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Submitted on 1 Jan 1990
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in the Ising spin glass Fe0.3Mg0.7Cl2
J.P. Redoulès, R. Bendaoud, A.R. Fert, D. Bertrand, J. Vétel, J.C.
Lasjaunias, J. Souletie, J. Ferré
To cite this version:
Static and
dynamic
evidence for
atransition
at
Tc
=0
in the
Ising spin glass
Fe0.3Mg0.7Cl2
J.P.
Redoulès(1),
R.Bendaoud(1),
A.R.Fert(1),
D.Bertrand(1),J. Vétel(1),
J.C.Lasjaunias(2),
J.Souletie(2)
and J.Ferré(3)
(1)
Laboratoire dePhysique
desSolides(*),
INSA,
Avenue deRangueil,
31077 ToulouseCedex,
France(2)
Centre de Recherche sur les Très BassesThmpératures
CNRS,
BP166X,
38042 GrenobleCedex,
France
(3)
Laboratoire dePhysique
desSolides(*),
UniversitdParis-Sud,
Bâtiment510,91405
Orsay
Cedex,
France
(Received
onJanuary
3, 1990,
revised onMay
23, 1990,
accepted
onMay
25, 1990)
Résumé. 2014 L’étude du
comportement
critique
du verre despin Ising Fe0.3Mg0.7Cl2
a été réalisée à l’aide de mesuresd’aimantation,
desusceptibilitd
alternative et de chaleurspecifique.
Les mesures desusceptibilitd
alternative ont été effectuéesjusqu’à
de très bassesfréquences
(0.02
Hzf
3000Hz)
grdce 21
la mise aupoint
d’undispositif
expdrimental
utilisant un convertisseuranalogique
numérique
16 bitsrapide.
Letemps
de relaxation 03C4 comme les coefficients a3 et a5 de lasusceptibilité
nonli-ndaire sont
puissances
l’un de l’autre etdivergent
comme desexponentielles
de 03B8/T.L’analyse
des résultats confirme donc les conclusions d’unepremière
étude ducomportement
critique
dynamique :
Fe0.30Mg0.70Cl2
appartient à
une classe d’universalité différente dessystèmes
3d etapparaît
commeexemple
de verre despin
2dIsing
caractérisé par une transition dephase à
Tc
= 0. Nous affirmons que lessingularites
observéesapparaissent
comme la limite naturelle à Tc = 0 des lois habituellesde
"scaling".
Nous nous différencions sur cepoint
desanalyses
présentées
récemment pour d’autressystèmes,
où uncomportement
semblable estinterprété
par une théorie ad hoc pour Tc = 0.Abstract. 2014 The critical behaviour of the
Ising spin glass
Fe0.3Mg0.7Cl2
has been studiedby
d.c.magnetisation,
a.c.susceptibility
andspecific
heat measurements.We have extended the range of ourprevious
a.c.susceptibility
measurements down to 0.02 Hzby using
a new set up which utilises thepossibilities
of a 16 bitanalog
todigital
converter. The relaxation time r and the coefficients a3 and a5 of the non linearsusceptibilities
are powers of each other anddiverge
likeexponential
functions of 03B8/T. This confirms our former statement thatFe0.3Mg0.7Cl2
is of a class different from that of traditional 3dsystems
and appears as anexample
of a real 2dIsing spin glass
with Tc = 0. We claimthat the essential
singularities
are obtained as the natural Tc = 0 limit of the usualassumption
of thescaling theory.
We differ at thispoint
from recentanalyses
in othersystems,
where similar evidence isinterpreted
in the framework of a differenttheory
ad hoc for the Tc = 0 case.Classification
Physics
Abstracts75.50L -75.40C - 75.40G - 64.60
1. Introduction.
Theory
predicts
a transition at finitetemperature
for 3dIsing spin glasses only.
