Molecular Design of n-Type Organic Semiconductors with Ultralow Electron Reorganization Energies

Abstract

Bottom-up design of n-type organic semiconductors with salient electron-transport properties is of fundamental importance. Here, with the aid of density functional theory, we demonstrate that condensing odd-membered carbon rings (5MR/7MR) to small polycyclic aromatic hydrocarbons (PAHs) can endow molecules with ultralow electron reorganization energies (λ < 100 meV). Studying 60 molecules, we find that introducing polycyclic fragments with built-in 5MR and 7MR to linear PAHs at the C α,β positions or to nonlinear PAHs in D 2h symmetry constitutes molecules with λ as low as 65 meV. A joint ACID and NICS analysis proves that the stronger the molecular aromaticity, the lower the λ will be. This is contrary to what has been previously found for p-type molecules. Furthermore, we propose "acupoints" on molecules for N-doping and cyanation, which can be used to precisely locate the substitution sites to reduce the LUMO energies (in favor of electron injection and air stability) of low-λ molecules while it does not elevate λ. These findings would help to reduce the synthetic blindness/cost and contribute to the bottom-up design of n-type small-molecule organic semiconductors.