Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-27T01:49:54.040Z Has data issue: false hasContentIssue false
  • English
  • Français

Directed Assembly of Model Block Copolymer-PCBM Blend System for Photovoltaic Applications

Published online by Cambridge University Press:  29 February 2012

G. Singh ,
M. M. Kulkarni ,
D. Smilgies ,
S. Sides ,
B. Berry ,
D. Raghavan ,
D.G. Bucknall ,
B Sumpter  and
A. Karim
G. Singh
Affiliation:
Department of Polymer Engineering, University of Akron, Akron, OH 44325
M. M. Kulkarni
Affiliation:
Department of Polymer Engineering, University of Akron, Akron, OH 44325
D. Smilgies
Affiliation:
Cornell High Energy Synchrotron Source (CHESS), Cornell University, Ithaca, New York 14853
S. Sides
Affiliation:
Tech-X Corporation, Boulder, CO 80303
B. Berry
Affiliation:
Department of Chemistry, University of Arkansas at Little Rock, Little Rock, AR 72204
D. Raghavan
Affiliation:
Department of Chemistry, Howard University, Washington DC 20059
D.G. Bucknall
Affiliation:
Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332
B Sumpter
Affiliation:
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, TN 37831
A. Karim
Affiliation:
Department of Polymer Engineering, University of Akron, Akron, OH 44325
Get access

Abstract

Block copolymers are considered to be highly attractive materials with regards to future applications of nanomaterials and nanostructures owing to their self-assembling nature. Block copolymers, when supplied with sufficient energy, phase separate at the nanoscales to form periodically ordered structures in the nanometer-scale range. A diversity of architectures can be accessed via composition control of individual block components. An exciting area of application for block copolymer self assembly is organic photovoltaic devices (OPV‟s) where it is expected that the very high interfacial area of the blocks with ∼10-20 nm domain spacing would be highly advantageous for exciton diffusion and separation. For this purpose BCPs composed of amorphous (non-conjugated) polymers can also serve as a template for directed assembly of nanoparticles. Zone annealing is a well established method predominantly utilized for metallurgical and semi-conductor purification processes, where recrystallization and oriented grain growth occur on the planar front formed by the cooling-edge of the zone. We have previously applied this process to create highly ordered BCP cylinders that are parallel to the substrate with orientational control, long range order and faster ordering kinetics than conventional thermal annealing. In the present paper, we extend this idea to block copolymer - [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blend system and report how the presence of PCBM nanoparticles influence the micro-phase separation behavior of cylinder forming poly(styrene-b-2-vinyl pyridine) under a dynamic thermal gradient field. A range of scattering techniques have been on the BCP:PCBM blend system, including grazing incidence small angle x-ray scattering (GISAXS) experiments to characterize in-plane and lateral ordering of BCP-PCBM blend system.

Keywords

polymerthin filmself-assembly
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 1390: Symposium H/I – Organic Photovoltaics–Materials to Devices , 2012 , mrsf11-1390-h13-54
Copyright
Copyright © Materials Research Society 2012

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

1. Bodycomb, J, Funaki, Y, Kimishima, K, Hashimoto, T. Macromolecules 1999, 32, 2075 Google Scholar
2. Berry, B. C., Bosse, A.W., Douglas, JF, Jones, RL, Karim, A. Nano letters 2007, 7, 2789 Google Scholar
3 Yager, K. G.; Fredin, N. J.; Zhang, X.; Berry, B. C.; Karim, A.; Jones, R. L. Soft Matter. 2010, 6, 92.Google Scholar
4 Yager, K. G.; Berry, B. C.; Page, K.; Patton, D.; Karim, A.; Amis, E. J. Soft Matter. 2009, 5, 622.Google Scholar
5 Shin, K.; Xiang, H.; Moon, S. I.; Kim, T.; McCarthy, T. J.; Russell, T. P. Science. 2004, 306, 76.Google Scholar
6 Kellogg, G.; Walton, D.; Mayes, A.; Lambooy, P.; Russell, T.; Gallagher, P.; Satija, S. Physical review letters. 1996, 76, 2503–2506.Google Scholar
7. Waller, J. H.; Bucknall, D. G.; Register, R. A.; Beckham, H. W.; Leisen, J.; Campbell, K., Polymer 2009, 50, 4199 Google Scholar