ABSTRACT
Complex assemblies of light-emitting polymer nanofibers with molecular materials exhibiting optical gain can lead to important advance to amorphous photonics and to random laser science and devices. In disordered mats of nanofibers, multiple scattering and waveguiding might interplay to determine localization or spreading of optical modes as well as correlation effects. Here we study electrospun fibers embedding a lasing fluorene-carbazole-fluorene molecule and doped with titania nanoparticles, which exhibit random lasing with sub-nm spectral width and threshold of about 9 mJ cm-2 for the absorbed excitation fluence. We focus on the spatial and spectral behavior of optical modes in the disordered and non-woven networks, finding evidence for the presence of modes with very large spatial extent, up to the 100 µm-scale. These findings suggest emission coupling into integrated nanofiber transmission channels as effective mechanism for enhancing spectral selectivity in random lasers and correlations of light modes in the complex and disordered material.
ABSTRACT
A straight synthetic route to fabricate hybrid nanocomposite films of well-dispersed CdS nanocrystals (NCs) in poly[2-methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) is reported. A soluble cadmium complex [Cd(SBz)2]2·MI, obtained by incorporating a Lewis base (1-methylimidazole, MI) on the cadmium bis(benzyl)thiol, is used as starting reagent in an in situ thermolytic process. CdS NCs with spherical shape nucleate and grow well below 200°C in a relatively short time (30 min). Photoluminescence spectroscopy measurements performed on CdS/MEH-PPV nanocomposites show that CdS photoluminescence peaks are totally quenched inside MEH-PPV, if compared to CdS/PMMA nanocomposites, as expected due to overlapping of the polymer absorption and CdS emission spectra. The CdS NCs are well-dispersed in size and homogeneously distributed within MEH-PPV matrix as proved by transmission electron microscopy. Nanocomposites with different precursor/polymer weight ratios were prepared in the range from 1:4 to 4:1. Highly dense materials, without NCs clustering, were obtained for a weight/weight ratio of 2:3 between precursor and polymer, making these nanocomposites particularly suitable for optoelectronic and solar energy conversion applications.
ABSTRACT
Polymer films embedding cadmium thiolate precursors have been irradiated with ultraviolet laser pulses resulting in the formation of cadmium sulfide crystalline nanoparticles through a macroscopically non-destructive procedure for the host matrix. Controlling the number of the incident laser pulses, the gradual increase of the size of the nanoparticles is accomplished, and consequently the progressive change of the emission characteristics of the formed nanocomposites. The X-ray diffraction and transmission electron microscopy measurements were used for the full characterization of the nanoparticles. This study compares two polymer matrices, poly(methyl methacrylate) and a cyclic olefin copolymer, and reveals the importance of each one for the emission characteristics of the formed cadmium sulfide nanocrystals. It is found that the poly(methyl methacrylate) matrix contributes to the increase of the trap states on the surface of the formed nanocrystals, causing the broadening of their emission. On the other hand the cadmium sulfide nanoparticles, grown into the cyclic olefin copolymer matrix, exhibit narrower emission spectra.
