Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-10T16:18:51.875Z Has data issue: false hasContentIssue false

Dielectric Properties of UV Cured Thick Film Polymer Networks through High Power Xenon Flash Lamp Curing

Published online by Cambridge University Press:  29 January 2014

Brian C. Riggs
Affiliation:
Department of Physics and Engineering Physics, Tulane University, New Orleans, LA 70118
Ravinder Elupula
Affiliation:
Department of Chemistry, Tulane University, New Orleans, LA 70118
Venkata S. Puli
Affiliation:
Department of Physics and Engineering Physics, Tulane University, New Orleans, LA 70118
Scott M. Grayson
Affiliation:
Department of Chemistry, Tulane University, New Orleans, LA 70118
Douglas B. Chrisey
Affiliation:
Department of Physics and Engineering Physics, Tulane University, New Orleans, LA 70118
Get access

Abstract

High-energy flash cure lamps process thick film materials (<10 um) over large areas (<100 cm2) within milliseconds and are capable to deliver higher energy and power densities (20 J/cm2 and 20 kW/cm2) allowing for a more complete curing and elimination of flaws that would exist in conventional treatment. Click reactions are especially attractive for patterned devices as they have minimal shape change during curing and have a more predictable structure compared to free radical acrylate polymerization. Pentaerythritol tetrakis(3-mercaptopropionate) and 2,4,6-Triallyloxy-1,3,5-triazine were combined at 3:4 by weight and then spin coated on copper foil substrates. The solutions were processed both thermally and with exposure to a xenon flash bulb. Thermal treatment consisted of heating the sample at 80°C on a hot plate over night. Flash curing was accomplished using a Novacentrix Pulseforge 1300 system. The flash lamp curing fluence and intensities were varied to determine their effects on degree of cross-linking, dielectric constant, breakdown field and energy storage. The degree of cross-linking was determined through comparative FTIR studies. Dielectric constant was measured using an Agilent 4294a impedance analyzer from 100 Hz-100 MHz with a two terminal setup. Breakdown strength and energy density measurements were taken using Radiant Technology's Precision Ferroelectric tester with a 10 kV source. The printed films averaged 1-3 microns thick as observed by an SEM cross section measurement. It was found that dielectric constant varies with both treatment intensity and fluence. Energy densities were calculated using the ideal capacitor equation and ranged from 1.5-4.8 J/cm3.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

