In Situ Probing the Relaxation Properties of Ultrathin Polystyrene Films by Using Electric Force Microscopy
Qian et al. Nanoscale Research Letters
In Situ Probing the Relaxation Properties of Ultrathin Polystyrene Films by Using Electric Force Microscopy
Xiaoqin Qian 0
Zihong Lin 0
Li Guan 0 1
Qiang Li 1
Yapei Wang 0
Meining Zhang 0
Mingdong Dong 0 1
0 Department of Chemistry, Renmin University of China , 100872 Beijing , China
1 Interdisciplinary Nanoscience Center (iNANO), University of Aarhus , DK-8000 Aarhus C , Denmark
The rapid development of nanoscience and nanotechnology involves polymer films with thickness down to nanometer scale. However, the properties of ultrathin polymer films are extremely different from that of bulk matrix or thin films. It is challenging to distinguish the changes of physical properties in ultrathin films using conventional techniques especially when it locates near the glass transition temperature (Tg). In this work, we successfully evaluated a series of physical properties of ultrathin polystyrene (PS) films by in situ characterizing the discharging behavior of the patterned charges using electric force microscopy. By monitoring the surface potential in real time, we found that the Tg of ultrathin PS films is clearly independent of film thickness, which are greatly different from that of thin PS films (film thickness larger than 10 nm).
Glass transition temperature; Ultrathin films; Surface potential; Electric force microscopy
-
Background
Thin polymer films display distinct differences from their
bulk matrix, including those related to crystallization [1, 2],
physical cross-linking in polymers [3], thermal expansion
coefficients [4?7], and physical aging [8?12]. Decreasing
the thickness of thin films below 10 nm, the physical and
chemical properties of ultrathin films are significantly
different in comparison with thin films due to the thickness
confinement effect [13?15]. To explore such a
thicknessdependent effect, a great deal of effort has been devoted
to investigating the molecular mobility and relaxation
dynamics within ultrathin polymer films [14, 16?18].
Previous studies have revealed that the surface relaxation
dynamics in ultrathin films were apparently different from
that in bulk materials and normal thin films [19, 20]. The
glass transition temperature (Tg) of ultrathin films was far
below the bulk Tg due to the enhanced mobility near the
free surface [13, 21?24]. For instance, the Tg of normal
thin polystyrene (PS) films deposited on silicon substrate
was found to drop by 20 K from the bulk Tg, while the
Tg almost dropped 70 K for freely standing thin PS
films [25]. A high surface-to-volume ratio, in which the
ultrathin films are dominated by the surface properties,
can considerably affect the relaxation dynamics near
the interface [26?29].
The anomalous thermal behavior observed in thin
films is closely related to the presence of surface and
interfaces [10]. Two models [7, 11, 12, 22, 30?33],
named as the three-layer model and the two-layer
model, have been widely used to explain the decrease of
Tg for nano-confined polymer films. In the three-layer
model, the interfacial layer, which is also described as
the dead layer, plays a great role in the relaxation behavior
[12, 34], and the conformation of the polymer chain
within interfacial layer is affected by the polymer-substrate
interaction. Polymer chains in the middle layer are
confined in the matrix, exhibiting the intrinsic
characteristics of the polymer matrix assumed to be the bulk Tg
[32].When the film thickness decreases to several
nanometers, the interfacial layer has disappeared; the thin
polymer film then could be illustrated by the two-layer
model. In the two-layer model, the top layer, which is
also regarded as a liquid-like layer, is supposed to
enhance the mobility of polymer chains and induce the
decrease of Tg [29].
Various kinds of techniques have been attempted to
quantitatively measure the Tg of ultrathin polymer films
? The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made.
