12, Septembfr 197$ Bicritical Tricritical: Ferroma Ets
12, Septembfr 197$ Bicritical Tricritical: Ferroma Ets
12, Septembfr 197$ Bicritical Tricritical: Ferroma Ets
1849
1850 KHA JEHPOUR, WANG, AND KROMHOUT 12
common tangent at BCP. ion anisotropy
In the models discussed in Refs. 5, 10, and 13,
the ordering fields are either physically fictitious R= QZ„S,(i)S,(j) QK„S,(i) S,(j) ~
&Q&
fields or experimentally uncontrollable. There-
fore one cannot investigate the vicinity of the BCP
in all directions experimentally. The features in
+~ Q [S,(i)1' — 4 g S(i),
. (2 1)
the vicinity of a BCP are of great interest, For where 4 and K are assumed positive. The trans-
example, it is shown- by Chang et al. ' that four verse coupling provides the possibility for the sys-
tricritical lines meet at a BCP in-a generalized tem to order in the basal plane perpendicular to the
metamagnetic model, The ordering fieMs to gen- z axis for certairi ranges of temperature and an-
erate these lines in all the above models are the isotropy. In the mean-field approximation (MFA)
staggered fields. the Hamiltonian (2. 1) can be written
In this paper we discuss an anisotropic uniazial
ferromagnetic model which exhibits, in addition to X„=-2(S,)S, -~2K(S, )S, +D(S,)
the ordinary critical phenomena, bicriticality at
—h S+(S,) yK(Si),
~
(2. 2)
H= 0 and tricriticality in a finite field. The Hamil-
tonian contains a single-ion term of the form where K=K(0)/&(0), h= pH/J(0), D=&/J(0), ~(0)
.
D(S,) The exchange interaction is also assumed =g& J,&,K(0) =g& K, &, and energies are measured
to be anisotropie. A magnetic field along either in units of &(0).
the parallel or the transverse direction generates It should be noted that while the basal plane is
two tricritieal lines which terminate at the BCP.
isotropic we have chosen a direction for the order-
Consequently, in a region near the BCP one expects
ing and have labeled it with the perpendicular sign;
a variety of critical (either Ising-like or xy-like), (S,) is the component of (8) on the basal plane.
bicritical, and tricritical behaviors, as well as the One can write Eq. (2. 2) in an even simpler form
crossovers between these behaviors.
Another interesting feature of the model is that X„=D(Sg)3 n, S, —n—~S, + eo, (2. 3)
when the anisotropy D is treated as a constant,
(H, , H, = 0, T) and (H, = 0, H„T) phase diagrams where
exhibit a tricritical point (TCP) for a wide range of n = h, +2(S, ),
the values of the parameters of the system. Here
one has a situation where the TCP and the wings n~= h, +2(S~), (2. 4)
are all within an experimentally accessible and eo-(S, ) +K(S, ) .
contro11able thermodynamic field space. This same
feature is shown in the Blume-Capel model in a The energy eigenvalues of X are the roots of the
transverse field (which is a special case of our secular equation
more general model) and has been discussed by the
authors elsewhere. '7 Xq —2DX~q+ (D —n~ n~ = 0
n~)Xq+D— . (2. 5)
In order to have a general picture of the phase
diagrams, we have carried out an investigation of. Equation (2. 5) can be solved by standard methods
this model in the mean-field approximation (MFA). to yield the result
The model Hamiltonian is discussed in Sec. II. We
have obtained the zero-field partition function as a
double expansion in the order parameters. The
zero-field phase diagrams in the whole range of the
=sD+s(D'+3n,'+3n', )'"cos[y+ 3m(k 1)]+e„-
transverse coupling && 0 is obtained in See. III, (2. 6)
where 4=1, 2, 3 and,
The range of values of K where the phase diagram
contains a BCP is found. The study of the system 1 2D' —18(n,'+n', )D+27n', D
in a finite magnetic field is the subject of Sec. IV. (D'+ 3n'+ 3n')"'
The behaviors of the system in a parallel and a
transverse field are treated separately, and the Equations (2. 6) and (2. 7} are used for numerical
corresponding phase diagrams are worked out, The calculations. For the special cases of H, = 0 (or
ranges of the parameters D and positive K where H, = 0) a simple expansion in (S, ) (or (S, )) can be
trieritieal behavior exists are found. Finally in easily obtained from Eq. (2. 5) in the vicinity of a
Sec. V the main points of the work are summarized. second-order phase transition. In general one. can
use Eq. (2. 6) to find a set of self-consistent equa-
P
expansion of energy eigenvalues about (S,) = 0 (or beeri vrorked out in Ref. 3.8. %e refer the reader
(S, ) =0) is a convenient approach to discuss the to that paper for the details of calculation.
