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Structure and mid-infrared optical properties of spin-coated polyethylene films developed for integrated photonics applications

Abstract

Polyethylene is a promising polymer for mid-infrared integrated optics due to its broad transparency and optimal refractive index. However, simple fabrication protocols that preserve its optical characteristics are needed to foster a wide range of applications and unlock its full potential. This work presents investigations of the optical and structural properties of spin-coated linear low-density polyethylene films fabricated under humidity-controlled conditions. The film thickness on polymer concentration dependence shows a non-linear behavior, in agreement with previously reported theoretical models and allowing predictive concentration-dependent thickness deposition with high repeatability. The surface roughness is on the nanometer-scale for all investigated concentrations between 1% and 10%. The crystallinity of the films was studied with the Raman spectroscopy technique. Mid-infrared ellipsometry measurements show a broad transparency range as expected for bulk material. Layer exposure to solvents revealed good stability of the films, indicating that the fabricated layers can outlast further fabrication steps. These investigations confirm the excellent properties of spin-coated thin films fabricated with our novel method, creating new opportunities for the use in photonic integrated circuits Published by Optica Publishing Group under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.

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Structure and mid-infrared optical properties of spin-coated polyethylene films developed for integrated photonics applications

Author: David, Mauro; Disnan, Davide; Lardschneider, Anna; Wacht, Dominik; Hoang, Hanh T.; Ramer, Georg; Detz, Hermann; Lendl, Bernhard; Schmid, Ulrich; Strasser, Gottfried; Hinkov, Borislav
Publisher: Optica Publishing Group
Year: 2022
DOI: 10.1364/OME.458667
Source: https://dspace.vut.cz/bitstreams/d3057020-04d7-4a71-ba03-f026d58e4218/download
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2168
S uc u e and mid-in a ed op ical p ope ies o
spin-coa ed polye hylene ilms de eloped o
in eg a ed pho onics applica ions
MAURO DAVID,1DAVIDE DISNAN,2ANNA LARDSCHNEIDER,1
DOMINIK WACHT,3HANH T. HOANG,1GEORG RAMER,3HERMANN
DETZ,1,4 BERNHARD LENDL,3ULRICH SCHMID,2GOTTFRIED
STRASSER,1AND BORISLAV HINKOV1,*
1Ins i u e o Solid S a e Elec onics, TU Wien, Vienna, Aus ia
2Ins i u e o Senso and Ac ua o Sys ems, TU Wien, Vienna, Aus ia
3Ins i u e o Chemical Technologies and Analy ics, TU Wien, Vienna, Aus ia
4Cen al Eu opean Ins i u e o Technology, B no Uni e si y o Technology, B no, Czech Republic
*bo isla [email p o ec ed]
Abs ac :
Polye hylene is a p omising polyme o mid-in a ed in eg a ed op ics due o i s b oad
anspa ency and op imal e ac i e index. Howe e , simple ab ica ion p o ocols ha p ese e
i s op ical cha ac e is ics a e needed o os e a wide ange o applica ions and unlock i s ull
po en ial. This wo k p esen s in es iga ions o he op ical and s uc u al p ope ies o spin-coa ed
linea low-densi y polye hylene ilms ab ica ed unde humidi y-con olled condi ions. The ilm
hickness on polyme concen a ion dependence shows a non-linea beha io , in ag eemen
wi h p e iously epo ed heo e ical models and allowing p edic i e concen a ion-dependen
hickness deposi ion wi h high epea abili y. The su ace oughness is on he nanome e -scale o
all in es iga ed concen a ions be ween 1% and 10%. The c ys allini y o he ilms was s udied
wi h he Raman spec oscopy echnique. Mid-in a ed ellipsome y measu emen s show a b oad
anspa ency ange as expec ed o bulk ma e ial. Laye exposu e o sol en s e ealed good
s abili y o he ilms, indica ing ha he ab ica ed laye s can ou las u he ab ica ion s eps.
These in es iga ions con i m he excellen p ope ies o spin-coa ed hin ilms ab ica ed wi h ou
no el me hod, c ea ing new oppo uni ies o he use in pho onic in eg a ed ci cui s
Published by Op ica Publishing G oup unde he e ms o he C ea i e Commons A ibu ion 4.0 License.
