Reducing substrate pinning of block copolymer microdomains with a buffer layer of polymer brushes

被引:106
作者
Harrison, C [1 ]
Chaikin, PM
Huse, DA
Register, RA
Adamson, DH
Daniel, A
Huang, E
Mansky, P
Russell, TP
Hawker, CJ
Egolf, DA
Melnikov, IV
Bodenschatz, E
机构
[1] Princeton Univ, Dept Phys, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
[3] Princeton Univ, Princeton Mat Inst, Princeton, NJ 08544 USA
[4] Univ Massachusetts, Dept Polymer Sci & Engn, Silvio O Conte Natl Ctr Polymer Res, Amherst, MA 01003 USA
[5] IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
[6] Cornell Univ, Atom & Solid State Phys Lab, Ithaca, NY 14853 USA
关键词
D O I
10.1021/ma991551g
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 study the range of orientational order of a single layer of cylindrical block copolymer microdomains annealed on several types of substrate. The orientational persistence length or nematic correlation length (xi) is evaluated using recently developed imaging and analysis methods to measure the grain size of the block copolymer microdomains. We show that the substrate can lower xi for block copolymers with a majority component that interacts strongly with the substrate, but this can be mitigated by attaching a buffer layer of polystyrene brushes to the substrate. In addition, we show that, for a block copolymer where the block that strongly interacts with the substrate is the minority component, the microdomain correlation length does not increase when substrates are treated with this buffer layer. We suggest that in this case the brushes do not increase xi not only because of the lower volume fraction of the strongly interacting component but also because there are block copolymer wetting layers at the free and substrate interfaces that decouple the microdomains from the substrate in a similar manner as the polystyrene brushes.
引用
收藏
页码:857 / 865
页数:9
相关论文
共 37 条
  • [1] AHAGON A, 1975, J POLYM SCI POL PHYS, V13, P1285, DOI 10.1002/pol.1975.180130703
  • [2] QUASI-STATIC MECHANICAL-PROPERTIES OF LAMELLAR BLOCK COPOLYMER MICROSTRUCTURE
    AMUNDSON, K
    HELFAND, E
    [J]. MACROMOLECULES, 1993, 26 (06) : 1324 - 1332
  • [3] ANNIS BK, 1992, MAKROMOL CHEM, V193, P2589
  • [4] RELATIONSHIP BETWEEN BIREFRINGENCE AND THE STRUCTURE OF ORDERED BLOCK COPOLYMER MATERIALS
    BALSARA, NP
    GARETZ, BA
    DAI, HJ
    [J]. MACROMOLECULES, 1992, 25 (22) : 6072 - 6074
  • [5] BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT
    BATES, FS
    FREDRICKSON, GH
    [J]. ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) : 525 - 557
  • [6] Chandrasekhar S., 1992, LIQUID CRYSTALS
  • [7] The use of force modulation microscopy to investigate block copolymer morphology
    Chen, JT
    Thomas, EL
    [J]. JOURNAL OF MATERIALS SCIENCE, 1996, 31 (10) : 2531 - 2538
  • [8] INTERFERENCE MICROSCOPY ON THIN DIBLOCK COPOLYMER FILMS
    COULON, G
    AUSSERRE, D
    RUSSELL, TP
    [J]. JOURNAL DE PHYSIQUE, 1990, 51 (08): : 777 - 786
  • [9] Grain growth and defect annihilation in block copolymers
    Dai, HJ
    Balsara, NP
    Garetz, BA
    Newstein, MC
    [J]. PHYSICAL REVIEW LETTERS, 1996, 77 (17) : 3677 - 3680
  • [10] Importance of local pattern properties in spiral defect chaos
    Egolf, DA
    Melnikov, IV
    Bodenschatz, E
    [J]. PHYSICAL REVIEW LETTERS, 1998, 80 (15) : 3228 - 3231