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Ferroelectric volume effect and surface induced fast instabilities for rapid electrooptical displays in liquid
crystals
Geoffroy Durand
To cite this version:
Geoffroy Durand. Ferroelectric volume effect and surface induced fast instabilities for rapid electroop-
tical displays in liquid crystals. Revue de Physique Appliquée, Société française de physique / EDP,
1986, 21 (11), pp.669-672. �10.1051/rphysap:019860021011066900�. �jpa-00245487�
Ferroelectric volume effect and surface induced fast instabilities for rapid electrooptical displays in liquid crystals
G. Durand
Laboratoire de
Physique
des Solides, Université de Paris-Sud, 91405Orsay
Cedex, France(Reçu
le 20février
1986,accepté
le 23 mai1986)
Résumé. - Il existe
aujourd’hui
unsystème qui
permet la commutationrapide à
la microseconde, dans les cristauxliquides,
sur de la lumièrepolarisée.
C’est la valve SC* bien connue,qui
utilise la ferroélectricité de volume d’un matériausmectique
C* chiral et un ancrage de surface faible. Un nouvel effet estprésenté, qui
donne naissance à des instabilités
polaires
de surface localisées. Certaines de ces instabilités induites par la surface existent encore pour des excitations alternatives hautefréquence (1 MHz).
Bien que leur mécanisme soit encore malcompris,
leur temps deréponse,
de typenématique,
est d’un ordre degrandeur
inférieur, à mêmechamp,
à celui des SC*. Le contrôle du mécanisme d’excitation par la surfacepermettrait d’envisager
une
application électrooptique
de ce nouvel effet.Abstract. 2014 One system exist which is
capable
of microsecondelectrooptical switching
inliquid crystals,
onpolarized light.
It is the well-known SC* valve, which uses a volume smectic ferroelectric material and a weak surfaceanchoring.
A new effect ispresented
whichgives
rise to localizedpolar
surface instabilities. Some of these surface induced instabilitiespersist
forhigh frequency (1 MHz)
AC excitation. Their mechanism is notyet understood. Their nematic-like response time is of an order of
magnitude
shorter, atequivalent
field, thanthe one of the SC*. A control of the surface excitation mechanism would
possibly
lead to newelectrooptical applications.
Classification
Physics
Abstracts61.30 - 73.90 - 68.45
Nematic
(N) liquid crystals
are nowwidely
used inelectrooptical displays [1].
This is due to threeproperties : 1)
theirstrong coupling
withlight
waves,
through
theirlarge birefringence, 2)
theirlarge sensitivity
to external electricfields,
because oftheir
large
dielectricanisotropy
and3)
their weakcurvature
elasticity
which allowslarge
distortions with small fields. The nematic materials for elec-trooptical applications
are now welloptimized,
toimprove
the contrast threshold andmultiplexability
of
displays. They
are used in well defined texture, orientedby
aking
ofepithaxy
fromcarefully
treatedboundary
surfaces. Thecorresponding anchoring
orthe nematic molecules at the surfaces is «
strong
», i.e. it will notchange
under the action of the command electricfield, during
thechange
of texturewhich
gives
rise to thedisplay.
One of themajor
drawback of these nematic
display
is theirlong
intrinsic response time due to their weak
elasticity
curvature. Ferroelectric smectic C*
liquid crystals
have been
proposed
to make fast submicrosecondelectrooptical
switches[2]. Recently,
we havedemonstrated in
Orsay [3]
the existence of surfacepolar instabilities,
under the action of an electricfield. A more or less distributed surface distortion is
observed,
with a mechanism related to the ferroelec- tric character of nematic-solidinterface,
and to the flexoelectricproperty
of nematics. As SC* thissystem
necessitates weakanchoring
conditions to work.Superimposed
to the surface flexo-ferroelec- tric instabilities we have observed other localized surface induced instabilities which canpresent
a fast responsetime,
in the microsecond range. The mechanism of these localized instabilities is not yetfully understood,
but their response time seemsnematic-like,
controlledby
thelarge
dielectric aniso-tropy
of theliquid crystal.
If wellcontrolled,
it couldlead to fast
electrooptical
effects. In this paper, wetry
to describe thephysical problems
involved in these fastelectrooptic switchings,
for both the mate- rials themselves and the associated weakanchoring
interfaces. We discuss in
particular
the thresholdeffects,
related to themultiplexability
of thesedisplays.