Fu he dis ibu ion o his wo k mus main ain a ibu ion o he au ho (s) and he published a icle’s i le,
jou nal ci a ion, and DOI.
1. In oduc ion
The mid-in a ed (mid-IR) spec al ange (
∼
2–20
µ
m) is a pa o he elec omagne ic spec um
o pa icula scien i ic and echnological in e es o sensing applica ions and op ical ee-space
communica ion. [1–3]. While lase sou ces ope a ing a hese wa eleng hs ha e de eloped in o
comme cially a ailable ins umen s o e he las yea s, he ad ancemen o in eg a ed ci cui s has
aced conside able challenges. A lo o wo k was dedica ed o op imizing op oelec onic de ices
[4–7], including no el ma e ials [8,9] and al e na i e a chi ec u es o mid-IR emission [10–12].
Howe e , nex -gene a ion in eg a ion s a egies [13,14], including implemen a ion o no el
anspa en ma e ials, we e ela i ely sca ce [15,16]. This is pa icula ly ue o he long-wa e
in a ed (LWIR) spec al ange, whe e an impo an a mosphe ic window is loca ed (8–14
µ
m).
The e, he ma e ial selec ion o highly anspa en ma e ials wi h sui able cha ac e is ics and
exis ing p ocessing p o ocols is e y limi ed [17,18]. This is pa icula ly he case conce ning he
in eg a ion o hese de ices on o Indium Phosphide (InP) subs a es o he ealiza ion o mid-IR
pho onic in eg a ed ci cui s (PICs). Semiconduc o - o Dielec ic Loaded Su ace Plasmon
Pola i on Wa eguides (S/D-LSPPW) ha e been ound o be a p omising solu ion o hese issues
#458667 h ps://doi.o g/10.1364/OME.458667
Jou nal © 2022 Recei ed 15 Ma 2022; e ised 15 Ap 2022; accep ed 21 Ap 2022; published 12 May 2022
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2169
[14,15]. Howe e , only a limi ed numbe o ma e ials can simul aneously o e high anspa ency
and low e ac i e index ( o educe in e ace e lec ions) o ma ch hei coun e pa ’s pe o mance
a elecom equencies (1.55
µ
m). Polyme s ha e a ac ed emendous in e es o in eg a ed
op ical applica ions o many yea s [19] bu so a lea ing ou he LWIR spec al ange. Thei
a o able op ical cha ac e is ics, such as high anspa ency and low e ac i e index, a e decisi e
ac o s o hei use in op oelec onic de ices and applica ions. PMMA and SU-8 a e o en
used dielec ic ma e ials o plasmonic de ices in he nea -IR [20–22]. Howe e , nei he o
bo h ma e ials can o e high anspa ency in he mid-IR spec al ange [23,24] due o nume ous
abso p ion lines especially loca ed in he LWIR (see Fig. 1).
Fig. 1.
Imagina y pa o he complex e ac i e index a a wa eleng h o
λ=
9.12
µ
m o
some o he mos anspa en polyme s in he LWIR. Da a aken om [36,37]
In con as , Polye hylene (PE) shows b oad anspa ency o a wide spec al ange [25]. I was
so a exploi ed as b oadband in e connec o [26], lexible an enna [27], and senso pla o m [28]
in he THz spec al egion (
>
20
µ
m). Theo e ical in es iga ions ha e shown i s g ea po en ial
as a co e ma e ial o DLSPPW a elecom and THz equencies [29] and as a cladding laye
o hyb id plasmonic THz wa eguides [30,31]. Howe e , o unlock i s ull po en ial in he
mid-IR wi h i s much smalle geome ical dimensions, i is necessa y o de elop ad an ageous
ab ica ion echniques ha o e epea able hin ilm deposi ion wi h excellen laye quali y. The
ilms a e expec ed o ha e a composi ion simila o he bulk ma e ial, wi h low su ace oughness
and con olled hickness, while main aining cons an e ac i e index and high anspa ency.
Mo eo e , sui able ilms mus supply he necessa y chemical and mechanical s abili y o ou las
ambien exposu e and u he p ocessing s eps.
