Lrelative to the short and
long
etalon and to the tworadiations,
we can eliminate the twocavity
lengths
and the reflectivephase
shifts03C8IR
and03C8R.
We obtain the ratio between the twofrequen-cies :
conséquent
changes
of1PR
and1PIR.
The difference between the two reflectivephase
shiftsOR
andÇIR
can be considered as a variation 6L of thecavity
optical
length
for the red and infrared radiations. For the infraredradiation,
the mirrors are more reflective than for the red one and thecavity
optical length
is shorter. From ourwavelength
measurements with the 10 cm étaloncavity
FPE,
we can deduce 6L at thebeginning
and at the end of theexperiment.
Ibe results aregiven
in table II. As the
hydrogen
and deuteriumwavelengths
are very close we have taken the mean of thehydrogen
and deuterium results relative to the same 2S-nDtwo-photon
transition. We have observed aslight
variation of 6L(about
0.03.nm)
during
theexperiment
and we take this effect into account in theuncertainty
of our final result.Table II. - Variation
of the
cavity
optical length
between the red andinfrared
radiation at thebegin-ning
and at the endof the
experiment.
2.4 FRESNEL PHASE SHIFT MEASUREMENT. - For a
plané-spherical
Fabry-Perot,
the Fresnelphase
shiftdepends
on thelength
of thecavity
and on the curvature R of thespherical
mirror[8] :
We have determined the Fresnel
phase
shiftby measuring
thefrequency
interval between thefundamental
TEMoo
mode and the first transverse modeTEMo1
(or
TEM,O)
of thecavity.
In-deed,
the resonance condition for theTEMn,m
mode is[8] :
We can deduce
In
principle
TEMO,
andTEMIO
aredegenerate by
symmetry. However,
due toimperfections
in the mirror curvature,
they
are notcompletely
degenerate.
Depending
on thealignment
of themodes which
give
different results for the relativefrequency
of the first transverse mode and theTEMoo
mode. We have made measurements for variousalignments
and the result is shown infigure
3,
which shows thedependence
of thisfrequency
différence upon the orientation of the two transmittedlight
spots
of theTEMol
mode. The Fresnelphase-shift
that we need is thengiven by
the mean value of the curve offigure
3[9].
We have made this measurement for eachstep
of theexperiment (10
cm, 50 cm and 10 cmetalon)
with the He-Ne laser. For the 50 cmetalon,
we have also made the measurement with thedye-laser
at 780 nm. The results aregiven
in table III. We have observed asignificant
variation between the two 10 cm etalon measurements. This is due tothe fact that we do not use
exactly
the samepoints
of the mirrors in the two cases. On the otherhand,
the two 50 cm etalon measurements are in verygood
agreement :
the variation with thewavelength
of the size of the laser beam inside thecavity
has anegligible
effect.Thble III. -
Frequency difference
(MHz)
between thefundamental
modeTEMoo
and thefirst
trans-verse mode
TEMm.
10 cm etalon
(first
measurment, 633nm)
: 200.776(67)
50 cm etalon
(633 nm)
: 109.851(13)
50 cm etalon
(780 nm)
: 109.853(13)
10 cm etalon
(last
measurement, 633nm) :
201.024(49)
Fig.
3. -Frequency
difference between the first transverse modes TEMO, and TEM1 o and the fondamental mode TEMoo vs. the orientation of the two spots of the transverse modes.2.5 RESULTS. 2013 We used
équation (3)
to détermine the infrared radiationfrequency.
In thetwo
preceding paragraphs
we have described the measurements of the Fresnelphase
shift 03A6 and-stabilized He-Ne laser and the six
two-photon
transitionwavelengths
which are measured.Indeed,
taking
into account our earlier determination of theRydberg
constant[11],
thesewavelengths
areknown with a relative
uncertainty
better than10-9.
Since theuncertainty
in a fractional ordermeasurement is about
10- 4
in the case of the 50 cm etalon and is smaller for the 10 cmetalon,
andsince the etalon
length
isinitially
known with a relativeuncertainty
of about10-3,
the fractionalorder data for these seven
wavelengths
are sufficient to determineunambiguously
theinteger
number N. The values of N aregiven
in table IVTable IV Values
of
theinteger
numbers N.As we have two sets of data for the 10 cm
etalon,
we canapply equation (3)
twice(firstly :
first 10 cm data and 50 cm
data;
secondly :
50 cm data and last 10 cmdata).
