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First-order quantum correction to the ground-state energy density of two-dimensional
hard-sphere Bose atoms
Sang-Hoon Kim
a,b
and Mukunda P. Das
b
a
Division of Liberal Arts & Sciences, Mokpo National Maritime University, Mokpo 530-729, Republic of Korea
b
Department of Theoretical Physics, RSPhysSE, Institute of Advanced Studies,
The Australian National University, Canberra, ACT 0200, Australia
(Dated: August 25, 2008)
Divergence exponents of the rst-order quantum correction of a two-dimensional hard-sphere Bose
atoms are obtained by an eective eld theory method. The rst-order correction to the ground-
state energy density with respect to the zeroth-order is given by E1/E0 |D2|
| ln |
, where
D is the spatial dimension, and is the gas parameter ( = na
D
). As D 2, =
= 1. We show
that the rst-order quantum correction of the energy density is not perturbative in low dimensions
of D < 2.2 regardless of any gas parameter which is much less that 1.
PACS numbers: 05.30.Jp, 21.60.Fw, 03.70.+k
Keywords: Boson systems, interacting boson model, quantum eld theory
I. INTRODUCTION
Weakly interacting uniform Bose gas is a fundamental topic of many-body Bose systems and has been studied for
more than ve decades. Bose-Einstein condensation(BEC) is known to be the only phase transition that does not
require interaction. However, in the real system an interaction exists even in very dilute Bose gases, and often the
diluteness is explained by a D-dimensional gas parameter: (D) = na
D
1, where n is the D-dimensional density
and a is the s-wave scattering length. At zero temperature the chemical potential, energy density, number density,
and speed of sound are written as an expansion in powers of the gas parameter .
A fundamental approximation method of a weakly interacting Bose system was introduced by Bogoliubov in 1947
[1]. In three-dimensions(3D) the ground-state energy density is given by
E0 +E1 + = E0 [1 +c1
+c2 ln + ] . (1)
Similarly, the number density in 3D is given by
n0 +n1 + = n0
1 +
8
3
. (2)
E
0
= 2
2
an
2
/m is the zeroth-order or mean-eld energy density. The rst-order quantum correction c
1
= 128/15
was rst obtained by Lee and Yang in 1957 for a hard-sphere Bose gas [2]. Later, it has been shown by Brueckner
et al. [3, 4] that above results are generally true for any short-range potential with scattering length a. The second-
order quantum correction c
2
= 8(4 3
3)/3
1 +
1
ln(1/)
+
. (4)
E
1
E
0
1
|D2|
| ln |
, (5)
where the exponents and
. Furthermore, since the rst-order quantum correction of the ground-state energy density converges in D=3 but
diverges in D=2, we may nd the dimensional border of the perturbative method which is eective between two and
three.
The paper is organized as follows: In Section II, we review the basic structure of EFT of a dilute Bose system in
non-integer dimensions between two and three [8, 14, 15]. In Section III, we reproduce the zeroth-order or mean-eld
results in D-dimensions. In section VI, we obtain the rst-order quantum correction in 2D and two exponents and
. Also we interpolate the rst-order quantum depletion between 2D and 3D. Finally, in section V we summarize
the results.
II. EFFECTIVE FIELD THEORY BY AN EFFECTIVE LAGRANGIAN
EFT is a general approach that can be used to analyze the low energy behavior of a physical system and takes
advantage of the separation of scales to make model-independent predictions [9, 10, 11]. The eective lagrangian that
describes the low energy physics is written in terms of only the long-wavelength degrees of freedom that includes every
non-renormalizable interactions, but to a certain order in a low energy expansion, only a nite number of operators
contribute to a physical quantity [14].
An uniform Bose gas can be described by eld theoretic method with Hamiltonian H N, where is the
chemical potential and N is the number operator. The number of atoms are conserved by the phase transformation:
(r, t) e
i
(r, t). The free energy in ground-state of the system is
F() = HN, (6)
where
= E() and N
) in the
ground-state (we set = 1 for convenience)
n() =
1
Z
_
D
D(
) e
iS[
,]
(7)
where
and are complex eld operators of bosons, S is the action from the Lagrangian [8], and Z is the grand-
canonical partition function given by
Z =
Z
D
D e
iS[
,]
. (8)
The grand-canonical ensemble of uniform Bose particles with a two-body interaction is governed by the action
S[
, ] =
Z
dt
Z
d
D
x
i
t
+
2
2m
+
1
2
g
, (9)
where m is the atomic mass, and g is the D-dimensional coupling constant which contains pairwise interaction between
atoms. In D-dimensions g is given by [16]
g(D) =
4
D/2
a
D2
m
1
2
2D
(1
D
2
)
D/21
+ (
D
2
1)
, (10)
where is the Gamma function. It satises the two limiting cases. In 3D, it has the well-know form
g(3) =
4a
m
. (11)
3
In 2D, it has the logarithmic form [17, 18]
g(2) =
4
m
1
ln(1/)
. (12)
When the temperature of a Bose system falls below the condensation temperature T
c
, we can write the quantum
eld in terms of a time-independent condensate and a quantum uctuation eld
= +
. (13)
The uctuation eld
can be conveniently written in terms of two real elds
1
and
2
=
1 +i2
2
. (14)
In the uniform system is the condensate order parameter and a real constant. It corresponds to a breaking of the
global U(1) symmetry and takes into account the Bogoluibov shift of the eld operator.