Se e al ypes o PE ha e been shown so a , and a e ypically classi ied acco ding o hei
densi y and b anching. The wo basic ypes a e High-Densi y PE (HDPE) and Low-Densi y PE
(LDPE). HDPE is cha ac e ized by igh ly packed molecules ha o m c ys alline pa ches, while
LDPE ypically has a highe deg ee o amo phous ac ions. In gene al, anspa ency ends o
dec ease wi h a highe deg ee o c ys alliza ion, as he ligh de lec s along c ys alline bounda ies
[32]. The e o e, he choice among he di e en PE ypes na u ally alls owa ds LDPE, mo i a ed
by i s highe ansmi ance compa ed o HDPE [33]. Nowadays, LDPE has almos en i ely been
eplaced by linea LDPE (LLDPE), which has a highe mel ing empe a u e and c ack s eng h
[34,35].
Spin coa ing is a s anda d echnique o p oduce high-quali y and uni o m polyme ilms o
adjus able hickness on a plane subs a e [38]. Howe e , he s a e-o - he-a echnology o
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2170
p oducing spin-coa ed PE ilms is cha ac e ized by complex and ime-consuming p ocesses,
including p ehea ed equipmen and employing oxic sol en s (e.g., Decalin) used a hei boiling
empe a u es, ollowed by se e al hou s o annealing [39–41]. Fu he mo e, only e y limi ed
da a al eady exis s, epo ing he mid-IR s uc u al and op ical p ope ies o PE, and none in
he case o laye s p oduced by spin-coa ing [42]. Finally, add essing mid-IR applica ions, he
hickness needs o be p edic ed p ecisely in he 100 nm – 6
µ
m ange, which has no ye been
ealized in li e a u e. In his con ex , we p esen an op imized ab ica ion echnique pe o med
by spin-coa ing o LLDPE wi h he scope o p ese ing i s ad an ageous op ical p ope ies
and ob aining high epea able esul s in e ms o laye hickness h ough con olling ambien
condi ions. The excellen op ical p ope ies o he ilms, and hei s abili y owa ds sol en
exposu e, con i m ha hin polye hylene laye s ob ained by ou spin-coa ing echnique can be
used o ealize he in eg a ion o c ucial building elemen s o PIC de ices.
2. Ma e ials and me hods
2.1. Ma e ials
Double side polished 2-inch Si (100) wa e s wi h 275
µ
m hickness we e used as subs a e
ma e ial. They we e clea ed in o 11
×
11 mm
2
pieces, cleaned in an ul asonic ba h wi h ace one,
insed in isop opanol, and d ied wi h ni ogen. Subsequen ly, 8 nm o Ti and 100 nm o Au
we e spu e ed (25 W, p
wo k =
8e-3 mba ) in mul iple cycles (30 s pe cycle), al e na ing wi h
cool-down pe iods o 60 s, un il eaching he desi ed ilm hickness.
LLDPE powde (ρ=0.906 g/mL, a e age Mw∼35000 and Mn∼7700, used wi hou u he
pu i ica ion) was pu chased om Sigma-Ald ich and dispe sed in oluene (Sigma-Ald ich,
anhyd ous, pu i y 99.8%).
2.2. Polyme ilm ab ica ion
The ab ica ion o he ilms was conduc ed in a humidi y-con olled glo e box (see Fig. 2). A
low cha o he ab ica ion p ocess is shown in Fig. 3.
Fig. 2.
Side (a) and op- iew (b) pic u es o he ab ica ion se up in he glo e box.
Tempe a u e and humidi y du ing ab ica ion we e moni o ed wi h a digi al hyg ome e . The
glo e box s abilizes he humidi y du ing he ab ica ion p ocess by a cons an supply o d y
ai lux and by he usage o silica gel g ains. The ela i e humidi y was kep a 15%
±
0.9%
du ing he p ocess.
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2171
Fig. 3.
Flow cha o he ilm ab ica ion p ocess. The LLDPE powde was dissol ed in
oluene wi h di e en weigh a ios, anging om 1% o 10%, and s i ed a 100
°
C un il
comple e dissolu ion. The empe a u e o he solu ion was acked wi h a p obe he mome e .
Be o e deposi ing he polyme solu ion, he subs a es we e p ehea ed on a ho pla e se o
120
°
C. The ilm was p oduced om he hea ed solu ion by using he dynamic dispense
me hod (i.e., deposi ing he polyme solu ion on he subs a e wa e du ing spinning) o a
ixed amoun o solu ion (100
µ
L). The spin-coa ing was ca ied ou a 1000 pm o 35 s
wi h 5 seconds o accele a ion o all coa ings, ollowed by a pos -baking a 120
°
C o 15
min o e apo a e any sol en esidual.
