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Crawling and spiraling of cholesteric fingers in electric field
P. Ribière, P. Oswald, S. Pirkl
To cite this version:
P. Ribière, P. Oswald, S. Pirkl. Crawling and spiraling of cholesteric fingers in electric field. Journal
de Physique II, EDP Sciences, 1994, 4 (1), pp.127-143. �10.1051/jp2:1994119�. �jpa-00247944�
Classification Physics Abst;a(.ts
61.30G 61.30J
Crawling and spiraling of cholesteric fingers in electric field
P.
Ribibre,
P. Oswald and S. Pirkl(*)
Laboratoire de physique, Ecole Normale Supdrieure de Lyon, 46Allde d'ltalie, 69364
Lyon
Cedex 07, France
(Received 7 July J993, receii,ed in final form 29 September J993, accepted J2 Or.tober J993)
Rdsum4. Nous montrons que deux types de doigts existent dans des dchantillons
hom£otropes
de cristaux liquides cholestdriques
d'anisotropie didlectrique positive
les doigts de premibre espkce danslesqueh
le champ de directeurs est continu, et les doigts de seconde espkce qui sonttopologiquement
singuliers
et de mdme nature que les sphdrulites (aussiappeldes
« bulles »cholestdriques).
Quand lespremiers
sont soumis hun champ dlectrique altematif basse frdquence, ils rampent lentement le long de leurs axes tandis que les seconds ddrivent perpendiculairement h
leurs axes et forment des spirales quand une de leurs extrdmitds est
pidgde
sur un ddfaut. Ce travail complbte les observations de spirales faites rdcemment h Nice parKamayd
et Gilli [8] ainsi que par Mitov et Sixou [9] dans des systbmes similaires.Abstract. We show that two types of
fingers
exist inhomeotropic
samples of cholestericliquid
crystals of positive dielectric anisotropy fingers of a first species in which the director field is continuous, and fingers of a second species which are topologically singular and of the same nature as spherulites (also called cholesteric bubbles). When the former aresubjected
to a lowfrequency
AC electric field,
they
crawl slowly along their axes whereas the latter driftperpendicularly
to theiraxes and forrn spirals when one of their ends is pinned on a defect. This work
supplements
spirals recently observed in Nice by Kamayd and Gilli [8] and by Mitov and Sixou [91 in similar systems.1. Introduction.
By confining
a cholesteric ofpositive
dielectricanisotropy
between twoparallel glass plates
which anchor molecules
strongly homeotropically
and/or,by subjecting
it to an electric field, it ispossible
to unwind itcompletely
and to obtain ahomeotropic
nematicphase [1-4].
Thisphase
transition isusually
first order and is controlledby
two parameters theapplied voltage
V and the confinement ratio C
=
d/p
of the thickness over thequiescent pitch.
In the parameterplane (C,
V ), thehomeotropic
nematic and the cholestericfingers
coexist on a critical linej~) Permanent address. University of Chemical Technology, 53210 Pardubice Czeck Republic.
V
=
V~(C
). The nematic is stable above this line whereas thefingers
are stable between this line and the C-axis. Ingeneral,
the director field inside thefingers
is continuous. Thesefingers
will be called cholesteric
fingers of
thefirst species (CF-I)
in contrast with thosehaving
adiscontinuity
inside, which we shall call cholestericfingers of
the secondspecies (CF-2).
Ourmain purpose is to show
experimentally
the existence of these two kinds offingers by
analyzing
theirdynamical properties.
So
far, only
CF-l's have been studiedintensively
becausethey
are much easier toproduce
than CF-2's, at least with conventional non
polymeric
materials. Moreover, there exists atopological
model on the unitsphere
S~[5]
which allows us toexplain
the varioustopological properties
of CF-l's as well as their mainoptical [6]
andenergetic properties [3, 4, 7].
On the critical line, the CF-I's do notlengthen
becausethey
have the same energy as thesurrounding
nematic
phase.
