Electronic and vibronic properties of a discotic liquid-crystal and its charge transfer complex

TL;DR

This study investigates the electronic and vibrational properties of a discotic liquid-crystal charge transfer complex, revealing groundstate charge transfer, vibronic relaxation processes, and implications for photovoltaic applications.

Contribution

It provides a detailed analysis combining experimental and theoretical methods to understand charge transfer and vibronic interactions in a prototypic DLC CT complex, highlighting mechanisms relevant for PV design.

Findings

Groundstate charge transfer with 10^-2 electron delocalization

Fast UV vibronic relaxation due to intramolecular coupling

Slower relaxation in the visible CT band involving nitro groups

Abstract

Discotic liquid crystalline (DLC) charge transfer (CT) complexes combine visible light absorption and rapid charge transfer characteristics within the CT complex, being favorable properties for photovoltaic (PV) applications. We present a detailed study of the electronic and vibrational properties of the prototypic 1:1 mixture of discotic 2,3,6,7,10,11-hexakishexyloxytriphenylene (HAT6) and 2,4,7-trinitro-9-fluorenone (TNF). It is shown that intermolecular charge transfer occurs in the groundstate of the complex: a charge delocalization of about 10-2 electron from the HAT6 core to TNF is deduced from both Raman and our previous NMR measurements (Reference 32), implying the presence of permanent dipoles at the donor-acceptor interface. A combined analysis of density functional theory calculations, resonant Raman and UV-VIS absorption measurements indicate that fast relaxation occurs in the UV region due to intramolecular vibronic coupling of HAT6 quinoidal modes with lower lying electronic states. Relatively slower relaxation in the visible region CT-band of the complex is also indicated, which likely involves motions of the TNF nitro groups. The fast quinoidal relaxation process in the hot UV band of HAT6 relates to pseudo-Jahn-Teller interactions in a single benzene unit, suggesting that the underlying vibronic coupling mechanism can be generic for polyaromatic hydrocarbons. Both the presence of CT dipoles and relatively slow relaxation processes in the CT band can be relevant concerning the design of DLC based organic PV systems.