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Title: Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor‐TCBD Push‐Pull System
Award ID(s):
2000988
NSF-PAR ID:
10320497
Author(s) / Creator(s):
; ; ; ;
Date Published:
Journal Name:
Angewandte Chemie International Edition
Volume:
60
Issue:
37
ISSN:
1433-7851
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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  1. null (Ed.)
  2. Abstract

    Attaining long‐lived charge‐transfer (CT) states is of the utmost importance for energy science, photocatalysis, and materials engineering. When charge separation (CS) is slower than consequent charge recombination (CR), formation of a CT state is not apparent, yet the CT process provides parallel pathways for deactivation of electronically excited systems. The nuclear, or Franck‐Condon (FC), contributions to the CT kinetics, as implemented by various formalisms based on the Marcus transition‐state theory, provide an excellent platform for designing systems that produce long‐lived CT states. Such approaches, however, tend to underestimate the complexity of alternative parameters that govern CT kinetics. Here we show a comparative analysis of two systems that have quite similar FC CT characteristics but manifest distinctly different CT kinetics. A decrease in the donor‐acceptor electronic coupling during the charge‐separation step provides an alternative route for slowing down undesired charge recombination. These examples suggest that, while infrequently reported and discussed, cases where CR is faster than CS are not necessarily rare occurrences.

     
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