This observation has been used to determineexperimentally
the criticalvoltage V~.
In
general, experiments
are carried out with an AC electric field. Itsfrequency
is chosenhigh enough (typically f
= I
kHz)
in order to avoid convection. For this reason, we assumed in ourprevious
calculations[3, 4]
thatelectrohydrodynamic
effects werenegligible.
Thisapproximation
isquite good
aslong
as we aredealing
with the « static »properties
offingers (topology,
domain of existence and limits of absolutestability
in the parameterplane,
also calledspinodal
lines). On the other hand, a careful examination of theirdynamical properties (growth
in the nematicphase)
reveals that fineelectrohydrodynamical
effects exist up torelatively high frequencies
(about lokHz).
Theseeffects,
which we shall examine in the present article, lead to thecrawling
of the CF- I's near the critical line and to the lateral drift ofthe CF-2's which form
spirals
when one of their ends ispinned
to a dustparticle.
Thisdifference of
dynamical
behavior allows us todistinguish
the two kinds offingers.
To our
knowledge, only spiral
formation has been mentioned and studied, firstby Kamayd
and Gilli
[8]
in a smectic Aphase
near a smectic A~cholestericphase
transition and then,by
Mitov and Sixou in a cholesteric
phase [9]. Although
theexperiment
of Mitov and Sixou isvery close to ours, these authors do not mention the existence of the two types of
fingers. By
contrast,
Kamay6
and Gilli describe two different types offingers
butthey
comparefingers
of the smectic Aphase
which formspirals
to those of the cholestericphase.
Thus, it islikely
that thefingers
of type two describedby
Gilli andKamayd
are different from thefingers
of thesecond
species
described in this article.The article is
organized
as follows. In section 2, webriefly
recall theexperimental procedure
and thephase diagram.
We then describe in section 3 thecrawling
of CF- l's and in sections 4 and 5 thespirals
that arespontaneously
formedby
CF-2's. Inparticular,
we shallemphasize
the fundamental
topological
differences that exist between thefingers
of the first and of the secondspecies.
We shall also see that there exists a strong link betweenspherulites
andfingers
of the second
species.
2.
Experimental phase diagram.
The cholesteric
liquid crystal
wasprepared by adding
a small amount(0.46 wtfG)
of the chiralcompound
S811(from
E.Merck)
to nematic BCB(4~n~octyl-4'~cyanobiphenyl
from BDHLimited).
The
experimental
cell has been described in aprevious
article [3]. It allows us tochange continuously
the distance between the two electrodes with an accuracy of 0. I ~Lm and toadjust
theirparallelism
to within 10-~ rad. The electrodes have been coated with silane ZLI 3124(E. Merck)
and all measurements have been made at 39 ± 0.I °C, I-e- 3 °C below thecholesteric-isotropic phase
transition. At this temperature,pi15.5
~Lm.The
phase diagram
isgiven
infigure
I. It was established as in reference[3] by observing fingers
of the firstspecies (sketched
inFig. 2)
which formspontaneously
when thevoltage
isquickly changed.
Four lines are visible. LineVz (C
is the critical line for coexistence between the twophases
: on this line, the CF-J's do notlengthen
because the twophases
have the same free energy. LinesVo
andV~
are thespinodal
limits of the nematicphase
and of thefingers,
respectively. Finally,
lineV,
separates twogrowth
modes of CF-l's : above it, thefingers lengthen
from their twotips,
while below their roundedtip splits continuously leading
to aflower-like pattern.
8
~
0V~
V~
V~
# V
b ~
>
4
> ,,-'
o
o-S I-o 1.5 2.0 2.5 3.o 3.5 4 o
C=d/p
Fig.
I.Experimental
phase diagram. LinesI',
(C)apply
to CF- l's whereas lineVI
(C relates to CF-2's. Stable
spirals
are observed in the shadedregion
of the phase diagram corresponding toi~~ + 0. V
< I'
< V
2 + 0.5 V.