We compare the response time of the bulk(SC*)
and .fast surface induced(N) displays,
whichturns out to be an order of
magnitude
morerapid
forthe same
field,
at roomtemperature.
The interest of the SC* ferroelectricsystem
is its linearcoupling
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/rphysap:019860021011066900
670
with an external electric
field,
which allows inprinciple
a bistable behaviour. The interest of fast surface induceddisplay
would be itssimplicity.
1. The ferroelectric SC *
electrooptic
valve.The SC*
liquid crystal
is asmectic,
i.e. alayered
material. In each
layer,
the rod-likeorganic
molecu-les have no
positionnal ordering.
There are tiltedby
an
angle 9 compared
to thelayers (Fig. 1).
Themolecules are
chiral,
i.e.they
have no more, on theaverage, the mirror
symmetry
which characterizes the N and smectic Aphases,
because of the presence, forinstance,
of anasymetric
carbon in the molecule.The
only symmetry
element which characterizes this monoclinicphase
is a two-foldflip-flop axis,
insidethe
layers
andperpendicular
to thelong
molecularaxis.
Along
this two-foldaxis,
if there exist any molecularpermanent
transverse electricdipole,
there is a
possibility
of existence for anaveraged macroscopic
electricpolarization
P. The SC* is thenferroelectric. Of course, if 0 =
0,
the SC* becomes aSA,
with molecules normal to thelayers.
P is thenzero. At a
SA ~ S*C
second ordertransition,
P mustvary in the
S*C phase
as P =Po 8, by symmetry. Pois
found to be
10-1 to 10- 2
of the transversepermanent dipole
of the molecule.The normal texture of a thick
S¿c sample
looks likethe one of a cholesteric. The
chirality
of the molecu- les induces a twist of theprojection
of n(the long
molecular
axis)
on the smecticlayers, resulting
in aheliconical
arrangement,
with amacroscopic pitch Z,
in the >m range. It ispossible
to supress this helix(which
is characterizedby
theobservation,
across itsaxis,
of dechiralization disclinationlines) by putting
the
sample
in between twoparallel glass plates, separated by
a distance dZ,
in the )JLm range. This is thegeometry
of the SC*electrooptical
valveproposed by
Clark andLagerwall [2] (Fig. 2).
n isuniform, parallel
to theplates.
The SC*layers
areFig. 1. - Geometry
of a smectic C*layer, showing
thecone of
half-angle
0, and the permanentpolarization
P.Fig.
2. -Principle
of the SC* valve.normal to the
plates. P,
inside thelayers,
is alsonormal to the
plates.
To provoque achange
oftexture, it is sufficient to
apply
alarge enough
electric field E across the
sample, opposed
to P.Above a certain threshold
Eth,
P willalign along
E . n will remain
parallel
to theplates,
but will have rotated of anangle 2 9, remaining
on the cone ofangle 0
which does not disturb the SC*ordering.
For2 0
= 450, using polarized light,
in crossedpolari-
zers, a
polarized light
beamgoing through
thesystem
will go from the total extinction to a totaltransmission,
if the new texturecorresponds
to ahalf-wave
plate. Calling
à the material birefrin- gence and À the wavelength
oflight,
thishappens
for d àn oooo-
À /2, easily
achieved with àn oooo-0.2,
À =0.6 11, d = 1.5 f.Lm. The
problem
is now to estimateEth5
and the response time of the device. Inprinciple,
in absence of
field,
the two states have the samevolume energy, so that one
expects Eth
to be relatedonly
to the elasticpotential
barrier to go from one texture to the other one. Infact,
in thisdevice,
onemust also
change
the molecular orientation on the twosurfaces,
whichimplies
a « weak »anchoring
surface energy. A
complication,
discussedby
Hands-chy
and Clark[4],
is related to thepolar
character of theanchoring,
i.e. at the surface the moleculesprefer
toalign
in such a direction that their trans- versepolarization
has a well defined directioncompared
to theboundary glass
electrodes. This allows for the existence of non-uniform textures(Fig. 3),
where P issplayed
from oneplate
to theother. Because of the weakness of the surface
anchoring,
the surface molecules are nolonger
restricted to remain
parallel
to the electrodes. The volume twist(on
the smectic C*cone) gives
apermanent torque
which tilts a little bit the molecules from thesurface, resulting
in four surface states, withcomplicated
defects between the associated various textures.The
explanation
of therapid (submicrosecond) switching
is notyet
well understood. We cantry
to make estimations. As n issupposed
to rotate on theSC* cone, any volume texture distortion can be described
by
a nematic-like standard curvature elasti-city.