On the otherhand,
theoreticians would rather favor a transition atTe =
0 for 2dIsing spin glasses
and notransition at all in cases of lower dimension or
Heisenberg
systems. However,
experimentally
it isnow
accepted
that thespin glass
transition occurs at finitetemperature
at d = 3 withHeisenberg
spins.
lypical
exponents
are 1 -3 , Q -
1, zv -
6 - 10.Feo.3Mgo.7CI2
spin
glass
hasproperties
which differ from the standard behaviour. Forexample
the field cooled
magnétisation
does not reach as flat aplateau
as in CuMn but it conserves aslight
negative
slope
in terms of thetemperature
and remainsstrongly
dependent
on thecooling
rate[1] .
Also,
our firstdynamic
data,
obtained fromFaraday
rotationexperiments
in thefrequency
range
1.5-80000 Hz[2, 3] ,
showed that the lowtemperature
slope
ofx" depends
more onfre-quency
than is usual. Furthermore wepointed
out that thedynamic
critical behaviour wasuncon-ventional,
not characteristic of a 3dIsing
spin
glass,
but more relevant of 2dIsing
spin
glasses
andwe were able to conclude from this
study
that we had with thissystem
the firstexample
of aspin
glass
transitionoccurring
atTe
= 0.Recently
other unconventional critical behaviours werereported
in a number ofsystems
anddiscussions arise as whether
they
can be taken asexamples
of a transition atT,, =
0 or whetherthey
call for a diflerentinterpretation
[4-6].
Because of the fundamental interest that there is in the discussion from thepoint
of view of thespin glass
transition as well as from thepoint
of view oftransitions in
general,
we havecompleted
our formerdynamic study
of theFeo sMgo ?Cl2
system.
We have
developed
anoriginal
method basedupon
theacquisition
of thesignal by
means of a16 bit
analog
todigital
converter andcomputer
dataprocessing
which allowed us to measure a.c.susceptibilities
down to 0.02 Hz with agood
accuracy. Thus therange
of ourprevious dynamic
study
was extendedsignificantly by
two decades at lowfrequencies.
In the
following
webriefly
describe the new lowfrequency
a.c.susceptibility
technique
andreport
our new data in acrystal
ofFeo.3Mgo.7CI2
over the 0.02 - 3000 Hzfrequency
range.
We thenrecall our non linear static
susceptibility
results[1]
andgive
new lowtemperature
specific
heatmeasurements on this
compound.
We show that thetemperature
dependence
of the characteristic relaxation time over the wholerange
between 0.02 and 80000 Hz is well describedby
an Arrheniuslaw and that the non-linear
susceptibilities
are describedby
essentialsingularities
[which
are, as weshow,
the naturalTe
= 0 limit of thepower
laws],
confirming
our former conclusion on the2d-Ising
like character of theFeo.3Mgo.7CI2
spin
glass.
We discuss our data in connection withrecently
published
results on othersystems
[4-6].
2.
Experimental procédures
and results.All the
samples
were issued from aFeo.3OMgO.70CI2 single crystal
grown
by
theBridgman
method.They
were cleaved in aglove
box filled with an4He
atmosphere
to avoidhydration during
prepa-ration.
2.1 DYNAMIC SUSCEPTIBILITY. - The
sample
used in our new lowfrequency experiments
wascomposed
of three identicaldisks,
6 mm in diameter and 3 mm inthickness,
the c-axis of thecrystal
being
perpendicular
to theplatelets.
These three disks were stacked in asample
holder toget
a 9 mm thicksample.
The a.c.
magnetic
field wassupplied by
a smallsuperconducting
coil ;
itsamplitude
was about 2 Oe for allexperiments
and it wasapplied along
the c-axis of thecrystal.
Thepick
up
coil,
It could be
weakly
shifted inside theprimary magnetic
field at thebeginning
of the measurementsto tune the
compensation
of the twoopposite windings,
the inducedvoltage being
zero in the absence ofsample.