Usually
linesV,
are determinedby using
a square wave ACvoltage
of I kHz. To our accuracy(usually
2 §G), theexperimental phase diagram
does notdepend
upon thefrequency
chosen in the range 0.I to loo kHz. Above this limit, dielectric effects
(diminishing
dielectricanisotropy
F~) occur and the measuredvoltages V,
increase.3.
Crawling
offingers
of the firstspecies.
It is well-known that each isolated CF-I of finite
length,
which does not contain apoint
defect.has two different
tips
a roundedtip,
called normal, because the twist inside has the samesign everywhere
as in the free cholesteric and asharp tip,
called abnormal, in which the twist islocally
ofsign opposite
to the free cholesteric[2, 3].
Between lines V~(C
) andV~(C
), the CF~l's shorten from their ends, whereas between lines
~~~(C
) andVj (C
),they lengthen.
In thefollowing,
we shall call v~ (hevelocity
of the normaltip
and u~ thevelocity
of the abnormaltip.
The velocities are chosen
positive
when thefingers lengthen.
Since the molecularconfigur-
ations in the twotips differ,
their velocities are alsoexpected
to differ. One can also introduce thelengthening velocity
of thefingers
: vj~~~~df/dt
where f is thelength
of thefinger.
Thisvelocity
ispositive
if thefinger length
increases andnegative
if it decreases. If thefinger
is rectilinear viength ~ r~ + c~. At V =V~,
thelengthening velocity
ofstraight fingers
vanishe.qby
200~m
al
1111111111111111
1it iii
itii it it I
iJll/"/
t iiiii I illll---~
,
"ii
i
/ /w~~--~~-~,, , , ' Ii
I
I'---"'I
t, ,, II
II11-"'~i
I>
'it
Ii
i,-,"iL
it ii
I
ii ' ,
ii ii
I' tii
I i i , i
it11,
/ /
i
Ii
I , Ii'L%,-'/ I
ii,,
<1,",~-'/i
i
I ~, , '"~--l'/
I
i I
I ' '~ --v'll/
I
it
iii ii llllll
f I
Ii it
I Ii I I I J JIi
ii ii ii
b)
Fig. 2. a) Cholesteric finger of the first species photographed between crossed polarizers. b) Director field of a CF-I in a vertical plane norrnal to its axis.
~~~~~~~~~~ ~~stmightf<ngerlensth "
~~
~ ~~~~ ~~S , ~length ~ ~ ~ ~z ~ ~z2 W ~.j1 ~ ~lcngth ~ ~ W~ enV ~
V~.
In
figure
3 we haveplotted tip
velocities v~ and v~ as a function of theapplied
RMSvoltage
atf
=
lkHz and C =1.48. In this
figure,
eachpoint
represents the average of severalmeasurements. We have checked that the
tip
velocities wereindependent
of thefinger length
as
long
as thefinger
is not too much curved at its two ends. Theexperimental dispersion
invelocity
measurements, of the order of ± 5 ~Lm/s, isprobably
causedby inhomogeneities
of the electrodes due to the surface treatment. One sees that both velocities v~ and v~ varylinearly
as afunction of the
voltage
in the whole range of accessiblevoltages (Vi
<V<V~).
Thedeviations from the linear law observed near
Vj
isprobably
causedby
thewidening
of thefinger tips
which will result insplitting
belowVi.
We also note that v~ and u~ do not vanishsimultaneously
on the critical line when V=
V~ (at
thisvoltage
v([[([~~~~~~~~ =0).
Thisunexpected
result shows that the rectilinearfingers
craw'l in thesample
w,hilekeeping
a~~~
'~~~
,
~~$~r~~~~ps
loo
~'
0
C
E
j
''~ '~
~'
'
£
", ",
/ §i
"" "
'
",
',',
' ', "
Vi V2 ',
",
~
''
',
" "
l.0 1-1 1.2 1.3 1.4 1.5
V(Volt)
Fig. 3. Velocities u~ and u~ of the norrnal and abnormal tips of CF-l's as a function of the applied RMS voltage ~l'= 1000 Hz, C
= 1.48).
constant
length (Fig.
