Ultrafast Electron Transfer at Organic Semiconductor Interfaces: Importance of Molecular Orientation

Alexander L. Ayzner, Dennis Nordlund, Do-Hwan Kim, Zhenan Bao, Michael F. Toney

Research output: Contribution to journalArticlepeer-review

49 Scopus citations


© 2014 American Chemical Society. Much is known about the rate of photoexcited charge generation in at organic donor/acceptor (D/A) heterojunctions overaged over all relative arrangements. However, there has been very little experimental work investigating how the photoexcited electron transfer (ET) rate depends on the precise relative molecular orientation between D and A in thin solid films. This is the question that we address in this work. We find that the ET rate depends strongly on the relative molecular arrangement: The interface where the model donor compound copper phthalocyanine is oriented face-on with respect to the fullerene C60 acceptor yields a rate that is approximately 4 times faster than that of the edge-on oriented interface. Our results suggest that the D/A electronic coupling is significantly enhanced in the face-on case, which agrees well with theoretical predictions, underscoring the importance of controlling the relative interfacial molecular orientation.
Original languageEnglish (US)
Pages (from-to)6-12
Number of pages7
JournalThe Journal of Physical Chemistry Letters
Issue number1
StatePublished - Dec 15 2014
Externally publishedYes

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUS-C1-015-21
Acknowledgements: This work was partially supported by the Center for Advanced
This publication acknowledges KAUST support, but has no KAUST affiliated authors.


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