The conservation of particle numbers requires that
has non-zero momentum component so that = and
= 0. Therefore, the condensate order parameter denes the density of condensed particles while
denes the
density of uncondensed particles. Then, the zeroth- and rst-order quantum correction to the density are given by
n0 =
2
, n1 =
. (15)
Substituting Eqs. (13) and (14) into Eq. (9) of the action S, we decompose the real part of the action into three
parts [8, 14, 15]:
S[, 1, 2] = S
clas
[] +S
free
[, 1, 2] +Sint[, 1, 2]. (16)
S
clas
is the classical part of the action. It does not contain any led operator:
S
clas
[] =
Z
dt
Z
d
D
x
1
2
g
4
. (17)
S
free
is the free part of the action. It is quadratic in
1
and
2
:
S
free
[, 1, 2] =
Z
dt
Z
d
D
x
1
2
(
12 1
2) +
1
2
1
2
2m
+X
1 +
1
2
2
2
2m
+Y
, (18)
where
/t, and the two new variable X and Y are
X = 3g
2
, (19)
Y = g
2
. (20)
The terms 3g
2
and g
2
in the X and Y are mean-eld self-energies of the system.
S
int
is the interaction part of the action. It is the remaining terms:
Sint[, 1, 2] =
Z
dt
Z
d
D
x
2J1 +
K
2
1(
2
1
+
2
2
)
g
8
(
2
1
+
2
2
)
2
, (21)
where
J = ( g
2
) = Y, (22)
and
K = g. (23)
The free part of the action in Eq. (18) gives rise to a propagator, which can be used in perturbative framework. If
we take the Fourier Transform in a momentum space, the uctuating part is given by
(t, r) =
1
X
n=
X
p
p
=
_
d
D
p/(2)
D
, and
n
= 2nT is the Matsubara frequency. Therefore, the propagator of the free
action S
free
is written as
G(, p) =
1
2
E
2
p
+iE
p
_
p
2
2m
Y i
i
p
2
2m
X
_
,
(25)
4
+
+
+ +
FIG. 1: Loop diagram of the two-body interaction. The zeroth, rst, and second loop from the left to right
with the dispersion relation
Ep =
s
p
2
2m
X
p
2
2m
Y
. (26)
This is a general form of the dispersion and includes every information of the energy spectrum in the two self-terms
X and Y . It is possible to diagonalize the propagator matrix in Eq. (25) by a eld redenition or renormalization,
which is equivalent to the Bogoliubov transformation in the operator method. However, such a redenition makes
the interaction terms in the action more complicated and increases the number of diagrams. Therefore, we use the
propagator matrix with o-diagonal elements to minimize the number of diagrams.
III. THERMODYNAMIC POTENTIAL AND ZEROTH-ORDER RESULTS
It is convenient to introduce the thermodynamic potential (, ). The thermodynamic potential contains the
information required to determine all of the thermodynamic functions. The free energy F() can be obtained by
evaluating at a particular value of .
The sum of the vacuum graphs is independent of the arbitrary background condensate . Thus, the sum of connected
vacuum diagram reduces to the sum of one-particle irreducible vacuum diagrams [8, 14, 15]:
F() = (, ()) (27)
From Eq. (6) the ground-state energy density is written by
E() = F() +n. (28)
By dierentiating the free energy, we obtain the density and chemical potential, too.
n() =
dF
d
, (n) =
dE
dn
. (29)
The n-loop contribution to the is denoted by
n
in FIG. 1. It is given by all one-particle irreducible vacuum
diagrams and can be expanded in the number of loops:
(, ) = 0(, ) + 1(, ) + 2(, ) + . (30)
If is evaluated at a value of the condensate, all one-particle reducible diagrams vanish. Then, the free energy density
in Eq. (27) is
F() = 0(, ) + 1(, ) + 2(, ) + . (31)
Using Eqs. (13) and (14), the condition of the condensate reduces to
1
=
2
= 0. This condition is equivalent
to
(, )
=
0(, )
+
1(, )
+
2(, )
+ = 0 (32)
The number density in Eq. (29) is obtained from the thermodynamic potential, too.