2.3. Film cha ac e iza ion
The a e age hickness o he ab ica ed ilms was measu ed a h ee di e en spo s on each sample
wi h a Vis-Nea -IR Ellipsome e (Woollam Alpha-SE, assuming n
LLDPE ∼
1.54 and measu ed
n
Au
). The measu emen s o he a e age ilm hickness o some o he hicke samples we e also
con i med wi h a su ace p o ilome e (B uke Dek ak XT, ip o ce 1 mg). The mo phology
analysis o he su ace o he LLDPE laye s was conduc ed wi h he p o ilome e i s and hen on
he nanome e scale using A omic Fo ce Mic oscope (AFM). The measu emen s o he analysis
wi h he su ace p o ilome e we e aken by scanning along he diagonal di ec ion o he sample.
Each scan was 8 mm long o ensu e a comple e o e iew o he su ace inhomogenei ies and
oughness dis ibu ion in he inne pa o he sample.
The s anda d p ac ice o eliably ex ac ing op ical and elec ical pa ame e s o o ganic hin
ilms is by spec ally esol ed ellipsome y in he spec al ange o in e es [43]. The e o e,
he op ical p ope ies o he ab ica ed laye s we e in es iga ed using a mid-IR ellipsome e
(IR-VASE, J.A Woollam) in he ange o 2–12 µm.
A e ilm ab ica ion, selec ed samples we e subme ged in deionized wa e and ace one o
se e al minu es. This s ep was pe o med o con i m he obus ness o he ab ica ed coa ings o
u he p ocessing s eps wi h espec o adhesion and delamina ion o he ilms.
Film c ys allini y was de e mined using Raman spec oscopy by i ing he CH
2
wis ing
band a ound 1300 cm
−1
, as ou lined by Lin e al. [44]. Raman spec a we e collec ed using
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2172
a con ocal Raman spec ome e using a 532 nm lase sou ce a 50 mW and a 100x (Zeiss EC
Epiplan-Neo lua , NA 0.9) objec i e, using 10 s in eg a ion ime and 10 a e ages. The spec um
was i wi h wo Gauss-Lo en z bands, one ixed a 1303 cm
−1
and he second loa ing be ween
1290 cm
−1
and 1295 cm
−1
. The amo phous con en was calcula ed as he a io o he a ea o he
1303 cm−1di ided by he sum o bo h bands.
3. Resul s and discussion
3.1. Fab ica ed samples
Syn hesis o PE-based hin ilms is ypically pe o med a empe a u es abo e 100
°
C, wi h
p ehea ed equipmen ollowed by long annealing imes [45,41,39,46,40]. S a e-o - he-a
echniques o spin coa ing LLDPE ypically equi e he p ehea ing o all he ins umen a ion
(subs a e, solu ion and spin coa e chuck) o e y high empe a u es (
>
150
°
C). Wang e al.
[39] in es iga ed he mo phology o ul a- hin LLDPE ilms coa ed on HF passi a ed silicon
wa e s. To p e en he ilms om c ys allizing, hey dissol ed polye hylene in boiling oluene
and spun-cas he h solu ion on hea ed subs a es (150
°
C). The ilms’ hickness was con olled
wi h he concen a ion (0.05–5%) and spin-coa ed wi h 2500 pm, ob aining ilms wi h hickness
be ween 10 and 460 nm. Two c ys alliza ion condi ions ha e been s udied o imp o e he su ace
quali y: non-iso he mal and iso he mal. The i s consis ed o hea ing he ab ica ed ilms in an oil
apped acuum o en a 140
°
C o 30 min o mel he ilms. The empe a u e was hen dec eased
o oom empe a u e o 12 h be o e exposing he sample o he a mosphe e. The iso he mal
p ocess was pe o med by annealing o e en highe empe a u es o 30 min and hen quickly
mo ing o ano he acuum o en se a 60 °C, whe e he samples we e u he annealed o 12 h
be o e exposing hem o oom empe a u e. Unde non-iso he mal c ys alliza ion condi ions, hey
ob ained la su aces wi h ypical sphe uli es. Howe e , a discussion on he su ace oughness o
he ab ica ed ilms is missing. They epo ed a high di e ence o 10–15 nm be ween he lamellae
