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The magnetic response of chaotic mesoscopic systems
Oded Agam
To cite this version:
Oded Agam. The magnetic response of chaotic mesoscopic systems. Journal de Physique I, EDP
Sciences, 1994, 4 (5), pp.697-730. �10.1051/jp1:1994171�. �jpa-00246942�
Classification Physics Abstracts
05.30F 75.70A 05.45 03.655
The magnetic response of chaotic mesoscopic systems
Oded
Agam
Departnlent of Physics, Technion, Haifa 32000, Israel
(Received
19 September 1993, accepted 27 January1994)
Abstract. The magnetic response of mesoscopic systems with ballistic motion of electrons thon is chaotic in the classical l1nlit is considered. Semiclassical methods are applied in order to derive a formula for the susceptibility which is expressed in terms of a finite number of classical
periodic orbits. This formula is used to study the fluctuations of the susceptibility in conlpar-
ison with the fluctuations of random systems. Some of the nlechanisms which lead to these fluctuations are discussed. At relatively high temperatures the fornlula for the susceptibility
reduces to a simple expression in which only few short periodic orbits dominate the behavior.
An experiment based on this result is proposed.
1. Introduction.
Mesoscopic systems were
extensively investigated
in recent yearsil,
2]. A mesoscopic system isusually large enough
to contain a number of electrons that may be considered asthermodynam- ically large,
but stillsufliciently
small to maintainphase
coherence over distancescomparable
to the size of trie
sample.
The elasticscattering
of thepartiales
from theimpurities
and from theboundary
generates behavior which isusually
chaotic in its dassical limit.Presently,
there is agrowing
interest inunderstanding
the imprints of trieunderlying
dassicaldynamics
on the quantum behavior of chaotic systems. Trieinvestigations
of such systems form the field of"quantum
chaos" [3-8]. In the nonlocalizedregime
triehigh
level wave functions of chaoticsystems
spread
over ail the system [9,10], therefore, they
are sensitive to theprecise
arrange-ment of the
impurities
as well as to theshape
of theboundary.
The energy spectrum, on trie otherhand, displays rigidity
andlong
range correlations. These correlations are thesubject
of several recentinvestigations.
Many
quantum eifects of mesoscopic systems aredirectly
related to thespectral
correlation function. Fordiffusing electrons,
this function was calculatedby
Altshuler and Shklovskiiiii]
using
aperturbative diagrammatic
method. An alternative derivation [12]applies
Gutzwiller's trace formula [13, 14] which expresses thedensity
of states in terms of a sum over classicalpenodic
orbits.Following Berry
[15] andapplying
ageneralization
ofHannay
and Ozono de Almeida sum rule [16] one is able to recover the saine results obtainedby diagrammatic
expansion.
Recent theoretical[17-20]
andexperimental
[21] studies show also that statisticalproperties
of the fluctuations of transport inirregular mesoscopic
structures, may beexplained
m the framework of the
periodic
orbittheory.
This paper focuses on the orbital
magnetic susceptibility
ofmesoscopic
systems. Several authorsinvestigated
thisproblem
for random systems[22-30].
One of the conclusions whichemerged
from these studies is that themagnetic
response in aspecific sample
is sensitiveto trie exact
configuration
of trieimpunties,
and that thesample
tosample
fluctuations areproportional
to kil where kF is the Fermi wavenumber and is the elastic mean freepath.
This result is somewhat counterintuitive since as the disorder decreases the fluctuations increase. In order to examine thisproblem
it is instructive tostudy
thesusceptibility
of cleanmesoscopic
systems. Thesample
tosample
fluctuations of themagnetic
response of such systems arise because of trie differentshape
of their boundaries. These are defined asôx= ((x (x))~),
where x is the
susceptibility
of some individualsample,
and (. .) represents ensemble averagmg associated with theroughness
of the boundaries. One expects that as becomessufficiently large compared
to the linear size of the system L, the fluctuations will cease to increase and will remainproportional
to kFL.In trie clean
limit,
it isimportant
todistinguish
between two extreme cases. One is the situation m which the classicaldynamics
of onepartiale
in thecorresponding
system is inte-grable,
while trie other is when it iscompletely
chaotic. In between these two cases are thesystems with mixed
dynanlics.
It tutus out that trie structure of their classicalphase
space isdirectly
related to themagnitude
of the fluctuations of thesusceptibility.
The fluctuations ofa system in which some of trie
corresponding periodic
orbits appear in continuons families of d parameters(e,g, integrable
systems with ddegrees
offreedom)
are ingeneral proportional
to
(kFL)1(~+d'
[31]. Forcompletely
chaotic systems theperiodic
orbits on the energy shell are isolated and the fluctuations in triesusceptibility
areproportional
to kFL. One purpose of this paper is to present a detailed derivation of this result. Theimpurities
in the random systems generate a chaotic classical motion.Therefore,
a propercomparison
between them and the clean systems reqmres the consideration of systems which in trie classical limit exhibit chaoticdynamics.
