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Optimizing the Grafting Density of Tethered Chains to Alter the Local Glass Transition Temperature of Polystyrene near Silica Substrates: The Advantage of Mushrooms over Brushes
被引:41
|作者:
Huang, Xinru
[1
]
Roth, Connie B.
[1
]
机构:
[1] Emory Univ, Dept Phys, Atlanta, GA 30322 USA
基金:
美国国家科学基金会;
关键词:
MOLECULAR-WEIGHT DEPENDENCE;
POLYMER NANOCOMPOSITES;
SURFACE DYNAMICS;
FILMS;
HOMOPOLYMER;
BEHAVIOR;
D O I:
10.1021/acsmacrolett.8b00019
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
We measured the local glass transition temperature T-g(z) of polystyrene (PS) as a function of distance z from a silica substrate with end-grafted chains using fluorescence, where competing effects from the free surface have been avoided to focus only on the influence of the tethered interface. The local T-g(z) increase next to the chain grafted substrate is found to exhibit a maximum increase of 49 +/- 2 K relative to bulk at an optimum grafting density that corresponds to the mushroom-to-brush transition regime. This perturbation to the local T-g(z) dynamics of the matrix is observed to persist out to a distance z approximate to 100-125 nm for this optimum grafting density before bulk Tg is recovered, a distance comparable to that previously observed by Baglay and Roth [J. Chem. Phys. 2017, 146, 203307] for PS next to the higher-T-g polymer polysulfone.
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页码:269 / 274
页数:11
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