Regular patterned surfaces from core-shell particles. Preparation and characterization

被引:19
作者
Synytska, Alla
Ionov, Leonid
Dutschk, Victoria
Minko, Sergiy
Eichhorn, Klaus-Jochen
Stamm, Manfred
Grundke, Karina
机构
[1] Dresden eV, Leibniz Inst Polymer Res, D-01069 Dresden, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[3] Clarkson Univ, Dept Chem, Potsdam, NY 13699 USA
来源
Characterization of Polymer Surfaces and Thin FIlms | 2006年 / 132卷
关键词
core-shell particles; modification; patterned surfaces; roughness; wettability;
D O I
10.1007/2882_037
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A simple route for fabrication of regularly patterned surfaces with specifically designed surface roughness and chemistry is reported using colloidal particles. The surface was built up from self-assembled submicrometer- and micrometer-sized monodisperse core-shell particles of different radius (0.1-10 mu m) forming ordered arrays. In this way, an increase in the vertical roughness is achieved with increasing particle radius, but without changing the Wenzel roughness factor. The morphology of the ordered particle arrays was characterized using an optical imaging method (MicroGlider), scanning force (SFM) and scanning electron (SEM) microscopy. The organic shell was either prepared by covalent grafting of polymer brushes or by chemisorption of a silane with a long fluoroalkyl tail. From FTIR-ATR, diffuse reflection IR spectroscopy, and capillary penetration experiments, it was concluded that the grafted polymer completely covers the surface of the silica particles. The solid surface tension of the organic shell obtained from contact angle measurements on smooth surfaces decreased in the following order: polystyrene brush-PS (gamma(sv) = 28.9 mJ/m(2)) > copolymer of polystyrene and 2,3,4,5,6-pentafluoropolystyrene brush-FPS (gamma(sv) = 24.3 mJ/m(2)) > chemisorbed (tridecafluoro-1, 1,2,2-tetrahydrooctyl) dimethylchlorosilane-FSI (gamma(sv) = 18.3 mJ/m(2)). Water contact angle measurements revealed an influence of the surface height roughness and the shell chemistry on the wettability. For all surfaces investigated, the contact angle hysteresis increased on the rough model surfaces compared to the smooth surfaces due to the increase of the advancing contact angle and the decrease of the receding angle. The lower the surface free energy of the shell chemistry, the smaller is the contact angle hysteresis on the closely packed surface arrays. Further the contact angles varied with increasing height roughness. A possible explanation for this behaviour is that the vertical roughness influences the curvature radius of the liquid in trapped air pockets at the solid-liquid interface as was already assumed in the literature for nanostructured metal surfaces and paraffin-coated steel balls.
引用
收藏
页码:72 / 81
页数:10
相关论文
共 44 条
[1]   SURFACE ROUGHNESS AS RELATED TO HYSTERESIS OF CONTACT ANGLES .1. THE SYSTEM PARAFFIN WATER AIR [J].
BARTELL, FE ;
SHEPARD, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1953, 57 (02) :211-215
[2]   Purity of the sacred lotus, or escape from contamination in biological surfaces [J].
Barthlott, W ;
Neinhuis, C .
PLANTA, 1997, 202 (01) :1-8
[3]   Rough wetting [J].
Bico, J ;
Tordeux, C ;
Quéré, D .
EUROPHYSICS LETTERS, 2001, 55 (02) :214-220
[4]   CONTACT ANGLES [J].
CASSIE, ABD .
DISCUSSIONS OF THE FARADAY SOCIETY, 1948, 3 :11-16
[5]   Ultrahydrophobic and ultralyophobic surfaces:: Some comments and examples [J].
Chen, W ;
Fadeev, AY ;
Hsieh, MC ;
Öner, D ;
Youngblood, J ;
McCarthy, TJ .
LANGMUIR, 1999, 15 (10) :3395-3399
[6]   Super-repellent composite fluoropolymer surfaces [J].
Coulson, SR ;
Woodward, I ;
Badyal, JPS ;
Brewer, SA ;
Willis, C .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (37) :8836-8840
[7]  
DAEHWAN J, 2002, LANGMUIR, V18, P6133
[8]  
Dettre R. H., 1964, ADV CHEM SER, V43, P136, DOI [10.1021/ba-1964-0043.ch008, DOI 10.1021/BA-1964-0043.CH008]
[9]   Ordered Arrays of large latex particles organized by vertical deposition [J].
Goldenberg, LM ;
Wagner, J ;
Stumpe, J ;
Paulke, BR ;
Görnitz, E .
LANGMUIR, 2002, 18 (08) :3319-3323
[10]   On the determination of the surface energetics of porous polymer materials [J].
Grundke, K ;
Augsburg, A .
JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY, 2000, 14 (05) :765-775