second-o&rder phase transitions. To do this one as- %'hen a transverse fieM is applied, again. two
sumes that (S, } (or (S,)) is finite: phases are possible, a canted phase and a phase
with moments only in the basal plane. In this case,
E, =e, + 24, X — X + ~ ~ ~
+so, (2. 8a) (S, ) is the appropriate order parameter, and one
16 $8 expands the partition function in powers of (S, ).
s +2~
4
E xa
&
+1 ( ) o
~ + +&to (2. 8b) III. PHASE TRANSITIONS IN ZERO EXTERNAL FIELD
D' (1 Using Eg. (2. 10), one can write the Landau free
energy
2 l, E'+ e.j
F = - (1/P) lnZ,
x —
D' j.
+ ~+~
4 s, s (e, s]~X +~ ~ ~
+so (2. 8c)
f=f fX yfrP+ftPX +fg fX + ~ ~ ~,
(3. 1.)
(3. 2)
("."-")
Zo
Although it may appear that Etis. (2. 8a) and
)-
(2. 8b) blow up as (S, 0, in the calculation of the ~ =-'. (3. 3d)
partition function one can show that all divergent
g23
terms from the two energy levels cancel each (S. Se)
Z 2Z
other, and so the free energy is actually an analytic
function of both (S, ) and (S, ). The final result can 1 Z',
be written as a double expansion of the partition fo Z 2Z 5)l
' (3, Sf)
function Z, for small values of (S, ) and (S, )'.
The coefficients fo, f4, and fo are functions of y
g ~agg
f
only. The dependence of on K is only through the
coefficient f~. One should note that knowledge of
= e 'o(Zo+ Z, X'+ Z, q'+ Zp X'+ Z,q'+Z, X'), sixth-order terms is needed only for checking the
stabibty at TCP.
(2. 10} The Landau free energies of the form (3.. 2) have
vrhere
been discussed by Liu and Fisher %'egner
Zo(y) =1+2e ", and
more recently by Bruce and Aharony. ~0 %e just
Zj(r) =r(1 e "), - (2. lib) mention the results for the case when f, & 0, which
is of relevance to our model. The continuous tran-
Zo(r) =r'e ', (2. 1lc) sition from the phase with g&0, X=O (Z phase) to
z, (r)=r[l-e (1 +r+o)r], (2, lid) the paramagnetic phase (P) happens when fo = 0; f~,
f& & 0,
Z4(r) =Jr'e ", (2. lie)
Zo(r) + 'r)],
=r [or 1+e '(1— - (2. 1 1f)
.
f, =b[D-D. (r)]=lr'[t- (r)], . (S. 4)
1 Z(0)
—
P= =
t kT D.(r) =4Z, /rz. t.(r) =4Z. /r*z. ,
, (S. 8)
One gets the same final results if one assumes (S,) i e. , at D.=D,{y) [or t=t, (y)].
to be finite and expands the energy eigenvalues in The transition from the & &0, q = 0 phase (T
(S. ). phase) to. the paramagnetic phase occurs at f~=O,
fn a field parallel to the e axis, (S~) is the ap- fo, fo o,'
propriate order parameter. A simple classical
calculation at &=0 shows that two phases are possi- f, = 'r[d d. (r)]=-(r'/«-)[t t.'(r)1, - (S. 8)
ble: (i) a phase with moments parallel to the applied
field, snd (ii) a canted phase in which the e com-
d=D/K (3. Va)
ponent vanishes chen h, tends to zero. The per-
turbation calculation corresponding to this ease has
1852 KHA JEHPOUR, WANG, AND KROMHOUT |2
to paramagnetic phase [Fig .1(d)]. The Z- P line
before meeting the T-P transition line has gone
2.Q-
through its TCP.