The a.c.
susceptibility
was measuredby
two different methods. Athigh
frequencies (f
=w/21r
>100
Hz)
a conventional lock-inamplifier
was used. At the lowfrequencies
(0.02
Hzf
100
Hz)
we used a 16 bitanalog
todigital
converter(ADC).
Atfrequencies
smaller than 3Hz,
1700 values of asignal e(t) proportional
to thepick
up
coilvoltage,
and of asignal
h(t) proportional
to theprimary
field were recorded for oneperiod
as shown infigure
1 for 0.02 and 0.1 Hz. From these data we deduceprecisely
theamplitude
ofe(t)
andh(t)
and theirphase
shiftallowing
to calculatethe real
XI
and theimaginary
part
y£§ of
thesusceptibility.
We have checked that this methodgives
the same results as lock-inamplifier
measurements at atypical frequency
of 100 Hz.Fig.
1. -The
pick
up coilvoltage
e(+)
and avoltage
u(+) proportional
to theprimary magnetic
field,
recorded versus thepoint
range over aperiod
for twoworking frequencies
0.1 Hz(a)
and 0.02 Hz(b).
Figures
2 and 3 show thetempérature
dependence
of thelongitudinal susceptibilities
XI w (T)
andXII (T)
at differentfrequencies.
Ondecreasing
thefrequency,
thecusp
inXI (T)
shiftsthe
high
frequency
range and to 0.10K/decade
in the lowfrequency
range. Thiscusp
isstrongly
sharpening
at lowestfrequencies :
at 0.02 Hz it is similar in width and inposition
to thecusp
wehave observed in static ZFC
susceptibility
measurementsby
using
aheating
rate of 0.2mK.s-1
[1] .
Theamplitude
of thedissipative
termX"
(T)
decreasesby
lowering
thefrequency ;
the value of the ratioX" (T)/Xl (T)
at maximum isroughly equal
to 3 x10-2
for our lowestfrequency
at0.02 Hz. The
signal
to noise ratioon X"
is ratherpoor
at lowfrequency
since it is measured from thepick-up
coilvoltage
which isproportional
to w.Fig.
2. - The realpart
xw {T)
of thecomplex
susceptibility
versustemperature
for variousfrequencies :
0.02 Hz(A),
0.1 Hz(B),
0.3 Hz(C),
3 Hz(D),
30 Hz(E),
113 Hz(F),
211 Hz(G),
1 kHz(H),
3 kHz(I)
and 10 kHz(J).
Our
previous
a.c.susceptibility
data in therange
1.5 - 80000 Hz were obtainedby
a methodFig.
3. - Theimaginary
part
x"
(T)
of thecomplex
susceptibility
versustemperature
for variousfrequen-cies : 0.1 Hz
(A),
1 Hz(B),
10 Hz(C),
113 Hz(D),
1 kHz(E)
and 3 kHz(F).
2.2 STATIC MAGNETISATION. - The
magnétisation
measurements wereperformed
for several values of themagnetic
field between 10 and 400Oe,
thesample being
cooled at a constant ratefrom 4.2 to 1 K. This field cooled
procedure
is known toprovide
data which remain close tothe
equilibrium
response
even in the nonergodic régime
where the relaxation time becomes of the order oflaboratory
times.However,
in thissystem,
thedependence
of themagnetisation
on the
cooling
rate at the lowesttemperatures
constrained us to reduce thetemperature
range understudy
to the range 1.7 - 4.2 K. The dataacquisition
was controlledby
computer,
allowing
measurements at well defined
températures :
the isothermalmagnétisation
curves wereeasily
deduced from the field cooled
magnétisation
data. The main results arepresented
in aprevious
2.3 SPECIFIC HEAT. - The measurements have been
performed
with a dilutionrefrigerator
us-ing
a transientheat-pulse technique
[7] .