idges and he la lamellae egion and a deg ee o he amo phous ac ion a ound 60%. Jeon and
K ishnamoo i [40] in es iga ed he indi idual e ec o con inemen and he mal his o y on he
supe molecula and lamellae mo phology a ia ion by pe o ming iso he mal c ys alliza ion wi h
di e en empe a u es. Fo his pu pose, hey i s dissol ed LLDPE in o boiling oluene and
pou ed he solu ion in o me hanol a oom empe a u e in o de o p ecipi a e he polyme a e
il a ion, ollowed by o e nigh d ying in a acuum o en a 110
°
C. Subsequen ly, he cleaned
LLDPE sample was hea ed o 160
°
C o 5 min and cooled a a a e o 100
°
C o ec ys alliza ion
and dissol ed in o boiling decalin (200
°
C) o 1 h. The solu ion was hen cooled and main ained
a a empe a u e o 160
°
C and spin coa ed a 1800 pm wi h he s a ic dispense me hod. To
p e en ea ly c ys alliza ion p io he spinning p ocess, he spinne chuck was also p ehea ed o
100–140
°
C. They obse ed ha he quali y o he ilms s ongly depended on he ime o he
accele a ion pe iod. A longe accele a ion imes he ilms we e no mac oscopically uni o m.
The concen a ion anged om 0.15 o 3.5%, and hey ob ained hickness anges be ween 20
o 800 nm. Fo iso he mal c ys alliza ion s udies, he spin-coa ed ilms we e mel ed o 2 h
a 160
°
C in a acuum o en, hen quickly mo ed o a second p ehea ed acuum o en whe e
hey we e iso he mally c ys allized o e a empe a u e ange o 90–119
°
C o 2 h, and quickly
quenched in o liquid ni ogen. As he ocus o he s udy was he mo phological ansi ions upon
c ys alliza ion p ocedu e, da a on he oughness and op ical p ope ies o he ilms a e missing.
Fo many op oelec onic applica ions, oughness, anspa ency, and epea abili y o a ab ica ion
me hod a e essen ial cha ac e is ics in o de o ob ain laye s wi h desi ed hickness and su icien
(su ace) quali y. Ambien condi ions may ha e a signi ican e ec on spin-coa ed ilm p ope ies.
Typically, spin-coa ing p ocesses o polyme s a e pe o med in esea ch lab ume hoods,
cha ac e ized by luc ua ing ela i e humidi y and empe a u e alues, bo h also depending
on ambien (wea he ) condi ions. In con as , glo e boxes limi empe a u e and humidi y
luc ua ions o a minimum. In gene al, he impac o he humidi y on he ilm hickness is a he

Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2173
known [47,48], and i can c ea e undesi ed hickness a ia ion and lowe laye quali y. The
a ia ion in hickness
∆
D o a spin-coa ed laye is ela ed o he Rela i e Humidi y (RH) h ough
∆
D
=
(1-RH)
β
, whe e
β
is an empi ically de e mined cons an . Indeed, om some p elimina y
expe imen s pe o med in a s anda d lab ume hood, we ob ained PE laye s wi h a a he b oad
hickness ange (be ween 200–500nm o w =2%). By pe o ming he ab ica ion in he glo e
box, humidi y luc ua ions ha a ec he hickness epea abili y a e a oided.
As discussed p e iously, s a e-o - he-a p ocesses in ol e dissolu ion a sol en boiling
empe a u es and p ehea ed equipmen . To a oid excess apo iza ion bu ensu e comple e
dissolu ion, we limi ed he empe a u e o he solu ion o 100
°
C (i.e., en deg ees below he
boiling poin o he sol en ). Howe e , when using he s a ic dispense me hod, we ob ained
inhomogeneous laye s wi h low op ical cla i y, in ag eemen wi h he indings in li e a u e [40].
We ound ha his issue is ci cum en ed by using he dynamic dispense me hod. In his way,
epea able homogenous laye s can be ob ained. Films ab ica ed wi h his me hod show no isible
inhomogenei ies o he naked eye (Fig. 4). Mo eo e , a e pos -baking, he syn hesized ilms
we e soaked in ace one and deionized wa e , p o ing s ong adhesion o he unde nea h subs a e.