[11, 18, 32, 34?38]. Particularly, the molecular motion
and relaxation dynamics in ultrathin polymer films have
been extensively investigated by many groups using some
intriguing techniques [18]. By using X-ray reflectivity,
Tsukasa et al. found that the Tg of ultrathin films was
almost independent of film thickness when it fell below
10 nm [18]. Keddie measured the Tg of ultrathin PS
films with the thickness less than 20 nm using
ellipsometry and found that the Tg was depressed from the
bulk values. [7] However, it is still challenging to
investigate the relaxation dynamics and Tg shifts in ultrathin
films, since the differences in properties near Tg become
rather smaller when using the traditional techniques as
stated above [39]. Increasing attention is then paid to
atomic force microscopy (AFM) method, which has the
advantages of systematically measuring relaxation
dynamics based on the mechanical and electrical characteristics
simultaneously with the observation of surface
morphologies. For example, Akabori et al. demonstrated how the
surface relaxation behavior depended on the thickness of
PS films using lateral force microscopy (LFM) [10].
Thermal molecular motion at the outermost surface of
the PS film was directly measured using scanning
viscoelasticity microscopy (SVM) [35]. The Tsurf g, which is
defined as the glass transition temperature at the surface,
decreased compared to the bulk Tbulk g [40].
In this work, patterned charges were introduced onto the
ultrathin PS films (less than 10 nm) by selectively charging
with a polydimethylsiloxane (PDMS) stamp. The surface
potential decay (SPD) of the patterned charges is in situ
monitored using electric force microscopy (EFM).
Compared to traditional methods, the discharging behavior is
more sensitive to the very small-scale motion of polymer
chains, especially in the ultrathin films, and the discharging
rate is closely related to the relaxation status of the polymer
films. Hence, the relationship between relaxation dynamics
and the behavior of the charge decay is identified in
ultrathin PS films, which is also proved to be greatly different
from that of normal thin PS films. The direct observation
of charge decay behaviors in ultrathin polymer films
provides a more sensitive approach to study the relaxation and
glass transition behaviors of polymer chains, and to
quantify a series of physical properties in ultrathin films.
Methods
Materials
All materials and chemicals are commercially available and
used as received. PS (Mw = 4000) was purchased from Alfa
Aesar, and chlorobenzene was purchased from Sinopharm
Chemical Reagent Beijing Co. The single-side polished
silicon wafer (<100>) doped with phosphorus (2 ? 4 ? cm)
was purchased from Silicon Quest International.
Polydimethylsiloxane (PDMS, Sylgard 184, Dow Corning Co.)
was used to fabricate the PDMS stamp.
Fabrication of Charge Patterns
Ultrathin PS films were prepared by spin-casting PS
solution on silicon wafers. The thickness of the ultrathin PS
films was determined by changing the concentration of PS
solution in chlorobenzene and the spin-coating speed.
Charge patterns were generated on the ultrathin PS films
using an electric microcontact printing (e-?CP) technique
[37]. A micro-patterned PDMS stamp was needed to inject
charges in the specific areas on ultrathin film [36].
The schematic fabrication processes of PDMS stamps
and patterned charges were illustrated in Fig. 1. PDMS
prepolymer was poured on an optical lithographed silicon
wafer with micro-structures and cured at a temperature of
348 K for 2 h. Then, the cured PDMS polymer was peeled
off from the silicon substrate, and a 10-nm Cr adhesive
layer and 100 nm Au conductive layer was deposited on
it, forming a conductive micro-patterned PDMS stamp.
The conductive PDMS stamp was then placed in close
contact with the PS film supported on Si substrate to form
a parallel-plate capacitor. A Keithley 2400 source meter
supplied a 10 kV cm?1 electrical field between the PDMS
stamp and the silicon substrate. The charge patterns were
successfully fabricated and characterized using EFM.
SPD Measurement
All topographies and surface potential images in this study
were recorded using a Dimension Icon system (Bruker,
USA) with an in situ heater/cooler accessory. A low
relative humidity between 20% and 30% was controlled by
trial and error to ensure that the patterned charges were
stored in a stable status. The charges decay properties
Fig. 1 a Schematic illustration of the fabrication of PDMS stamps and
b the in situ monitoring of discharging behavior
were characterized in situ using EFM. A 30 ?m ? 30 ?m
area was scanned to obtain sufficient patterns for reliable
statistics. The measurements were conducted at a
constant heating rate of 2 K/min starting from the room
temperature (298 K) to the desired temperature. An
adequate waiting time of 3 min and a temperature interval
of 10 K are adopted to avoid possible measuring errors by
trial and error. The surface potential was measured, and
the histograms of the captured data were counted to get
accurate and reliable results.