4). Thisphenomenon
is not an artifact due to a thicknessgradient
in thesample
because both c~ and v~ areindependent
of the orientation of thefingers
in thesample plane.
Furthermore,neighbouring parallel straight fingers
oriented head to footalways
move inopposite
directions. We shall call the abnormaltip velocity
v~ = v~, thecrawling velocity
~ ~~~~ ~/ ~/ ~~ ~st~aighlfinger
crawl 2 length
The
crawling velocity
is acomplex
function of thesample
thickness and of thefrequency.
Infigure
5 weplotted
v~~~~j versusfrequency
for various values of the confinement ratio C=
d/p. Surprisingly,
u~~~~j canchange sign
when the thickness is increased. In contrast, thecut-off
frequency
above whichcrawling disappears (defined
as thefrequency
at whichv~~~~j is half of its
low-frequency
value) isroughly independent
of the thickness andequals
lo kHz. In
figure
6, weplotted
v~~~~,j as a function of the criticalvoltage V~
atf
= I kHz. This
curve confirms the
crawling velocity
inversion atV~
m 1.85 Vcorresponding
to Cm 2. We
also note that v~~~~j vanishes when
V~
- 0, asexpected.
Crawling
is not theonly
manifestation ofelectrohydrodynamic
effects.Indeed,
one very often observes the formation ofrotating spirals
in oursamples
after along period
(several hours ingeneral).
Thesespirals
involvesingular fingers
as will be shown in the next section.4. Characterization of the cholesteric
fingers
of the secondspecies.
In this section, we focus on
fingers
that formspirals
when theapplied voltage
is held at a valueclose to
V~.
Thesespirals
have been observedpreviously,
firstby Kamay6
and Gilli in asmectic A
phase [8],
and thenby
Mitov and Sixou in a cholestericphase [9]. They
are formed from newfingers
which have almost the sameoptical
contrast as the classicalfingers
of the firstspecies.
This canexplain why
Mitov and Sixou do not mention the two types offingers.
Moreover, the nucleation time of
spirals
is muchlonger
in ourexperiment
than in theexperiment
of Mitov and Sixou(it
varies from half an hour atf
=
lo Hz to several hours at
f
= I
kHz).
Thisprobably
comes from the value of the electric field, much smaller in ourexperiment (typically
E= 600
V/cm)
than in theirs(E
1
10~
V/cm ).a
b
c
d
50 iLm
Fig.
4. -Crawlingfinger
of the firstspecies.
The time interval between twophotographs
is 2 mn(u~~~~j = 20.4 ~m/min, V V~ 3.8 V, f 000 Hz).
-'~ . .
'c 0
E
"E "
~ lo
)
~
(
. V~=
1.58
V,
C=1.72"
m
V~=1.85 V,
30 ~
"
MV~= 4.10
10~
10~
10~ 10~
10~
f
(Hz)ig.
5.
C
=d/p
I 1.5 2 2.5 3
,'~ i,
, ,
,
,~
,,
~- , ,
, ,
b ,'
~
,E
~
- ,
= ,
~ ,
e ',
u ,
>
~',
',
i,,
,,~
20
"~,,
),
30
2 3 4
V~ (V)
Fig. 6. Crawling velocity as a function of the critical voltage at f
= 1000 Hz.
In the
following,
we focus on the difference between the two types offingers
and describe how todistinguish
them.Figure
7 shows aregion
of thesample
in which the two types offingers
coexist. Their widthsare very close and
they
are almostindistinguishable
whether between crossedpolarizers (al
or innon-polarized light (b).
