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Dynamics of the director alignment in cholesterics under applied magnetic field
J. Marignan, G. Malet, O. Parodi
To cite this version:
J. Marignan, G. Malet, O. Parodi. Dynamics of the director alignment in cholesterics under applied magnetic field. Journal de Physique, 1976, 37 (4), pp.365-368. �10.1051/jphys:01976003704036500�.
�jpa-00208431�
DYNAMICS OF THE DIRECTOR ALIGNMENT
IN CHOLESTERICS UNDER APPLIED MAGNETIC FIELD
J.
MARIGNAN,
G. MALET and O. PARODIGroupe
dedynamique
desphases
condensées(*),
Laboratoire decristallographie
Université des sciences et
techniques
duLanguedoc, place Eugène-Bataillon,
34060Montpellier,
France(Rep
le 26septembre
1975,accepté
le 25 novembre1975)
Résumé. 2014 Nous étudions, au moyen des théories élastiques et
hydrodynamiques,
le mouvementde rotation des molécules, provoqué par l’action d’un champ
magnétique
relativement faible sur unéchantillon
cholestérique
d’épaisseur déterminée avec ancrage fort aux parois. La solution est unefonction sinusoidale simple, dont l’amplitude
dépendant
du temps est caractérisée par un temps de relaxation de l’ordre de 10-1 s.Abstract. 2014 By means of static and hydrodynamic theories, we study the rotary motion of the molecules in a cholesteric slab (of given thickness and strong anchored surfaces),
subject
to a weak magnetic field. The tilt angle ~(z, t) of the molecules is a simple sine wave with a timedependent
amplitude characterized by a relaxation time of the order of 10-1 s.Classification
Physics Abstracts
7.130
1. Introduction. - In a recent letter
[ 1 ],
we havebriefly presented
the mainexperimental
and theoretical resultsconcerning
thedynamics
of the firstGrandjean-
Cano line under weak
magnetic
fields. The theoreticalapproach
to thisproblem
was based ondividing
thedynamical study
in two parts :alignment
of director without any motion of theline,
andthen,
translation of the line.The purpose of this paper is to present in a more
complete
form the theoreticalanalysis
of the firstpoint (director adjustment).
In absence of any
perturbing forces,
the cholestericmesophase
possesses atypical
helical structure. Thepossibility
ofuntwisting
the cholestericspiral by
amagnetic
field H was first notedby
Frank[2].
Thecoupling
betweensusceptibility
xa(xa
>0)
and a staticmagnetic
field normal to the helicalaxis,
tends to unwind thespiral
structure,and,
as a consequence, thespatial period
increases. When themagnetic
fieldreaches a critical value
Hc,
the cholestericliquid crystal
takes a nematicconfiguration.
This cholesteric- nematic transition has been first observedby
Sack-mann et al.
[3].
The variation of thepitch
with magne- tic field has been measured in a few cases[4, 5].
Astatic
theory
of this effect has beengiven by
De Gennes
[6]
andMeyer [7].
The continuumtheory
was
completed by hydrodynamical
studies on fluctua-tions of cholesterics in a static
magnetic
field[8, 9].
An
experimental
and theoreticalstudy
hasalready
been
performed by
Prost[10]
on cholestericdrops,
(*) Laboratoire associe au C.N.R.S.
i.e. in the case where one of the
limiting
surfaces is afree-surface.
In this paper we
study
the case of a cholesteric filmplaced
between two treatedsurfaces,
with stronganchoring.
Hence ouranalysis
and results arequite
different from those obtained
by
Prost.In section 2 of the present paper, we rework the static
theory by introducing
a cholesteric slab of finit thickness and stronganchoring
at walls. In section 3we present, for twist
mode,
a verysimple
solution of motionequation
of the director under weakmagnetic
fields
(H Hc).
2. Static
theory.
- Let us start with a cholestericsample
of thickness d =Po/2 (Po being
the unper- turbedpitch).
We assumethat,
at the walls there is oneeasy direction for the
molecules, parallel
to the x-axisand that strong
anchoring prevails (Fig. 1).