In an
early
work on thissubject
[32],Dingle
considered themagnetic
response of a nonin-teracting
electron gas confined to move in acylinder
of radius R where a uniformmagnetic
field is
applied parallel
to the axis of thecylinder.
He showed that the behavior of this systemdepends
on the ratio of thecyclotron
radius at the Fermi energy,l~,
to the linear size of the system R. When R » Rc("large systems")
there is a smallsteady diamagnetism together
with some small terms
periodic
in the field which aresignificant only
at low temperature.The latter
correspond
to de-Haasvan-Alphen
oscillations [33,34].
At the other limit R<Rc("small systems")
he found alarge steady diamagnetism
and someoscillatory
terms whichbecome
sigmficant
at very low temperature.(In fact,
the rotational symmetry of the system may account forperfect diamagnetism [29].)
A moregeneral
case oflarge
systems where the electrons are confined to move in acylinder
ofarbitrary
section was consideredby
Robnik athigh
temperatures [35]. Sivan and Imryinvestigated large
two dimensional systems at very low temperature [36], while Nakamura and Thomas studiednumerically
billiard systems withboth circular and
elliptic shapes
[37].The model
investigated
in the present paper consists m anoninteracting
electron gas confined to in a small two dimensional chaotic billiard ofarbitrary shape.
The electronic motion isassumed to be
completely ballistic, namely,
the elastic mean freepath
due to the(static) impurities
is infinite. The levelsbroadening
because of inelastic processes issupposed
to benegligible compared
to the thermal energy, i-e- the inelastic mean freepath
is also assumed to be infinite. The spm orbitcouphng
will beignored.
The
problem
will beanalyzed using
semiclassical methods. It tums out that thisapproach
clarifies the mechanism which leads to trielarge
fluctuations in thesusceptibility.
Recent re- summationtechniques
which enable to extract from Gutzwiller's trace formula trie semiclassical informationregarding
indiuidual energy levels of chaotic systems will be used. This issue andsome other related
topics
are summarized in section 2. In section 3 weanalyze magnetic
re-sponse due to a
single
Aharonov-Bohm flux fine. The main result there is ageneral
formula for thesusceptibility expressed
in terms of a finite number ofperiodic
orbits. Athigh
temperaturesit reduces to a
simple expression
in whichonly
trie shortestperiodic
orbits bave substantial contribution. It is dear from trie latter that triesusceptibility
is anoscillating
function of the flux and of the Fermi wavenumber with atypical amplitude proportional
tokFL.
A formula for the low temperatureregime
is obtainedapplying
theBerry-Keating
resummation method[38].
The fluctuations in this limit are shown to
be,
ingeneral, proportional
tokFL@@.
Some of trie mechanisms which lead toanomalously large
fluctuations of thesusceptibility
in this energyregime
will be related to "scars" and to avoidedcrossings.
In section4,
these resultsare
generalized
to the case of a uniformmagnetic
field. Inparticular
it is shown that for a wide range of fieldstrengths,
trie response is very similar to that of amagnetic
flux fine.Finally,
aproposed experiment,
and some related openproblems
are discussed in section 5.2. Semiclassical
quantization.
The semidassical
approximation
concerns trieleading
terms ofexpansions
in which àplays
trie rote of a small parameter,therefore,
it reflects theunderlying dynamics
of thecorrespond- ing
classical system. Trie characterization of thisdynamics
is crucial since trie appropriatesemiclassical method of
quantization depends
on trie nature of thisdynamics.
Integrable
systems of Ndegrees
of freedom contain Nindependent
constants of motion m involution. Theirphase
space motion is confined to a N dimensional torus, and semidassicalquantization
of these systems may be obtainedusing
Einstein-Brillouin-Keller(E.B.K) theory [39].
In this case, each energy level of the spectrum arises from a set of values of the irreducibleaction
integrals
associated with the differentperiods
of trie motion.Chaotic systems, on the other hand, do not contain besides trie energy any constant of mc- tion. A
typical trajectory
of these systems covers trie whole energy shellergodically, therefore,
E-B-K method ofquantization
isinadequate
for this case.Yet,
chaos introduces another sort ofsimplicity,
and semidassicalquantization
may beformulated,
rathersimply,
in terms of trieisolated
periodic
orbits of the dassicaldynamics.
Gutzwiller's trace formula[13, 14],
which expresses thedensity
of states as a sum over theseorbits,
is the main trot in the field of chaos quantization.Generic systems,
however,
are neither chaotic norintegrable.
Theirphase
space structure is a mixture ofregular
and chaoticdomains, consequently,
semidassical quantization of thesesystems is more
complicated.
