Paul Liska

Highly Efficient Dye-Sensitized Solar Cells Based on Carbon Black Counter Electrodes

Carbon black was employed as the catalyst for triiodide reduction on fluorine-doped tin oxide glass substrates (FTO-glass) used as counter electrodes in platinum-free dye-sensitized solar cells. The fill factors were strongly dependent on the thickness of the carbon layer, and the light energy conversion efficiency also increased up to a thickness of 10 μm. The charge-transfer resistance (R ct ) of the carbon counter electrode decreased with the thickness of the carbon layer. The R ct for the thicker carbon layer is less than three times that for the platinized FTO-glass. The highest cell efficiency was 9.1% under 100 mW cm -2 light intensity (1 sun AM 1.5 light, J sc = 16.8 mA cm -2 , V oc = 789.8 mV, fill factor = 0.685).

High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye

An indoline dye (D205), the synthesis method of which is disclosed in this report, gave high-efficiency organic dye-sensitized solar cells (9.52%) using an anti-aggregation reagent (chenodeoxycholic acid).

Nanocrystalline dye-sensitized solar cell/copper indium gallium selenide thin-film tandem showing greater than 15% conversion efficiency

Multijunction stacked (tandem) solar cells can increase the overall photovoltaic conversion efficiency by optimal utilization of the solar spectrum in individual cells. We demonstrate that a photovoltaic tandem cell comprising a nanocrystalline dye-sensitized solar cell as a top cell for high-energy photons and a copper indium gallium selenide thin-film bottom cell for lower-energy photons produces AM 1.5 solar to electric conversion efficiencies greater than 15%.

Mediator Transport in Multilayer Nanocrystalline Photoelectrochemical Cell Configurations

Reference LPI-ARTICLE-1999-019doi:10.1149/1.1391698View record in Web of Science Record created on 2006-02-21, modified on 2017-05-12

Acid versus base peptization of mesoporous nanocrystalline TiO2 films: functional studies in dye sensitized solar cells

We report an analysis of the influence of acid/base conditions employed in the synthesis of TiO2 nanoparticles upon the performance of dye sensitised photoelectrochemical solar cells fabricated from these particles. The functional properties of the TiO2 nanoparticles in these devices are investigated by potential step chronoamperometry, transient laser spectroscopy, and photovoltaic device characterisation. We find that base peptization conditions employed in the sol–gel fabrication of the TiO2 nanoparticles result in a reduction in film electron density under negative applied bias, correlated with slower interfacial recombination losses and a higher device open circuit voltage.

Voltage enhancement in dye-sensitized solar cell using (001)-oriented anatase TiO2 nanosheets

A nanocrystalline TiO2 (anatase) nanosheet exposing mainly the (001) crystal faces was tested as photoanode material in dye-sensitized solar cells. The nanosheets were prepared by hydrothermal growth in HF medium. Good-quality thin films were deposited on F-doped SnO2 support from the TiO2 suspension in ethanolic or aqueous media. The anatase (001) face adsorbs a smaller amount of the used dye sensitizer (C101) per unit area than the (101) face which was tested as a reference. The corresponding solar cell with sensitized (001)-nanosheet photoanode exhibits a larger open-circuit voltage than the reference cell with (101)-terminated anatase nanocrystals. The voltage enhancement is attributed to the negative shift of flatband potential for the (001) face. This conclusion rationalizes earlier works on similar systems, and it indicates that careful control of experimental conditions is needed to extract the effect of band energetic on the current/voltage characteristics of dye-sensitized solar cell.

Highly active meso-microporous TaON photocatalyst driven by visible light

TaON was found to be ca. 20 times more active as a visible light activated photocatalyst for the oxidation of methanol, when compared to the well studied UV-visible activated TiO2 (P25) catalyst.

The Electronic Role of the TiO2 Light-Scattering Layer in Dye-Sensitized Solar Cells

Dye-sensitized solar cells have been fabricated with different kinds of TiO2 films including SiO2 coated and bare TiO2 microparticles as light-scattering layer (LSL). Results show that the LSL barely affects the cells dark current, whereas under illumination, it made a significant contribution to the total photocurrent. Photo-voltage decay measurements performed under bias illumination show the density of electronic states (DOS) of the LSL to be two times smaller than that of a transparent nanoparticle layer (TNL). Strikingly, DSCs fabricated from a 4.5μm thick LSL alone showed a conversion efficiency of 5% despite of being pale pink in color. This impressive performance is attributed to light containment in the LSL and a low density of defect electronic states.

Efficient spectral sensitisation of polycrystalline titanium dioxide photoelectrodes

Reference LPI-ARTICLE-1987-021View record in Web of Science Record created on 2006-02-21, modified on 2017-05-12

Optically Transparent FTO-Free Cathode for Dye-Sensitized Solar Cells

The woven fabric containing electrochemically platinized tungsten wire is an affordable flexible cathode for liquid-junction dye-sensitized solar cells with the I3(-)/I(-) redox mediator and electrolyte solution consisting of ionic liquids and propionitrile. The fabric-based electrode outperforms the thermally platinized FTO in serial ohmic resistance and charge-transfer resistance for triiodide reduction, and it offers comparable or better optical transparency in the visible and particularly in the near-IR spectral region. The electrode exhibits good stability during electrochemical loading and storage at open circuit. The dye-sensitized solar cells with a C101-sensitized titania photoanode and either Pt-W/PEN or Pt-FTO cathodes show a comparable performance.