Results and Discussion
Charge patterns in accord with the electrode template
are successfully fabricated as illustrated in Fig. 1b. The
ultrathin PS film is scratched to create some grooves for
the measurement of film thicknesses (Fig. 2a). As an
excellent polymer electret, PS film is able to store electric
charges for a long time. It should be noted that only the
areas contacted by the stamp can be electrically injected.
Charge patterns are successfully fabricated without any
morphological deformation, as shown in Fig. 2b. Both
positive and negative charges with uniform patterns
could be successfully injected onto the ultrathin PS
films, as shown in Fig. 2c, d. Unless otherwise specified,
negative charge patterns are chosen in the following
experiments, owing to their long life time, than positive
charge patterns at a given temperature.
The in situ surface potential images corresponding to
electric charges with time extension or against temperature
increase are recorded by EFM (Fig. 3). Accordingly, the
charge dissipation is slow at low temperature, while it is
accelerated upon the increase of temperature. At a
relatively high temperature, e.g., 358 K, the charges are mostly
Fig. 2 AFM topography images and surface potential of ultrathin PS
films obtained in a single measurement. a The scratched film for
thickness measurement. b AFM morphology of charged ultrathin PS
film. c Surface potential images of charged ultrathin PS film with
positive charge and d negative charge
dissipated in a few minutes, along with the disappearance
of surface potentials.
The charge decay behavior referring to chain relaxation
dynamics is quantitatively evaluated. As previously
demonstrated, polymer chains in the ultrathin films
begin to relax and loosen once the temperature is beyond
a threshold, which accordingly accelerates the discharging
behavior [36]. At a moderate temperature of 318 K which
may not induce local dewetting [36], typical time-lapse
isothermal SPD curves of an ultrathin PS film with the
thickness of 6 nm are summarized in Fig. 4a. The
discharging has a similar decreasing tendency with
changing the initial surface potential. The charge decay is
fast at the early stage yet tends to reach an equilibrium
state over time. The overall characteristic decay time is
estimated as tens of minutes. Notably, the discharging
behavior begins at much lower temperature (318 K)
than the bulk Tg or Tg of normal thin PS films, which
indicates that local movement of polymer chains occurs
much earlier. This phenomenon is also confirmed by
other reported researches [18, 22, 41].
The temperature dependence of the discharging behavior
is crucial to ultrathin film relaxation properties, especially
at the segmental level. The discharging behavior is closely
related to the polymer chain mobility, which are intensified
under temperature stimulation especially for ultrathin
films. Fig. 4b illustrates the isothermal SPD versus time at
different constant temperatures of 303, 308, and 318 K for
ultrathin PS film (6 nm). The inset of normalized results
shows that the charge dissipation tendencies are nearly the
same at 303, 308, and 318 K. However, as to normal thin
PS films (more than 10 nm), higher temperature leads to
sharper decay behaviors. Moderate temperatures of 328,
338, and 348 K are chosen for normal thin PS films of
20 nm, and the isothermal SPD curves over time at
different temperature are illustrated in Fig. 4c. The charge decay
behavior is accelerated under a higher temperature, which
is caused by the intensification of polymer chain mobility
under temperature stimulation.