In some cases one may consider theregular
and the chaotic parts of thephase
spaceseparately,
andapply correspondingly
the E-B-K or the Gutzwiller'squantization
methods. A remarkableexample
of thisapproach
is the semiclassicalquantization
of the hehum atom [40]. A different route for
quantizing
such systems is based on time demaintechniques
which whererecently developed
[41].According
to this method the spectrum isobtained from the Fourier transform of the autocorrelation
function,
<#(0))#(t)
>,expressed
in terms of the Van-Vleck propagator, where
)#(0)
> is some initial Gaussian wavepacket.
Trie systems this paper is
dealing
with are two dimensional closed chaotic billiards. Trie semiclassicalapproximation
for theirdensity
of states is obtainedby tracing
trie Green functionusing
thestationary phase
approximation. The result may be written as a sum of a smoothbackground
andoscillatory corrections,
P(E)
~P(E)
+Posc(E). (2.1)
The first term
originates
from shortorbits,
1-e- orbits with actions which are small relative to&. It is
given approximately by
trie Thomas-Fermiexpression, fl(E)
~j / / dPdqô(E
7i(q>
P))>(2.2)
where
7i(q, p)
is the Hamiltonian of trie system, and(q, p)
are trie coordinates and momenta.For closed
billiards,
trieanalytic expressions
for triehigher
corrections offl(E)
are also known [42]. Trieoscillatory contribution, po~c(E),
is related to trie classicalperiodic
orbits of triesystem [13]
pose
(E)
= Re£ Aj e~~~~~J (2.3)
grà
J
The sum over j includes ail trie
penodic orbits, Sj
is the action of thej-th orbit, Aj
is anamplitude
which characterizes the behavior of trietrajectories
in thevicinity
of thatorbit,
and 'tj is trie Maslov
phase
deterniinedby
thefocusing patins
close toj.
In the case where ail theperiodic
orbits(on
the energyshell)
areisolated,
this contribution may beconveniently expressed
in terms of thedynaniical
zeta function [43],(s(E),
aspos~(E)
=
Im£ log((s(E)). (2.4)
This
function,
aise called trieSelberg
zetafunction,
is defined as aproduct
overprimitive periodic
orbits (1.e. orbits which do not retracethemselves),
(s(E)
=
fl fl
1exp()Sp(E) i'tp
+j)up)
,
(2.5)
P-P-o J
~
where the
subscflpt
p denotes theseorbits, Sp(E)
is thecorresponding action,
'tp is the Maslovphase,
and up is trieinstability
exponent associated with the hneanzed motion m trievicinity
of the
periodic
orbit.The introduction of
(s(E)
isextremely
useful. Forexample,
the semidassicalquantization
rule for chaotic systems may be formulated as
(~(E)
= 0.
(2.6)
Unfortunately,
triedynamical
zeta function suffers from severe convergenceproblems
due to theexponential growth
in trie number ofperiodic
orbits as their period increases. In order todarify
this point, it is convenient to represent(~(E)
as a sum overpseudo-orbits, (~(E)
=
£c~ek~". (2.7)
Each
pseudo-orbit,
labeled hereby
~t, is a linear combination of primitive orbits where~1
represents trie vector of the repetition numbers of the
primitive
orbits,(rp)~
=
(ri,
r2> r3,).
Thus trie
pseudo-orbit
action isS~
=£ rpsp, (2.8)
lrpl«
and trie
corresponding period
isgiven by 7j
=ôS~/ôE.
Forlong
orbits andpseudo-orbits
ofergodic
systems7j
andS~
areproportional
andsatisfy
trie relation~~
~~lll~
~~~~where D is the number of
degrees
of freedom of the system(two
in ourcase), fl(E)
is the classicalphase
space volunie with energy less thanE,
fl(E)
=/ / dpdq8[E 7i(q, p)], (2.10)
and
fl'(E)
is its derivative with respect to the energy. In the aboveequation,
8 is the unit step function.Formula
(2.7)
is obtainedby expanding
trieproduct (2.5)
andcollecting
trie various terms.The
resulting amplitudes
aregiven by
[43]CH "
fl ~~(j~~~~f~le~irp~p
~~~~"
~~
~~~ ~ ~~~~(2,Il)
They
decreaseexponentially
with theperiod
r ase~Î~
where is the metric entropy associatedwith the average value of the
instability
exponents. On the otherhand,
trie number ofpseudo-
orbits
proliferates exponentially
with theirperiod
as e~T~ where hT is thetopological
entropy.Since hT > À, absolute convergence of the sum
(2.7)
is obtainedonly
forcomplex
values of ilà satisfying
[38]~
~~~~~
~~&
~~~
22fl(El'
~~'~~~Convergence
of trie seniiclassical expansion forcomplex
values of the energy was discussedby
Eckhardt and Aurell [44].
