Visualizing charge separation in bulk heterojunction organic solar cells
D. Amarasinghe Vithanage,
A. Devižis,
V. Abramavičius,
Y. Infahsaeng,
D. Abramavičius,
R. C. I. MacKenzie,
P. E. Keivanidis,
A. Yartsev,
D. Hertel,
J. Nelson,
V. Sundström and
V. Gulbinas ()
Additional contact information
D. Amarasinghe Vithanage: Chemical Physics, Lund University Box 124
A. Devižis: Center for Physical Sciences and Technology
V. Abramavičius: Center for Physical Sciences and Technology
Y. Infahsaeng: Chemical Physics, Lund University Box 124
D. Abramavičius: Vilnius University
R. C. I. MacKenzie: FRIAS, School of Soft Matter Research, University of Freiburg
P. E. Keivanidis: Center for Nano Science and Technology at PoliMi, Istituto Italiano di Tecnologia
A. Yartsev: Chemical Physics, Lund University Box 124
D. Hertel: Physical Chemistry, University of Cologne
J. Nelson: FRIAS, School of Soft Matter Research, University of Freiburg
V. Sundström: Chemical Physics, Lund University Box 124
V. Gulbinas: Center for Physical Sciences and Technology
Nature Communications, 2013, vol. 4, issue 1, 1-6
Abstract:
Abstract Solar cells based on conjugated polymer and fullerene blends have been developed as a low-cost alternative to silicon. For efficient solar cells, electron–hole pairs must separate into free mobile charges that can be extracted in high yield. We still lack good understanding of how, why and when carriers separate against the Coulomb attraction. Here we visualize the charge separation process in bulk heterojunction solar cells by directly measuring charge carrier drift in a polymer:fullerene blend with ultrafast time resolution. We show that initially only closely separated (
Date: 2013
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3334
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DOI: 10.1038/ncomms3334
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