I
~
~ '~
'
~
~
b
50 pm
Fig. 7. Region of the sample where the two types of finger coexist. Between crossed
polarizers
(a) aswell as without
polarizers
(b), CF-l's and CF-2's are difficult to distinguish. The small arrow shows a CF-I and the large one a CF-2. C= 3.13, V 3.9 V.
A convenient way to differentiate them is to observe their behavior when the
applied
electricfield is
suddenly changed.
This method is used to measureaccurately
the~pinodal
limitV~(C
) of CF-l's : indeed, above this limit, CF-l's breakspontaneously
in numerousplaces
anddisappear
within a few tenths of a second, whereas betweenV~
andV~,
CF-l's aremetastable and shorten. The same
experiment
can beperformed
with the CF-2's afterthey
have formedfully developed spirals (Fig.
8). One then observes that CF-2's are still metastable atvoltages
muchlarger
thanV~,
which means that theirspinodal
limitVI (C
is muchhigher
than that,V~(C
), of CF-l's(Fig, ii.
Note thatVI
(C ) is more difficult to measure thanV~(C
because CF-2's shorten veryquickly
atlarge voltages.
When thevoltage
is increased fromV~
toV~,
the width of CF-2's decreasesslowly
whileremaining comparable
to that of CF-a
b
ec
f
soo pm
Fig. 8. The same spiral photographed at increasing voltages (C
= 3.13, circularly polarized light).
From a-f, V 4.2, 4.6, 5. 5.8, 6.4 and 6.8 V ~f
=
000 Hz ).
l's. In contrast, their width decreases very
quickly
aboveV~ (Fig. 9)
thefinger
looks like a thin thread atlarge voltage.
This observation suggests that there is asingularity
inside thefinger.
30
"
fi
25
. D CF-I
Q
~~ Q
_
15
I
~
m
. .
V3 " " .
~
4.5 5.0 5.5 6.O 6.5 7.O
V
(Volt)
Fig. 9.- Width A of the cholesteric
fingers
of the two species as a function of thevoltage
(C
= 3.13, f = 000 Hzl.
Another evidence of the difference in
topology
between the two types offingers
concernstheir ends when
they
form segments of finitelength.
Whereas CF-l's have two differenttips,
arounded one and a
pointed
one(Fig. 4,
we exclude from the discussionfingers having
apoint
defect inside), CF-2's
always
have two similar roundedtips (Fig. lo).
In order to make the segments ofCF-2,
wesubject
aspiral
tovoltage VI during
a fraction of a second and we thenabruptly
decrease thevoltage
to a valueslightly
aboveV~.
Each segment of CF-2 shortenssymmetrically
from its two ends until aspherulite
is formed lo, iii(Fig,
10).By
contrast, at thisvoltage,
any segment of CF-Idisappears by collapse
of its twotips
ofopposite signs.
The transformationCF-2-spherulite
is irreversible.Indeed, growing
afinger
from aspherulite
at smallvoltage
never leads to a CF-2 but to a CF-I segment with two roundedtips
and apoint
defect in the middle of the
finger
(seeFig.
4c of Ref.[3]).
It is also
possible
to measure thevoltage VI
for which thelength
of a small segment of CF-2 remainsstationary.
This criticalvoltage
isslightly larger
thanV~
(about 0, IV).
This meansthat CF-2's are
slightly
more stable than CF-l's. If thevoltage
is decreased belowVi,
CF-2's undulate as do CF-l's belowV~.
Thisinstability
leads toundulating spirals
(Fig. II). By subjecting
anundulating spiral
to alarge voltage,
it ispossible
to break itregularly
and to nucleatestrings
ofspherulites (Fig.
12).5.
Spiral dynamics.
We first mention that there is
always
one or several dustparticles
in the center of eachspiral,
on which the end of the
moving
CF-2 ispinned.
When the dustparticles
arestrongly
anchoredon a
glass plate, they
do not move. If not,they
can rotate. This rotation israrely
continuous and isaccompanied by
a chaotic motion of the centre ofgravity
of theparticle.
