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Submitted on 1 Jan 1978
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NMR MEASUREMENTS ON LIQUID 3He
CONFINED IN ALUMINA AND PLATINUM
POWDERS AND GRAFOIL
H. Godfrin, G. Frossati, D. Thoulouze, M. Chapellier, W. Clark
To cite this version:
JOURNAL DE PHYSIQUE Colloque C6, supplement au n° 8, Tome 39, aout 1978, page C6-287
NMR MEASUREMENTS ON L I Q U I D 3H e CONFINED IN ALUMINA AND PLATINUM POWDERS AND GRAFOIL
XX ++
H. Godfnn, G. Frossati, D. Thoulouze, M. Chapellier and W.G. Clark
C.N.R.S., BP 166X 38042 Grenoble - France
**DPG/SRM Orme dee Mevisiers, 91190 Saolay - Fvanee
++
Physios Dept., UCLA California 90024, U.S.A.
Résumé.- Nous présentons des mesures de la susceptibilité et du temps de relaxation Ti de l'3He liquide confiné dans du grafoil, dans de la poudre d'alumine de 400 A et dans de
la poudre de platine de 8u. Nous observons une susceptibilité de Curie-Weiss correspon-dant à une monocouche d'^He adsorbé qui serait responsable du fort taux de relaxation. Ces effets sont supprimés par quelques couches d,l*He.
Abstract.- We report susceptibility and Ti measurements of liquid 3He confined in grafoil, 400 A alumina powder, and 8u platinum powder. We observe a Curie-Weiss susceptibility corresponding to a monolayer of adsorbed 3He that would be responsible for the high
re-laxation rate. These effects are suppressed by a few ^He layers.
Ahonen et al. /I/ showed recently that the susceptibility of liquid ^He confined between mylar foils or in carbon powders, at temperatures in the mK range, can be described by the expression X = TjCa + B> where B is the Fermi liquid (tempe-reature independent) susceptibility of the "bulk"
A
3He, and -=—5- the Curie-Weiss susceptibility of
the adsorbed 3He layers. The parameter 0 was found
to be positive on mylar (vO.5 IDRI and on carbon particles (MD.8 m K ) .
We report here CW NMR susceptibility mea-surements on 3He confined in grafoil, 400 A
alumi-na powder and 8u platinum powder, and pulsed NMR measurements of Tj performed on the same samples. The 3 NMR coils were placed in an araldite cell, located in the mixing chamber of a dilution refri-gerator HI. Thermal contact was achieved by means of copper plates, through the 3He cell, with sin-tered silver powder on both sides.
The surface of the grafoil sample was 1.1 m % and the surface of alumina 4.1 m measured by the B.E.T. technique. The sintered silver in the cell and filling line had a surface of 2.7 m2.
The CW NMR measurements were performed at 757 and 923.2 kHz (233 and 285 Gauss) using a low level Q-meter. The susceptibility is obtai-ned by integration of the absorption signal, and given in arbitrary units. We use a commercial IT bridge for the Tj measurements, at 250 kHz (77 Gauss).
The temperature T was given by the Curie susceptibility of the platinum powder measured either by CW or pulsed NMR. The Curie constant of
the platinum thermometer was determined by cali-bration against the CMN susceptibility, measured with the mutual inductance technique above 10 mK.
The cell was flushed with 3He, and filled at IK with "pure" 3He (<100 ppm 4H e ) . All the
measurements were performed at zero pressure. In the last part of the experiment we added ^0.3 % of ^He. This amount is equivalent to 2.7 layers, with M O1 9 atoms/m2 x layer /3/.
SUSCEPTIBILITY MEASUREMENTS : In grafoil and A
alumina, the Curie-Weiss term =—r becomes larger than the bulk susceptibility B for temperatures below 10 mK (Figure 1, curve 1). In the platinum powder, even at 2.6 mK, the Curie-Weiss contribu-tion was not relevant.
The addition of 4He reduces drastically the Curie-Weiss term (Figure 1, curves 3 and 4 ) ; it vanishes practically in grafoil (98 % reduction of A ) , but less in alumina (80 % reduction).
In the last case, this figure was only 70 % in the few hours after the ^He was added, and the "stable" value of 80 % was reached after one day. A similar effect was observed in grafoil.
Within the accuracy of the measurements (M % below 20 mK and ^3 % at higher temperatures) in the temperature range 2.6 mK - 100 mK, we
A
observe no deviation from the fit x = ifZK + B for
pure 3He and x = f- + B <f~« B) f°r 3He + ^He.