Thesample (a single crystal piece
of 0.832 g inweight)
wasglued
to the siliconsample
holder with a controlled amount(10 mg)
ofApiezon
N grease whichprotected
thesample
from moistureduring
thepreparation
of theexperiment.
Due to thelarge
heatcapacity
of thesample,
the time constant of theexponential
decay
of thetemperature
transients varies from 10 minutes at 7 K to several hours at 0.1
K,
whichcorresponds
to thequasi-adiabatic conditions. Also the contribution of addenda was
generally negligible (less
than 1 %below 5
K).
The curve of thespecific
heat measured in the range 0.1 - 7 K is shown infigure
4.Fig.
4. - In-In3. Discussion.
3.1 DYNAMIC SUSCEPTIBILITY COLE-COLE ANALYSIS. -
Following
Saito et aL[8],,
severalau-thors have
analysed
thesusceptibility
ofspin
glasses
with anempirical law
which was firstintro-duced for dielectrics
[9] :
For wT 1 the out of
phase
susceptibility
reduces to :For
a (T )
= 1 we recover the usualDebye
result for asingle
relaxation time. A smallera (T)
results from a distribution of relaxation times which becomes broader as a decreases to zero.
Figures
5a and 5brepresent
our dataplot
oflog(x£§ )
vs.log(w)
at differenttemperatures
be-tween 1 and 4
K,
measured eitherby
theFaraday
rotationtechnique
or with the new setup.
The différent isothermscorrespond
to vertical sections of the différent curves shown infigure
3. As wedecrease the
temperature
the lowfrequency
tail ofx"(w)
shiftsup
and flattens out. It isasymp-totically
well describedby
astraight
line ofslope o:(T),
which is consistent with apower
law of thetype
describedby
équation (2).
Thefigure
6 shows howet(T) dépends
on thetempérature.
Wenotice some mismatch between the data obtained at T = 2.8 K
by
the twomethods ;
this mayre-ftect a
slight
difference in the concentrations of the two differentsamples
and in the thermometercalibrations which have been used for these two sets of
experiments.
In usual
spin glasses
theparameter
a(T)
variesabruptly
near thephase
transitiontempera-ture
Te,
the existence of a transition at finitetempérature
being
associated to anabrupt
broad-ening
atTc
of the relaxation timespectrum.
Forexample, a(T) -
1 at 1.1Te
and 0.1 at 0.9Te
in(Tix V1-x)203 [8].
Similar results have been alsoreported
inEuo.4Sro.6S
[101
orin
CdCr2-xln2-2xS4[11] .
InFeo.30Mgo.7oCI2, in
contrast,
a(T)
smoothly
varies,
approximately
likeT2
in theexperimental
range 1.8 - 4 Kwhere it reaches a value close to one(figure
6).
Dekkeret al.
[4]
have observed a similar behaviour in thelayered compound
Rb2CUO.78Coo.22F4
(a
varies like T in thiscase)
which is alsointeresting
to test the2d-Ising
behaviour. Theprogressive
broad-ening
of the relaxation timespectrum
indicates that there is no transition at finitetemperature.
Like Dekker et al we have determined
Tcc(T)
whichappears
in the Cole Cole law(equation
1).
In thehigh
température
regime (T >
3.5K)
where the width of the distributioncollapses
tozero, we find that
r,,(T)
isequivalent
to the value of the relaxation time T determinedby
othersmethods
(see
later).
As thetemperature
decreases and the distribution broadens Tcc becomes much smaller than T(for example
we observe Tcc -10-7
s and T - 1 s for T = 2K).
This is consistent with theanalysis
of Saito et al.[8]
and Alba et al.[11] :
the relaxation time Teedepends
strongly
on the width of the relaxation timespectrum
and has no clearphysical
meaning
when thetemperature
isdecreased ;
itrepresents
sometypical
relaxation time which is far from theaveraged
relaxation time(notice
thelogarithmic
scale in the curvegiving
the distribution of Tassociated with the Cole Cole law
[9]
).