n() =
. (33)
The free energy can also be expanded in powers of quantum corrections around the mean-eld value F
0
():
F() = F0() +F1() +F2() + . (34)
The loop expansion in Eq. (31) does not coincide with the above expansion of F() in powers of quantum corrections
because of its independence of . To obtain the expansion of F in powers of quantum corrections, we must expand
the condensate around its classical minimum
0
, which satises
0(, 0)
= 0. (35)
5
By expanding Eq. (32) in powers of
0
, and solving for , we obtain the quantum expansion for the condensate:
= 0 +1 +2 + , (36)
where
n
is the nth-order quantum correction. For instance, the rst-order quantum correction for the condensate
1
is obtained from the expanding of Eq. (35) around
0
. The nonzero terms are
0(, )
=
2
0(, 0)
2
( 0) +
1(, 0)
+ = 0. (37)
Then,
1
in Eq. (36) is written as
1 =
1(, 0)
2
0(, 0)
1
. (38)
Therefore, keeping up to the terms of the second order and
0
1
, the rst three terms of the free energy
density is
F
0
() =
0
(,
0
), (39)
F
1
() =
1
(,
0
), (40)
F
2
() =
2
(,
0
) +
1
(,
0
)
1
+
1
2
0
(,
0
)
2
2
1
. (41)
The mean-eld thermodynamic potential is given by the terms in the classical action in Eq. (17) as
0(, ) =
1
V
S
clas
=
2
+
1
2
g
4
. (42)
From Eq. (35) we obtain the classical minimum
0
as
0 =
r
g
(43)
Therefore, the mean-eld free energy density in D-dimensions is obtained from Eq. (39)
F0() = 0(, 0) =
2
2g
. (44)
The mean-eld number density is obtained from Eq. (7) as
n(0) =
F(0)
=
0
g
(45)
The mean-eld ground-state energy density in D-dimensions is obtained from Eq. (28)
E
(D)
0
=
2
0
2g
+n0 =
1
2
g(D)n
2
. (46)
In 3D, since g(3) = 4a/m from Eq. (11), the mean-eld energy density is
E
(3)
0
=
2an
2
m
. (47)
In 2D, since g(2) = 4/mln(1/) from Eq. (12), the mean-eld energy density is
E
(2)
0
=
2an
2
mln(1/)
. (48)
Therefore, this method reproduced the well-known mean-eld energy densities in Eqs. (1) and (3) successfully.
6
IV. FIRST-ORDER QUANTUM CORRECTION
The rst-order quantum correction of the ground-state energy is obtained in the following way. Substituting Eq.
(43) into Eqs. (19) and (20), we obtain the two variables X and Y at the minimum of
0
.
X = 3g
2
0
= 2, (49)
Y = g
2
0
= 0. (50)
The propagator and the dispersion relation in Eqs. (25) and (26) becomes
G(, p) =
1
2
E
2
p
+iE
p
_
p
2
2m
i
i
p
2
2m
+ 2
_
,
(51)
and from Eq. (45)
Ep =
s
p
2
2m
p
2
2m
+ 2
. (52)
These are the original Bogoliubov results. E
p
is gapless and is linear for small wave-vectors. For large wave-vectors,
the dispersion relation becomes E
p
p
2
/2m+2 p
2
/2m+2g(D)n. Therefore, the 2g(D)n represents the mean-eld
energy in D-dimensions due to interaction with the condensed particles.
In the Bogoliubov approximation one makes a pair approximation to the Hamiltonian by neglecting terms with
three and four operators [1]. On the other hand, in the Beliaev approximation, one goes one step further by calculating
the leading quantum corrections to the quasi-particle spectrum [4]. This is done by including all one-loop diagrams.
The free energy can be written with the inverse of the propagator. From Eq. (8)
Z = exp
i
Z
dt
Z
d
D
xdetG
1
(, p)
. (53)
Therefore,
F = Tr lnG
1
(, p). (54)
Note that ln detA = Tr ln A for any matrix A. The one-loop contribution to the thermodynamic potential in D-
dimensions,
1
= i ln Z, is obtained by the following way.
1
(, ) =
i
2
_
d
2
_
d
D
p
(2)
D
ln det G(, p)
1
=
1
2
_
d
D
p
(2)
D
E
p
. (55)
From Eq. (40), we have the free energy component
F1() = 1(, 0) =
1
4m
I0,1(), (56)
where = 4m = 4mgn and I
i,j
are loop integral function in D-dimensions, which is dened as [8, 14]
I
(D)
i,j
() =
_
d
D
p
(2)
D
p
2i
p
j
(p
2
+)
j/2
, (57)
where i and j are integers. This I
i,J
is expressed by Gamma function, too.