Weconsider the case where the static
magnetic
field isalong
the oxdirection;
the helical axis oz is then normal to theapplied
field. This is a situation of pure twist with thefollowing
components of the director n :FIG. 1. - Cholesteric slab of thickness d, under static magnetic field parallel to the easy axis and normal to the helical axis oz.
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphys:01976003704036500
366
Q(z)
is theangle
between n and the x-axis. The boun-dary
conditions are Q = 0 for z = 0 and T = 1tfor z = d.
The Frank free energy
(per
unit area in the xoyplane),
can be written in the presence of the field[6] :
K2
is the twist elastic constant, qo the wave vectorcorresponding
to H =0, (qo
= 2nIPo).
2.1 EQUILIBRIUM CONFORMATION OF CHOIESTERIC.
-
Minimizing
the free energy, eq.(2 .1 ),
inQ(z),
onefinds the
equilibrium
condition :where ç = (K2IXa)1/2 jH
is themagnetic
coherencelength.
Multiplying by
2dcpjdz,
andintegrating,
one findsthe
following
firstintegral :
where C is a constant
integration.
Introducing ql =
Q -(n/2)
and owe
finally
write the firstintegral
of eq.Recalling
thatand
integrating
eq.(2.3),
onegets
thefollowing implicit equation
for the modulus k :where
K(k)
is thecomplete elliptic integral
of the first kind[11].
The
integral
of eq.(2.3)
can beexpressed
as :where
F( t/J, k)
is the normalelliptic integral
of the first kind. The constant zo is fixedby
theboundary
condi-tions. We
finally find, making
useof eq. (2.4) :
where am
(u, k)
is a Jacobianelliptic
function of argument u and modulus k.2.2 EQUILIBRIUM FREE ENERGY. -
Taking again
§
= qJ-, n/2
andusing
eq.(2.3)
onefinds,
afterintegration of eq. (2 .1 )
Or, introducing
thecomplete elliptic integral
of thesecond kind
E(k) :
2.3 WEAK MAGNETIC FIELD APPROXIMATION. -
Under weak
magnetic fields, ç
- oo and k - 0. Wecan then use the
expansion
ofK(k), neglecting
all termsof order
higher
thank3 :
and eq.
(2.4)
becomeswhich leads to :
and
finally :
Define now u as the argument of the am function in the r.h.s. of eq.
(2.5) :
Then,
from eq.(2.4),
one hasIntroduce the Jacobi’s nome q :
One can now
expand
am(u, k)
in Fourier series :Finally making
use of the four eq.(2. 10)
and(2. .11 ),
eq.(2. 5)
becomes :-
In the
expression
for thefree-energy (2.6),
one canexpand E(k),
Using
now thedevelopments of k - 2 and k -1
from eq.(2. 8),
one finds :Eq. (2. 6)
then reduces to :It must be noted that the same results could have been found
by inserting directly
into eq.(2.1)
theexpression
for Qgiven by
eq.(2.12).
3.
Hydrodynamic theory
under weakmagnetic
field.- Let us now consider the case where a
magnetic
field H is
applied
at time t = 0. At t = 0 the helical structure is stillundistorted, corresponding
to thewave vector qo =
n/d.
Theequilibrium
distortionunder field H is
given by
eq.(2.12).
Introducing
a timedependent amplitude a(t)
of thesimple
sine wave, we then can choose :with the
help
of eq.(3.1),
eq.(2.1)
isreadily integrated
and one gets : .
Jl(2 a(t))
is the Bessel function of first kind of order 1.Let us assume that the cholesteric
liquid crystal
isincompressible
and that all friction processes in the fluid are isothermal. Thedissipation Tg resulting
from these processes is
given by
the fundamentalequation of nematodynamics [12] :
A is the shear rate
tensor, a’
thesymmetric
part of the viscous stress tensor, h the molecularfield,
N thevelocity
of the director relative to the fluid.It can be shown from the Leslie
equations
that forpure twist there is no
hydrodynamic
backflow. Then the tensor Adrops
out and the evolutionequation
of the director
gives :
where yi
is a Leslie friction coefficient and N =dn/dt.
The entropy source
TS
is thereforeUsing
now eq.(3.1),
one getsThe
dissipation TS
isequal
to the decrease in storedfree-energy
The time derivative of
F(t)
is from eq.(3.2) :
Replacing J1’(2 a) by Jo(2 a) - ( 1 /2 a) J1(2 a),
andexpanding
the Bessel functionsJo
andJ1
andneglect- ing
terms ina2 (a2 1),
one finds :We now substitute eq.