3.2 STATIC AND DYNAMIC CRITICAL BEHAVIOUR. - In a
spin glass, expanding
the static mag-netisation in terms ofH/T
[12] :
the first order Curie constant ai is a constant but a3, a5, ...
diverges
like finitepowers
of thecoherence
length
e.
Assuming
that for a transition at finitetempérature Te
the cohérencelength
Fig.
5. - Plots of theimaginary
partx"(w)
of thesusceptibility versus w
for various températures :a)
fromFig.
6. -Température dependence
of theexponent
a of the Cole-Cole law obtained from the fits ofx"(w)
described in the text. Circles
(,o) correspond
to thepresent
expérimental
a.c. measurements, squares(3)
correspond
toFaraday
rotation measurements.we have:
On another
hand,
thedynamic scaling hypothesis
states that the relaxation time is also apower
of the coherencelength
and hence of the reducedtemperature t:
For the
specific
heat,
one has:(the
temperature
independent
criticalexponent a
should not be mistaken for thetemperature
dependent
a (T )
of the Cole-Colelaw).
In a
previous
paper
[1] ,
we havepresented
the results of theanalysis
of themagnetisation
interms of odd
powers
ofH/T
assuggested
in reference[12].
We have shown that the third ordera3 and the fifth order a5 Curie constants vary
respectively by
one and two orders ofmagnitude
between 2.5 and 1.7 K. Such adivergence
was considered as asign
for aphase
transition but we haddifficulties to determine
precisely
a transitiontempérature.
We shall examineagain
these results in connection with theanalysis
of the relaxation time of thesystem
deduced from a.c.susceptibility
measurements.
In our former a.c.
susceptibility
study
[2,3],
wemainly
considered thetemperature Tf,
relatedto the onset of
irreversibilities,
wheretge =
IX" /XI
had a
constant small value(10-2 ),
andas-suming
thattge
=wr/2r
[13],
we deduced thecorrespondance
betweenTf
and the characteristicrelaxation time T of the
system :
T(Tf)
=0.01/w.
Because of the scatter on the measurement offrom the
analysis
of thebreakaway point
betweenxfj
and xeq , assuggested by
Carré et aL[14].
They
write thatTmax(% )
=Ilx/ú}
at thetempérature 11
where :Figure
7presents
thetemperature
dependence
ofOx
inFeo.3MgO.7CI2.
In a recentpaper,
Bon-temps
et aL[15]
have shown that in the limit c.vT « 1 these two criteria used to determine the,r(T)
law areequivalent.
In most
accepted
spin glasses, fixing successively
Tc
at diflerent finitevalues,
theexponents
and -y, on onehand,
theexponent
zv and the characteristic time To, on the otherhand,
can be calculatedby
fitting
a3(T),
a5(T)
andT(T)
withequations (5)
and(6) respectively.
It isgenerally
observed that there isonly
one value ofTe
which minimises thevariances ;
theexponent y
isgenerally
of the order of3,
Q
of the order of 1 and theexponent
zvranges
between 6 and 10[16] .
Asfigure
8 .ashows,
with our newdynamic
data inFeO.3Mgo.7CI2,
the smaller theTc
wechose the smaller the error. When
Te
decreases thecorresponding
exponent
zvsteadily
increaseslike
0 /Tc
where 0 - 50 K(Fig.
8.b).
This is consistent with a transition atTe
= 0. Indeedin the
high
temperature
"paramagnetic" regime, e ought
to remain ananalytic
function ofT-1
(T /Ta ,...,
1 +(zvTc)/T
+ ... = 1 -fOIT
-f-...).
This constraint whichimposes
tha t zvdiverges
like
OIT,
leads to an Arrhenius law for thedynamic (and
to essentialsingularities
for ail staticproperties) [17] :
_-Consistently
with the above discussion we find(fig.
