Interplay between Ordering Effects and Solar Cell Performance IN PBDTTPD Polymers
Pierre M. Beaujuge a
a King Abdullah University of Science and Technology (KAUST) - Saudi Arabia, 4700 King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia
International Conference on Hybrid and Organic Photovoltaics
Proceedings of 6th International Conference on Hybrid and Organic Photovoltaics (HOPV14)
Ecublens, Switzerland, 2014 May 11th - 14th
Organizers: Michael Graetzel and Mohammad Nazeeruddin
Oral, Pierre M. Beaujuge, presentation 268
Publication date: 1st March 2014

Among Organic Electronics, solution-processable π-conjugated polymers are proving particularly promising in bulk-heterojunction (BHJ) solar cells with fullerene acceptors such as PCBM.[1] In the past few years, we have found that varying the size and branching of solubilizing side-chains in π-conjugated polymers impacts their self-assembling properties in thin-films. Beyond film-forming properties, nanoscale ordering in the active layer governs material and device performance. For example, in poly(benzo[1,2-b:4,5-b’]dithiophene–thieno[3,4-c]pyrrole-4,6-dione) (PBDTTPD), side-chain substituents of various size and branching impart distinct molecular packing distances (i.e., π–π stacking and lamellar spacing),[2] varying degrees of nanostructural order in thin films,[2] and preferential backbone orientation relative to the device substrate (Fig.1).[3,4] While these structural variations seem to correlate with BHJ solar cell performance, with power conversion efficiencies ranging from 4% to 8.5%,[2,3,5] we believe that other contributing parameters – such as the local conformations between the polymer and the fullerene, and the domain distribution/composition across the BHJ (i.e., pure/mixed phases) – should also be taken into account.[6,7] Other discrete modifications of PBDTTPD’s molecular structure affect polymer performance in BHJ solar cells with PCBM, and our recent developments emphasize how systematic structure-property relationship studies impact the design of efficient polymer donors for BHJ solar cell applications.[8-10]



[1] P. M. Beaujuge, and J. M. J. Fréchet, JACS, 2011, 133, 20009. [2] C. Piliego, T. W. Holcombe, J. D. Douglas, C. H. Woo, P. M. Beaujuge, and J. M. J. Fréchet, JACS, 2010, 132, 7595. [3] C. Cabanetos, A. El Labban, J. A. Bartelt, J. D. Douglas, W. R. Mateker, J. M. J. Fréchet, M. D. McGehee, and P. M. Beaujuge, JACS, 2013, 135, 4656. [4] J. Warnan, A. El Labban, O. Ratel, C. Cabanetos, C. Tassone, M. F. Toney, and P. M. Beaujuge, 2014, Submitted. [5] J. A. Bartelt, J. D. Douglas, W. R. Mateker, A. El Labban, C. J. Tassone, M. F. Toney, J. M. J. Fréchet, P. M. Beaujuge, and M. D. McGehee, Adv. Energy Mater., 2014, Accepted. [6] J. A. Bartelt, Z. M. Beiley, E. T. Hoke, W. R. Mateker, J. D. Douglas, B. A. Collins, J. R. Tumbleston, K. R. Graham, A. Amassian, H. Ade, J. M. J. Fréchet, M. F. Toney, and M. D. McGehee, Adv. Energy Mater., 2013, 3, 364. [7] K. R. Graham, C. Cabanetos, J. P. Jahnke, M. N. Idso, A. El Labban, G. O. Ngongang Ndjawa, B. F. Chmelka, A. Amassian, P. M. Beaujuge, M. D. McGehee, 2014, Submitted. [8] J. Warnan, C. Cabanetos, A. El Labban, M. R. Hansen, C. Tassone, M. F. Toney, and P. M. Beaujuge, 2014, Submitted. [9] J. Warnan, A. El Labban, C. Cabanetos, E. Hoke, C. Risko, J-L. Brédas, M. D. McGehee, and P. M. Beaujuge, Chem. Mater., 2014, Accepted. [10] J. Warnan, C. Cabanetos, R. Bude, A. El Labban, Liang Li, and P. M. Beaujuge, 2014, Submitted.
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