posted on 2025-01-29, 13:07authored byAditi Kumar, Rohan J. Hudson, Nikita A. Shumilov, Chao-Yang Lin, Trevor A. Smith, Nathaniel J. L.
K. Davis, Eric C. Le Ru, Michael B. Price, Paul A. Hume, Justin M. Hodgkiss
The organic semiconductor Y6 has been extensively used
as an acceptor
in organic photovoltaic devices, yielding high efficiencies. Its unique
properties include a high refractive index, intrinsic exciton dissociation,
and barrierless charge generation in bulk heterojunctions. However,
the direct impact of the crystal packing morphology on the photophysics
of Y6 has remained elusive, hindering further development of heterojunction
and homojunction devices. Herein, we study the photogenerated species
in multiple distinct Y6 crystal packing geometries via transient absorption
spectroscopy and photovoltaic measurements of the corresponding single-component
devices. Our results reveal that “co-facial” interactions
drive the generation of charge-transfer states in neat films of Y6
and that exciton dissociation can be switched on and off by controlling
these interactions. Additionally, we find that a combination of long-range
order and more co-facial packing interactions accelerates the charge-transfer
generation process and increases the exciton to charge-transfer conversion
efficiency. These insights provide valuable structure–property
relationships for optimizing device performance.