The temperature-dependent SPD curves for ultrathin
PS films with different film thicknesses are illustrated in
Fig. 5a. The discharging behaviors are quite similar when
ultrathin PS film thickness reduces from 10 to 6 nm. Both
linear and very sharp decay tendencies are obtained when
the temperature increases from room temperature (298 K)
to 328 K. With temperature continuously increasing, the
sharp discharging behaviors tend to be gentle until
patterned charges are nearly exhausted. According to the
previous studies, the interface layer which is near the
substrate could be negligible [11, 18], while the top layer and
middle layer are regarded as the free surface layer and
bulk layer [42], respectively. Polymer chains on the top
surface layer have larger free space and higher mobility,
which is much more active and independent of the
bulkFig. 3 Surface potential images of patterned charges on ultrathin PS films with a thickness of 6 nm a with time extension under a constant
temperature of 318 K and b under different temperatures for 3 min
like layer [10, 35, 39, 43, 44]. Hence, there is fast dynamics
near the free surface compared to normal thin films and
bulk matrix [13, 23, 45, 46], and most charges dissipate
very quickly at the beginning stages. However, with the
continuous dissipation of patterned charges, a reduction
in the driving forces for the segmental relaxation could
lead to a reduced discharging behavior, which conversely
weakens the discharging behavior.
The discontinuous changes in the physical properties
are always regarded as the glass transition temperature.
For example, similar researches have proved that the
temperature at the discontinuous changing of thermal
expansivity or fluorescence intensity is regarded as the
Tg [4, 18, 22, 47?50]. The transition temperatures in
Fig. 5a are regarded as the Tg for ultrathin PS film with
different film thicknesses. However, the Tg (328 K) in
Fig. 5a is almost independent of thickness for ultrathin
PS films, when the thickness is less than 10 nm. This
result is also consistent with previously reported
researches [18]. The two-layer model also indicates that
the free surface layer (which is also regarded as
liquidlike layer) exists when the thickness is below 10 nm, and
it is independent of the overall film thickness [51].
Therefore, the film thickness of ultrathin PS films shows
nearly independent of the discharging behaviors [22].
The observation of film thickness independences of Tg
in ultrathin PS films is abnormal compared to reported
results of normal thin polymer films, including PS thin
films [4, 7, 32]. We then conduct experiments to identify
the Tg of normal thin PS films, and the results are shown
in Fig. 5b. Charge decay tendencies of normal thin PS
films are well-defined exponential curves. A slow decay
is observed at lower temperature, which is supposed to
be related to confined movement of polymer segments.
As the temperature increases, the movements of
molecular chains are intensified, resulting in a sharp decay
over the temperature range from 323 to 358 K. When
the temperature further increases above 358 K, the SPD
curves remain constant, which should be related to that
the polymer main chains completely relax and trapped
charges exhausted.
The SPD curves could be fitted as an exponential
equation, in which the surface potential is as a function
of temperature. The Tg of normal thin PS films could be
calculated by the following equation:
Where ? is the measured surface potential of the thin
PS film, ?0 is the initial surface potential (the patterned
charges), and ?r is the residual potential when the
discharging curves approaching flat. T is the applied
temperature on the PS films, and dT is the temperature
width of glass transition region. Td is the Tg that related
to film thickness, at which charge decay is fastest.
The results in Table 1 show the calculated Tg shifts
with decreasing film thickness, which are far lower than
the Tg of the bulk matrix. The Tg of bulk PS film in this
work is estimated to be 363 K using the differential
scanning calorimetry (DSC). However, when the film
thickness falls below 10 nm, the Tg remains constant
and is also far lower than the one for normal thin PS
films and bulk material.
For normal thin films, the structural relaxations, which
are associated with a variety of small dynamics, is
influenced by the interfacial and size confinement effects [22,
52]. However, it is regarded that there are only free
surface layers and bulk-like layer for ultrathin polymer films
[19], which results in weak interactions between the
polymer chains.
In order to clearly interpret the polymer chain mobility
and the discharging behavior with film thickness
decreasing, a schematic illustration is proposed as shown in Fig. 6.
The discharging of patterned charges is closely related to
the polymer chain?s mobility. The SPD tendencies are
monitored in situ using EFM, as shown in Fig. 6a?c, and
the relaxation dynamics and Tg could be estimated.
