The fate of electron–hole pairs in polymer:fullerene blends for organic photovoltaics
Jonghe-Risse, Jelissa De
Brauer, Jan C.
KAUST DepartmentPhysical Sciences and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/622033
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AbstractThere has been long-standing debate on how free charges are generated in donor: acceptor blends that are used in organic solar cells, and which are generally comprised of a complex phase morphology, where intermixed and neat phases of the donor and acceptor material co-exist. Here we resolve this question, basing our conclusions on Stark effect spectroscopy data obtained in the absence and presence of externally applied electric fields. Reconciling opposing views found in literature, we unambiguously demonstrate that the fate of photogenerated electron-hole pairs-whether they will dissociate to free charges or geminately recombine-is determined at ultrafast times, despite the fact that their actual spatial separation can be much slower. Our insights are important to further develop rational approaches towards material design and processing of organic solar cells, assisting to realize their purported promise as lead-free, third-generation energy technology that can reach efficiencies over 10%.
CitationCausa’ M, De Jonghe-Risse J, Scarongella M, Brauer JC, Buchaca-Domingo E, et al. (2016) The fate of electron–hole pairs in polymer:fullerene blends for organic photovoltaics. Nature Communications 7: 12556. Available: http://dx.doi.org/10.1038/ncomms12556.
SponsorsM.C., M.S., J.C.B. and N.B. thank the Swiss National Science Foundation (PP00P2_150536) and the University of Fribourg for funding. N.B., J.D.J.-R and J.-E.M are grateful to NCCR-MUST, a research instrument of the Swiss National Science Foundation, for support. N.S. is supported by a European Research Council (ERC) Starting Independent Researcher Fellowship under the grant agreement No. 279587. E.B.-D. is funded by a SABIC Post-Doctoral Fellowship at King Abdullah University of Science and Technology. We thank Prof. Martin Heeney (Imperial College, London, UK) for providing the pBTTT polymer, and we thank Prof. E. Vauthey and R. Letrun (Univ. of Geneva, Switzerland) for use of their fluorescence up-conversion set-up and help with the experiment. We thank Dr A. Devizis (Center for Physical Sciences and Technology, Vilnius) for having built the EDA set-up and for useful discussion.
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