To be able to obtain real
eigenenergies
from(2.6),
ananalytic
continuation of(s(E)
into the real1là
axis isrequired.
The rifain conclusion from studiesconceming
this issue is that the sum(2.7)
overpseudo-orbits
should beeffectively
truncated [38,45-49]. Generally,
it will include ailpseudo-orbits
ofperiod
smaller than trieHeisenberg
time.Yet,
a considerable reduction inthe number of
pseudo-orbits
may be obtainedusing
functional relations that exist within the quantumtheory,
and thelongest
orbitrequired (labeled
hereby ji)
bas aperiod equal
to half of trieHeisenberg time,
6
"1> (2'13)
where /h
=1/fl(E)
is trie mean level spacing. Trie resummed formula which will bepresented
here wasrecently
obtainedby Berry
andKeating
[38].They
considered trie semiclassicalspectral determmant, D(E),
which is related to triedynamical
zeta functionby
D(E)
=e~~"'~~~'(s(E), (2,14)
where
fiÎ(E)
is the smooth level staircaseapproximately
givenby
the classicalphase
space volume of energy less than E dividedby h~, namely,
NIE)
c~")(~
=j((. 12.15)
J~~ fl
~(£ ~a)
~_ d~
~~ ~~À/( ÎÎ
~
~%~ ~'~
0 2000 4000 E
o ()
~~
_
- c
~ uJ
- ~
©
~
6000 8000 E
Fig. l.
(a)
The billiard together with a typical periodic orbit.(b)+(c)
the corresponding spectraldeterminant for u= I,à, and L=2m= h=1. It is calculated using
(2,16)
from 17347 penodic orbits.The tuning parameter is set to K~
= 5 ~
~~~~~~.
The vertical bars along theenergy axis mark the
à(1/&)2
exact eigenvalues.
Here A is trie area of the
billiard,
and m is thepartide
mass. Like for(s(E),
the zeros of thespectral
determinantprovide
the semiclassicalapproximation
for theeigenenergies.
Theadvantage
of this function is that,semiclassically,
it is real for real values of E [43], and unlike(s(E)
it is invariant under thechange
- -& [38].Exploiting
theseproperties, Berry
andKeating
were able to continueanalytically
thespectral
determinant. Theleading
term of theresulting asymptotic
formula is~~~~
'~' ~~~
~~~ ~~~~~~~~~~~~~~Q(ÎÎÎÎÎ~Î ~'
~~ ~~~where
((~t,
&,E)
=
S~
grfiÎ(E), (2.17)
ôi
and
~
Q(l~>
à>l~)~ l~~ +1) ~/l
)2
~~~~'
~~'~~~h
Inspection
of this formula reveals that thecomplementary
errer function term cutssmoothly
the infinite sum over
pseudc-orbits.
The center of the smoothed cutoif(2.13)
may be found fromiii, à, E)
=0,
and the width of thesmoothing region
is determinedby
K which is a free finetuning
parameter. This width is minimal when K~=
~ ~~
fiÎ(E).
à
à(1/à)2
The
applicability
of formula(2,16)
is demonstrated infigure
1. The system consist in apartiale
of mass m movingfreely
inside a two dimensional chaoticbilliard,
which is a closed version of the openhyperbola
billiard studiedby
Sieber and Steiner [50].figure
la shows the billiardtogether
with atypical periodic
orbit. Thecorresponding spectral determinant,
calculated in the semiclassical
approximation
from 17347periodic
orbits(the
shortest among those which bounce thehyperbola boundary
segment up to 13times),
is drawn mfigures
16 and lc. Trie exacteigenvalues
of the systeni, obtainedby solving
trieShrôdinger equation
numerically,
are indicatedby
vertical barsalong
trie energy axis, and trie zeros ofD(E) give
thecorresponding
semiclassicalapproximation.
In thisfigure,
122 of them are shown and found ingood
agreenient with the exacteigenenergies.
Even after the resummation, the number of
periodic
orbitsrequired
for the calculation of thespectral
determinantproliferates exponentially
with the energy. Thisproliferation
is themajor
obstacle incalculating
thespectral
deterniinant athigh energies. Using
argumentsrelated to the
pruning
ofpseudo,orbits, BogomoIny proposed
a way forreducing
their number for agiven
accuracy [51].However,
it is still not clear whether thisapproach, indeed, improves
the accuracy to work ratio [52].
Part of the
analysis presented
in thefollowing
section, is formulated in terms of thedynamical
zeta function rather than in terms of the
spectral
determinant. A resummed formula for this function may beeasily
obtained from(2.14)
and(2.16).
