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相关论文: Slow dynamics near glass transitions in thin polym…

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The glass transition temperature $T_{\rm g}$ and the temperature $T_{\alpha}$ corresponding to the peak in the dielectric loss due to the $\alpha$-process have been simultaneously determined as functions of film thickness d through…

软凝聚态物质 · 物理学 2009-10-31 Koji Fukao , Yoshihisa Miyamoto

The glass transition temperature $T_g$ and the temperature $T_{\alpha}$ corresponding to the peak in the dielectric loss due to the $\alpha$-process have been simultaneously determined as functions of film thickness $d$ through dielectric…

软凝聚态物质 · 物理学 2009-10-31 Koji Fukao , Yoshihisa Miyamoto

Dielectric relaxation and thermal expansion spectroscopy were made for thin polystyrene films in order to measure the temperature $T_{\alpha}$ corresponding to the peak in the loss component of susceptibility due to the $\alpha$-process and…

软凝聚态物质 · 物理学 2007-05-23 Koji Fukao , Yoshihisa Miyamoto

Dynamics of thin films of poly(vinyl acetate) (PVAc) and poly(methyl methacrylate) (PMMA) have been investigated by dielectric relaxation spectroscopy in the frequency range from 0.1Hz to 1MHz at temperatures from 263K to 423K. The…

软凝聚态物质 · 物理学 2009-11-07 Koji Fukao , Shinobu Uno , Yoshihisa Miyamoto , Akitaka Hoshino , Hideki Miyaji

Glass transition process gets affected in ultrathin films having thickness comparable to the size of the molecules. We observe systematic broadening of glass transition temperature (Tg) as the thickness of the polymer film reduces below the…

软凝聚态物质 · 物理学 2009-11-11 M. Bhattacharya , M. K. Sanyal , Th. Geue , U. Pietsch

We investigate the relaxation behavior of thin films of a polyamide random copolymer, PA66/6I, with various film thicknesses using dielectric relaxation spectroscopy. Two dielectric signals are observed at high temperatures, the…

软凝聚态物质 · 物理学 2015-06-11 Natsumi Taniguchi , Koji Fukao , Paul Sotta , Didier R. Long

The glass transition temperature and its connection to statistical properties of confined and free-standing polymer films of varying thickness containing unentangled to highly entangled bead-spring chains are studied by molecular dynamics…

软凝聚态物质 · 物理学 2023-09-21 Hsiao-Ping Hsu , Kurt Kremer

The glass transition temperature and relaxation dynamics of the segmental motions of thin films of polystyrene labeled with a dye, 4-[N-ethyl-N-(hydroxyethyl)]amino-4-nitraozobenzene (Disperse Red 1, DR1) are investigated using dielectric…

软凝聚态物质 · 物理学 2009-11-13 Rodney D. Priestley , Linda J. Broadbelt , John M. Torkelson , Koji Fukao

We present a study of orientational relaxation dynamics in thin films of a low-molecular-weight glass-former as a function of temperature and film thickness. The relaxation is probed by second-harmonic generation after release of a poling…

软凝聚态物质 · 物理学 2009-11-10 Elio Cecchetto , Daniele Moroni , Blandine Jerome

Recent experiments have demonstrated that the glass transition temperature of thin polymer films can be shifted as compared to the same polymer in the bulk, the amplitude and the sign of this effect depending on the interaction between the…

统计力学 · 物理学 2007-05-23 D. Long , P. Sotta

A simple and predictive model is put forward explaining the experimentally observed substantial shift of the glass transition temperature, Tg, of sufficiently thin polymer films. It focuses on the limit of small molecular weight, where…

软凝聚态物质 · 物理学 2009-11-07 Stephan Herminghaus , Karin Jacobs , Ralf Seemann

We present results of molecular dynamics (MD) simulations for a non-entangled polymer melt confined between two completely smooth and repulsive walls, interacting with inner particles via the potential $U_{\rm wall}\myeq (\sigma/z)^9$,…

软凝聚态物质 · 物理学 2009-11-07 F. Varnik , J. Baschnagel , K. Binder

We measure the isothermal rejuvenation of stable glass films of poly(styrene) and poly(methylmethacrylate). We demonstrate that the propagation of the front responsible for the transformation to a supercooled-liquid state can serve as a…

软凝聚态物质 · 物理学 2023-12-12 Saba Karimi , Junjie Yin , Thomas Salez , James A Forrest

Describing the dynamics and thermodynamics of amorphous materials near the glass transition is a major challenge in soft-matter physics and polymer engineering. Here, we show that the dependence of the dielectric alpha-relaxation time on…

软凝聚态物质 · 物理学 2025-04-28 Valeriy V. Ginzburg , Oleg V. Gendelman , Riccardo Casalini , Alessio Zaccone

We have investigated the reduction of the glass transition temperature, $T_g$, for thin supported films of particularly small molecular weight ($M_W$ = 2 kg/mol) polystyrene, and found good agreement with earlier studies on larger…

软凝聚态物质 · 物理学 2009-09-25 Ralf Seemann , Karin Jacobs , Stephan Herminghaus

The glass transition temperature ($T_g$) of polymer thin films has been a subject of controversy in the last two decades. (Pseudo)thermodynamic determinations of $T_g$ generally suggest a significant depression, whereas the molecular…

软凝聚态物质 · 物理学 2011-08-02 V. M. Boucher , D. Cangialosi , A. Alegría , J. Colmenero

In an earlier preprint (V. V. Ginzburg, O. V. Gendelman, R. Casalini, and A. Zaccone, arxiv:2409.17291), we demonstrated that the dynamic (relaxation time) and volume equations of state for many amorphous polymers are near-universal -- each…

软凝聚态物质 · 物理学 2025-01-03 Valeriy V. Ginzburg , Oleg V. Gendelman , Riccardo Casalini , Alessio Zaccone

The molecular mobility of glassy and supercooled liquid states of clotrimazole is studied using broadband dielectric spectroscopy for a wide range of temperatures and frequency. The dielectric loss data of clotrimazole below T$_{g}$, do not…

软凝聚态物质 · 物理学 2016-09-12 N S K Kumar , G Govindaraj , U Sailaja

In stark contrast with the conventional understanding of the glass transition, where the transition from glass to liquid appears as a dynamic process where atoms/molecules cooperatively relax into the equilibrium phase, we experimentally…

The viscoelastic properties of thin polymeric films represent a central issue, especially for nanotechnological applications. In particular, it is highly relevant the dependence of viscoelasticity on the temperature. For polystyrene it is…

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