These a e common s eps pe o med in clean ooms du ing pho oli hog aphy-based p ocesses o
he ab ica ion o pho onic de ices, making he coa ings’ s abili y o hese sol en s essen ial o
u he de elopmen s. In con as , he laye s ab ica ed ou side he glo e box o en expe ienced
delamina ion and showed adhesion p oblems a e he pos -bake s ep.
Fig. 4.
Mac oscopic pic u es o ab ica ed samples in he glo e box wi h deposi ion
pe o med be o e spinning (a), (b), and du ing spinning (c),(d).
3.2. Film hickness and concen a ion dependence
F om a de ice design pe spec i e, i is desi able o be able o p edic he hickness o he ab ica ed
laye s wi h ela i ely high p ecision om simple, measu able quan i ies. Typically, his is done by
changing he concen a ion o he solu ion and/o he o a ional speed o he spin coa ing p ocess.
In i s app oxima ion, he hickness depends mo e s ongly on he concen a ion, and he e o e
we decided o ix he o a ional speed o 1000 pm (a a he low alue as we aimed o ela i ely
hick ilms). Wi h ou me hod, i was possible o epea edly ex ac he non-linea ilm hickness
dependence as a unc ion o he LLDPE concen a ion om he ilms ab ica ed. To desc ibe his
beha io , we used he ela ion p oposed by Chen [47] ha models he hickness-dependence o a
spin-coa ed laye om sol en ype, solu ion, and spin coa ing pa ame e s:
D=K0µ0.36ω−0.50 (︃Eλ
Cµ)︃0.6
(1)
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2174
whe e Dis he ilm hickness,
K0
is a cons an o ola ile o ganic sol en s,
µ
is he iscosi y
o he coa ing solu ion,
ω
is he o a ional speed, Eis he sol en -e apo a ion a e,
λ
is he
la en hea o e apo a ion and
Cµ
is he sol en hea capaci y. E en hough he ela ionship
be ween iscosi y and polyme concen a ion can be a he complex [45,49,50], i is possible o
app oxima e i by a powe -law unc ion [45,51,52]. The e o e, he da a we e i ed o:
logD =C+0.36α(w )(2)
whe e Cis a pa ame e ha includes all he cons an s om Eq. (1), w is he concen a ion,
and
α
ep esen s he coe icien desc ibing he phenomenological powe law ha cha ac e izes
concen a ion and iscosi y. In gene al, he iscous beha io o a solu ion can be es ima ed wi h
good p ecision o highe concen a ions, by expanding he iscosi y-concen a ion equa ion in o
a Taylo se ies [50]:
µ=µ0(1+[µ]w +kH[µ]2w 2+· · ·) (3)
whe e
[µ]
is he in insic iscosi y and
kH
is he Huggins cons an . Figu e 5shows he ob ained
esul s when i ing he hickness o he model. F om ou measu emen s, we could ex ac wo
dis inc alues o
α
ha di ide he solu ion in o wo egimes. We ob ained a alue o
α=
2.8
o concen a ions anging be ween 1 and 4%, indica ing ha he solu ion in his concen a ion
ange can be conside ed iscoelas ic [52]. Fo concen a ions abo e 5% we ex ac ed a alue o
α=
7.72. This ela i ely high alue indica es ha he solu ion is in a highly concen a ed egime,
ypically cha ac e ized by en angled mac omolecules [49,50,52].
w
(%) D (nm) 

1 138 ± 1 2.83
2 271 ± 4 2.83
4 560 ± 11 2.83
6 1246 ± 13 7.72
8 2670 ± 2 7.72
10 5186 ± 17 7.72
(a) (b)
Fig. 5.
(a) Film hickness dependence on LLDPE concen a ion including expe imen al
da apoin s ( ed c osses) and i s o he model in bo h ob ained egimes (solid line). All ilms
we e ab ica ed in he glo e box. (b) Table epo ing he p ecise hickness alues measu ed
wi h he ellipsome e .
To es he epea abili y o ou ab ica ion me hod, we ab ica ed 10 coa ings wi h mass po ion
o 10%. The a e age measu ed hickness was 5159
±
87 nm, showing he excellen epea abili y
o ou ab ica ion p ocess.