I 0- 'I 0- ~
I 0 i.o N The determination of the flop line in all above
Z
cases is done by comparing the two free energies
0.5 I.O 0,5 I.O
corresponding to the two phases of Z and & order-
-I,O -
z -I.O - -1.0 -I.O- ing. At ~= 0 the flop transition takes place when
D = 4(WK- K}.
(o) (b) (c) (d)
The coordinates of BCP in the D-T plane for any
FIG. 1. Phase diagrams in (D, t) plane for different value of K& 0. 462 can be found from Fig. 2. In this
K values. The BCP is the intersection of the two critical figure D, (y) and d, (y) are plotted as a function of y.
lines (solid) and flop line (dashed), T and Z deisgnate Since K=D, /d, at BCP, one should find the value of
the phases with orderings in the basal plane and along
y such that the ordinates for the two curves has a
the s axis, respectively. (a) K=1.25, (b) K=1. 00, (c)
K=0. 6, and (d) K=0. 35. ratio equal to K. Then t, can be found from y, = P,D,
= D~/t~.
One should note the similarity of the phase dia-
grams in the D-t plane, with those of an anisotropic
c
4 ~S p
c
4K' antiferromagnet in a parallel external field. As in
yg ~
yg Z
the case of an antiferromagnet, the flop line sepa-
The paramagnetic phase is stable against a transi- rates two phases one with xy symmetry (T phase)
tion to the above phases when both f~ and fa are and the other Ising-like (Z phase). Phase diagrams
positive. In general, a phase with both &+0 and similar to Fig. 1(b) (near the flop line) have been
g&0 would be stable only if suggested by Bruce and Aharony'o for structural
phase transitions in perovskites, with basically the
a'=(2') -f4fs'0 (3 9) same symmetries as mentioned above.
Numerical calculation shows that for all values of IV. PHASE TRANSITIONS IN A FINITE FIELD
the parameter y &0, g&0. Consequently, the canted
phase (h= 0) is never stable for our model. The A. E&0.462
transition between @&0, X=0 phase (Z phase) and l. .Field along s uxis
& &0, g= 0 phase (T phase) is of first order (flop
transition) and occurs whenever In the presence of a magnetic field along the s
axis two possible phases exist: one with moments
fs = ( fs/f4)"f2 (3. 9) along the field and the other with canted magnetic
provided f, and f4 are positive. One can easily show moments, The second-order phase transition be-
that f, is always non-negative (i. e. , a T-P phase tween the two phases can be easily understood by
transition is always of second order) while f, taking (S, ) as the order parameter and expanding
changes sign at D = 0. 924 and t= 0. 67, (which is the the free energy as a Taylor series in powers of
Blume-Capel TCP). Equation (3. 9), is the equa- (S, ). The equation for the critical line is found by
tion of the flop line close to the point where it meets setting the coefficient of the second-order term
with the two second-order transition lines. When equal to zero, with the condition that the coefficient
f4&0 the iwo critical lines f~=O and f2=0 and the
flop line meet at the bicritical point (BCP) (D, , t~). Dc dc
When f4& 0 the phase diagram ceases to contain a
BCP. This happens when K& 0. 462. At K=0. 462,
f, ~fz =f4= 0. The possible phase diagrams in the
D-~ plane are shown in Fig. One can distinguish l. 2.0
the following cases:
K&1. In this case the flop line is below the t
axis, and is bent slightly downwards [Fig 1(a)]. .
K= 3. . The flop line is along the D= 0 axis, and
BCP is located on temperature axis at /=+3. For
L)&0one finds the &phase and a&0, the Z phase
[»g 1(b)].
0, 462& K& 1, %e have a BCP in the D & 0 region 0.0' - y'
of D-t plane, as shown in Fig. 1(c}. The flop line 0.0 0.4 0.8 l.2 l.6 2.0
bends upward. FIG. 2. Plot of Dc Eq. (3 4) a" dc Ej (3 6) a
0. 462 &K&0. In this case the critical line f~=0 functions of y =D/t. This plot is used to obtain the BCP
meets a first-order phase transition line of Z phase for K& 0. 462.
BICRI TICAL AND TRIC Rr THECAL I HZ NOME XA IN. ..