It is alsoimportant
to mention that
spirals
are much less numerous than the dustparticles
present in thesample they
also,rarely cling
to the sameparticles
from oneexperiment
to the next. Most of thespirals
are
single
(as inFig. 8)
and areequally
left-handed orright-handed
(if thesample
is turned over a left-handedspiral
transforms into aright-handed
one). Some of them are doubleit
b
c
~~
d
50 pm
Fig. lo- Evolution of a CF-2 at C 3.13, V
= 4.3 V and f 000 Hz. A spherulite forms after the two similar ends meet each other.
(Fig, 13a)
or eventriple (Figs,
13b, cl. We have also observedsingle ~pirals
twice as thick as usual(Fig. 13d). By observing
theirdisappearance
atlarge voltage,
we have seen thatthey
were
composed
of two CF-2'splaced
sideby
side. Themultiple spirals
are rare, so we shall focus in thefollowing
on the more commonsingle
ones.Stationary spirals
are observed in a smallvoltage
range,usually
betweenVi
andVI
+ 0.5 V(hatched region
in thephase diagram
of
Fig,
I). Atlarger voltages,
CF-2'seasily unpin
from dustpanicles
andspirals quickly
disappear.
~ 500 pm ~ 500 pm
Fig. ii. Fig. 12.
Fig. ii. al
Undulating spiral
(C= 3,13, V
= 4 V and f
= 000 Hz). This undulation
spontaneously
develops when the voltage is decreased belowVi.
hi The same spiral at V= 4,I V. At this voltage, the
spiral
is stable.Fig, 12. By
subjecting
an undulating spiral (photograph (a), I' = 3.8 VI to a large voltage (close to V~~ = 7 VI during a fraction of a second, it is possible to break it into small, regularly spaced pieces. If the voltage is decreased before all of these pieces have disappeared, it is possible to obtain strings ofspherulites (photograph (b), V
=
4.2 V). Each
spherulite
comes from the collapse of a piece of CF-?.C
= 3.13.
We have first
analyzed
theshape
ofsingle spirals. They
canalways
be fitted togood
accuracy
by
an Archimedianspiral
whosepolar equation
is p(H)
=
3L(H wt).
Thepitch
of thespiral
is .S=
2 arJ~ and w is its
angular velocity.
The transversevelocity
of thefinger
atinfinity
is v~,=
3Lw. In
figure14a (resp,14b),
weplotted
w(resp,
i~~~) as a function of
voltage
i'for differentspirals
observed in the samesample (C
=
3,13).
While w(and consequently
:f and 3L) vary from onespiral
to another (thesequantities probably depend
on the size and on themobility
of the dustparticle
whichpins
eachspiral),
v~~ isindependent
of thespiral
chosen (this feature was also underlinedby Kamayd
and Gilli[8]).
Moresurprisingly,
v~,is also
independent
of thevoltage
in the small range which can beinvestigated.
On the otherhand,
v~~depends
on C andf
as shown infigure
15. Inparticular,
v~, decreasesstrongly
above acut-off
frequency
of about 3 kHz and vanishes above loo kHz. This cut-offfrequency
isr
a
b
csoo pm
d
Fig. 13. a) Double spiral (C 3,13, I' 4? V) b) triple
spiral
(C= 3.13, V 4.2 V) cl the
same triple spiral at V 4.5 V. The three branches have split off from the center where no dust particle is visible note that the ends of the three branches are identical d) thick simple
