Volume 42, Issue 6 pp. 1106-1113
Article

Brillouin scattering studies of polymeric nanostructures *

R. Hartschuh

R. Hartschuh

Department of Polymer Science, University of Akron, Akron, Ohio 44325

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Y. Ding

Y. Ding

Department of Polymer Science, University of Akron, Akron, Ohio 44325

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J. H. Roh

J. H. Roh

Department of Polymer Science, University of Akron, Akron, Ohio 44325

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A. Kisliuk

A. Kisliuk

Department of Polymer Science, University of Akron, Akron, Ohio 44325

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A. P. Sokolov

A. P. Sokolov

Department of Polymer Science, University of Akron, Akron, Ohio 44325

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C. L. Soles

Corresponding Author

C. L. Soles

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8541

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8541Search for more papers by this author
R. L. Jones

R. L. Jones

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8541

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T. J. Hu

T. J. Hu

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8541

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W. L. Wu

W. L. Wu

Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8541

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A. P. Mahorowala

A. P. Mahorowala

IBM T. J. Watson Research Center, Yorktown Heights, New York 10598

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First published: 02 February 2004
Citations: 31
*

Contribution from the March 2003 Meeting of the American Physical Society—Division of Polymer Physics, Austin, Texas

This article is a US Government work and, as such, is in the public domain in the United States of America.

Abstract

For a range of applications, polymers are now being patterned into nanometer-sized features. In these applications, the robust mechanical properties of the nanostructures are critical for performance and stability. Brillouin light scattering is presented as a nondestructive, noncontact tool used to quantify the elastic constants in such nanostructures. We demonstrate this through a series of thin films and parallel ridges and spacings (gratings) with ridge widths ranging from 180 to 80 nm. For the set of films and structures presented here, the room-temperature elastic moduli did not change with decreasing film thickness or grating ridge width, and this implied that one-dimensional and two-dimensional confinement-induced changes of the mechanical properties were not significant down to feature sizes of 80 nm. Additionally, Brillouin spectra of submicrometer gratings revealed new modes not present in the spectra of thin films. The origin of these new modes remains unclear. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 1106–1113, 2004

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