Glass Transition Temperature Of Ultrathin Polymer Films On Silicon

1995 ◽  
Vol 381 ◽  
Author(s):  
Wen-Li Wu ◽  
William E Wallace ◽  
John Van Zanten

AbstractThe glass transition temperature, Tg, of polystyrene (PS) thin films on silicon wafers with different surface preparations was determined in order to explore the effect of interfacial interaction energy on local chain dynamics. To enhance interface behavior, the film thickness included in this work was as low as 50 Å. PS with monodisperse molecular weights was chosen as a model polymer. Two different silicon surfaces were prepared: sulfuric acid-clean and hydrogen passivated. Tg of thin films was determined by monitoring the film thickness as a function of temperature. Tgwas identified as the temperature where the thermal expansion coefficient underwent an abrupt change. X-ray reflectivity was used to determine film thickness with a precision of a few angstroms. Tg of PS was found to depend strongly on the initial film thickness, as well as the substrate surface.

2014 ◽  
Vol 70 (a1) ◽  
pp. C885-C885
Author(s):  
Krassimir Stoev ◽  
Kenji Sakurai

The glass transition takes place in amorphous materials (like polymers) during heating or cooling, and can be described as reversible transition from a hard and brittle state into a rubber-like state. Although physical properties of the material change significantly during the glass transition, this is not a phase transition of the material. The temperature at which the transition between the glassy and rubbery state occurs is called the glass transition temperature, and this temperature is always lower than the melting temperature. Thermodynamically, the glass transition is associated with transfer of heat between the system and its surrounding and with an abrupt volume change. Previously it was shown that the glass transition temperature of nano-films is different from that of bulk materials [1], which signifies the importance of determining this parameter for such systems. In the current work, we use quick X-ray reflectivity (qXRR) measurements to determine the glass transition temperature of polyvinyl acetate (PVAc). PVAc is rubbery synthetic polymer with the formula (C4H6O2), a density of 1.18 g/cm3, and a glass transition temperature for bulk material of 30oC [2]. Regular X-ray reflectivity measurements are based on θ/2θ scans at grazing incidence and typically require 0.5-1.5 h for a single scan. The qXRR technique is based on simultaneous measurement of the whole angular x-ray reflectivity profile and is suitable for in-situ measurement without moving the sample and/or the x-ray optics. Thus, the qXRR technique allows for very fast measurement of the x-ray reflectivity curves (duration of each scan is typically 0.1–20 sec [3]), which permits studying the time evolution of chemical, thermal, and mechanical changes at the surface and interface of different materials. X-ray reflectivity measurements give information about both density and thickness of thin films, and are suitable for studying glass transition phenomena. Nano-thickness PVAc layers on a Si substrate were examined with the qXRR technique, with x-ray reflectivity scans (each 10-seconds in duration) being recorded while temperature was changed from 20 to 50oC (total of 331 scans over 7 hours and 46 minutes). In the current paper, the experimental setup, the data-processing, and the analysis of the results from the qXRR measurements will be presented.


2011 ◽  
Vol 287-290 ◽  
pp. 2234-2239 ◽  
Author(s):  
Sil Ro Jin ◽  
Jong Keun Lee

The effects of the polyhedral oligomeric silsequioxanes (POSS) in stacked poly(methyl methacrylate) (PMMA) film samples were investigated in two different film thicknesses, ~50 and ~660 nm. The types of the POSS include methacryl-, octaisobutyl-, and octasilane-POSS. The glass transition temperature (Tg) and isothermal physical aging was depressed by the reduction of film thickness. Among POSS molecules used in this work, methacryl-POSS was the greatest effect in both Tgand relaxation enthalpy (DHRelax) due to the physical aging. The Kohlrausch-Williams-Watts (KWW) relaxation function was used to further understand the effect of POSS and film thickness on the physical aging.


2007 ◽  
Vol 40 (22) ◽  
pp. 7755-7757 ◽  
Author(s):  
Jong-Young Lee ◽  
Kristin E. Su ◽  
Edwin P. Chan ◽  
Qingling Zhang ◽  
Todd Emrick ◽  
...  

Polymer ◽  
2010 ◽  
Vol 51 (1) ◽  
pp. 129-135 ◽  
Author(s):  
M. Erber ◽  
A. Khalyavina ◽  
K.-J. Eichhorn ◽  
B.I. Voit

2017 ◽  
Vol 40 (1) ◽  
Author(s):  
Marceau Hénot ◽  
Alexis Chennevière ◽  
Eric Drockenmuller ◽  
Kenneth Shull ◽  
Liliane Léger ◽  
...  

2006 ◽  
Vol 977 ◽  
Author(s):  
Rahmi Ozisik ◽  
Tong Liu ◽  
Richard W. Siegel

AbstractGlass transition temperature of polyetherimide (PEI) thin films and nanoporous PEI samples was investigated using differential scanning calorimetry. In both of these systems, the glass transition temperature decreased with respect to the bulk value. In the nanoporous system, scanning electron microscope images were used to characterize pore size distribution, and Monte Carlo simulations were performed to calculate the nearest neighbor pore-to-pore distances. Pore-to-pore distances and thin film thickness values were used to establish a quantitative analogy between thin films and nanoporous system.


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