Mechanism of Density Evolution of Polystyrene Adsorbed Layers on the Substrate

被引:1
作者
Bai, Lu [1 ]
Jiang, Zhenwei [1 ]
Fan, Liang [1 ]
Zhou, Xianjing [1 ]
Xu, Jianquan [1 ]
Tan, Junjun [2 ]
Wei, Feng [3 ]
Ye, Shuji [2 ]
Wang, Xinping [1 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Chem & Chem Engn, Key Lab Surface & Interface Sci Polymer Mat Zhejia, Hangzhou 310018, Peoples R China
[2] Univ Sci & Technol China, Dept Chem Phys, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[3] Jianghan Univ, Inst Interdisciplinary Res, Sch Optoelect Mat & Technol, Wuhan 430056, Peoples R China
基金
中国国家自然科学基金;
关键词
THIN POLYMER-FILMS; IRREVERSIBLE ADSORPTION; GLASS-TRANSITION; DYNAMICS; CHAIN; SURFACE; SUPPRESSION; GRAPHITE; RIGIDITY; ADHESION;
D O I
10.1021/acsmacrolett.4c00470
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The density evolution of polystyrene (PS) adsorbed layers on phenyl-modified SiO2-Si substrates was investigated. The thickness and density of flattened layer on substrates with above 75% phenyl content increased over annealing time and could approach 4.7 nm and 1.37 g/cm3 at equilibrium, respectively, which were much higher than those on SiO2-Si. The annealing time for flattened chains to reach equilibrium increased with an increasing phenyl content on the substrate. The interface sensitive sum frequency generation vibrational spectroscopy (SFG) technique revealed that both the amount and the strength of the interfacial pi-pi interaction between the phenyl groups of substrates and in PS chains increased with annealing time. This resulted in more stretched chains perpendicularly, leading to a denser and thicker adsorbed layer with a closest-packing structure, driven by favorable enthalpy processes. Our work provides important insight into the densification mechanism of adsorbed flattened layers.
引用
收藏
页码:1539 / 1544
页数:6
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