spiral
formed by two CF- 2'splaced
side by side (C 3.13, V=
4 VI.
A
j
O. 8 D Spiral2
h Spiral3
a A
c
~ ~
+ a
(a)
# °
8 ~
a
+ A
~ A
+
+ a
+ ~
A +
~ A
+
I
~
4.O 4.1 4.2 4.3 4.4 4.5 4.6
V
(Volt)
25
20 h $ $ ~ ~ " k
~ ~
- +
C 15
E
( (b)
+
~D Spira12 h Spira13
4.O 4.1
V (Volt)
Fig. 14.-a) Angular velocity w as a function of voltage V for different spirals (C
= 3.13, f =1000 Hz). b) Transverse drift velocity v~~ as a function of voltage V for the same spirals (C
= 3.13, f
=
000 Hz).
comparable
to that we foundpreviously
for thecrawling
of the CF-l's.Finally,
we note thatv~~ decreases
strongly
with C and seems to vanish at C~ l.3. This result, obtained
by extrapolating
v~~(CI to zero, suggests thatspirals
shoulddisappear
when C ~ l.3.6. Tentative
topological
model for CF-2's.Our observations show
clearly
that CF-2's are different from CF-l's inspite
of theirresemblance
through
themicroscope.
Themajor
observation is that thecollapse
of any CF-2 segmentgives
birth to aspherulite (also
called cholestericbubble).
In reference[I ii,
we havesuggested
that thesingularity along
thespherulite
axis isactually
twopoint
defects ofopposite
strength.
In the present article, we propose that CF-2's have the sametopology
asspherulite~
in theplane perpendicular
to thefinger
axis. The twopoint
defects now arereplaced by
two25
-j
~
~~~~
o
2 3 4
c=d/p
D D o a D
- O
T °
Cl a
E
ii
~
~~~
<r
5 a
a
io~
iO~io~ io~ io~
f
(Hz)
Fig.
15. al Transverse drift velocity v~~ as a function of C at voltage V=
VI
~f =1000 Hz).b) Transver~e drift velocity v~~ as a function of frequency f (C = 3.13, V = 4.15 VI.
singular
lines or disclinations(of strengths
S= + I and S
=
Ii joining
the two ends of thefingers. Figure
16a shows the director field in a verticalplane perpendicular
to thefinger
axis whilefigure
16b shows the director field in the medianplane parallel
to theglass plates.
Onesees in
figure
16b that the two ends of thefinger
are identical, in contrast with CF-l's whichhave two different
tips.
Inspite
of this fundamental difference, itclearly
appears,by
comparing figures
2b and 16a, that director fields inside bothfinger
types resemble each other, whichexplains why they
are so difficult todistinguish through
themicroscope. Moreover,
bothdirector fields
identically
match thehomeotropic
nematicphase.
Thisexplains why
theabnormal
tip
of a CF-I can merge into the side of a CF-2,just
as it would have with a CF-I, and form a T-like sidebranch (seeFig.
2a)[3].
7. Conclusion.
The main conclu~ion of this article is that there exist
experimentally
twofinger types
:fingers
of the first
species
which aretopologically
continuous andfingers
of the secondspecies
whichI I I I I I I
I / / i I I I I I I
I / /
J i II I
I i II I I
I I
J, ~
4
~, , i I
I I
I J
i , iI I
I ~ iI I
I I
J , II
J J ,i I
I I
/ -,I I i
J -,I I
I
i i iI I
i ,I
I
I > 7 II I
I > 7 II
~,
-, /l
~,~'/ l
I ~%~--ll1 ~~--~ll I
I ~'~~---~>--~---ll 7 I
I ~"" ~ / llllf I
I ~"'i I I till / I
I I I I I I I I I I I I I I
a)
b)
Fig, 16. Director field in a cholesteric finger of the second species a) section by a plane perpendicular
to the
finger
axis b) section by a median plane parallel to the glass plates. The two ends of thefinger
areidentical in contrast with cholesteric
fingers
of the first species.are
singular.
The former havedifferently shaped
ends and crawlalong
their axes in an AC electric field. The latter have similarends, collapse by leaving spherulites,
and moveperpendicularly
to their axes. This transverse motion may lead tospirals.
The
question
now is toexplain
theorigin
of theseelectrohydrodynamic phenomena.
Acknowledgments.
We thank L. S. Tuckerman for fruitful discussions. This work was
supported by
DRETContract No. 92/1313/DS/SR.
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