A morphology map based on phase evolution in polymer blend films

被引:32
作者
Chung, HJ
Wang, H
Composto, RJ [1 ]
机构
[1] Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[2] Univ Penn, Res Struct Matter Lab, Philadelphia, PA 19104 USA
[3] Michigan Technol Univ, Dept Mat Sci & Engn, Houghton, MI 49931 USA
关键词
D O I
10.1021/ma051513z
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 present a novel morphology map based on pattern development mechanisms in polymer blend films. Six distinct mechanism are found for poly(methyl methacrylate) (PMMA): poly (styrene-ran-acrylonitrile) (SAN) films for thickness values and bulk compositions between 50-1000 nm and phi 5(PMMA) = 0.3-0.8, respectively. In regime A (phi(PMMA) = 0.3), PMMA is completely depleted from the midlayer by preferential wetting, resulting in a stable PMMA/SAN/PMMA trilayer. With increasing phi(PMMA) (0.4-0.7), pattern development is driven by phase separation in the midlayer, which produces circular domains, irregular domains, and bicontinuous patterns denoted as regimes B, C, and D, respectively. Here, shape factors are used for the first time to quantitatively distinguish these regimes. In regime E (phi(PMMA) = 0.8), the SAN phase is the minority component in the midlayer and breaks up into droplets in a smooth PMMA film. In regime F (phi(PMMA) = 0.4 or 0.5; d < 80 nm), films initially develop a trilayer structure, which then ruptures upon dewetting of the SAN midlayer. Trilayer stability is analyzed using a free energy model that attributes dewetting to capillary fluctuations at the PMMA/SAN interface. This study of pattern development mechanisms will serve as a guideline to control morphology shape and feature size, which are both critical design parameters for technological applications such as organic devices and membranes.
引用
收藏
页码:153 / 161
页数:9
相关论文
共 61 条
[1]   Phase segregation in polymer thin films: Elucidations by X-ray and scanning force microscopy [J].
Ade, H ;
Winesett, DA ;
Smith, AP ;
Qu, S ;
Ge, S ;
Sokolov, J ;
Rafailovich, M .
EUROPHYSICS LETTERS, 1999, 45 (04) :526-532
[2]   Surface topography and composition of deuterated polystyrene-poly(bromostyrene) blends [J].
Affrossman, S ;
Henn, G ;
ONeill, SA ;
Pethrick, RA ;
Stamm, M .
MACROMOLECULES, 1996, 29 (14) :5010-5016
[3]   Interactions of nanoscopic particles with phase-separating polymeric mixtures [J].
Balazs, AC .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1999, 4 (06) :443-448
[4]  
Binder K, 1999, ADV POLYM SCI, V138, P1
[5]  
BINDER K, 1974, PHYS REV LETT, V33, P1006, DOI 10.1103/PhysRevLett.33.1006
[6]   MOTIONS OF DROPLETS ON HYDROPHOBIC MODEL SURFACES INDUCED BY THERMAL-GRADIENTS [J].
BRZOSKA, JB ;
BROCHARDWYART, F ;
RONDELEZ, F .
LANGMUIR, 1993, 9 (08) :2220-2224
[7]   Polymer electronics: the skill lies in the blending [J].
Cacialli, F ;
Stoneham, M .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2002, 14 (47) :V9-V11
[8]   Correlating structure with fluorescence emission in phase-separated conjugated-polymer blends [J].
Chappell, J ;
Lidzey, DG ;
Jukes, PC ;
Higgins, AM ;
Thompson, RL ;
O'Connor, S ;
Grizzi, I ;
Fletcher, R ;
O'Brien, J ;
Geoghegan, M ;
Jones, RAL .
NATURE MATERIALS, 2003, 2 (09) :616-621
[9]   Lattice Boltzmann study of spinodal decomposition in two dimensions [J].
Chin, J ;
Coveney, PV .
PHYSICAL REVIEW E, 2002, 66 (01) :1-016303
[10]   High-stability ultrathin spin-on benzocyclobutene gate dielectric for polymer field-effect transistors [J].
Chua, LL ;
Ho, PKH ;
Sirringhaus, H ;
Friend, RH .
APPLIED PHYSICS LETTERS, 2004, 84 (17) :3400-3402