An Expeditious Synthesis of Near‐Infrared‐Absorbing Imide‐Based Graphene Nanoribbons and Their Photothermal Properties

Abstract

Graphene nanoribbons (GNRs) with low band gap and strong near‐infrared (NIR) absorption are potential candidates for optoelectronic and biomedical applications. In this context, imide‐based GNRs are promising, but there are no rational design principles that yield these robust GNRs with strong NIR absorption. Here, we demonstrate a rational synthesis route to achieve NIR‐absorbing imide‐based robust GNRs by exploring the bay region of polyperylene (PP). Using the oxidative Diels‐Alder reaction, we have successfully introduced mono and diimide functional groups on PP. After cyclodehydrogenation, the resultant GNRs, benzoperylene imide GNR (BPI‐GNR) and coronene diimide GNR (CDI‐GNR), show oscillatory edge geometry with strong NIR absorption (up to 1000 nm) and optical band gap of ~1.3 eV. Computational studies also indicate that imide substituents play an important role in fine‐tuning the optoelectronic properties of GNRs. Moreover, these GNRs are solution‐processable and can be made into thin films via spray coating. Owing to the strong NIR absorption and imide substitutions, BPI and CDI‐GNRs show good photothermal conversion with excellent cyclic stability.