Asimplified
expression, in which thecomplementary
error function isreplaced by
asharp cutoif,
isgiven by (s(E)
t£
(cpeÉ~"
+Îe~~'~~~~~~k~"Î (2.19)
n<y
3. The
magnetic
response of Aharonov-Bohm billiards.In this
section,
weinvestigate
themagnetic
response of a two dimensionalnoninteracting
electron gas, due to a
single
Aharonov,Bohm flux hne. Theconfining potential
of the electronsis a chaotic billiard of area A
lying
in the ~yplane.
Themagnetic
flux#,
located at somepoint (~o, vo)
within thebilhard,
is related to the vectorpotential
Asatisfying
1#à(~ ~o)à(y
vo " V x A.(3.1)
Its components
expressed
inpolar
coordinates(r,Ù,z)
where(~o, go)
is chosen as theorigin
are Ar =Az =0, and Ao
=#/2grr.
The
thermodynamic properties
of the system are determmedby
thecorresponding
one par, tiffedensity
of statesp(E),
and may be derived from thegrand potential
[53]fl = -T
/dE p(E)
In(1
+e~l)
,
(3.2)
where the temperature units chosen here and henceforth are such that the Boltzman constant kB is umty, and il is the chemical
potential.
For two dimensional systems at low temperature(T<i~)
here considered it may beapproximated by
the Fermi energy,ilmEF. Equation (3.2)
is correct for
spinless partides. Nevertheless,
in Aharonov-Bohmbilliards,
the effect of thespin
amounts tomultiply by
a factor of 2 theintegral
in(3.2).
In what follows this factor will beignored.
Consider first the case of zero temperature. To the
ground
state of the system with##
0corresponds
nonzeroplanar
currentdensity j~(r).
It generates amagnetic
moment M per-pendicular
to theplane
of thebilliard, given by
Biot-Savart law M=
/d~rr
xj~.
For 2cnoninteracting
electrons this moment is built up front moments associated with thesingle
elec-tron states
#~
of energy En below the Fermi energy.Namely,
M=
£~~~~~
Mn with Mn=
~
<
#n)rvo)#n
>, where r and arepolar
coordinates with theorigm
located at the flux 2chne,
and vo is thetangential
component of thevelocity
operator v. Thethermodynamic
current which flows around the flux fine is In =-côEn lai.
Let us define thequantity: ùn
=
-A~~"
ai
=-~
<#~)
~ vo)#~
>. Ingeneral
M~ andùn
aredifferent, however,
for thecase of a uni-
c 2grr
form magnetic field where # is taken as the total flux
through
the two dimensionalsample
they
coincide. Inanalogy
with the standard definition of thesusceptibility
as the denvative of themagnetic
moment with respect to thefield,
we define the response due to a flux hneby
x=
£ £ ù~.
Fornonzero temperature it is
~
E~<E~
x = -A
([il
~~,~
(3.3)
The
starting
point for the semidassicalanalysis
is the Gutzwillerapproximation
forp(E) expressed
in terms of the dassicalperiodic
orbits of the system [13].Substituting (2.1)
in(3.2)
and
integrating by
partsyields
thegrand potential
as a sum of smooth andoscillatory
termsanalogous
to thedensity
of states:fl ci ù + flo~~.
(3.4)
The smooth part
corresponding
to the contribution of short orbits isù
=
/
dE~~ $~~
,
(3.5)
1 + e T
where
fiÎ(E)
is the smooth level staircase(2.15).
Theoscillatory
term commg from theperiodic
orbits isexpressed
in terms of thedynamical
zeta function(2.5)
asflosc = Im
/
dE ~°~~(~Î~ (3. 6)
« 1 + e T
The semidassical
approach requires
the exactdependence
of various dassical quantities in the flux. Here it issimple,
since the dassicaldynamics
is not affectedby
the flux fine. Inparticular,
thephase
space volume isindependent
of the flux. This leads to the invariance of smooth level staircase,fiÎ(E,#)
=
fiÎ(E)
[54].Consequently,
theonly
contribution to thesusceptibility,
in the semidassicallimit,
comes from the dassicalperiodic
orbits of the system.Substituting (3.6)
in(3.3), diiferentiating
with respect to theflux,
andconverting
theintegral
into a Matsubara sum
(by integrating along
the contour shown inFig. 2),
we obtain ageneral
formula for the
susceptibility
of chaotic billiards:x c~
i2xoiRe( 1[~llii~j
~
~llii~j
~_~~~~~~
(3.7)
Here q~
=
<I<D
denotes the reduced flux 1-e- themagnetic
flux measured in units of the flux quantum#o
"~~,
Ko"
~~
~
is the Landau
susceptibility
in twodimensions,
/h=
~~~~
e 12grmc mA
is the mean level
spacing,
and(Î~~(E;q~)
denotes thej-th
denvative of thedynamical
zeta function with respect to q~. The Matsubarafrequencies
are Enlà
withEn =
(2n
+1)grT. (3.8)
The use of
Cauchy
theorem for the conversion of theintegral (3.6)
into a sum over the residues(3.7)
isjustified by
thefollowing properties
of thedynamical
zeta function and its derivatives:(1) lim~-m (s(ee~~;q~) =1 for
gr/2
> > 0;(ii)
in the same hmit the derivatives (Î~~(ee~~;q~)decay exponentially; (iii)
the contribution from theintegral along
theimagmary
axis may be1>nE
Matsubara
frequencies
+ + + + + + +
2nT(
~~~ j
Re Ezeros of trie dynani (cal zeta function
Fig. 2. The contour of trie integral which leads to equation
(3.7).
