Molecular Dynamics in 1-and 2-D Confinement as Studied for the Case of Poly(Cis-1,4-Isoprene)

被引:12
|
作者
Mapesa, Emmanuel Urandu [1 ]
Popp, Ludwig [1 ]
Kipnusu, Wycliffe Kiprop [1 ]
Tress, Martin [1 ]
Kremer, Friedrich [1 ]
机构
[1] Univ Leipzig, Inst Expt Phys 1, Mol Phys Grp, D-04103 Leipzig, Germany
关键词
Anodic Aluminum Oxide (AAO); Broadband Dielectric Spectroscopy (BDS); Dynamic glass transition; Nanostructured electrodes; Normal mode; Poly(cis-1; 4-isoprene)(PI); Segmental mode; Terminal subchains (TSC); GLASS-TRANSITION MEASUREMENTS; THIN POLYMER LAYERS; AC-CHIP CALORIMETER; DIELECTRIC-SPECTROSCOPY; LENGTH SCALE; TEMPERATURE-DEPENDENCE; CIS-POLYISOPRENE; RELAXATION DATA; T-G; FILMS;
D O I
10.1080/1539445X.2014.928320
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Broadband Dielectric Spectroscopy (BDS) is used to probe the molecular dynamics of Type A polymer, poly(cis-1,4-isoprene), when confined in the 1-dimensional (1D) exploring space of thin layers and the 2-dimensional (2D) constraining geometry of unidirectional anodic aluminum oxide (AAO) nanopores. For both cases, it was observed that the structural relaxation remains bulk-like in its mean relaxation rate, although the distribution of its relaxation times is broadened in 2D confinement. Furthermore, the fluctuation of the end-to-end vector is interrupted, with the 1D case being relatively less pronounced. By this clear-cut comparison, it is demonstrated that the effects of confinement on molecular dynamics depend, inter alia, on the dimensionality of the restricting space.
引用
收藏
页码:S22 / S30
页数:9
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