Josep Albero

Catalysis of Recombination and Its Limitation on Open Circuit Voltage for Dye Sensitized Photovoltaic Cells Using Phthalocyanine Dyes

In order to increase the energy efficiency of dye-sensitized solar cells beyond 10%, an improved dye needs to be developed with greater light absorption in the red and near-infrared. Many dyes have been tested for this purpose; however, no dye with significant absorption beyond 750 nm has functioned properly. We have examined a series of ruthenium phthalocyanines, a dye class with large and tunable absorption in the red. For these dyes we observe a large reduction in the output voltage of the cells relative to the benchmark dye (N719). By examination of photovoltage transients and charge density measurements, we demonstrate that this reduction in voltage is caused by a 100-fold increase in the rate constant for recombination (iodine reduction) at the TiO2/electrolyte interface. N719, however, does not seem to catalyze this reaction. By examination of the literature, we propose that catalysis of the recombination reaction may be occurring for many other classes of potentially useful dyes including porphyri...

Structure-function relationships in unsymmetrical zinc phthalocyanines for dye-sensitized solar cells.

A series of unsymmetrical zinc phthalocyanines bearing an anchoring carboxylic function linked to the phthalocyanine ring through different spacers were designed for dye-sensitised solar cells (DSSC). The modification of the spacer group allows not only a variable distance between the dye and the nanocrystalline TiO(2), but also a distinct orientation of the phthalocyanine on the semiconductor surface. The photovoltaic data show that the nature of the spacer group plays a significant role in the electron injection from the photo-excited dye into the nanocrystalline TiO(2) semiconductor, the recombination rates and the efficiency of the cells. The incident monochromatic photon-to-current conversion efficiency (IPCE) for phthalocyanines bearing an insulating spacer is as low as 9%, whereas for those with a conducting spacer an outstanding IPCE 80% was obtained.

Quantum Dot-Dye Bilayer-Sensitized Solar Cells: Breaking the Limits Imposed by the Low Absorbance of Dye Monolayers

Here, we present a new DSSC design, consisting of sequential QDs and dye sensitization layers, that opens the path toward high optical density DSSCs that cover a significant part of the solar spectrum. The new configuration is enabled by the application of an amorphous TiO2 layer between the two sensitizers, allowing both electron injection from the outer absorber and fast hole extraction from the inner sensitizing layer. Utilizing two sensitizing layers, we obtain a 250% increase in cell efficiency compared to a QD monolayer cell.

Efficient and limiting reactions in aqueous light-induced hydrogen evolution systems using molecular catalysts and quantum dots.

Hydrogen produced from water and solar energy holds much promise for decreasing the fossil fuel dependence. It has recently been proven that the use of quantum dots as light harvesters in combination with catalysts is a valuable strategy to obtain photogenerated hydrogen. However, the light to hydrogen conversion efficiency of these systems is reported to be lower than 40%. The low conversion efficiency is mainly due to losses occurring at the different interfacial charge-transfer reactions taking place in the multicomponent system during illumination. In this work we have analyzed all the involved reactions in the hydrogen evolution catalysis of a model system composed of CdTe quantum dots, a molecular cobalt catalyst and vitamin C as sacrificial electron donor. The results demonstrate that the electron transfer from the quantum dots to the catalyst occurs fast enough and efficiently (nanosecond time scale), while the back electron transfer and catalysis are much slower (millisecond and microsecond time scales). Further improvements of the photodriven proton reduction should focus on the catalytic rate enhancement, which should be at least in the hundreds of nanoseconds time scale.

Light‐Driven Organocatalysis Using Inexpensive, Nontoxic Bi2O3 as the Photocatalyst

The development of enantioselective catalytic processes that make use of sunlight as the energy source and nontoxic, affordable materials as catalysts represents one of the new and rapidly evolving areas in chemical research. The direct asymmetric α-alkylation of aldehydes with α-bromocarbonyl compounds can be successfully achieved by combining bismuth-based materials as low-band-gap photocatalysts with the second-generation MacMillan imidazolidinone as the chiral catalyst and simulated sunlight as a low-cost and clean energy source. This reaction also proceeded with high efficiency when the reaction vial was exposed to the morning sunlight on a clear September day in Tarragona, Spain.

111 oriented gold nanoplatelets on multilayer graphene as visible light photocatalyst for overall water splitting

Development of renewable fuels from solar light appears as one of the main current challenges in energy science. A plethora of photocatalysts have been investigated to obtain hydrogen and oxygen from water and solar light in the last decades. However, the photon-to-hydrogen molecule conversion is still far from allowing real implementation of solar fuels. Here we show that 111 facet-oriented gold nanoplatelets on multilayer graphene films deposited on quartz is a highly active photocatalyst for simulated sunlight overall water splitting into hydrogen and oxygen in the absence of sacrificial electron donors, achieving hydrogen production rate of 1.2 molH2 per gcomposite per h. This photocatalytic activity arises from the gold preferential orientation and the strong gold–graphene interaction occurring in the composite system.

Charge transfer kinetics in CdSe quantum dot sensitized solar cells.

We report the charge transfer dynamics for CdSe quantum dot (QD) sensitized solar cells. The effect of QD sensitization mode in recombination kinetics has been measured and their implications in solar cell performance analyzed.

Interfacial charge transfer dynamics in CdSe/dipole molecules coated quantum dot polymer blends

We report our results on the influence of the dipole moment of small molecules anchored to the surface of CdSe nanocrystals, over the interfacial charge recombination dynamics in CdSe/P3HT (P3HT : poly-3-hexylthiophene). The polarizability of the CdSe/P3HT interface is key to achieving efficient charge separation and slow back electron transfer, two of the most important processes to boost the photocurrent and voltage in CdSe/P3HT photovoltaic devices.

Photocatalytic Activity of Au/TiO2 Photocatalysts for H2 Evolution: Role of the Au Nanoparticles as a Function of the Irradiation Wavelength

An investigation of hydrogen production with a series of Au/TiO2 photocatalysts reveals that the Au nanoparticles play different roles depending on the wavelength of the light irradiation. Under visible-light irradiation, the photoactivity is primarily controlled by the intensity of the Au surface plasmon band, whereas under UV irradiation the Au nanoparticles act as co-catalysts with TiO2 .

Photo-induced charge recombination kinetics in low bandgap PCPDTBT polymer:CdSe quantum dot bulk heterojunction solar cells

The interfacial charge transfer recombination processes under working conditions that limit the device performance in polymer:CdSe quantum dot bulk heterojunction hybrid solar cells have been measured. The recombination lifetimes for electrons and holes in the device show an exponential dependence in a similar way to that observed for other molecular based solar cells such as bulk heterojunction organic solar cells (OSC) and dye sensitized solar cells (DSSC). The implications of this unprecedented observation on the design of novel devices are discussed as well as the relationship between the charge accumulation in these devices under operation and the device open-circuit voltage.