In addition to photoluminescence, pyrene molecules also display electroluminescence (EL).[15] The electrical conductivity of the pyrene-embedded PPy nanoparticles was 3.5 S cm ±1 .In EL devices, a PPy conducting layer can be used as a good hole-transporting layer (HTL). In general, EL devices doped with PPy as the HTL yield higher luminance efficiencies and lower turn-on voltages. [16] It seems that a pyrene-embeddedPPy nanoparticle layer could be utilized as a good HTL (owing to the conducting ability of PPy) and also as an emitting layer (EML) due to the EL properties of pyrene. Pyrene-embedded PPy nanoparticles can therefore be called HTL/EML nanohybrids. In addition, the emission color can be tuned by introducing other organic dyes, such as rhodamine B (red) and fluorescein (green).In conclusion, photochromic dye±conducting polymer core± shell nanomaterials were fabricated using microemulsion micelles as nanoreactors. PPy nanoparticles (7±13 nm in diameter) embedded with a pyrene core were successfully synthesized. As the pyrrole monomer polymerized, pyrene molecules were phase-separated and gathered together toward the interior of the micelle. The adsorption state of pyrene was tunable over a wide range with a small amount of pyrene, because of the nanosized reaction site of the micelles and the packing constraint of pyrene crystal. The emission colors of the nanohybrids were controllable from violet to blue by changing the amount of embedded pyrene. Our methodology provides a facile and effective way for controlling the adsorption state of organic dyes, and also presents a new concept in use of the HTL/EML nanohybrids in EL devices.
ExperimentalSynthesis of Pyrene-Embedded PPy Nanoparticles: 3 g of decyltrimethylammonium bromide (DeTAB) was magnetically stirred in 40 mL of H 2 O at 3 C. Pyrene, in quantities of 0.5, 3, 5, and 10 mg, was mixed into 1.0 g (14.9 mmol) of pyrrole monomer. The mixture was added dropwise to the surfactant solution. FeCl 3 (5.561 g, 34.3 mmol) was dissolved in a small amount of distilled water and the solution was added to the reaction mixture. Chemical polymerization proceeded for 3 h at 3 C. The reaction product was moved to a separating funnel and excess methyl alcohol was added to remove the surfactant and residual ferric chloride. A small amount of isooctane was added to promote the precipitation of the PPy nanoparticles, owing to the enhanced hydrophobicity. The upper solution containing surfactant and unreacted ferric chloride was discarded and the nanoparticle precipitate was dried in a vacuum oven at room temperature. For comparison, pure PPy nanoparticles, without any embedded pyrene, were also synthesized. For the photoluminescence experiments, pyrene and pyrene-embedded PPy nanoparticles were dispersed in benzene and methyl alcohol (spectrophotometric grade), respectively.Instrumental Analysis: The TEM images and EDX data were taken using a Philips CM-20 microscope coupled with an EDX facility. Emission spectra were obtained with a Shimadzu RF-5301 PC spectrofluorophot...