FIG. 3. Schematic phase diagrams in the (D, h.„t) and (D, h~, t) hyperplanes (K & 0. 462). The hatched regions are the
coexistence surfaces. R2 and R& denote the two-dimensional critical surface of order 2, and the one-dimensional criti-
cal surface of order 3 (tricritical line), respectively (Ref. 12). In each phase diagram two R~ surfaces meet at the
BCP ( Rp)
0.5 I.O
I
l. 5
%ith a fieM applied in the transverse direction,
while Pg, =0, we have a three-dimensional phase
FIG. 4. (D, h, ) cross sections of Fig. 3(a) for X=0. 6 diagram in the (D, h, , f) field space, as given sche-
at different temperatures. The bvo t=0. 0 lit, s a and b matically in Fig. S(b). The surface of the second-
meet at infinity and enclose the canted phase. Solid lines order transition can be obtained by a perturbative
and dashed lines represent, respectively, the second- expansion similar to the one discussed in Ref. 18.
order and the first-order phase boundaries. The dotted Again we would have the free energy expanded in
line is the projection of the line of tricritical points in even powers of (S,). Vanishing of the second-order
Fig. 3(a) on the (D, h ) plane. term in the expansion gives the critical point, while
the fourth-order term is positive. The equation of
surface of second-order transitions thus obtained is
at the transition point if it is of the second order. (4/zo)(bo e "o+ bg e "~ + h, e "2) = 1, (4 6)
The second-order part of curve b is given by
where
h, =D+2(K-1) . (4. 6)
o= —
D
a
kl
bi =-
X4g
&2 (4 9)
The lines of first- and second-order transitions join X&)
OA l. 2— /
/
0.2 I. I
/
hq hz
O. l 0.3 0.5 0.7 O. l 0.2 0.3 0.4 0.5
FIG. 6. P, h~) phase diagrams for K=0. 6. These
phase diagrams are cross sections of Fig. 3(b). For t FIG, 8. (D, hg) phase diagrams for K=0. 35. The first-
& 0. 924, the phase diagram consists only of a second- order l.ines (dashed) Pq and PR terminate the second-
order line. The dotted line is the locus of the tricritical order (solid) boundary of the canted phase at point P.
points. As t increases the canted phase region decreases.
0.25-
~ ~
~
0=0.5
der parameter.
0.20- A phase diagram in the (D-h, ) plane at constant t
for K=O. 35 and D & Do is shown in Fig. 8; it con-
O. I5-
sists, for all temperatures, of two coexistence
O. IO- lines QP (between the canted and the paramagnetic
phases) and PR (between the states with longitudinal
0.05- moments only), and a second-order transition line
0=0.75
a Sp. These three li. nes intersect one another at
O. l 0.3 0.5 0.7 0.9 poi. nt I'. As temperature is raised, the point I'
FIG. 7. (h~, t) phase diagrams for K'=0. 6 and various moves down and the area of the region of canted
values of anisotropy D. Solid l. ines and dashed lines phase decreases. This area shrinks to zero at
represent, respectively, the second, and the first-order f =0. 6V (independent of the value K). The phase
phase boundaries. The dotted line is the projection of diagram exhibits no TCP for any value of K i.n this
the tricritical line on the (h~, T) plane. range.
1856 KHA JEHPOUR, WANG, AND KROMHOUT
ation prevails at the BCP of our model. restriction delimits a complete scan of the vicinity
The assumption of homogeneity near a BCP (or a of the BCP in all directions. The model discussed
Ro) has important consequences. In addition to the in this paper, though not suffering. from this re-
bicritical scaling laws, the tangency of the critical striction, is subjected to another limitation in the
lines to the flop line may be of special importance. study of BCP: A controlled variation of D in a real
Also of interest is the competition between critical, magnet, if not impossible, is rather difficult (al-
bicritical, and tricritica) behaviors in the vicinity though there are evidences that D can be varied by
of the BCP, which results in crossovers between applying a pressure to the crystal ).
these different criticalities. Hankey et al. , ' Perhaps the most interesting feature of this model
based on the simultaneous validity of the scaling is the TCP behavior. Since the ordering field is
groups of critical points of order 2 (ordinary criti- experimentally accessible, the wing CXS's are
cal point) and 3 (tricritical point) with that of or- wholly in the experimental fi, eld space. The range
der 4, have arrived at the "double and triple scal- of the parameters Kand D to permit a TCP in an
ing functions" for the singular part of the Gibbs external field is significantly large. Therefore, a
potential, and have discussed the corresponding search for a system with the model Hamiltonian
crossover regions. Most of the systems exhibiting (2. I) is highly desirable.