Fig. 4 Time-elapsed isothermal discharging tendencies of ultrathin and
normal thin PS films at different constant temperatures. a SPD of
ultrathin PS film (6 nm) at 318 K with different initial surface potentials.
b SPD of ultrathin PS film (6 nm) at 303, 308, and 318 K. c SPD of
normal thin PS film (20 nm) at 328, 338, and 348 K. The normalized SPD
with surface potential at 0 time as the reference is shown in the inset
Two model theories are proposed to explain the
phenomenon of the Tg depression with film thickness
reducing. It is regarded that the dead layer in the
threelayer model has almost no mobility [22]. Therefore, the
Fig. 5 Temperature-dependent SPD curves of a ultrathin PS films
with different thickness of 6, 9, and 10 nm and b normal thin PS
films with thicknesses of 21, 43, and 78 nm
shift of Tg is contributed both by surface layer (Tsurf g)
and bulk layer (Tbulk g), in which the surface layer is
thought as a region of enhanced mobility [28, 29].
Polymer chain ends at the air-polymer interface tends to
move toward the surface, which leads to the increase of
free volume and acceleration of chain mobility [30].
Therefore, the Tsurf g of surface is much lower than the
Tbulk g [38, 40]. The film thickness dependence of the
Tg is illustrated as following [18]:
Where D is the total thickness of the films and A is
the surface thickness (free surface layer) of polymer film.
Table 1 The Tg of PS films with various film thicknesses
Transition temperature (Tg/K)
Fig. 6 Diagram of patterned charges characterized polymer chains?
mobility and film thickness dependence of the Tg in thin and ultrathin
polymer films. a Initial topographic polymer film, b selectively charged
polymer film, c charges release, d, e film thickness dependent on local
relaxation dynamics of normal thin films, f and ultrathin films
Therefore, when the film thickness decreases, the
relative fraction of Tsurf g to total Tg increases and leads to an
overall decrease of Tg in normal thin PS film [30, 53], as
shown in Fig. 6d, e. However, when film thickness
continuously decreases below 10 nm, the dead layer
disappears (Fig. 6f ), the interaction between surface and bulk
layer is weak, and the free surface layer contributes mostly
to the depression of Tg. As has been reported, the
thickness of the free surface layer is assumed to be constant,
which is independent of the thickness of films [18, 22].
Thus, the Tg of ultrathin PS film keeps constant.
The employment of the charge patterns as a more
sensitive indicator to directly monitor the relaxation behavior
could be feasible and precise, since the signals can be
amplified and the transition points can be easily observed.
However, it is worth noting that there is still some
controversy about the relaxation dynamics and Tg of ultrathin
polymer films. More challenging and rigorous studies
should be conducted to quantitatively calculate the Tg of
ultrathin polymer films.
Conclusions
In summary, the relaxation properties and Tg of
ultrathin PS film are characterized by directly monitoring the
properties of the charge decay. When film thickness falls
below 10 nm, linear discharging behaviors are obtained,
and the Tg of ultrathin PS films is clearly independent of
film thickness. This phenomenon is greatly different
from that of the normal thin PS films, in which the Tg
depresses with decreasing film thickness. To sum up,
the discharging behavior of patterned charges provides a
more precise approach to directly observe the relaxation
dynamics and detect the Tg both for ultrathin and thin
PS films. These results could be beneficial for
understanding the relaxation dynamics of ultrathin polymer
films, especially when the glass transition is considered.
Abbreviations
AFM: Atomic force microscopy; DSC: Differential scanning calorimetry;
EFM: Electric force microscopy; e-?CP: Electric microcontact printing;
LFM: Lateral force microscopy; PDMS: Polydimethylsiloxane; PS: Polystyrene;
SPD: Surface potential decay; SVM: Scanning viscoelasticity microscopy; Tg: Glass
transition temperature; Tsurf g: Glass transition temperature at surface
Acknowledgements
This research was financially supported by the National Key Research and
Development Program of China (Grant No. 2016YFC0207104), the National
Natural Science Foundation of China (Grant No. 21528501, 21304107),
Science-technology Program of State Grid Corporation of
China(521700140004), the Danish National Research Foundation, and the
AUFF NOVA project.
