Increased efficiency of luminescent solar concentrators after application of organic wavelength selective mirrors.

Organic wavelength-selective mirrors are used to reduce the loss of emitted photons through the surface of a luminescent solar concentrator (LSC). A theoretical calculation suggests that application of a 400 nm broad reflector on top of an LSC containing BASF Lumogen Red 305 as a luminophore can reflect 91% of all surface emitted photons back into the device. Used in this way, such broad reflectors could increase the edge-emission efficiency of the LSC by up to 66%. Similarly, 175 nm broad reflectors could increase efficiency up to 45%. Measurements demonstrate more limited effectiveness and dependency on the peak absorbance of the LSC. At higher absorbance, the increased number of internal re-absorption events reduces the effectiveness of the reflectors, leading to a maximum increase in LSC efficiency of ~5% for an LSC with a peak absorbance of 1. Reducing re-absorption by reducing dye concentration or the coverage of the luminophore coating results in an increase in LSC efficiency of up to 30% and 27%, respectively.

Patterned dye structures limit reabsorption in luminescent solar concentrators.

This work describes a method for limiting internal losses of a luminescent solar concentrator (LSC) due to reabsorption through patterning the fluorescent dye doped coating of the LSC. By engineering the dye coating into regular line patterns with fill factors ranging from 20 - 80%, the surface coverage of the dye molecules were reduced, thereby decreasing the probability of the re-emitted light encountering another dye molecule and the probability of reabsorption. Two types of fluorescent dyes with different quantum yields were used to examine the effects of patterning on LSC performance. The effect of various dimension and geometry of the patterns on the efficiency and edge emission of LSC are presented and analyzed.

Control of Alq3 wetting layer thickness via substrate surface functionalization.

The effects of substrate surface energy and vapor deposition rate on the initial growth of porous columnar tris(8-hydroxyquinoline)aluminum (Alq3) nanostructures were investigated. Alq3 nanostructures thermally evaporated onto as-supplied Si substrates bearing an oxide were observed to form a solid wetting layer, likely caused by an interfacial energy mismatch between the substrate and Alq3. Wetting layer thickness control is important for potential optoelectronic applications. A dramatic decrease in wetting layer thickness was achieved by depositing Alq3 onto alkyltrichlorosilane-derivatized Si/oxide substrates. Similar effects were noted with increasing deposition rates. These two effects enable tailoring of the wetting layer thickness.

Formation and aqueous surface wettability of polysiloxane nanofibers prepared via surface initiated, vapor-phase polymerization of organotrichlorosilanes.

The formation of high aspect ratio organosiloxane fibers of nanodimensionality via the surface-induced vapor-phase polymerization of vinyltrichlorosilane is reported. We also demonstrate the versatility of our method by producing fibers of various densities, polydispersities, and lengths. Nanofibers were characterized using SEM, EDX, XPS, TOF-SIMS, and variable-angle FTIR. Advancing aqueous contact angle measurements were used to evaluate the nanofiber surface wettability.