bi criticality (uniaxial antiferromagnets and an- A study of this model in the light of the recent
isotropically stressed perovskites' ) suffer from works by Fisher and Nelson, Nelson, Kosterlitz,
the restriction that the ordering field is either fic- and Fisher, and Bruce and Aharony wi. ll be pub-
ti.tious or uncontrollable in the laboratory. This lished later.
Supported in part by the Committee on Faculty Research Commun. 12, 779 (1973).
Support. K. S. Liu and M. E. Fisheg, J. Low. Temp. Phys. 10,
~Supported in part by National Science Foundation under 665 (1973).
Grant No. GH-40174. 9F. Wegner, Solid State Commun. 12, 785 (1973).
'Ph, Kohnstamm, in HandMch dew Pky sik, Vol. 10, A. D. Bruce and A. Aharony, phys. Rev. B 11, 478
edited by H. Geiger and K. Scheel (Springer, Berlin, (1975).
1926), p. -223; I. R. Krichevskii et al. , Russ. J. Phys. ~~8. Ba,usch, Z. Phys. 254, 81 (1972).
Chem. 37, 1046 (1963); G. S. Radyshevskaya et al.', ' T. S. Chang, A. Hankey, H. E. Stanley, Phys. Rev.
J. Gen. Chem. USSR 32, 673 (1968); see also R. B. B 8, 346 (1973); A. Hankey, T.' S. Chang, and H. E.
Griffith and B, Qidom, Phys. Rev. A 8, 2173 (1973), Stanley ibiH' 8 1178 (1973)
and references cited therein. F. Harbus, A. Hankey, H. E. Sta, nley, and T. S.
2E. H. Graf, M. Lee, J. D. Reppy, Phys. Bev. Lett. Chang, Phys. Rev. B 8, 273 (1973).
19, 417 (1967); I. S. Jacobs and P. E. Lawrence, Phys. D. Nelson, J, M, Kosterlitz, and N. E. Fisher, Phys.
Rev. 164, 866 {1967); G. GoeQner and H. Meyer, Phys. Rev, Lett. 33, 813 {1974).
Rev. Lett. 26, 1534 {1971);D. P. Landau, B, E. Keen, n*(d) = (4+3. 176 e')/(1+1, 294 e) up to order c (e =4-d).
B. Schneider, and W. P. Wolf, Phys. Bev, B 3, 2310 See Befs. 5 and 14.
{1971);M. Blume, V. J. Emery, and R. B. Griffith, ~~The real. nature of the staggered fields in certain anti-
Phys. Rev. A 4, 1071 {1971). ferromagnets is discussed in M. :Blume, L. M. Corliss,
3C. J. Gorter and T. Van Peski-Tinbergen, Physica J. M. Hastings, and E. Schiller, phys. Rev. Lett. 32,
(Utr. ) 22, 273 {1956). 554 {1974).
4G. A. Smolenski, Fiz. Tverd. Tela 4, 1095 (1962) fSov. M. R, H. Khajehpour, R. A. Kromhout, and Yung-Li
Phys. — Solid State 4, 807 {1962)]. Wang, J. Phys. A 8, 913 (1975).
M. E. Fisher and D. B. Nelson, Phys. Bev. Lett. 32, Yung-Li Wang and M. R. H. Khajehpour, Phys. Rev.
1350 (1974); A. Aharony and A. D, Bruce, ibid, 33, B 6, 1778 (1972),
1350 (1974). 9M, Blume, J. V. Emery, and B, B, Griffith, Phys.
6Ch. Wissel, Phys. Status SolidiB51, 699 (1972), and Rev. A 4, 1071 (1971).
references cited therein. D. Meier, M. Kornezos, and S. A, Friedberg, ~P
~H. Weitzel, , Z. Kristallogr. 131, 239 (1970); H. A. Conf. Proc. 2, 1316 {1974).
Qbermayer, H. Dachs, and H. Schroke, Solid State