The volume elastic barrierdensity
energy is of the order ofK/d2,
with the Frank constant K oooo-10- 6
cgs,which gives
a response time of the order ofFig.
3. - Thepolar anchoring
of a SC*. P is nowsplayed
from the upper to the lower
plate.
TN =
d2 11/K, were 11 -
0.1 cgs is a standard visco-sity.
This time TN is atypical
nematic like curvature relaxationtime,
in the10- 3
s range and not in the iis, sothat,
at threshold where thecoupling
electricenergy
density -
E . P compares to the barrier energydensity,
one does notexpect
any submicrose- cond behaviour. What seems tohappen
forlarge
electric field
pulses,
of duration Tp TN, is that the energy barrier is localized close to thesurfaces,
where a
rapid
localized twist occurs, on a thicknessdE.
The surfaceanchoring
energy does notplay probably
alarge
role. Itsstrengh Ws - ! K fJ2 is
characterized
by
theextrapolation length L,
whichgives
the distance overwhich a surfacetorque
from the weakanchoring
compares with a curvaturetorque,
for adistortion 0
of the molecular orienta- tionns at
the surface. L isknown,
for «strong » anchoring,
to be in the 0.1 >m range, and to extend to the 03BCm range for weakanchoring.
In this case, Lcompares with
d,
and the weak surface energy does notchange significantly
thedynamics
of the effect.We can estimate the thickness of the surface
layer dE by saying that,
for fixedstrong anchoring,
thecurvature energy
density
associated withdF
mustcompare with the ferroelectric energy
density
-- E . P. This result into EP ~
K d 2
so that thelesponsc time for
large pulses
issimply T p - 11 / EP .
To
get
into theT(2013ljLs)
range, one has toncrease
E/Eth as TN/T.
One does observe[5]
aE-
response
time,
but also aE- 2, which
is notexplained by
this model.Anyway,
because of the weak ancho-ring,
the response time ispurely
nematic-like. One would obtain the same short response time with a standard nematic distorted on a short distancedE.
The short response time is not related to the volumepotential
barrier. This makes difficult themultiplexing
of adisplay
withSC*,
which appears topresent
a very weakapparent
threshold at DC. For very lowfrequencies,
this threshold can even go to zero, in presence of surface disclinationlines,
whichallow for a surface reorientation whithout any
jump
above the elastic
potential
barrier. Toimprove
themultiplexing
it has beensuggested
to stabilize the unwound SC* helixby
external AC electric fields[6].
Inpractice
this would increase the powerconsumption
ofelectrooptical devices,
which seemsan
important
drawback.Finally,
thepresent
use of therapid
SC* valve iscomplicated by
all the surface states associated with thepolar anchoring.
Themastering
of surface treatment to induce theright
weak surface orientation is now far from
complete.
An intensive work is
curently
under way in manyapplied
laboratories to solve theseproblems.
2. The surface induced fast instabilities of nematics
(SIFI).
We have
recently
observed inOrsay [3] polar
surfaceinstabilities under the action of an electric field on
cyanobiphenyl compounds.
The molecules are ali-gned
in thehomeotropic geometry,
i.e. n is normalto the electrodes. This surface orientation is obtained
using
a DMOAP silane treatment. A surfacepolari-
zation can exist at a nematic-solid
interface,
becausethe inversion
symetry
of the bulk material is broken.The
origin
of this surfacepolarization
can be apermanent
polarization
of thesilane,
thepolarization
associated with the
gradient
of orderparameter
at theinterface,
orsimply
the flexoelectricpolarization.
This surface
polarization PS
iscoupled
with n so thatan
applied
fieldopposite
toPs can
induce a molecu-lar surface tilt
(Fig. 4).
Inpractice,
because of thelarge
dielectricanisotropy
of thematerial,
thismechanism cannot lead to
high
contrast instabilities and seems not usefull forpractical application.
Inaddition to this
polar
surfaceinstability,
whichappears
optically
to draw a chart of the variation of the surfaceanchoring
energy on theelectrodes,
wehave observed localized
instabilities,
of disk-likeshape
of diameter ~ 50-200 03BCm. At lowfrequencies (
1kHz)
thesepoints
are also excitedby
a localizedpolar mechanism,
which could beunipolar charge injection, resulting
in a vortex flow which would tilt the director n and result into thelarge
observedcontrast. Some of these
points
can be excited in AC up to onekilohertz,
others up to onemegahertz
withfield - 1
V/03BCtm.
