Ultrafast electron transfer at organic semiconductor interfaces: Importance of molecular orientation
- Stanford Univ., Stanford, CA (United States); SLAC National Accelerator Laboratory, Menlo Park, CA (United States)
- SLAC National Accelerator Laboratory, Menlo Park, CA (United States)
- Soongsil Univ., Seoul (Korea)
- Stanford Univ., Stanford, CA (United States)
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.
- Research Organization:
- SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC)
- Grant/Contract Number:
- 2011-0031628; KUS-C1-015-21
- OSTI ID:
- 1215420
- Journal Information:
- Journal of Physical Chemistry Letters, Vol. 6, Issue 1; ISSN 1948-7185
- Publisher:
- American Chemical SocietyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Web of Science
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