shown
(integrating by parts)
to be of trie ordere~~F/~, therefore,
it may beneglected
when T<EF.We now
investigate
thedependence
of(~(E;
q~) on the flux. For this purpose it is sufficient to examine thedependence
for anarbitrary periodic
orbit as themagnetic
fluxchanges.
Consider first trie zero flux liniitq~ = 0. In this case the system exhibits time reversai
invariance,
and this synimetry is reflected in trieperiodic
orbits structureby
the fact that there are two types of orbits. There are orbits that trace themselves backalong
the samepath.
These exhibita time reversai invanance. On the other hard orbits which do not have this symmetry may be traced in two
opposite directions,
and therefore to every such orbitcorresponds
a time reversed counterpart. The time reversai symmetry presents itself in the Gutzwiller formulaby
the property that such
pairs
of orbits are characterizedby exactly
the same dassical quantities.When q~
#
0 thisdegeneracy
is lifted. Triemagnetic
flux fine is introduced in trie equationsby replacing
theoriginal
momentum p=mvby
p=mv-~A,
where A is the vectorpotential
c
which satisfies
(3.1).
Thisreplacement
leads to a fluxdependence
of theperiodic
orbits actions of the form [55]Sp(q~) =
jÎ pdq
=Sp hwpq~, (3.9)
where
Sp
isindependent
of q~ andcorresponds
to the zero fluxvalue,
and Wp is triewinding
number of trie orbit around trie flux fine at (~o>go)-
Note that trie other relevant classicalquantities, namely,
theinstability
exponent and the Maslovphase
are not aifectedby
the flux fine.The
change
m the time reversaiproperties
of trie system is related to thepossible change
in the actions of pairs of time reversed orbits. The opposite
signs
of theirwinding
numbers lead to a diiference m their actions.Yet,
wheneverq~ is an
integer
(1.e#
is aninteger multiple
of
#o),
there will be aphase
coherence between the orbit and its time reversed counterpart.Therefore,
the variousthermodynamic properties
of this system arepenodic
functions ofq~
[56].
Inserting
expression(3.9)
for the action into the approximate formula(2.19)
andtaking
thederivatives with respect to q~
yields
((J)j
E.~)
r~~£ ~(J>~#s~(~)
~
~u)*~~2«fit(E)-js~(~)j j~
~~)~
~ <m
~ ~
where the
pseudo-orbits actions, S~(q~),
aregiven by
formula(2.8)
withSp replaced by Sp(q~),
and theamplitudes
arec))
= c~(-2griW~)?
,
(3.Il)
where c~ is
given by (2.Il),
andW~
is thepseudo-orbit winding number, W~
=£ rpwp. (3.12)
lrpl«
Note that at q~ = 0,
(Î~~(E;
q~) vanishes. It follows from the lineardependence
of theamplitudes cÎ~
on thewinding numbers,
whichimplies
that the contributions from a pair of time reversedpseudo-orbits
add updestructively.
At q~=0 theseexactly
cancel each other.Forniula
(3.7)
for thesusceptibility
of chaotic billiards will now beinvestigated.
We assumea
large enough
Fermi energy (1.e. kFL »1 where kF is the Fernii wavenumber),
muchlarger
than the thermal excitations
(EF
»T).
Under thisassumption,
thepseudo-orbits
actions evaluated at EF + iEn may beexpanded
to first order in En/EF
asS~(EF
+iEn)
mS~(EF) +17j(2n
+1)grT, (3.13)
where
7j
=ôS~/ôE
is thepseudo-orbit period.
This expansion holdsonly
for the low Mat- subarafrequencies
for which n <$.
It tums out that contributions from
large
n terms arenegligibly
small as will beargued
whengr the contribution of the varions Matsubarafrequencies
will be calculated(see
discussionfollowing (3.29)).
Theimaginary
part of(3.13)
results in anexponential damping
of thecorres/onding pseudo-orbit
contribution. For the lowestfrequency (n
=0)
it isproportional
toe~MG,
while forhigher frequencies
it is much stronger. Thisdamping imphes
that athigh
temperatureonly
the shortestpseudo-orbits
contributesignifi- cantly
to thesusceptibility.
