journal article·2014-06-25

Enhanced Permittivity and Energy Density in Neat Poly(vinylidene fluoride-trifluoroethylene-chlorotrifluoroethylene) Terpolymer Films through Control of Morphology

O’Neil L. Smith, Yunsang Kim, Mohanalingam Kathaperumal, Matthew R. Gadinski, Ming-Jen Pan, Qing Wang, Joseph W. Perry

Publisher page

Abstract

Polymer materials with large dielectric constants are desirable for the development of high energy density capacitors. We show that the dielectric properties of poly(vinylidene fluoride-trifluoroethylene-chlorotrifluoroethylene) [P(VDF-TrFE-CTFE)] can be improved by the use of processing conditions that favor formation of a highly crystalline morphology of the nonpolar α-phase. Through the use of spin coating, thermal treatment above the melting temperature, and quenching, we were able to attain a highly crystalline, α-phase rich morphology that has a quite large dielectric constant of 77 ± 10 at 1 kHz. The final morphology and phase composition of the terpolymer films depend strongly on the postprocessing thermal treatment and the quality of the solvent. Evaluation of the polarization behavior of the terpolymer films as a function of electric field reveal that the polymer exhibits a relaxor-ferroelectric behavior and has a substantial energy density of 9.7 J/cm(3) at fields of up to approximately 470 V/μm. Under millisecond pulsed charge-discharge measurements a 3-fold increase in energy density (27 J/cm(3)) is obtained at high fields (∼600 V/μm). Our study demonstrates that the processing conditions and morphology of fluorinated terpolymer films are controlling factors for achievement of high dielectric permittivity and energy density that are critical for high performance capacitors.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Dielectric materials and actuators · Advanced Sensor and Energy Harvesting Materials · Ferroelectric and Piezoelectric Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Chemistry and Biochemistry, and Center for Organic Photonics and Electronics, Georgia Institute of Technology, Atlanta, Georgia 30332, United States

School of Materials Science and Engineering, and Center for Organic Photonics and Electronics, Georgia Institute of Technology, Atlanta, Georgia 30332, United States

Department of Materials Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States

Naval Research Laboratory, 4555 Overlook Avenue, Washington, D.C. 20375, United States

Funding

Office of Naval Research

References (40)

Show source-provided references
1. Cao Y. · IEEE. T. Dielect. El. Insul. · 2004 · 11 · 79710.1109/TDEI.2004.1349785 ↗
2. Wang Q. · J. Polym. Sci., Polym. Phys. · 2011 · 49 · 142110.1002/polb.22337 ↗
3. Nalwa H. S. · 1999
4. Barber P. · Materials · 2009 · 2 · 169710.3390/ma2041697 ↗
5. Sarjeant W. J. · Proc. IEEE · 2001 · 89 · 84610.1109/5.931475 ↗
6. Sarjeant W. J. · IEEE. T. Plasma Sci. · 1998 · 26 · 136810.1109/27.736020 ↗
7. Starkweather H. W. · Macromolecules · 1992 · 25 · 687110.1021/ma00051a023 ↗
8. Yao K. · IEEE. T. Ultrason. Ferro. · 2011 · 58 · 196810.1109/TUFFC.2011.2039 ↗
9. Chu B. · Science · 2006 · 313 · 33410.1126/science.1127798 ↗
10. Ho J. · IEEE. T. Dielect. El. Insul. · 2007 · 14 · 129510.1109/TDEI.2007.4339492 ↗
11. Rabuffi M. · IEEE. T. Plasma Sci. · 2002 · 30 · 193910.1109/TPS.2002.805318 ↗
12. Wu S. · Adv. Mater. · 2013 · 25 · 173410.1002/adma.201204072 ↗
13. Wu S. · Appl. Phys. Lett. · 2014 · 104 · 07290310.1063/1.4865931 ↗
14. Lorenzini R. G. · Polymer · 2013 · 54 · 352910.1016/j.polymer.2013.05.003 ↗
15. Zhu L. · Macromolecules · 2012 · 45 · 293710.1021/ma2024057 ↗
16. Lovinger A. J. · Polymer · 1987 · 28 · 61710.1016/0032-3861(87)90478-2 ↗
17. Xia F. · Adv. Mater. · 2002 · 14 · 157410.1002/1521-4095(20021104)14:21<1574::AID-ADMA1574>3.0.CO;2-# ↗
18. Xu H. S. · Appl. Phys. Lett. · 2001 · 78 · 236010.1063/1.1358847 ↗
19. Lu Y. Y. · J. Am. Chem. Soc. · 2006 · 128 · 812010.1021/ja062306x ↗
20. Chung T. C. · Macromolecules · 2002 · 35 · 767810.1021/ma020504c ↗
21. Gregorio R. · J. Mater. Sci. · 1999 · 34 · 448910.1023/A:1004689205706 ↗
22. Sencadas V. · J. Macromol. Sci. B · 2009 · 48 · 51410.1080/00222340902837527 ↗
23. Branciforti M. C. · J. Polm. Sci. Polym. Phys. · 2007 · 45 · 279310.1002/polb.21239 ↗
24. Sencadas V. · J. Non-Cryst. Solids · 2006 · 352 · 222610.1016/j.jnoncrysol.2006.02.052 ↗
25. Bao H. M. · Macromolecules · 2007 · 40 · 237110.1021/ma062800l ↗
26. Ranjan V. · Phys. Rev. Lett. · 2012 · 108 · 087802-110.1103/PhysRevLett.108.087802 ↗
27. Ranjan V. · Phys. Rev. Lett. · 2007 · 99 · 047801-110.1103/PhysRevLett.99.047801 ↗
28. Su H. B. · Phys. Rev. B · 2004 · 70 · 064101-1
29. Lu Y. · Macromolecules · 2006 · 39 · 696210.1021/ma061311i ↗
30. Kim P. · ACS Nano · 2009 · 3 · 258110.1021/nn9006412 ↗
31. Kim Y. · ACS Appl. Mater. Interfaces · 2013 · 5 · 154410.1021/am303162u ↗
32. Lovinger A. J. · Science · 1983 · 220 · 111510.1126/science.220.4602.1115 ↗
33. Hasegawa R. · Polym. J. (Tokyo, Jpn.) · 1972 · 3 · 60010.1295/polymj.3.600 ↗
34. Tashiro K. · Polymer · 1984 · 25 · 19510.1016/0032-3861(84)90326-4 ↗
35. Skoog D. A. · 2007
36. Cheng Z. Y. · Macromolecules · 2002 · 35 · 66410.1021/ma0112265 ↗
37. Weibull W. · J. Appl. Mech-T. Asme. · 1951 · 18 · 29310.1115/1.4010337 ↗
38. Dissado L. A. · IEEE Trans. Electr. Insul. · 1984 · 19 · 22710.1109/TEI.1984.298753 ↗
39. Xia F. · Appl. Phys. Lett. · 2004 · 85 · 171910.1063/1.1786364 ↗
40. Gao K. C. · 2004