I
(D)
i,j
=
1
(4)
D/2
`
D+2ij
2
D+2i2j
2
`
D
2
`
j
2
D+2i2j
2
. (58)
Note that in D=3, I
(3)
0,1
() =
5/2
/15
2
, I
(3)
1,1
() =
3/2
/3
2
, and I
(3)
1,1
() =
3/2
/6
2
. It has the useful relation
of the rst derivative
d
d
I
(D)
i,j
() =
j
2
I
(D)
i+1,j+1
(). (59)
Ground-state energy density is expressed as
E
0
+E
1
+ =
1
2
gn
2
+
1
4m
I
(D)
0,1
() + . (60)
7
-2.5
-2
-1.5
-1
-0.5
0
0.5
1
1.5
2 2.2 2.4 2.6 2.8 3
q
u
a
n
t
u
m
c
o
r
r
e
c
t
i
o
n
,
l
o
g
(
1
/
0
)
Dimension, D
=10
-2
=10
-4
=10
-6
FIG. 2: The rst-order quantum correction of the ground-state energy density in D-dimensions in the logarithmic scale. The
divergence in D=2 is clear. itself is a function of the dimensions.
Therefore, the contribution of the rst-order quantum correction in D-dimensions is obtained as
E
1
E
0
=
D+2
2
_
_
D+1
2
_
(D+1)/2
_
D
2
_ {mg(D)}
D/2
n
D/21
=
2
D
(D
2
2D2)/4
D+2
2
_
_
D+1
2
_
D/21
_
D
2
_ _
2
2D
_
1
D
2
_
D/21
+
_
D
2
1
__
D/2
. (61)
Note that = (n
0
+n
1
+ )a
D
.
Substituting D=3, we obtain the well-known rst-order quantum correction of the ground-state energy density in
3D as
E1
E0
=
128
15
. (62)
Taking the limit of D = lim
0
+ 2(1 + ), we obtain the rst-order quantum correction of the ground-state energy
density in 2D as
E1
E0
+ 1
1
ln(1/)
1. (63)
For the singularities of the function at non-positive argument, we used the following expansions
(n +) =
(1)
n
n
+h(n + 1) +O()
, (64)
where h(n+1) = 1+1/2+1/3+ +1/n
E
and
E
= 0.5772... is the Euler constant. In particular, () = 1/
E
.
Also, we used the approximations:
1 + ln.
In 2D there is a divergence, and we can obtain the two exponents of the divergence in Eq. (5) as =
= 1. We
plotted E
1
/E
0
in FIG. 2 as the functions of the dimensions and gas parameter in the logarithmic scale. From the FIG.
2 it is clear that the expansion in Eq. (3) satisfy the perturbative condition of E
1
/E
0
1 only when D > 2.2. In low
dimensions of D < 2.2, the rst-order ground-state energy density is not perturbative regardless of the magnitude of
the gas parameter.
The number density is obtained from Eqs. (13)-(15) as
n =
2
+
1
2
2
1
+
2
2
. (65)
Therefore, taking the one-loop eects into account
n
0
+n
1
= n
0
+
i
2
_
d
2
d
D
p
(2)
D
_
p
2
/2m+ 2mE
2
p
/p
2
2
E
2
p
+iE
p
_
= n
0
+
1
4
I
1,1
(4mgn) +
1
4
I
1,1
(4mgn)
= n
0
_
1 +
D
2
_ _
2
_
D+1
2
_
_
D1
2
__
2
3
(D+2)/2
_
D
2
_ (mg)
D/2
n
(D2)/2
0
_
. (66)
8
0
0.02
0.04
0.06
0.08
0.1
0.12
2 2.2 2.4 2.6 2.8 3
Q
u
a
n
t
u
m
d
e
p
l
e
t
i
o
n
,
n
1
/
n
0
Dimension, D
=10
-4
FIG. 3: The rst-order quantum correction of the number density at = 10
4
as a function the dimensions.
Then, the rst-order quantum correction of the number density in D-dimensions is obtained as
n
1
n
0
=
(D
2
2D2)/4
2
3D
D
2
_ _
2
_
D+1
2
_
_
D1
2
__
_
D
2
_ _
2
2D
_
1
D
2
_
D/21
+
_
D
2
1
__
D/2
D/21
. (67)
In 3D we obtain the well-known rst-order quantum depletion as
n1
n0
=
8
3
. (68)
In 2D taking the limit of D = lim
0
+ 2(1 + ), we obtain the rst-order quantum depletion as
n
1
n
0
+
1
1
ln(1/)
. (69)
We used the approximations: (
D
2
) 1/ and 2(
D+1
2
) (
D1
2
) 2
| ln |
analytically as =
na
2
instead Nogueiras Choice of pa na
2
, where p is the momentum.
[17] S.-H. Kim, C. Won, S. D. Oh, and W. Jhe, cond-mat/9904087 (1999).
[18] E. H. Lieb, R. Seiringer, and J. Yngvason, Commun. Math. Phys. 224, pp. 17-31 (2001).