(3.3)
and(3.5)
into eq.(3.4),
and obtain :
Taking
now into account theboundary
conditiona(O)
=0,
one finds :where the relaxation time i is
given by
368
The solution
a(t) gives
theexpected equilibrium
value for the tilt
angle Q(z, t).
Note that this relaxation time is
quite typical
ofsuch processes. A similar
expression
had beenalready
found
by Fan,
Kramer andStephen
andby
Prost.4. Conclusion. - In the
experiments reported
in aprevious
paper[1]
we have used cholesterol cinna- mate diluted in anequimolar
mixture of4-methoxy 4’-pentyl
tolane and4-propoxy-4’-heptyl
tolane. Forsuch a
sample
one has thefollowing
values : y 1 ~ 2poises (1), d ~
10 pm andK2 - 5 x
10-7dyne [13] ;
then the relaxation time i would be of order 10 -1 s.
In this
previous
paper on the motion ofGrandjean-
Cano lines under weak
magnetic fields,
our basicassumption
was that the relaxation time for the directoralignment
was much shorter than the relaxa- tion times for the lines motion.This last relaxation was found to be of order
102
s.We therefore find that our
assumption
wascompletely justified.
An
experimental
confirmation of the present theo- retical results is not easy to find. As far as thepitch
ismuch greater than the
wavelength,
and themagnetic
(1) Achard, M. F., Gasparoux, H., private communication.distortion
small,
the so-called adiabaticapproximation
for
light propagation along
the helical axis holds.This means that a small
magnetic
distortion has noeffect on the
light polarisation
at the exit-face. On the otherhand, light
refractionby
a cholestericprism
should be very sensitive to a distortion of the helical structure. An
experimental study relying
on this ideais to be done in our
laboratory.
It is worth
finally
topoint
out that our results arequite
different from those foundby
Prost. This isessentially
due to the difference inboundary
condi-tions. In Prost case, the presence of a free surface allowed for the escape of free walls. Hence a critical field
appeared.
In our case, the presence of a stronganchoring
on bothplates
forbids such an escape, and this is the reasonwhy
the nematic-cholesteric transi- tion cannot takeplace
in aperfect sample.
Of course,in real
samples,
for veryhigh magnetic fields,
thisconstraint should be relaxed
by
the appearance of disclination lines which would thus allow the transi- tion to occur.Acknowledgments.
- It is apleasure
for us to thankhere Drs M. F. Achard and H.
Gasparoux
who havekindly
measured for us the twist viscous coefficient y 1.References
[1] MALET, G., MARIGNAN, J. and PARODI, O., J. Physique Lett.
36 (1975) L-317.
[2] FRANK, F. C., Discuss. Faraday Soc. 25 (1958) 1.
[3] SACKMANN, E., MEIBOOM, S. and SNYDER, L. C., J. Am. Chem.
Soc. 89 (1967) 5982.
[4] DURAND, G., LÉGER, L., RONDELEZ, F. and VEYSSIÉ, M., Phys. Rev. Lett. 22 (1969) 227.
[5] MEYER, R. B., Appl. Phys. Lett. 14 (1969) 208.
[6] DE GENNES, P. G., Solid State Commun. 6 (1968) 163.
[7] MEYER, R. B., Appl. Phys. Lett. 12 (1968) 281.
[8] FAN, C., KRAMER, L. and STEPHEN, M., Phys. Rev. A 2 (1970)
2482.
[9] PARSON, J. D. and HAYES, C. F., Phys. Rev. A 9 (1974) 2652.
[10] PROST, J., Thèse, Bordeaux (1973).
[11] Our notations about elliptic integrals are from : Handbook of elliptic integrals for engineers and physicists. By BYRD, P. F. and FRIEDMANN, M. D. (Ed. Springer-Berlin)
1971.
[12] DE GENNES, P. G., The physics of Liquid Crystals (Clarendon
Press. Oxford) 1974.
[13] MARIGNAN, J., MALET, G. and PARODI, O., J. Phys. (to be published).