TY - JOUR
T1 - Direct and Energy-Transfer-Mediated Charge-Transfer State Formation and Recombination in Triangulene-Spacer-Perylenediimide Multichromophores
T2 - Lessons for Photovoltaic Applications
AU - Balawi, Ahmed H.
AU - Stappert, Sebastian
AU - Gorenflot, Julien
AU - Li, Chen
AU - Müllen, Klaus
AU - Andrienko, Denis
AU - Laquai, Frédéric
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/7/11
Y1 - 2019/7/11
N2 - We study the dynamics of primary photoexcitations in three symmetric donor-spacer-acceptor-spacer-donor multichromophores with increasing oligophenylene spacer length, following selective donor or acceptor excitation. Energy levels of the donor and acceptor moieties are tailored to facilitate splitting of the excited state into a lower-lying charge-transfer (CT) state, mimicking the functionality of a donor-acceptor interface for charge generation, thus resulting in long-lived charge separation. Ultrafast electronic energy transfer (ET) from the donor followed by fast hole (back)transfer from the acceptor populates the molecules' CT states. However, the CT efficiency is found to be close to unity, independent of the donor or acceptor photoexcitation. The ratio of CT and recombination rates, which reflects the population of CT states, increases with the oligophenylene spacer length for both direct hole transfer and hole transfer following ET, boosting the population of CT states under continuous excitation. We observe the population of high-lying "dark" excited states following ET from the donor to the acceptor. The "dark" states successively undergo CT and form CT states of higher energy, with decreased recombination rates, while maintaining the high charge generation efficiency. Changes in CT reaction rates are rationalized within the Marcus theory, with driving forces and reorganization energies evaluated by density functional theory and polarizable continuum models. The present study demonstrates the importance of energetically higher-lying states, which cannot be directly photoexcited yet are accessible through ET from local excited states. Similar processes are anticipated in other donor-acceptor systems, which allow for both energy and CT processes, such as bulk heterojunctions of the polymer and small-molecule donor/nonfullerene acceptor typically used in photovoltaic systems.
AB - We study the dynamics of primary photoexcitations in three symmetric donor-spacer-acceptor-spacer-donor multichromophores with increasing oligophenylene spacer length, following selective donor or acceptor excitation. Energy levels of the donor and acceptor moieties are tailored to facilitate splitting of the excited state into a lower-lying charge-transfer (CT) state, mimicking the functionality of a donor-acceptor interface for charge generation, thus resulting in long-lived charge separation. Ultrafast electronic energy transfer (ET) from the donor followed by fast hole (back)transfer from the acceptor populates the molecules' CT states. However, the CT efficiency is found to be close to unity, independent of the donor or acceptor photoexcitation. The ratio of CT and recombination rates, which reflects the population of CT states, increases with the oligophenylene spacer length for both direct hole transfer and hole transfer following ET, boosting the population of CT states under continuous excitation. We observe the population of high-lying "dark" excited states following ET from the donor to the acceptor. The "dark" states successively undergo CT and form CT states of higher energy, with decreased recombination rates, while maintaining the high charge generation efficiency. Changes in CT reaction rates are rationalized within the Marcus theory, with driving forces and reorganization energies evaluated by density functional theory and polarizable continuum models. The present study demonstrates the importance of energetically higher-lying states, which cannot be directly photoexcited yet are accessible through ET from local excited states. Similar processes are anticipated in other donor-acceptor systems, which allow for both energy and CT processes, such as bulk heterojunctions of the polymer and small-molecule donor/nonfullerene acceptor typically used in photovoltaic systems.
UR - http://www.scopus.com/inward/record.url?scp=85068416204&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.9b05149
DO - 10.1021/acs.jpcc.9b05149
M3 - Article
AN - SCOPUS:85068416204
SN - 1932-7447
VL - 123
SP - 16602
EP - 16613
JO - JOURNAL OF PHYSICAL CHEMISTRY C
JF - JOURNAL OF PHYSICAL CHEMISTRY C
IS - 27
ER -