9)
that if wetry
torepresent
ln(rmaR)
vs.ln( 1- TIT)
for differentattempt
valuesof Tc
(0.5
K,
1 K or 1.5K),
thelarger
theTe
wechose,
thelarger
the
curvature. The bestlinearity
is obtained in the Arrheniusplot
ofln(T)
vs.11T (fig. 10)
which
yields 0
= 57 K and Ta - 1.5 x10-12
s .The same result follows from
figure
11 which is the differential form of theequation (6).
As To has been eliminated in the
differentiation,
it ispossible
to obtain in onestep
the best value of the two otherparameters Te
and zv(or 0). According
toequation (6)
P,(T)
shouldgive
astraight
line. Theintercept
of this line withthe y
= 0 axis isTe
and withthe y
= 1 axisTe
+ 0. The datareported
onfigure
11 lead to:Te
= 0 ± 0.5 K whichimplies
an Arrhenius behaviour with(J ’" 63 :i: 7 K.
The static data
agree
well with this conclusion.Figure
12 shows that a5 is indeed apower
of a3as
equation
(5)
tells us and from thisplot
ofIn(a5)
versusln(a3),
whoseslope
is2+/3/¡,
we obtain/?/Y=0.2.
We also findthat,
in anattempt
to fit thetemperature
dependence
of a3 with thepower
law,
the best variance is obtained forTe
=0,
although
asatisfactory
fit is noticed in the range0 - 1.4
K,
due to theuncertainty
on the static data. We find thus that a3 and therefore a5, like T,can be described
byan
essentialsingularity
of the forma2n+,(T) =
a2n+leXP(02n+,/T)
where(J2n+l
=n0q - (n -
1)Op [(J-y
=yT,
and Op
=/3Te]
follows fromequation
(5).
From the data offigure
13,
we find0q
= 8.3 K so thatOu
= 1.7 K.In the
spirit
of theprevious
analysis
we wouldexpect
that a becomes infinite whenTe
---+ 0and that the anomalous contribution reduces to a
Schottky anomaly :
which would become
exponentially
small onapproaching
Tc
= 0 andpresents
abump
at1001/2
Fig.
7. - Values of the ratio(xeq - Xiw)
/Xeq
versus temperature for variousfrequencies :
0.02 Hz(A),
0.1 Hz
(B),
0.3Hz,
(C),
3 Hz(D),
10 Hz(E),
30 Hz(F),
113 Hz(G),
211 Hz(H),
500 Hz(I), 1
kHz(J),
3 kHz(K)
and 10 kHz(L).
Wearbitrary
fix theirreversibility
onset at thevalue A x
=10-2.
(this
relation is theTc
---+ 0 limit of a =2 - -y - 2(3
which can be written(Jo:/Tc
= 2 -(J’Y /Tc
-20plT,).
We have measured thespecific
heat ofFeo.3MgO.7CI2
down to 0.1 K toverify
thisequa-tion.
Figure
4 shows theexperimental
data corrected from the lattice contribution : the curveexhibits a rounded maximum at T ,-...; 4.5 K and also a
hump
at about 1 K. This last smallanomaly
probably
corresponds
to aSchottky anomaly
which is also observed in similarcompounds
and has been attributed to thepresence
of someimpurities
[18].
Our data extend to lower concentrationsthe measurements of
Wong
et aL[19]
andthey
agree
qualitatively.
At lowertemperature,
we donot observe the
expected exponential
behaviour but we notice that there is a dominantFig.
8. - For differentattempt
values of Te we calculate(a)
the variance and(b)
theexponent
zv of theajustment
ofTmax(T’)
by
a power law of t = 1 -T,,IT.
Ibe best values ofexponent
zv tend to increase like0 /Tc
v4th 0 = 50 K when Tc,approaches
zero for which the variance is minimum(inset).
spin glass
where very littleentropy
is contained in the "critical contribution" which is controlledby
alarge
exponent a
",,3 and where the dominant contribution which accounts for most of theentropy
is also describedby
a smallpower
of thetemperature.