Author?s Contributions
XQQ performed all the AFM measurement and data analysis and wrote the
manuscript. ZHL provided valuable discussions and helped with the result
analysis. LG, QL, YPW, MNZ, and MDD contributed in the analysis and
interpretation of the data. All authors read and approved the final manuscript.
1. Reiter G , Castelein G , Sommer JU , Rottele A , Thurn-Albrecht T ( 2001 ) Direct visualization of random crystallization and melting in arrays of nanometersize polymer crystals . Phys Rev Lett 87:22610
2. Wang HP , Keum JK , Hiltner A , Baer E ( 2009 ) Confined crystallization of PEO in nanolayered films impacting structure and oxygen permeability . Macromolecules 42 : 7055 - 7066
3. Kim SD , Torkelson JM ( 2002 ) Nanoscale confinement and temperature effects on associative polymers in thin films: fluorescence study of a telechelic, pyrene-labeled poly(dimethylsiloxane) . Macromolecules 35 : 5943 - 5952
4. Singh L , Ludovice PJ , Henderson CL ( 2004 ) Influence of molecular weight and film thickness on the glass transition temperature and coefficient of thermal expansion of supported ultrathin polymer films . Thin Solid Films 449 : 231 - 241
5. Kahle O , Wielsch U , Metzner H , Bauer J , Uhlig C , Zawatzki C ( 1998 ) Glass transition temperature and thermal expansion behaviour of polymer films investigated by variable temperature spectroscopic ellipsometry . Thin Solid Films 313 - 314 : 803 - 807
6. Soles CL , Douglas JF , Jones RL , Wu WL ( 2004 ) Unusual expansion and contraction in ultrathin glassy polycarbonate films . Macromolecules 37 : 2901 - 2908
7. Keddie JL , Jones RAL , Cory RA ( 1994 ) Size-dependent depression of the glass-transition temperature in polymer-films . Europhys Lett 27 : 59 - 64
8. Lin Y , Liu LP , Cheng JQ , Shangguan YG , Yu WW , Qiu BW , Zheng Q ( 2014 ) Segmental dynamics and physical aging of polystyrene/silver nanocomposites . RSC Adv 4 : 20086 - 20093
9. Pfromm PH , Koros WJ ( 1995 ) Accelerated physical ageing of thin glassy polymer films: evidence from gas transport measurements . Polymer 36 : 2379 - 2387
10. Akabori K , Tanaka K , Kajiyama T , Takahara A ( 2003 ) Anomalous surface relaxation process in polystyrene ultrathin films . Macromolecules 36 : 4937 - 4943
11. DeMaggio GB , Frieze WE , Gidley DW , Zhu M , Hristov HA , Yee AF ( 1997 ) Interface and surface effects on the glass transition in thin polystyrene films . Phys Rev Lett 78 : 1524 - 1527
12. Forrest JA , Dalnoki-Veress K ( 2001 ) The glass transition in thin polymer films . Adv Colloid Interface 94 : 167 - 196
13. Ellison CJ , Torkelson JM ( 2003 ) The distribution of glass-transition temperatures in nanoscopically confined glass formers . Nat Mater 2 : 695 - 700
14. Forrest JA , Svanberg C , Revesz K , Rodahl M , Torell LM , Kasemo B ( 1998 ) Relaxation dynamics in ultrathin polymer film . Phys Rev E 58 : R1226 - R1229
15. Nguyen HK , Prevosto D , Labardi M , Capaccioli S , Lucchesi M , Rolla P ( 2011 ) Effect of confinement on structural relaxation in ultrathin polymer films investigated by local dielectric spectroscopy . Macromolecules 44 : 6588 - 6593
16. Yoon H , McKenna GB ( 2014 ) Substrate effects on glass transition and free surface viscoelasticity of ultrathin polystyrene films . Macromolecules 47 : 8808 - 8818
