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https://hdl.handle.net/20.500.14279/1514
Title: | Composition and annealing effects in polythiophene/fullerene solar cells | Authors: | Choulis, Stelios A. Kim, Youngkyoo Nelson, Jenny K. |
metadata.dc.contributor.other: | Χούλης, Στέλιος Α. | Major Field of Science: | Engineering and Technology | Field Category: | ENGINEERING AND TECHNOLOGY | Keywords: | Solar cells;Fullerenes;Photoluminescence;Atomic force microscopy;Polychlorinated biphenyls | Issue Date: | Mar-2005 | Source: | Journal of Materials Science, 2005, vol. 40, no. 6, pp. 1371-1376 | Volume: | 40 | Issue: | 6 | Start page: | 1371 | End page: | 1376 | Journal: | Journal of Materials Science | Abstract: | We have fabricated organic solar cells with blends of regioregular poly(3-hexylthiophene) (P3HT) and 1-(3-methoxycarbonyl)-propyl-1-phenyl-(6,6) C 61 (PCBM) as electron donor and electron acceptor, respectively. Blend composition and device annealing effects were investigated with optical absorption and photoluminescence spectroscopy, atomic force microscopy, photocurrent spectroscopy, and current-voltage characteristic measurements on devices under monochromatic or air mass (AM) 1.5 simulated solar light illumination. The highest efficiency was achieved for the 1:1 (P3HT:PCBM) weight ratio composition. The good performance is attributed to an optimized morphology that enables close intermolecular packing of P3HT chains. Inferior performance for the 1:2 composition is attributed to poorer intermolecular packing with increased PCBM content, while phase segregation on a sub-micron scale was observed for the 1:4 composition. The power conversion efficiency (AM 1.5) was doubled by the thermal annealing of devices at 140°C to reach a value of 1.4% | URI: | https://hdl.handle.net/20.500.14279/1514 | ISSN: | 15734803 | DOI: | 10.1007/s10853-005-0568-0 | Rights: | © Springer Science | Type: | Article | Affiliation: | Imperial College London | Affiliation : | Imperial College London | Publication Type: | Peer Reviewed |
Appears in Collections: | Άρθρα/Articles |
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