3.3. Mo phology analysis o ilms
LLDPE ypically p esen s a deg ee o c ys allini y anging om 20% o 50% [32,39,44] and,
he e o e, na u ally ends o a ange in o a mo e amo phous phase. Since he scope o ou wo k is
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2175
o a ain homogenous and anspa en coa ings, we did no need o ocus on achie ing a maximal
deg ee o c ys alliza ion, because i would ha e been coun e p oduc i e, as desc ibed in he
in oduc ion.
AFM su ace scans o he ab ica ed LLDPE ilms o di e en polyme concen a ions a e
p esen ed in Fig. 6. Di e en a angemen s o chains along he su ace can be iden i ied om
he heigh p o ile eco ded wi h he AFM. The b igh a eas a e connec ed o a highe polyme
chains concen a ion. Howe e , since we did no pe o m any iso he mal o non-iso he mal
c ys alliza ion p ocess, no highly s uc u ed and o de ed mo phology based on sphe uli es can
be obse ed. F om Fig. 6, i can be seen ha inc easing he pe cen age o LLDPE dissol ed in
he solu ion esul s in an enla gemen o he polyme mic os uc u e. The su ace ea u es o
he LLDPE hin ilms become mo e p ominen as he polyme concen a ion inc eases, wi hou
a ec ing he gene al cha ac e is ics o he chain a angemen . Fu he mo e, he su ace’s heigh
eco ded by he AFM inc eases by he enla gemen o he mic os uc u e.
Fig. 6.
AFM images o LLDPE hin ilm su aces o di e en mass concen a ions. The
change in o de ing o he s uc u es in he di e en egimes can be obse ed.
In o de o e alua e he quali y o he laye s, we de e mined he mean oughness as a unc ion
o he polyme concen a ion om he AFM measu emen s (Fig. 7). E en hough he su ace
oughness inc eases wi h concen a ion, i emains below 15 nm o all concen a ions.
The su ace o he ilms, analyzed by he p o ilome e , does no e eal inhomogenei ies on he
mm-scale ac oss he samples. Such “wa y-like” luc ua ions o he hickness ha e been obse ed
in p e ious s udies on PE coa ings [39] and a e associa ed wi h he Gibbs-Ma angoni e ec .
3.4. Film c ys allini y
The amo phous con en o he ilm was ound o dec ease wi h inc easing LLDPE concen a ion
in he coa ing solu ion (see Fig. 8) om a ound 80%(m/m) a 1% concen a ion down o a ound
65%(m/m) a 10% ( i ed spec um is p o ided in Supplemen 1). Simila ly, he a iance o
amo phous con en was ound o dec ease wi h inc easing PE con en . Howe e , as Raman
spec a ep esen he make up o an a ea smalle han 500 nm in diame e , he dec ease in s anda d
de ia ion can be in e p e ed as being in pa dependen on he homogenei y o he ilm. A highe
Resea ch A icle Vol. 12, No. 6 / 1 Jun 2022 / Op ical Ma e ials Exp ess 2176
Fig. 7.
Mean oughness (S
a
) e sus concen a ion o he di e en concen a ions o LLDPE.
concen a ion o he s ock solu ion leads no only o a dec ease in amo phous ac ion o he ilm,
bu also o mo e homogeneous ilms.
Fig. 8.
Mass ac ion o amo phous con en o he ilm, as de e mined om con ocal
Raman spec oscopy. E o ba s ep esen he s anda d de ia ion o measu emen s aken in
5 di e en loca ions.
3.5. Mid-in a ed op ical cha ac e iza ion
The wa eleng h-dependen mid-IR e ac i e index and pe mi i i y p o ile o a ypical LLDPE
ilm ab ica ed in he glo e box is shown in Fig. 9( he able wi h he da a is p o ided in
Supplemen 1). We hus expec ed hei p esence due o he in insic polyme in e band ansi ions
[3]. The high anspa ency o he ab ica ed ilms is expe imen ally con i med, indica ing he
excellen op ical p ope ies o he ab ica ed laye s a mid-IR o LWIR equencies.
This da a p esen s he i s mid-IR ellipsome y measu emen o spin-coa ed LLDPE and
con i ms he po en ial o ou ab ica ion echnique o p oducing obus , con ollable, and
ime-e icien LLDPE coa ings. Due o he op imal e ac i e index cha ac e is ics, hey can
be employed as passi a ion laye s, an i e lec ion-coa ing, and wa eguides (cladding o co e)