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DOE OSTI · 1383301

Organometallics Roundtable 2011

Gladysz, John A.·Ball, Zachary T.·Bertrand, Guy·Blum, Suzanne A.·Dong, Vy M.·Dorta, Reto·Hahn, F. Ekkehardt·Humphrey, Mark G.·Jones, William D.·Klosin, Jerzy·Manners, Ian·Marks, Tobin J.·Mayer, James M.·Rieger, Bernhard·Ritter, Joachim C.·Sattelberger, Alfred P.·Schomaker, Jennifer M.·Yam, Vivian Wing-Wah
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bio-inspiredcatalysis (heterogeneous)catalysis (homogeneous)charge transportenergy storage (including batteries and capacitors)hydrogen and fuel cellsmaterials and chemistry by designsolar (fuels)synthesis (novel materials)

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Gladysz, John A., Ball, Zachary T., Bertrand, Guy, Blum, Suzanne A., Dong, Vy M., Dorta, Reto, Hahn, F. Ekkehardt, Humphrey, Mark G., Jones, William D., Klosin, Jerzy, Manners, Ian, Marks, Tobin J., Mayer, James M., Rieger, Bernhard, Ritter, Joachim C., Sattelberger, Alfred P., Schomaker, Jennifer M., Yam, Vivian Wing-Wah. 2011-12-19. Organometallics Roundtable 2011. https://doi.org/10.1021/om201234x

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DOE OSTI2020

Photoinduced electron transfer from zinc meso -tetraphenylporphyrin to a one-dimensional perylenediimide aggregate: Probing anion delocalization effects

Organic photovoltaics incorporating non-fullerene acceptors based on perylenediimide (PDI) now rival fullerene acceptor-based devices in performance, although the mechanisms of charge generation in PDI-based devices are not yet fully understood. Fullerene-based systems are proposed to undergo electron transfer directly from the photoexcited donor into a band of delocalized acceptor states, thus increasing charge generation efficiency. Similarly, anion delocalization has been shown to enhance the rate of electron transfer from a photoexcited donor to two electronically coupled PDI acceptors. Here we investigate how additional electron acceptors may further increase the rate of electron transfer from the donor zinc meso-tetraphenylporphyrin (ZnTPP) to an aggregate of PDI acceptors (PDI[Formula: see text]. Femtosecond transient visible and mid-infrared absorption spectroscopies show that the rate of electron transfer from 1 *ZnTPP to the PDI assembly ZnTPP 2 -PDI 3 is statistically identical to that of the previously examined ZnTPP-PDI 2 . A Marcus theory analysis indicates that the parameters governing electron transfer are nearly identical for the two molecules, suggesting that the maximum electron transfer rate enhancement has been achieved in a cofacial PDI dimer because the ZnTPP directly couples to the first two PDI acceptors whereas the coupling to the third PDI is too weak.

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