The
analysis
of the static anddynamic
critical data inFeo.3MgO.7CI2
comforts ourprevious
con-clusions that this
system
isrepresentative
of a class ofuniversality
different from that of usualspin
glasses
andpresumably
the same as for 2dIsing
systems
whereTe
= 0. Morerecently
un-traditional behaviours have been
reported
in otherspin
glasses,
e.g.
by
Dekker et aL[4]
orGeschwind et al
[5].
The samedependence
of the f.c.magnetisation
on thecooling
rate isre-ported
inRb2CUO.78Coo.22F4
andFeO.3MgO.7CI2 ;
it limits totemperature
over 3.2 K and 1.7 Krespectively
the window where reliable static measurements can be obtained.They
howeverex-hibit definite differences which are more
easily recognised
andanalysed
in thefigure
14. We havepresented P, (T)
versus the dimensionlesstemperature
T /()
normalisedby
0 which is ameasure
of the interaction for several
spin glasses.
The usualscaling
hypothesis (Eq. (4))
leads toparallel
straight
lines which intersect theTIO
axis atT/0
=(ZII)-l.
So that we have one line for agiven
universality
class.Accepted spin
glasses
including
simulations or 3dIsing
spin
glasses
arereputed
to have their zv between 6 and
10,
i.e.they
lie between CuMn 4.0% and aluminosilicate on theplot
infigure
14. Inpractice
we find in thisrange
manyRKKY
systems
and a number of classicalFig.
9. - Plotsof -LnTmax(r)
versusLn(T - Tc )/T
for three values of Tc : 0.5K,
1 K and 1.5 K. The solid lines aresimple guides
to the eyes.of the
scaling hypothesis :
thisimplies,
asexplained
inequation
9,
that zvdiverges
likeOIT,
sothat
(1 -
Tc/T)-8/Tc
-exp«(JjT)
and we findaccordingly
that a3, as and T are allpower
of each other and describedby
essentialsingularities
as weexpect
when we reach a lower critical dimension.The same
plot
shows that othersystems
such asRb2CUO.78CO0.22F4
orCdo.6Mno.4Th
arediffer-ent and we would be
prompted by
thisplot
tointerpret
them with untraditionalexponents
(zv
-30 and zv -15 inRb2CUO.78CO0.22F4
andCdo.6Mno.4’Iè
respectively).
The authorsreject
these valuesas
unphysically large
on the basis of a tradition which is enforcedby
thetheory
andpractice
offer-romagnets.
Following
Fisher and Huse[20],
they
argue
that for this transition T -Toexp(W/T)
where
W,
i.e.ln(r),
rather r is apower
of e.
This leads to afamily
of solutions of the formD a ...
r =
Toexp ( 201320132013 )
with among them the Fulcher law for o- = 1 and the solution that Binder(T - To )
and
Young
[21]
promoted
forTo
= 0. Within this frameworkP, (T)
is apower
law as we have :PT (T )
=BloT [(T -
TO)IB]’+’
[17].
It iseasy to understand that for a
given
experimental
Fig.
10. - Plot of-LnTmax(T’)
versus 11T. Thestraight
linecorresponds
to the fit with an Arrhenius lawand ro = 1.5 x
10-12S (J = 57 K.
from its
tangent
and the Fisher and Husetheory
therefore willprovide
afamily
of solutions al-ternative to the one thatprovided by
the criticalslowing
down: forexample,
rather than withTe
= 2.8 K andzv=32,
assuggested
by
figure
14,
Dekker et al.prefer
to fit their data with theequation
of Binder andYoung
(To
=0)
and find cr=3.2. Thequestion
is not todeny
thatalterna-tives exist to the
slowing
downequation
whichprovide
acomparable
fit to the data. However wedo not want a different
theory
for each of the different data shown infigure
14. Thedisturbing
point
finally
withFeo. 3()MgO.70CI2
and a number of othersystems
is that we are confronted withdifferent values of the
exponents
which we do not know how tojustify
by
an obvious differencein either the
spin
or thespace
dimension.Perhaps,
the reason for our discomfort is that we arewilling
to extend tospin
glasses
anargument
(essentially
the Harriscriterion)
which is valid forferromagnets
but may bewrong
withspin glasses
when frustration ispresent.
