Impact of Molecular Orientation and Spontaneous Interfacial Mixing on the Performance of Organic Solar Cells

Guy Olivier Ngongang Ndjawa, Kenneth Graham, Ruipeng Li, Sarah M Conron, Patrick Erwin, Kang Wei Chou, George Burkhard, Kui Zhao, Eric T. Hoke, Mark E Thompson, Michael D. McGehee, Aram Amassian

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

A critically important question that must be answered to understand how organic solar cells operate and should be improved is how the orientation of the donor and acceptor molecules at the interface influences exciton diffusion, exciton dissociation by electron transfer and recombination. It is exceedingly difficult to probe the orientation in bulk heterojunctions because there are many interfaces and they are arranged with varying angles with respect to the substrate. One of the best ways to study the interface is to make bilayer solar cells with just one donor-acceptor interface. Zinc phthalocyanine is particularly interesting to study because its orientation can be adjusted by using a 2-nm-thick copper iodide seed layer before it is deposited. Previous studies have claimed that solar cells in which fullerene acceptor molecules touch the face of zinc phthalocyanine have more current than ones in which the fullerenes touch the edge of zinc phthalocyanine because of suppressed recombination. We have more thoroughly characterized the system using in situ x-ray photoelectron spectroscopy and found that the interfaces are not as sharp as previous studies claimed when formed at room temperature or above. Fullerenes have a much stronger tendency to mix into the face-on films than into the edge-on films. Moreover we show that almost all of the increase in the current with face-on films can be attributed to improved exciton diffusion and to the formation of a spontaneously mixed interface, not suppressed recombination. This work highlights the importance of spontaneous interfacial molecular mixing in organic solar cells, the extent of which depends on molecular orientation of frontier molecules in donor domains.
Original languageEnglish (US)
Pages (from-to)5597-5604
Number of pages8
JournalChemistry of Materials
Volume27
Issue number16
DOIs
StatePublished - Aug 10 2015

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