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A Promising Ketone Containing Alternating Copolymer for Organic Photovoltaics

Published online by Cambridge University Press:  27 February 2013

Ranjith Kottokkaran ,
Arun D Rao  and
Praveen C Ramamurthy
Ranjith Kottokkaran
Affiliation:
Department of Materials Engineering, Indian Institute of Science, Bangalore-560012, INDIA.
Arun D Rao
Affiliation:
Department of Materials Engineering, Indian Institute of Science, Bangalore-560012, INDIA.
Praveen C Ramamurthy
Affiliation:
Department of Materials Engineering, Indian Institute of Science, Bangalore-560012, INDIA.
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Abstract

An alternating copolymer containing dithienylcyclopentadienone, thiophene and benzothiadiazole was synthesized by palladium (0) catalyzed Stille coupling reaction. Structural characterization of the synthesized alternating copolymer was carried out by NMR and FTIR spectroscopy. This solution processable copolymer shows an excellent thermal stability and has a broad absorption range from 300-800 nm. High LUMO energy level and low band gap of the synthesized copolymers suggest that, this copolymer will be a better donor material for application in organic photovoltaics. Particle size analysis and molecular weight determination of the synthesized copolymer through dynamic light scattering experiment indicates that, high molecular weight copolymer was obtained by this polymerization route. Photovoltaic devices were fabricated from the blend of copolymer and phenyl-C61- butyric acid methyl ester as the active material. Fabricated photovoltaic device results show that this alternating copolymer is a promising candidate for use in organic photovoltaics.

Keywords

polymerphotovoltaicsemiconducting
Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1500: Symposium O – Next-Generation Polymer-Based Organic Photovoltaics , 2013 , mrsf12-1500-o03-19
Copyright
Copyright © Materials Research Society 2013

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References

REFERENCES

Jung, J. W., Jo, J. W., Liu, F., Russell, T. P. and Jo, W. H., Chem. Commun. 48, 6933 (2012).CrossRefGoogle Scholar
Winder, C. and Sariciftci, N. S., J. Mater. Chem. 14, 1077 (2004).CrossRefGoogle Scholar
Ranjith, K., Swathi, S. K., Kumar, P. and Ramamurthy, P. C., J. Mater. Sci. 46, 2259 (2011).CrossRefGoogle Scholar
Walker, W., Veldman, B., Chiechi, R., Patil, S., Bendikov, M. and Wudl, F., Macromolecules 41, 7278 (2008).CrossRefGoogle Scholar
Swathi, S. K., Ranjith, K., Kumar, P. and Ramamurthy, P. C., Sol. Energy Mater. Sol. Cells 96, 101 (2012).CrossRefGoogle Scholar
Kumar, P., Ranjith, K., Gupta, S. and Ramamurthy, P. C., Electrochimica Acta 56, 8184 (2011).CrossRefGoogle Scholar
Ranjith, K., Swathi, S. K., Malavika, A. and Ramamurthy, P. C., Sol. Energy Mater. Sol. Cells 105, 263 (2012).CrossRefGoogle Scholar
Ranjith, K., Swathi, S. K., Kumar, P. and Ramamurthy, P. C., Sol. Energy Mater. Sol. Cells 98, 448 (2012).CrossRefGoogle Scholar
Zhang, M., Yang, C., Mishra, A. K., Pisula, W., Zhou, G., Schmaltz, B., Baumgarten, M. and Mullen, K., Chem. Commun. 17, 1704 (2007).CrossRefGoogle Scholar