One may define a threshold temperature,Tth, according
to therequirement
that the Upper bound on thesedamping
factors(which corresponds
to the short- estperiodic orbit)
is of ordere~~.
Since the shortestpenodic
orbitlength
is of order 2L thiscondition leads to the definition of the threshold temperature:
~~
(Î)2~~~~'
~~'~~~where
fl
=
/À/L
is ageometrical
factor of orderunity.
There are,therefore,
three relevant energy scales in theproblem:
(1) the niean levelspacing /h; (ii)
the threshold teniperatureTth
associated with the tinte it takes for a partide at the Fernii energy to cross the
sample; (iii)
the Fermi energy EFfQS ~(kFL)~.
When the Fermi energy issulficiently high,
so that kFL » (2gr)~,4gr
these scales are well
separated, namely, /h«Tth
<EF.At
high
temperatures(T>Tth)>
the thermal fluctuations wash ont structures in the energy scale of the mean level spacing, andonly
shortperiodic
orbits contributeeifectively
to thesusceptibility.
We then expect asimple dependence
on the parameters. As the temperature decreases below Tthlonger periodic
orbits become more important, and at very low tempera- tures(T
</h)
ail orbits(of period
smaller than half of theHeisenberg time)
havesignificant
contributions.
Fig. 3. A schematic illustration of a billiard with rough boundary
(thick
fine), and some of the shortest penodic orbits(thin
fines), which almost cover the energy shell uniformly. L is the linear dimension of the billiard, A is its area, and LR is the scale associated with the roughness of the boundary. The latter is assumed to be large conlpared to the Fermi wavelength.In what
follows,
an estimation for themagnitude
of thesusceptibility,
in two ranges of temperature, /h > T and Tth < T, is calculated. For this purpose, some statisticalproperties
of theperiodic
orbits arerequired (cf. Appendix A),
and thefollowing
discussion will beconfined to billiards for which the
boundary
iscomplicated enough
so that one may consider thecorresponding
set of the shortestperiodic
orbits(e.g.
the orbits which bounce theboundary twice)
ascovering
the energy shell almostuniformly
in an ensemble of billiards. Anexample
of such billiardtogether
with some of the shortestperiodic
orbits is illustrated infigure
3. Inaddition,
it will be assumed that the scale associated with theroughness
of theboundary,
LR>is
large compared
with the Fermiwavelength.
We shall also introduce two types of ensembleaveraging,
(. and((. )).
The first represents anaveraging
over some externat parameter related to theroughness
of theboundary
and is an average over an ensemble ofbilliards,
while the second indudes also an additional averaging over the flux.3.1 THE HIGH TEMPERATURE REGIME T > Tth. It is clear tram the above discussion
that at temperatures
sufficiently high
so that T > Th issatisfied,
the shortestperiodic
orbits dominate the behavior. In this case one mayexploit
the natural cutoif of theperiodic
orbitsum
(2.3)
due to the temperature in order to derive asimpler
formula for thesusceptibility
which does not require the resummed expression of the zeta function.
Substituting (2.3)
in(3.2)
andusing (3.3)
leads tox cf
12xo )Re £ £ Îo (? (2«Wj )~e~+~~~J, (3.15)
j ?
~ ~
where the sum is over ail the
pefiodic
orbits(primitive
andrepeated),
andAj, Tj
andWj
are the
j-th periodic
orbitamplitude, penod,
andwinding
numberrespectively.
In the range of teniperature here considered, the rifain contribution comes from the lowest Matsubara fre-quency n =0, and the
higher frequencies
may beneglected.
Thenusing
first order expansion of the actions similar to(3.13)
we obtain:x t
12xo )Re £ ? (2grWj)~e~ÎÎ+fi~~~~J
Tth 1 T « EF(3.16)
~ J
A
simpler
form of thisformula,
where thedependence
on the varions parameters isdearer,
is obtainedby substituting
theexplicit
form of the actions(at
zeroflux) Sj(EF)
"
PFLj
whereoD
CQ
*S~
à
', , , /
- ' / ' /
', /"' / ' /", ,~
o
-0.4 -0 2 0 0.2 0 4
#
Fig. 4. The fluctuations of the susceptibility ôx> in units of x*
"
Îxo)kFL,
as function of the reducedflux ~=
#/#o
for various values of the temperature. The sohd fine corresponds to T=Tth, the dashed Iine to T=2Tth, and the dotted fine to T=3Tth. The threshold temperature, Tth, is given by(3,14).
pF =
àkf
is the Fermi momentum andLj
is thelength
of theorbit,
as well as the fluxdependent
partgiven by (3.9).
