AI Article Synopsis

  • The text discusses how structural similarities in organic molecules lead to narcissistic self-sorted phenomena, enhancing exciton dissociation and charge separation in solar cells.
  • It presents two π-conjugated derivatives, one being a zinc-porphyrin linked to benzothiadiazole (PB) as the acceptor and anthracene (PA) as the donor, which form unique 1D nanofibers and aggregates.
  • The study highlights that the electrical properties of these self-sorting assemblies are influenced by the electrostatic potential differences between PA and PB, achieving a conductivity of 0.14 S cm, which aids in the development of more effective photovoltaic materials.

Article Abstract

The narcissistic self-sorted phenomenon is explicitly attributed to the structural similarities in organic molecules. Although such relevant materials are rarely explored, self-sorted structures from macrocyclic π-conjugated-based p- and n-type organic semiconductors facilitate the increase of exciton dissociation and charge separation in bulk heterojunction solar cells. Herein, we report two extended π-conjugated derivatives consisting of zinc-porphyrin-linked benzothiadiazole acting as an acceptor (PB) and anthracene as a donor (PA). Despite having the same porphyrin π-conjugated core in PA and PB, variations in donor and acceptor moieties make the molecular packing form one-dimensional (1D) self-assembled nanofibers H- and J-type aggregates. Interestingly, a dissimilar aggregate of PA and PB exists as a mixture (PA + PB), promoting narcissistic self-sorted structures. Electrochemical impedance investigation reveals that the electronic characteristics of self-sorting assemblies are influenced by the difference in electrostatic potentials for PA and PB, resulting in a transitional electrical conductivity of 0.14 S cm. Therefore, the design of such materials for the fabrication of effective photovoltaics is promoted by these extraordinary self-sorted behaviors in comparable organic π-conjugated molecules.

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http://dx.doi.org/10.1039/d4nr00991fDOI Listing

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