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Hybrid nanostructures comprising conjugated polymers (CPs) and plasmonic metals show excellent performance in light harvesting. However, the energy transfer mechanism of the CP film to nearby metal nanoparticles, especially knowledge of the characteristic distance, is still unclear. Here, quenching of the emission of a CP film in proximity to a monolayer of graphene-nanodot-supported silver nanoparticles (GND-Ag NPs) is investigated. Uniform Ag NPs with D = 3.2 nm were grown on GNDs in situ under mild light irradiation, and a series of bilayer structures of GND-Ag NPs/CPs were constructed by spin-coating blue, green and red light-emitting poly(9,9-dioctylfluorene) (PFO), poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) and poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV),respectively, on top of the GND-Ag NP plane. The spacer distance was controlled by the layers of assembled polyelectrolytes. Both steady and transient photoluminescence (PL) spectra showed emission quenching of the bilayer structures, providing the maximum efficiency of 99% for the F8BT films. The surface density of GND-Ag NPs and the spacer distance-dependent PL quenching data were analyzed within the plasmonic resonant energy transfer model, and the extracted characteristic distances are 6 nm, 3 nm and 10 nm for the PFO, F8BT and MEH-PPV systems, respectively. Current-sensing atomic force microscopy shows that the GND-Ag NPs/F8BT film exhibits enhanced electrical conductivity. These results are believed to be important for the development of plasmonic enhanced polymer photovoltaics and photocatalysis.