Then one findsx m
24xo) £' (? e~$(2grWj)~ cos(kFLj -'tj) cos(2grWjq~), (3.17)
j J
where here
£(
denotes a sum overpairs
of time reversed orbits. This formula showsthat,
ingeneral,
x is anoscillatory
function of the Fermi wavenumber and of the flux. For the shortest orbitsAj/Tj
is of orderunity
andLj
m 2L,therefore,
theamplitude
of these oscillations at T =Tth isproportional
to kFL and it decreasesexponentially
ase~~/~th
for T > Tth. In orderto estimate the
magnitude
of thesample
tosample
fluctuations we shall considerôX "
À~. (3.18)
Its calculation
(given
inAppendix A)
is based on two results: one is theHannay
and Ozorio de Almeida sum rule [16] which expresses thedensity
of the periodic orbitsweighted by
theiramplitudes
as asimple
function of theirperiods,
and the other is a result ofBerry
and Robnik [55]according
to which thewinding numbers, Wj,
ofperiodic
orbits of chaotic billiardssatisfy
a discrete Gaussian distribution. The
corresponding
vanance a~ is found to beproportional
to the orbits
period
t,namely
~~
~ÎÎ~'
~~'~~~where VF is the Fermi
velocity,
and C is a constantapproximately give
j Cm 0.215. The average over theroughness
of the fluctuationfunction, ôx,
takes the form~~
m
@
~I(T,
q~) Tth < T < EF
(3.20)
Xo ~
where
I(T,
q~) is aperiodic
function ofq~ for which an exact formula is
given
inAppendix
A(Eq.
(A.14)).
It ispresented
infigure
4. Note that ôX is aperiodic
function ofq~ with
periodicity 1/2.
Thisperiodicity
is a consequence of the coherent interference of the orbits and their time reversed counterparts which takesplace
notonly
atinteger
values of q~ but also at halfintegers
which
correspond
to false timebreaking
symmetry [55]. In order to estimate themagnitude
ofthe fluctuations it is instructive to consider
ôy
which is the same function defined in(3.18)
but with(.
.)replaced by ((. .)).
It isstraightforward
to show thatôy
satisfies a similar formula but withI(T,
q~)replaced by
asimpler
functionÎ(T) given by (A.17).
Inparticular,
as shown at the end ofAppendix A,
at T =Tth
ityields
~~
=
3@e~~CkF/À
m
2kFL. (3.21)
ÎXO
Note that kFL is of the order of the square root of the number of electrons in the system, thus at the threshold temperature the fluctuations in the
susceptibility
are ingeneral
verylarge compared
to )xoÎ. Theasymptotic
behavior for T »Tth
may be also deduced from(A.17),
and in thisregime
the average of the fluctuations decreasesexponentially
as)
m
4.5kF/À
~e~Î
Th< T < EF
(3.22)
XOÎ Tth
The temperature for which the fluctuations are of order of the Landau
susceptibility
xo isapproximately
TmTthIn(4.5kFL)
1-e-typically larger
than Th.3.2 THE Low TEMPERATURE REGIME T < /h. Consider now the low temperature
regime
T < A. It is
iniportant
to note that unlikehigh
temperatures where the fluxdependence
of the chemicalpotential
is very weak(and
therefore wasignored),
here it is very strong. Thereason is that in order to maintain the nuniber of
partides
constant, the chemicalpotential
niust lie in the middle between two energy
levels,
therefore it must follow the variations of the energy levels due tochanges
in the flux. Athigh
temperatures, on the otherhand,
the chemicalpotential
is aifectedby
the occupation of many levels in the energy interval of size T. The flux does not affect the meandensity
of states and therefore it does not affect the chemicalpotential
as well. Note also that
fixing
the number of electrons whileconsidering
thegrand potential (3.2)
isjustified
in the limit oflarge
number ofpartides
where the diiferences between thethermodynamic properties
derived from the canonical and from thegrand
canonical ensemblesare small.
In order to obtain a dosed formula for the
susceptibility
in the low temperature regime,we shall
apply Berry
andKeating
resummation method [38]. Since this method wasalready
described(see
also Ref.[57]),
here it willonly
be outlinedbriefly.
Letù
be definedas
T E -E
fl =
/
dER(E) In(1
+ e T
), (3.23)
«
where
R(E)
is the resolvent givenby
~~~~ ~
E +
iÎ E~'
~~'~~~and
E~
are theeigenenergies
of the system (E is an infinitesimalpositive number).
The imag- mary part ofù
is thegrand potential
defined in(3.2).
An important relation satisfiedby ù
isthe exact functional
equation:
ù(-à)
=
fl*(&). (3.25)
It is due to the fact that the
eigenvalues
En are invanant while Echanges
sign under à reversai[38, 57].
Let1
be related to fl as in(3.3), namely
ô2~j
~~ ~
ôj2
' ~~'~~~EF,T
JOURNAL DE PHYSIQUE T 4 N' ~ MAY 1994