No description available.

In this work, we study the technique of Titanium Dioxide(TiO2) work electrode of the dye sensitized solar cells. The research contained four parts. (I)Fabrication of porous TiO2 with sol-gel method. (II)Compare the efficiency between dense layer non-dense layer. (III)Study the characteristics of nanometer photocatalyzer layer with silver atom on porous layer. (IV)Replace the commercial dye with the novel Discotic Liquid Crystal(DLC) material which we synthesized. We compared different TiO2 particle size, and discovered the efficiency of 20nm particle which made Degussa reached 3.31%. After joining dense layer, the efficiency can be up to 3.75%. Finally, we sprayed a silver atom layer, the device efficiency increase to 4.13%. Because of the cost of the commercial dye, we replace the dye with DLC which were synthesized by ourselves. The efficiency is up to 0.46%. We offer a feasible direction in low cost and high-efficiency at present.

Thesis (M.S.)--Rutgers University, 2008. / "Graduate Program in Physics." Includes bibliographical references (p. 83-87).

Dye-sensitized solar cells (DSSC) have drawn much attention due to their higher versatility and lower production cost compared to inorganic photovoltaics. The top performers of DSSC have achieved power conversion efficiency over 10%, which is comparable to amorphous silicon solar cells. In this work, new photosensitizers and nanostructure for improving the photovoltaic performance of DSSC were developed and evaluated. Two series of cyclometalated ruthenium(II) complex photosensitizer were presented and their photosensitizing properties in DSSC were studied. Eight cyclometalated ruthenium(II) terpyridine complexes with three carboxylic acid groups on the terpyridine ligand were synthesized. Series A (M1 to M4) consist of C,N,N’ ligands substituted with phenyl group whereas series B (M5 to M8) consist of C,N,N’ ligands substituted with m-fluorophenyl group. All of the complexes exhibited broad aborption spectra covering the whole visible spectrum. The complexes in series B generally showed better photovoltaic performance than those in series A in the DSSCs. DSSC fabricated from M7 achieved the highest Voc, Jsc and power conversion efficiency among other DSSC, which were 0.56 V, 7.30 mAcm-2 and 2.63 % respectively. Truxene-core donor--acceptor dyes were presented and their photosensitizing properties in DSSC were studied. Eight dyes with either one donor two acceptors system (T2, B2, T2R and B2R) or two donor one acceptor system (T1, B1, T1R and B1R) were synthesized. Dyes with two acceptors have high molar extinction coefficients originated from the charge-transfer transition band, which are almost two times higher than those with only one accceptors. Both the enhanced absorption and better anchoring geometry on TiO2 contribute to the better photovoltaic performance of the two acceptors dyes in the DSSCs. Devices fabricated from B2 and volatile solvent electrolyte exhibited the best photovoltaic performance among the truxene-core dyes. The Voc, Jsc, FF and power conversion efficiency of the device were 0.59 V, 9.69 mAcm-2, 0.63 and 3.62 % respectively. Dyes based on cyanoacrylic acid anchoring groups (T1, T2, B1 and B2) were found to perform better than those based on rhodanine-3-acetic acid dyes (T1R, T2R, B1R and B2R) in both donor--acceptor configurations. ITO nanorod/TiO2 nanoparticle composite films with the three different types of ITO nanorod with different length (150 nm, 600 nm and 1.5 μm) were fabricated on FTO glass substrate. The transmittance and sheet resistance of the ITO nanorod array on the FTO glass substrate were found decreased with increasing the length of the ITO nanorod. When the ITO nanorod/TiO2 nanoparticle composite films were applied as the anode in DSSCs, the device fabricated from 600 nm ITO nanorod with TiO2 ‘double layer‘ film showed enhanced photocurrent generation. The improved photocurrent generation is suggested to be due to an improved charge collection efficiency at the ITO nanorod back electrode. / published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

No description available.

Thesis (M.S.)--West Virginia University, 2008. / Title from document title page. Document formatted into pages; contains v, 37 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 33-37).

Thesis (Ph. D.)--Rutgers University, 2010. / "Graduate Program in Materials Science and Engineering." Includes bibliographical references.

Thesis (Ph. D.)--Rutgers University, 2008. / "Graduate Program in Physics and Astronomy." Includes bibliographical references (p. 153-161).

No description available.

Dye-sensitised solar cells (DSCs) have the potential to be a low cost solar cell candidate due to the relatively low cost of materials and ease of processing. Also, unlike traditional silicon solar cells, DSCs can be lightweight and flexible, and perform well in diffuse sunlight and indoors which make them an extremely attractive prospect. This thesis investigates the time intensive heating stages associated with the fabrication of a DSC which are currently a bottleneck for translating this technology from the laboratory to an industrial scale. In addition some steps associated with the fabrication of a DSC share similarity to other technologies so these methods could be extremely applicable and versatile. Near infrared (NIR) radiative heating was used here to drastically reduce the heating times associated with DSC fabrication steps. NIR heating involves the absorption of NIR photons by the free electrons of an infrared absorbing substrate which releases thermal energy rapidly. NIR radiation has previously been used for the heating of metallic substrates but this is the first time it has been used to heat glass based substrates, which significantly broadens the potential applications of NIR heating. Upon 12.5 s of NIR exposure FTO and ITO coated glass reached significantly high temperatures, temperatures corresponding well to those required for the DSC heating steps. NIR radiation was used to sinter TiO2 working electrodes and thermally platinise counter electrodes on FTO glass in 12.5 s, 144 times faster than the conventional oven heating of 30 minutes. When assembled into DSC devices these electrodes performed identically to their oven equivalents. When combined with a faster dyeing process this enabled the overall laboratory manufacturing time of a DSC to be reduced from 123 min to 5 min with no compromise in efficiency which is an extremely promising step for the viability of DSC commercialisation.