17. Labahn D , Mix R , Schonhals A ( 2009 ) Dielectric relaxation of ultrathin films of supported polysulfone . Phys Rev E 79:011801
18. Miyazaki T , Nishida K , Kanaya T ( 2004 ) Thermal expansion behavior of ultrathin polymer films supported on silicon substrate . Phys Rev E 69:061803
19. Keddie JL , Jones RAL ( 1995 ) Glass transition behavior in ultrathin polystyrene films . Isr J Chem 35 : 21 - 26
20. Lu XL , Mi YL ( 2015 ) Glass transition behavior of spin-coated thin films of a hydrophilic polymer on supported substrates . Chinese J Polym Sci 33 : 607 - 612
21. Priestley RD , Ellison CJ , Broadbelt LJ , Torkelson JM ( 2005 ) Structural relaxation of polymer glasses at surfaces, interfaces, and in between. Science 309 : 456 - 459
22. Fukao K , Miyamoto Y ( 2000 ) Glass transitions and dynamics in thin polymer films: dielectric relaxation of thin films of polystyrene . Phys Rev E 61 : 1743 - 1754
23. Paeng K , Richert R , Ediger MD ( 2012 ) Molecular mobility in supported thin films of polystyrene, poly(methyl methacrylate), and poly(2-vinyl pyridine) probed by dye reorientation . Soft Matter 8 : 819 - 826
24. Hall DB , Hooker JC , Torkelson JM ( 1997 ) Ultrathin polymer films near the glass transition: effect on the distribution of relaxation times as measured by second harmonic generation . Macromolecules 30 : 667 - 669
25. Forrest JA , Dalnoki-Veress K , Stevens JR , Dutcher JR ( 1996 ) Effect of free surfaces on the glass transition temperature of thin polymer films . Phys Rev Lett 77 : 2002 - 2005
26. Ediger MD , Forrest JA ( 2014 ) Dynamics near free surfaces and the glass transition in thin polymer films: a view to the future . Macromolecules 47 : 471 - 478
27. Pu Y , Ge SR , Rafailovich M , Sokolov J , Duan Y , Pearce E , Zaitsev V , Schwarz S ( 2001 ) Surface transitions by shear modulation force microscopy . Langmuir 17 : 5865 - 5871
28. See YK , Cha J , Chang T , Ree M ( 2000 ) Glass transition temperature of poly(tert-butyl methacrylate) langmuir-blodgett film and spin-coated film by X-ray reflectivity and ellipsometry . Langmuir 16 : 2351 - 2355
29. Grohens Y , Brogly M , Labbe C , David MO , Schultz J ( 1998 ) Glass transition of stereoregular poly(methyl methacrylate) at interfaces . Langmuir 14 : 2929 - 2932
30. Kim JH , Jang J , Zin WC ( 2001 ) Thickness dependence of the glass transition temperature in thin polymer films . Langmuir 17 : 2703 - 2710
31. Dalnoki-Veress K , Forrest JA , de Gennes PG , Dutcher JR ( 2000 ) Glass transition reductions in thin freely-standing polymer films: a scaling analysis of chain confinement effects . J Phys IV 10 : 221 - 226
32. Forrest JA , Mattsson J ( 2000 ) Reductions of the glass transition temperature in thin polymer films: probing the length scale of cooperative dynamics . Phys Rev E 61 : R53 - R56
33. van Zanten JH , Wallace WE , Wu WL ( 1996 ) Effect of strongly favorable substrate interactions on the thermal properties of ultrathin polymer films . Phys Rev E 53 : R2053 - R2056
34. Angell CA ( 1991 ) Relaxation in liquids, polymers and plastic crystals-strong/fragile patterns and problems . J Non-Cryst Solids 131 : 13 - 31
35. Satomi N , Takahara A , Kajiyama T ( 1999 ) Determination of surface glass transition temperature of monodisperse polystyrene based on temperaturedependent scanning viscoelasticity microscopy . Macromolecules 32 : 4474 - 4476