The results for the six studied transitions aregiven
in table V The second columngives
the difference between the second and the first determinations. This difference is due to theageing
of the mirrors. The third columngives
the mean of the two results. This is the value that we haveadopted.
Thequoted uncertainty
does not include the reference laseruncertainty.
It is thequadratic
sum of :i)
theuncertainty
of thecomparison
between the He-Ne lasers(about
10-11),
ii)
theuncertainty
of the atomic
frequencies (statistical
uncertainty
anduncertainty
of the theoreticallineshape
asexplained
in[3] ),
iii)
theuncertainty
of the Fresnelphase
shift measurements(about
1.2 x 10-11 ),
iv)
the statisticaluncertainty
of the fractional order measurements andv)
theuncertainty
due tothe
ageing
of the mirrors(half
the value of the first column of Tab.V).
A more detailedanalysis
of the uncertainties will begiven
in section 3.3.
Rydberg
constant detennination.3.1 DETERMINATION OF THE
2S1/2 - nD5/2
ATOMIC SPLITTING. - Th détermine the2S1/2
-nD5/2
atomicsplitting
from thefrequency
measurementsreported
in tableV,
we have to make several corrections. These corrections aregiven
in table VI.i)
Second orderDoppler
effect.
This correction has been discussed in paper II[3] .
As we havemeasured the
velocity
distribution in the metastable atomicbeam,
we can calculateprecisely
thesecond-order
Doppler
effect forhydrogen
and deuterium.ii)
2Si/2
hyperfine
splitting.
As we have measuredonly
the most intensehyperfine
component,
’Iàble V -Resonance frequencies of
thetwo-photon
transitions(column
3)
anddifference (D)
be-tween the last and the
first
measurements(column
2).
1àble VI. -
Corrections for
the second-orderDoppler effect
and thehyperfine splittings
(MHz).
is very well known for
hydrogen
[12]
and deuterium[13]
and thecorresponding
corrections are+ 44.389 MHz and + 13.641 MHz
respectively.
üi)
nD5s/2
hyperfine splitting.
We do not resolve thehyperfine
structure of thenD5/2
state. Thissplitting
can be calculated with the Fermi formula[14] .
Forexample
we obtain 142.6 kHz for the8Ds/2
level inhydrogen .
As the initial level of thetwo-photon
transition is aparticular
hyperfine
level(for
instance F;
= 1 forhydrogen),
the intensities of the twohyperfine
transitions2S1/2(Fi
=1) -
nDs/2(FJ)
(Ff
= 2 andFf
= 3 forhydrogen)
are notproportional
to thedegeneracy
2Ff
+ 1 of the excitedhyperfine
level but to :3.2 CALCULATION OF THE RYDBERG CONSTANT. - The corrections
given
in table VI lead tosix values of the
2Si/2 - nD5/2
splittings corresponding
to the six transitionsinvestigated.
Wehave used the
experimental
value of thehydrogen
2SLamb
shift(1057.851(2)
MHz[15] )
and the theoretical value(1057.229
MHz)
of the deuterium one, calculatedusing
reference[16],
to deducethe
2Pi/2 - nDS/2
frequencies.
We have thencompared
thesefrequencies
to thosereported
by
Erickson[17]
after correction for the 1986 recommended values of the fine structure constant,the
proton/electron,
and thedeuteron/proton
mass ratios[18] :
The measured
frequencies
lead to sixindependent
determinations of theRydberg
constantgiven
in table VII. Thequoted
uncertainties do not include the reference laseruncertainty.
Ascan be seen from this
table,
our sixindependent
measurements ofRoc
arequite
self-consistent.1àking
into account the reference laseruncertainty,
our final result is:Uble VII. - Determination
of the Rydberg
constant.The
precision
is 1.7 x10-1°
and 4.3 x10-11
withrespect
to our reference laser. This resultis
slightly
smaller(about
4.4 x10-11)than
ourpreliminary
resultpublished
in 1988[19] .
