Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-18T04:46:26.535Z Has data issue: false hasContentIssue false

Behavior of Block Copolymers in Thin Films

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

The uses of polymeric materials in today's world are vast. Polymers are finding applications in the microelectronics industry as dielectric insulators and photoresists, in the aerospace and automobile industry as lightweight substitutes for metals, and in biotechnology as replacement components for bone, heart, and other organs. These are just a few of the many end uses of polymers.

Often, a polymer may have a particular, desirable property but processing of the polymer is difficult or the polymer's surface characteristics are undesirable. To circumvent such shortcomings there are several options. The first is to synthesize a new material, which is quite costly and time consuming. Alternatively, two polymers with complimentary properties can be mixed. Unfortunately, most polymer pairs are immiscible unless there are specific interactions (e.g., hydrogen bonding) between the two components. Consequently, coarse phase separation is often observed, leading to an ill-defined material. Finally, two chemically distinct homopolymers can be joined together at one point, forming a block copolymer. While phase separation may occur, the scale of the domains is restricted to the sizes of the individual homopolymers, which is typically on the tens of nanometers scale. The added advantage of this approach is that the size of the different blocks can be altered, varying the concentration of the different components. For copolymers that “microphase” separate, this variation in composition leads to a variation of the morphology of the microdomains ranging from spherical to cylindrical to lamellar.

Type
Technical Features
Copyright
Copyright © Materials Research Society 1989

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Green, P.F., Palmstrom, C.J., Mayer, J.W., and Kramer, E.J., Macromolecules 18 (1985) p. 501.CrossRefGoogle Scholar
2.Mills, P.J., Green, P.F., Palmstrom, C.J., Mayer, J.W., and Kramer, E.J., Appl. Phys. Lett. 45 (1984) p. 9.CrossRefGoogle Scholar
3.Schmitt, R.L., Gardella, J.A., Magill, J.H., Salvati, L., and Chin, R.L., Macromolecules 18 (1985) p. 2675.CrossRefGoogle Scholar
4.Thomas, H.R. and O'Malley, J.J., Macromolecules 12 (1979) p. 323.CrossRefGoogle Scholar
5.Hasegawa, H. and Hashimoto, T., Macromolecules 18 (1988) p. 589.CrossRefGoogle Scholar
6.Henkee, C.S., Thomas, E.L., and Fetters, L.J., J. Mat. Sci. 23 (1988) p. 1685.CrossRefGoogle Scholar
7.Coulon, G., Russell, T.P., Deline, V.R., and Green, P.F., Macromolecules, 22 (1989) p. 2581.CrossRefGoogle Scholar
8.Russell, T.P., Coulon, G., Deline, V.R., and Miller, D.C., Macromolecules, in press.Google Scholar
9.Whitlow, S.J. and Wool, R.P., Macromolecules, 22 (1989) p. 2648.CrossRefGoogle Scholar
10.Valenty, S.J., Chera, J.J., Olson, D.R., Webb, K.K., Smith, G.A., and Katz, W., J. Am. Chem. Soc. 106 (1984) p. 6155.CrossRefGoogle Scholar
11.Sinko, S.J., Bryan, S.R., Griffis, D.P., Murray, R.W., and Linton, R.W., Anal. Chem. 57 (1985) p. 1198.CrossRefGoogle Scholar
12.Goldblatt, R., Scilla, G., Park, J., Johnson, J.F., and Huang, S.J., J. Appl. Polym. Sci. 35 (1988) p. 2075.CrossRefGoogle Scholar
13.Scilla, G., unpublished results.Google Scholar
14.Vanzo, E.J., J. Polym. Sci. A-4 (1966) p. 1727.CrossRefGoogle Scholar
15.Bradford, E.B. and Vanzo, E.J., J. Polym. Sci., Polym. Chem. Ed. A1-6 (1986) p. 1661.Google Scholar
16.Wittmann, J.C., Lotz, B., Candau, F., and Kovacs, A.J., J. Polym. Sci., Polym. Phys. Ed. 20 (1982) p. 1341.CrossRefGoogle Scholar
17.Quan, X. and Koberstein, J.T., J. Polym. Sci., Polym. Phys. Ed. 25 (1987) p. 1381.CrossRefGoogle Scholar