36. Zhao D , Peng JX , Tang XF , Zhang DD , Qiu XH , Yang YL , Wang YP , Zhang MN , Guan L , Cao TB ( 2013 ) Charge-induced local dewetting on polymer electrets studied by atomic force microscopy . Soft Matter 9 : 9702 - 9709
37. Jacobs HO , Whitesides GM ( 2001 ) Submicrometer patterning of charge in thin-film electrets . Science 291 : 1763 - 1766
38. Kajiyama T , Kawaguchi D , Tanaka K ( 2003 ) Polymer chain diffusion at a temperature below its bulk glass transition temperature . Chinese J Polym Sci 21 : 141 - 146
39. Kawana S , Jones RAL ( 2001 ) Character of the glass transition in thin supported polymer films . Phys Rev E 63:021501
40. Tanaka K , Hashimoto K , Kajiyama T , Takahara A ( 2003 ) Visualization of active surface molecular motion in polystyrene film by scanning viscoelasticity microscopy . Langmuir 19 : 6573 - 6575
41. Hammerschmidt JA , Gladfelter WL , Haugstad G ( 1999 ) Probing polymer viscoelastic relaxations with temperature-controlled friction force microscopy . Macromolecules 32 : 3360 - 3367
42. Peng DD , Nancy Li RX , Lam CH , Tsui OKC ( 2013 ) Two-layer model description of polymer thin film dynamics . Chinese J Polym Sci 31 : 12 - 20
43. Yang Z , Clough A , Lam CH , Tsui OKC ( 2011 ) Glass transition dynamics and surface mobility of entangled polystyrene films at equilibrium . Macromolecules 44 : 8294 - 8300
44. Sasaki T , Misu M , Shimada T , Teramoto M ( 2008 ) Glass transition and its characteristic length for thin crosslinked polystyrene shells of rodlike capsules . J Polym Sci Pt B Polym Phys 46 : 2116 - 2125
45. Crider PS , Majewski MR , Zhang J , Oukris H , Israeloff NE ( 2008 ) Local dielectric spectroscopy of near-surface glassy polymer dynamics . J Chem Phys 128 : 044908
46. Mann I , Yu XF , Zhang WB , Van Horn RM , Ge JJ , Graha MJ , Harris FW , Cheng SZD ( 2011 ) What are the differences of polymer surface relaxation from the bulk ? Chinese J Polym Sci 29 : 81 - 86
47. Forrest JA , Dalnoki-Veress K , Dutcher JR ( 1997 ) Interface and chain confinement effects on the glass transition temperature of thin polymer films . Phys Rev E 56 : 5705 - 5716
48. Mattsson J , Forrest JA , Borjesson L ( 2000 ) Quantifying glass transition behavior in ultrathin free-standing polymer films . Phys Rev E 62 : 5187 - 5200
49. Keddie JL , Jones RAL , Cory RA ( 1994 ) Interface and surface effect on the glasstransition temperature in thin polymer films . Faraday Discuss 98 : 219 - 230
50. Yang Q , Chen X , He ZW , Lan FT , Liu H ( 2016 ) The glass transition temperature measurements of polyethylene: determined by using molecular dynamic method . RSC Adv 6 : 12053 - 12060
51. Pye JE , Rohald KA , Baker EA , Roth CB ( 2010 ) Physical aging in ultrathin polystyrene films: evidence of a gradient in dynamics at the free surface and its connection to the glass transition temperature reductions . Macromolecules 43 : 8296 - 8303
52. Priestley RD , Broadbelt LJ , Torkelson JM ( 2005 ) Physical aging of ultrathin polymer films above and below the bulk glass transition temperature: effects of attractive vs neutral polymer-substrate interactions measured by fluorescence . Macromolecules 38 : 654 - 657
53. Kim JH , Jang J , Zin WC ( 2000 ) Estimation of the thickness dependence of the glass transition temperature in various thin polymer films . Langmuir 16 : 4064 - 4067