Tuning from unipolar (p-type or n-type) to ambipolar charge transport efficiency in bowl-shaped perylene-derivatives: a DFT study

Abstract

A series of bowl-shaped dicyclopenta perylene (DCPP) derivatives have been theoretically constructed by indeno-substitution at the peri-positions of DCPP, and suitably functionalizing with aza-, fluoride and imide-groups to enhance the electron transport behavior in the materials. To further ensure the solubility and stability of these organic compounds, we incorporated triethylsilylethynyl (TES) groups in the designed structures. The factors such as degree of aromaticity, electronic structure, molecular packing motif, intermolecular charge coupling, and charge transfer rate are essential in determining the charge transporting ability. The low-lying LUMO-levels (< -4.0 eV) and high electron affinities (> 3.0 eV) of a few DCPPs ensure efficient electron injection from the metal electrodes. These molecules are arranged in bowl-in-bowl columnar packing, which is suitable for facilitating the intermolecular charge transport in the crystal. As a result, we observed enhanced hole-transport behavior in DCPP-9 ({\mu}h = 6.296 cm2V-1s-1), electron transport in DCPP-TES-6 ({\mu}e = 0.142 cm2V-1s-1) and ambipolar nature of DCPP-12 and DCPP-TES-12. The DCPP-derivatives are also optically active in the UV-visible region, which is confirmed from the TD-DFT analysis. Inspired from their non-centrosymmetric molecular geometry and optical activity, we also investigated their non-linear optical (NLO) responses, which may pave their way towards applications in photonics and optoelectronics.