The characteristics of field effect transistors (FETs) fabricated using two-dimensional (2D) transition-metal dichalcogenides (TMDCs) can be modulated by surface treatment of the active layers. In this study, an ionic π-conjugated polyelectrolyte, poly­(9,9-bis­(4′-sulfonatobutyl)­fluorene-alt-1,4-phenylene) potassium (FPS-K), was used for the surface treatment of MoSe2 and WS2 FETs. The photoluminescence (PL) intensities of monolayer (1L)-MoSe2 and 1L-WS2 clearly decreased, and the PL peaks were red-shifted after FPS-K treatment, suggesting a charge-transfer effect. In addition, the n-channel current of both the MoSe2 and WS2 FETs increased and the threshold voltage (V th) shifted negatively after FPS-K treatment owing to the charge-transfer effect. The photoresponsivity of the MoSe2 FET under light irradiation (λex = 455 nm) increased considerably, from 5300 A W–1 to approximately 10 000 A W–1, after FPS-K treatment, and similar behavior was observed in the WS2 FET. The results can be explained in terms of the increase in electron concentration due to photogating. The external quantum efficiency and photodetectivity of both FETs were also enhanced by the charge-transfer effect resulting from surface treatment with FPS-K containing mobile cations (K+) and fixed anions (SO3 –), as well as by the photogating effect. The variation in charge-carrier density due to the photogating and charge-transfer effects is estimated to be approximately 2 × 1012 cm–2. The results suggest that π-conjugated polyelectrolytes such as FPS-K can be a promising candidate for the passivation of TMDC-based FETs and obtaining enhanced photoresponsivity.

Organic–inorganic metal halide perovskites (OMHPs) are promising active materials suitable for highly efficient solar cells, photodetectors, light-emitting diodes, and sensors. In this study, methylammonium lead iodide (MAPbI3) thin sheets (TSs) were synthesized as OMHPs using both hybrid vapor-solution method for optical study and anti-solvent solution method for the photodetector. π-Conjugated polyelectrolyte (π-CPE), such as poly­(9,9-bis­(4′-sulfonatobutyl)­fluorene-alt-1,4-phenylene) potassium (FPS-K), was spin-coated on the MAPbI3 TS, and functionalized gold nanoparticles (Au-NPs) were hybridized. The laser confocal microscope photoluminescence (PL) intensity of the MAPbI3 TS was significantly enhanced after hybridization with Au-NPs/FPS-K, owing to the passivating effect of the FPS-K and the generation of extra-photoexcited charges by local surface plasmon resonance (LSPR) coupling with Au-NPs. These results were supported by the variation in the exciton lifetime measured from the time-resolved PL decay curves. The photocurrent of the MAPbI3 photodetector increased up to 1.1 × 104 times, and the photoresponsivity (R) and photodetectivity (D*) increased by 70 and 13 times, respectively, with the hybridization of Au-NPs/FPS-K. The highest D* of the Au-NPs/FPS-K/MAPbI3 photodetector was measured to be 7.5 × 1010 Jones at 735 nm excitation. The power and wavelength dependencies of R and D* for the MAPbI3 photodetector were also significantly improved by the Au-NPs/FPS-K hybrid. These results support the development of high-performance perovskite photodetectors utilizing LSPR coupling with the π-CPE layer.