Whatis,
in the firstplace,
thespace
dimension of aspin glass ?
In a disorderedsystem
with short range interactionswe know from the
percolation
theory
that thespace
dimension is different at shortrange
and atlong
range withrespect
toe,
-(p -
p,)-l’
the correlationlength
of thepercolation
problem.
Fig.
11. - Plot ofPï(T) = -bLnT/bLnr
versus T. Thestraight
line is asimple âuide
to the eyes.of the
percolation
cluster.If e
>e,
it has the dimension ofspace.
In aspin glass
themagnetic
problem
makesaverages
at allranges,
smaller than a maximum one, whichis e,
so that the shortrange
and thelong
range
are mixed foreach e
in aproportion
which maydepend
on how closeto the
percolation
threshold we are.Perhaps
rather than the notion ofspace
dimension it would beappropriate
to introduce some sort of dimension of the disorder which would evolve with theproximity
of thepercolation
threshold.The situation is
particularly
tricky
in the bidimensionalsystems
such asFeo.3Mgo.7CL2
orRb2Cuo.78Coo.22F4.
The two dimensional character of theantiferromagnetic
FeCl2 system
is well established. It results from thegreat
ratio(Jl / -
JI -
10)
between theintraplane
ferromag-netic
exchange
JI
and theinterplane antiferromagnetic
interactionJi .
It is more dubious that thischaracter
persists
in therange
of concentrations near the 2dpercolation
threshold where thespin
glass
effect occurs. As in most disorderedsystems
there is a clear différence between the shortrange order which
prevails
athigh
temperature
and the order whichfinally
sets in. The effect ofJi
is feltmainly through
the constitution of short range 2dferromagnetic
clusters which then may well interact in the third dimension also. We arepresently checking
thepossibility
ofexponents
varying continuously
with concentration ininsulating spin glasses :
such apossibility
seems to besupported by
theexperimental
evidence since thecompounds
with lower concentration inMg
show a flat
plateau,
as isgenerally
observed insystems
with a transition at finiteTc.
In RKKYFig.
12. - Plot of Ina,5 vs In a3.
Fig.
13. - Arrheniusplot
of In a3problem might depend
on theway
the interaction decreases with the distance due to the effect ofa mean free
path
limitation or ofexchange
enhancement. Conclusion.Our new
dynamic
data in theFeO.3MgO.7CI2
spin glass
have allowed us to enforce the evidence for a transition atTc
= 0 in thisIsing
system.
Its critical behaviour is different from that observedin
typical
3dIsing
systems
asFeO.35MgO.65Br2
[22]
orFeo.25Zno.75F2
[23]
and we describe itby
Fig.
14. -Plataf PT(T) 1I.Y. T/8 farFeo.3Mgo.7CI2, Rh2CuO.78Coo.22F4 [4], Cdo.6Mno.41è [5], Feo.sMno.STi03
[24],
amorphous
aluminosilicateAI2Mn3Si3012
[25]
and CuMn 4.6%[26].
References
[1]
BENSAMKAF.,
BERTRANDD.,
FERT A.R. and REDOULESJ.R,
J.Phys.
C : Solid StatePhys.
19(1986)
4741.[2]
FERREJ.,
POMMIER J. and BERTRANDD.,
Advances inMagneto-Optics,
J.Magn.
Soc.Japan
11(1987)
83.