Large electrostrictive strain at gigahertz frequencies in a polymer nanoactuator: Computational device design
Abstract
Using molecular dynamics with a first-principles-based force field (denoted MSXX), we show that large electrostrictive strains (similar to 5%) at extremely high frequencies (over similar to 10^(9) Hz) can be achieved in a poly(vinylidene-fluoride) nanoactuator if the packing density of the polymer chains is chosen appropriately. We control the packing density by assembling the polymer chains on a silicon < 111 > surface with one-half coverage. Under these conditions, the equilibrium, zero electric field conformation of the polymer contains a combination of gauche and trans bonds. This structure can be transformed to an all-T conformation by applying an external electric field. Such molecular transformation is accompanied by a large deformation in the direction of the polymer chains. The device shows typical electrostrictive behavior with strain proportional to the square of the polarization.
Additional Information
© 2005 American Institute of Physics. Received 16 September 2004; accepted 7 December 2004; published online 15 February 2005. This work was supported by DARPA, program manager: Carey Schwartz.Files
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Additional details
- Eprint ID
- 3475
- Resolver ID
- CaltechAUTHORS:STRAapl05
- Defense Advanced Research Projects Agency (DARPA)
- Created
-
2006-06-08Created from EPrint's datestamp field
- Updated
-
2021-11-08Created from EPrint's last_modified field
- Other Numbering System Name
- WAG
- Other Numbering System Identifier
- 0611