We do not know now the exactmechanism of these surface induced fast instabilities
(SIFI)
athigh frequencies.
To check the response of the SIFI we have measured theamplitude Ep
of arectangular pulse
of durationap
,whichgives
thethreshold of the
effect,
or its full contrast(appea-
rance of one
fringe
in greenlight).
We observe(Fig. 5)
an increase ofEp
likeTp 1/2.
This is characte- ristic of a nematic likebehaviour,
with a balancebetween dielectric and viscous
torque 1 Tp
=E./4 7r ) E;/’Y1. With Ea -10,
one can explain
quantitatnely
the date offigure
5.Comparing
theSC* bistable
display
and theSIFI,
we can say thatboth mechanisms
present
nematic-like responsetime ;
the SIFIgives
at roomtemperature
the same response time at full contrast than the SC* at 60- 70 °C.Keeping
in mind that this difference intemperature
results in an order ofmagnitude change
for the
viscosity
we can say that the SIFI is an order ofmagnitude
faster than then SC* valve.3. Conclusion.
The SC*
liquid crystal
valve of Clark andLagerwall
is now well known to
produce rapid electrooptical switching, using polarized light.
It uses a ferroelectricFig.
4. -Principle
of thepolar
surfaceinstability. Ps
tends to
align along
E,forcing
a surface tilt 0 of themolecules.
672
Fig.
5. -Amplitude Ep
of an electric fieldpulse
of duration T, for threshold and full contrast, for SIFI at room temperature. To compare, thecorresponding
values for the SC * valve arerepresented
at 68 °C. For shortpulse,
the SC *valve needs an order of
magnitude larger
excitation.property
which allows ahighly
sensitive linear cou-pling
with an external electric field. It also necessi- tates weak surfaceanchoring.
Its behaviour is notcompletely
understood. It seems topresent
little orno
threshold,
theswitching being
related to theheight
of a lowpotential
barrier. Itsrapid dynamics
is
probably
controlledby
a thin elastic surfacelayer
breakdown. Its use is
complicated by
the existence of many surface states, connected with surfacepolar anchoring.
Materials with areasonably large
rangeof
temperature,
with anacceptable
tiltangle
and alow
enough viscosity
at roomtemperature
seem toexist,
at least in the form of mixtures.Multiplexibility
of the SC* is not a solved
question.
A new surfaceinduced fast
instability (SIFI)
in nematics hasjust
been discovered in
Orsay.
It cangive
the samecontrast as the SC* valve. It has a short response
time,
forhigh field,
up to the )JLS range. Its response to fieldpulses
can be an order ofmagnitude
fasterthan the one of a
SC*,
at roomtemperature.
Its mechanism is notyet clear, giving polar
effects atlow
frequencies
and nonpolar
athigh frequencies.
Ifwe can control its
mechanism,
the SIFI could become usefull for fastelectrooptical switching.
Note
finally
that for bothsystems
therapid switching
effects are related to the
high applied
field and to theliquid crystal-solid
electrode interfaceproperties.
Future progress in
rapid electrooptic switching implies
at betterunderstanding
of interface ancho-ring properties.
Acknowledgments.
1 thank M.
Monkade,
Ph.Martinot-Lagarde,
B.Barbero and J. F. Palierne for
interesting
discussionand
partial
disclosure of their results beforepublica-
tion.
References
[1]
For ageneral description
ofliquid crystals
see : thePhysics
ofLiquid crystals,
P. G. de Gennes,Oxford
(1974).
[2]
CLARK, N., LAGERWALL, S., Ferroelectrics 59(1984)
25. In fact, this
special
issue of Ferroelectricgives
agood
review of thephysics
andchemistry
of SC*.
[3]
MONKADE, M., MARTINOT-LAGARDE, Ph., DURAND,G.,
Europhys.
Lett. 2(1986)
299.[4]
HANDSCHY M., CLARK, N., Ferroelectrics 59(1984)
69.
[5]
CLARK, N., HANDSCHY, M., LAGERWALL, S., Mol.Cryst. Liq. Cryst.
94(1983)
213.[6]
LE PESANT, M., DUBOIS, J. C., MOUREY, B., HARENG, M., DECOBERT, G.,Proceedings
ofthe