This isdue to three reasons:
i)
The second-orderDoppler
effect correction has been calculated with the measuredvelocity
distribution and not with
an a priori
one(correction
of about -0.6 x10-11)
ii)
TheRydberg
constant calculation wasmade
with an old value of the fine structure constanta-1 =
137.03604(correction
of about -1.3 x10-11)
Table VIII.
Comparison
with other recent measurements.Thèse values are all corrected
using
the new definition of c and theexperimental
ratiome /mp.
In table VIII our result is
compared
to ourprevious
one[11]
and to those obtainedby
differentgroups since 1978 from excitation either of the Balmer-a and
-,Q
transitions[20-24]
or of the 1S-2S transition[25-28].
Since our 1986 measurement there is a verygood
agreement
which is illustratedin
figure
4.3.3 UNCERTAINTIES ANALYSIS. - The various contributions to the total
uncertainty
are listedin table IX. In this table the first two items do not come from our
experiment
andgive
thepresent
limitation to the method
(about
1.9 x10-11 ) .
Forhydrogen
the 2S Lamb shiftexperimental
un-certainty
is 2 kHz[15].
Nevertheless,
taking
into account another lessprecise
measurement[29]
(1057.845 (9)
MHz),
we haveadopted
a 10 kHzuncertainty
for thehydrogen
2S Lamb shiftmea-surement. As the Q.E.D.
uncertainty
of the2Pi/2
level energy calculation is about 3 kHz[17],
the total
uncertainty
due to the Lamb shift and the energy level calculations is about 1.5 x10-11,
which is the value indicated in table IX. For deuterium the Lamb shift calculationuncertainty
is = 14 kHz(quadratic
sum of the 9 kHz Q.E.D.uncertainty
and of the 11 kHz nuclear sizeuncertainty)
and the total Lamb shift and energy calculations
uncertainty
is = 1.8 x10-11.
In table IX the other items
depend
upon ourexperiment.
The statisticaluncertainty
is the standard deviation of our sixindependent
results. The Starkeffect,
second-orderDoppler
effect and theoreticallineshape
uncertainties have been discussed in paper II[3].
Incomparison
withour
previous
measurement[11]
theimprovement
in the Stark effectuncertainty
is checkedby
thestudy
of the 2S-20Dtwo-photon
transition whichgives
an upper limit(2
mV/cm)
to thestray
electric fields. The uncertainties due to the
ageing
of themirrors,
to the Fresnelphase
shiftmea-surement and to the
comparison
between the He-Ne lasers have been discussed in this paper.Finally
the moreimportant uncertainty
is due to the standard laser(1.6
x10-1°) . With
respect
Fig.
4. -Comparison
of our result with recenthigh
precision
measurements of theRydberg
constant.TABLE IX. Uncertainties
(part
in1011 ).
3.4 ISOTOPIC SHIFTS. - Our
experiment
alsoprovides
threeisotopic
shifts which aregiven
intable X. The
quoted
uncertainties are much smaller than those on each261/2 - nD5/2
measure-ment, since various
systematic
errors cancel. From these threeisotopic
shifts,
we can deduce threeindependent
measurements of theproton/électron
mass ratio. Our mean value :mP/me
=1836.152
59(24)
is in excellentagreement
with the moreprecise
onemp/me
=1836.152701(37)
of VanDyck
et aL[30].
Theuncertainty
of our measurement is the rms sum of thefollowing
(6.3
x10-8)
and second-orderDoppler
effect(2
x10-8).
Figure
5 shows thecomparison
of ourresult with other recent measurements
[30-33].
’Tàble X. -
Isotopic shifts.
Fig.
5. -Comparison
of our result with recent determinations of theproton/electron
mass ratio.4. Conclusion.
We have made a new measurement of the
Rydberg
constant, the mostprecise
one at thepresent
time. It is limited
by
theprecision
of thewavelength
andfrequency
standard in the visible range.This shows that the
present
realization of the meter is nolonger
satisfactory
in theoptical
domainand that more
precise frequency
standards arerequired.
Acknowledgements.
The authors are indebted to Prof. B.
Cagnac
for much fruitful adviceduring
thisexperiment.
Wethank Drs R Juncar and Y. Millerioux from the Institut National de
Métrologie
for the loan of aetalon. This work is
partially supported by
the Bureau National deMétrologie.
One of us(JCG)
is
grateful
to the Brazilian FinancialAgency
CAPES for ascholarship.
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