Block copolymers under cylindrical confinement

被引:268
作者
Xiang, HQ [1 ]
Shin, K [1 ]
Kim, T [1 ]
Moon, SI [1 ]
McCarthy, TJ [1 ]
Russell, TP [1 ]
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
关键词
D O I
10.1021/ma049299m
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Microphase-separated block copolymers were introduced as melts into nanoscopic cylindrical pores in alumina membranes via capillary action. The geometric confinement of both lamellar and cylindrical microdomain morphologies of styrene/butadiene block copolymers, PS-b-PBD, was investigated by transmission electron microscopy. Well-developed microphase-separated structures were formed within the resulting nanorods. Polymers that exhibit cylindrical microdomains in the bulk orient with cylindrical microdomains along the nanorod axis due to the preferential segregation of the PBD block to the walls of the pores. The period and packing of the microdomains differ from those observed in the bulk due to an incommensurability between the pore geometry and the natural period and hexagonal packing of the copolymer microdomains. With polymers exhibiting bulk lamellar morphology, confinement forces the formation of concentric cylinders oriented along the nanorod axis. The number of concentric cylinders depends on the ratio of the nanorod diameter to the equilibrium period of the copolymer. Because of the preferential segregation of PBD at the alumina. surface, either PBD or PS can form the central core. These results indicate a method by which copolymer microdomains can be manipulated in a simple manner for the fabrication of isolated nanostructures.
引用
收藏
页码:5660 / 5664
页数:5
相关论文
共 26 条
[1]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[2]   ORDERING OF BLOCK-COPOLYMER MELTS IN CONFINED GEOMETRY [J].
BROWN, G ;
CHAKRABARTI, A .
JOURNAL OF CHEMICAL PHYSICS, 1995, 102 (03) :1440-1448
[3]   Morphology of ultrathin supported diblock copolymer films: Theory and experiment [J].
Fasolka, MJ ;
Banerjee, P ;
Mayes, AM ;
Pickett, G ;
Balazs, AC .
MACROMOLECULES, 2000, 33 (15) :5702-5712
[4]   Phase separation in confined systems [J].
Gelb, LD ;
Gubbins, KE ;
Radhakrishnan, R ;
Sliwinska-Bartkowiak, M .
REPORTS ON PROGRESS IN PHYSICS, 1999, 62 (12) :1573-1659
[5]   Self-assembly of the symmetric diblock copolymer in a confined state: Monte Carlo simulation [J].
He, XH ;
Song, M ;
Liang, HJ ;
Pan, CY .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (23) :10510-10513
[6]   Asymmetric block copolymers confined in a thin film [J].
Huinink, HP ;
Brokken-Zijp, JCM ;
van Dijk, MA ;
Sevink, GJA .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (05) :2452-2462
[7]   Observed surface energy effects in confined diblock copolymers [J].
Kellogg, GJ ;
Walton, DG ;
Mayes, AM ;
Lambooy, P ;
Russell, TP ;
Gallagher, PD ;
Satija, SK .
PHYSICAL REVIEW LETTERS, 1996, 76 (14) :2503-2506
[8]   MONTE-CARLO STUDY OF THIN-FILMS OF THE SYMMETRICAL DIBLOCK-COPOLYMER MELT [J].
KIKUCHI, M ;
BINDER, K .
EUROPHYSICS LETTERS, 1993, 21 (04) :427-432
[9]   POLYMER MICROSTRUCTURES FORMED BY MOLDING IN CAPILLARIES [J].
KIM, E ;
XIA, YN ;
WHITESIDES, GM .
NATURE, 1995, 376 (6541) :581-584
[10]   Phase behavior in thin films of cylinder-forming block copolymers [J].
Knoll, A ;
Horvat, A ;
Lyakhova, KS ;
Krausch, G ;
Sevink, GJA ;
Zvelindovsky, AV ;
Magerle, R .
PHYSICAL REVIEW LETTERS, 2002, 89 (03) :355011-355014