Spectroscopic near-infrared photodetectors enabled by strong light–matter coupling in (6,5) single-walled carbon nanotubes

Abstract

Strong light-matter coupling leads to the formation of mixed exciton-polariton states, allowing for a rigorous manipulation of the absorption and emission of excitonic materials. Here, we demonstrate the realization of this promising concept in organic photodetectors. By hybridizing the E₁₁ exciton of semiconducting (6,5) single-walled carbon nanotubes (SWNTs) with near-infrared cavity photons, we create spectrally tunable polariton states within a photodiode. In turn, we are able to red-shift the detection peak that coincides with the lower polariton band. Our photodiodes comprise a metal cavity to mediate strong coupling between light and SWNTs and utilize P3HT and PC₇₀BM as the electron donor and acceptor, respectively. The diodes are formed either via mixing of SWNTs, P3HT, and PC₇₀BM to create a bulk heterojunction or by sequential processing of layers to form flat heterojunctions. The resulting near-infrared sensors show tunable, efficient exciton harvesting in an application-relevant wavelength range between 1000 nm and 1300 nm, with optical simulations showing a possible extension beyond 1500 nm.