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

REFERENCES

Wang, C., Lee, W.-Y., Nakajima, R., Mei, J., Kim, D. H., and Bao, Z., “Thiol–ene Cross-Linked Polymer Gate Dielectrics for Low-Voltage Organic Thin-Film Transistors,” Chem. Mater., vol. 25, no. 23, pp. 48064812, Dec. 2013.10.1021/cm403203kCrossRefGoogle Scholar
Kim, J.-S., Lee, S., Hwang, Y. H., Kim, Y., Yoo, S., and Bae, B.-S., “Photo-Curable Sol-Gel Hybrid Film as a Dielectric Layer by a Thiol-ene Reaction in Air or N2 for Organic Thin Film Transistors,” Electrochem. Solid-State Lett., vol. 15, no. 5, p. G13, 2012.10.1149/2.021205eslCrossRefGoogle Scholar
Senyurt, A., Wei, H., and Phillips, B., “Physical and mechanical properties of photopolymerized thiol-ene/acrylates,” Macromolecules, vol. 39, no. 19, pp. 3941, 2006.10.1021/ma060507fCrossRefGoogle Scholar
Ko, J. M., Kang, Y. H., Lee, C., and Cho, S. Y., “Electrically and thermally stable gate dielectrics from thiol–ene cross-linked systems for use in organic thin-film transistors,” J. Mater. Chem. C, vol. 1, no. 18, p. 3091, 2013.10.1039/c3tc30297kCrossRefGoogle Scholar
Lowe, A. B., “Thiol-ene ‘click’ reactions and recent applications in polymer and materials synthesis,” Polym. Chem., vol. 1, no. 1, p. 17, 2010.10.1039/B9PY00216BCrossRefGoogle Scholar
Burlingame, Q., Wu, S., Lin, M., and Zhang, Q. M., “Conduction Mechanisms and Structure-Property Relationships in High Energy Density Aromatic Polythiourea Dielectric Films,” Adv. Energy Mater., p. n/a–n/a, Apr. 2013.10.1002/aenm.201201110CrossRefGoogle Scholar
Chu, B., Zhou, X., Ren, K., Neese, B., Lin, M., Wang, Q., Bauer, F., and Zhang, Q. M., “A dielectric polymer with high electric energy density and fast discharge speed.,” Science, vol. 313, no. 5785, pp. 334–6, Jul. 2006.10.1126/science.1127798CrossRefGoogle ScholarPubMed
Tang, H. and Sodano, H., “Ultra High Energy Density Nanocomposite Capacitors with Fast Discharge Using Ba0. 2Sr0. 8TiO3 Nanowires,” Nano Lett., vol. 13, pp. 13731379, 2013.10.1021/nl3037273CrossRefGoogle ScholarPubMed
Wu, S., Li, W., Lin, M., Burlingame, Q., Chen, Q., Payzant, A., Xiao, K., and Zhang, Q. M., “Aromatic polythiourea dielectrics with ultrahigh breakdown field strength, low dielectric loss, and high electric energy density.,” Adv. Mater., vol. 25, no. 12, pp. 1734–8, Mar. 2013.10.1002/adma.201204072CrossRefGoogle ScholarPubMed
Zhou, X., Chu, B., Neese, B., Lin, M., and Zhang, Q., “Electrical Energy Density and Discharge Characteristics of a Poly(vinylidene fluoride-chlorotrifluoroethylene)Copolymer,” IEEE Trans. Dielectr. Electr. Insul., vol. 14, no. 5, pp. 11331138, Oct. 2007.10.1109/TDEI.2007.4339472CrossRefGoogle Scholar
Yang, Z., Wicks, D. a., Hoyle, C. E., Pu, H., Yuan, J., Wan, D., and Liu, Y., “Newly UV-curable polyurethane coatings prepared by multifunctional thiol- and ene-terminated polyurethane aqueous dispersions mixtures: Preparation and characterization,” Polymer (Guildf)., vol. 50, no. 7, pp. 17171722, Mar. 2009.10.1016/j.polymer.2008.12.018CrossRefGoogle Scholar
Northrop, B. H. and Coffey, R. N., “Thiol-ene click chemistry: computational and kinetic analysis of the influence of alkene functionality.,” J. Am. Chem. Soc., vol. 134, no. 33, pp. 13804–17, Aug. 2012.10.1021/ja305441dCrossRefGoogle ScholarPubMed
Cramer, N. B., Reddy, S. K., Cole, M., Hoyle, C., and Bowman, C. N., “Initiation and kinetics of thiol-ene photopolymerizations without photoinitiators,” J. Polym. Sci. Part A Polym. Chem., vol. 42, no. 22, pp. 58175826, Nov. 2004.10.1002/pola.20419CrossRefGoogle Scholar
Cramer, N. B. and Bowman, C. N., “Kinetics of thiol-ene and thiol-acrylate photopolymerizations with real-time fourier transform infrared,” J. Polym. Sci. Part A Polym. Chem., vol. 39, no. 19, pp. 33113319, Oct. 2001.10.1002/pola.1314CrossRefGoogle Scholar
Cramer, N. B., Scott, J. P., and Bowman, C. N., “Photopolymerizations of Thiol - Ene Polymers without Photoinitiators,” pp. 5361–5365, 2002.Google Scholar
Wang, Y., Zhou, X., Lin, M., and Zhang, Q. M., “High-energy density in aromatic polyurea thin films,” Appl. Phys. Lett., vol. 94, no. 20, p. 202905, 2009.10.1063/1.3142388CrossRefGoogle Scholar
Wang, Y., Zhou, X., Chen, Q., Chu, B., and Zhang, Q., “Recent development of high energy density polymers for dielectric capacitors,” IEEE Trans. Dielectr. Electr. Insul., vol. 17, no. 4, pp. 10361042, Aug. 2010.10.1109/TDEI.2010.5539672CrossRefGoogle Scholar