In grafoil ~ = 3.0 mK, 0 = (0.58 ± 0.14)mK A
-and in alumina ^ = 9.2 mK, 0 = (0.030 ± 0.10)mK, o
for both frequencies.
20
If we calculate the number of adsorbed
3 ~ e
layers, following the procedure of reference
/l/, we find 0.9 layers on grafoil and
1on alumi-
na.
Fig.
l :The susceptibiligy of liquid 3 ~ e
at zero
pressure confined in
400
A
alumina powder, vs.
temperature T, at 923.2 kHz.
A
Curve
1 : pure 3 ~ e ,fitted by X
=G
+ BCurve 2 : 3 ~ e
+
4 ~ e
results, after a few hours
Curve 3 : 3 ~ e
+
4 ~ e
results, after one day, fitted
T 1
MEASUREMENTS : The results are summarized in
Figure 2. In all the samples, T1 increases with T
in all the temperature range (3
mKto
100 mK)in
pure 3 ~ e .
When 4 ~ e
is added, T1 increases by one
to two orders of magnitude at low temperatures and
shows a maximum at 20
mK.The same bahaviour of
T1 in pure 3 ~ e
has been observed in a cell filled
with copper wires /4/ and in platinum powders
/5/.The relaxation of the magnetization, after a 90"
pulse, was not exponential; the T1 values given
here are the short time constants measured just
after the pulse; we supposed that the slowly rela-
xing part of the magnetization wias due to 3 ~ e
far
from the powder
.
Comparing the thermal behaviour of T1
in platinum with the one in grafoil and alumina,
one can deduce that the confined liquid and the
adeorbed layers in each substrate relax with a
single T1, in agreement with known values of the
spin diffusion coefficient. The relaxation takes
place at the level of the adsorbed 3 ~ e
layers,
probably on magnetic impurities at the surface of
the substrates.
Fig. 2 : The spin lattice relaxation time T1 vs.
temperature, for pure 3 ~ e
in :
l)platinum;
2) alumina;
3) grafoil and 3 ~ e
+4 ~ e
in
4)
plati-
num;
5)alumina;
6)grafoil.
Dotted line minimum measurable T1.
CONCLUSION.- We measure on different substrates a
magnetic susceptibility corresponding to a mono-
layer of adsorbed 3 ~ e
with ferro-magnetic interac-
tions, responsible for the high relaxation rates.
Adding 4 ~ e ,
the Curie-Weiss term vanishes and Tl
increases; this is coherent with the picture
1of a replacement of the 3 ~ e
adsorbed layers by 4He.
However, it is difficult to understand that
2 or 3 layers of 4 ~ e
are necessary to eliminate
the Curie-Weiss contribution. There ltesults also
provide an experimental support to theoretical
predictions /6/ that relate the magnetic suscepti-
lity of 3 ~ e
and substrates to the relaxation time
T1 and the "magnetic" Kapitza resistance, allowing
R e f e r e n c e s
/ l / Ahonen, A.I., Kodama, T., K r u s i u s , M., Paalanen, M.A., Richardson, R.C., Schoepe, W., Takano, Y . , J . Phys. C
2
(1976) 1665.Ahonen, A.I., Kokko, J . , Lounasmaa, O.V.,
Paalanen, M.A., Richardson, R.C., Schoepe, W., Takano, Y . , i n "Quantum F l u i d s and S o l i d s " E d i t e d by S.B. T r i c k e y , E.D. Adams and J . W . D u f t y , (Plenum P r e s s , New-York) 1977.
/ 2 / F r o s s a t i , G., G o d f r i n , H., H Q b r a l , B., Schumacher, G . , Thou- l o u z e , D., Proc. of t h e HakonL I n t e r n a t i o n a l Symposium o n ULT P h y s i c s
-
J a p a n ( 1 977).131 Daunt, J . G . e t a l . , "Monolayer and Submonolayer helium f i l m s " . E d i t e d by J.C. Daunt and E. L e r n e r , (Plenum P r e s s , New York)
1973.
/ 4 / R a m , H., P e d r o n i , P . , Thomson, J.R., Meyer, H., J . Low Temp. Phys.
2
(1970) 539./ 5 / Varoquaux, E . , P r i v a t e c o r m n i c a t i o n .
/ 6 / BQal-Monod, M.T., M i l l s , D.L., J . Low Temp. Phys.
30
(1978) 289./ 7 / BLal-Monod, M.T., M i l l s , D.L., t h i s c o n f e r e n c e . / 8 / HGbral, B., t h e s i s , Grenoble (1978).
191 Hbbral, B., F r o s s a t i , G., Godfrin, H., Schumacher, G., Thoulouze
D . , t h i s c o n f e r e n c e .
/10/ BLal