Lenneke H. Slooff

Luminescent Solar Concentrators - A review of recent results

Luminescent solar concentrators (LSCs) generally consist of transparent polymer sheets doped with luminescent species. Incident sunlight is absorbed by the luminescent species and emitted with high quantum efficiency, such that emitted light is trapped in the sheet and travels to the edges where it can be collected by solar cells. LSCs offer potentially lower cost per Wp. This paper reviews results mainly obtained within the framework of the Full-spectrum project. Two modeling approaches are presented, i.e., a thermodynamic and a ray-trace one, as well as experimental results, with a focus on LSC stability.

Determining the internal quantum efficiency of highly efficient polymer solar cells through optical modeling

A power conversion efficiency of 4.2% (AM1.5, 1000W∕m2) is measured for an organic solar cell based on an active layer of an alternating copolymer, containing a fluorene and a benzothiadiazole unit with two neighboring thiophene rings, and a fullerene derivative. Using optical modeling, the absorption profile in the active layer of the solar cell is calculated and used to calculate the maximum short circuit current. The calculated currents are compared with measured currents from current-voltage measurements for various film thicknesses. From this the internal quantum efficiency is estimated to be 75% at the maximum for the best device.

I-V Performance and Stability Study of Dyes for Luminescent Plate Concentrators

In this paper, both the performance and stability of luminescent flat plate concentrator (LFPC) plates in combination with mc-Si photovoltaic cells are studied. It is shown that the electrical current of a silicon solar cell attached to the luminescent plate is improved by a factor 1.5 using a LFPC containing a single dye. It is also shown that most of the dyes are not stable in the polymer plates that are currently used. Screening of the stability of several other dyes indicates that the stability is strongly dependent on the type of dye and the polymer matrix, e.g., additives or the monomer residues.

Efficiency Enhancement of Solar Cells by Application of a Polymer Coating Containing a Luminescent Dye

One of the major loss mechanisms in state of the art photovoltaic cells is spectral loss resulting from inefficient use of ultraviolet photons and the lack of absorption of infrared photons by the solar cell. For a Si solar cell, e.g., spectral losses alone result in over 55% loss of the energy of the solar spectrum. Converting the spectrum of the incoming light such that it has a better match with the absorption spectrum of the solar cell can reduce spectral losses, especially in the case of a small absorption band, such as for dye sensitized solar cells and polymer solar cells. In this paper it is shown that the ultraviolet response of a multicrystalline silicon solar cell and polymer solar cell can be enhanced by application of a polymer coating doped with a luminescent dye. An increase in the power conversion efficiency is obtained for coatings with luminescent dyes with an absorption onset <450 nm. Coatings with luminescent dyes that absorb at higher wavelengths give rise to lower power conversion efficiencies. When applied to a dye sensitized solar cell, a decrease in the cell performance is observed.

The luminescent concentrator illuminated

Luminescent concentrator (LC) plates with different dyes were combined with standard multicrystalline silicon solar cells. External quantum efficiency measurements were performed, showing an increase in electrical current of the silicon cell (under AM1.5, 1 sun conditions, at normal incidence) compared to a bare cell. The influence of dye concentration and plate dimensions are addressed. The best results show a 1.7 times increase in the current from the LC/silicon cell compared to the silicon cell alone. To broaden the absorption spectrum of the LC, a second dye was incorporated in the LC plates. This results in a relative increase in current of 5-8% with respect to the one dye LC, giving. Using a ray-tracing model, transmission, reflection and external quantum efficiency spectra were simulated and compared with the measured spectra. The simulations deliver the luminescent quantum efficiencies of the two dyes as well as the background absorption by the polymer host. It is found that the luminescent quantum efficiency of the red emitting dye is 87%, which is one of the major loss factors in the measured LC. Using ray-tracing simulations it is predicted that increasing the luminescent quantum efficiency to 98% would substantially reduce this loss, resulting in an increase in overall power conversion efficiency of the LC from 1.8 to 2.6%.

Performance of Single Layer Luminescent Concentrators with Multiple Dyes

A ray tracing simulation has been developed for luminescent solar concentrators. By fitting to measurements on the devices, parameters such as the quantum efficiency of the dyes employed can be determined. Once a complete description of the device is available it becomes clear where the losses originate from and directions for the improvement of the devices can be given

Reduction of escape cone losses in luminescent solar concentrators with cholesteric mirrors

The Luminescent Solar Concentrator (LSC) consists of a transparent polymer plate containing luminescent particles. Solar cells are connected to one or more sides of the polymer plate. Part of the light emitted by the luminescent particles is guided towards the solar cells by total internal reflection. About 25% of the dye emission is typically emitted within the optical escape cone of the matrix material and is lost due to emission from the top. We study the application of selectively-reflective cholesteric layers to reduce these losses. We have implemented these mirrors in the ray-tracing model for the LSC. The simulations show that an optimum in performance can be obtained by selecting an appropriate centre wavelength of the cholesteric mirror. External Quantum Efficiency measurements were performed on LSC devices with a mc-Si, GaAs or InGaP cell and a dichroic mirror. This mirror shows a similar behavior as the cholesteric mirror. The results show that for a 5x5 cm2 LSC the mirror does improve the EQE in the absorption range of the dye.

Improving Polymer Based Photovoltaic Devices by Reducing the Voltage Loss at the Donor-Acceptor Interface

The costs of large area, organic photovoltaic devices are stronly related to their module efficiency. Even for niche markets, such as consumer electronics, efficiency is imperative since the available area is limited. Therefore, if polymer photovoltaics is to become a mature technology, it is key to increase the power conversion efficiency of the devices. In our contribution an analysis is given of the energy loss factors in P3HT:[C6O]PCBM cells. The main loss occurs as a voltage loss at the donor-accpetor interface. Since this loss factor is linked to the HOMO-LUMO levels of the system, it is impossilble to reduce this loss using the same material combination. We present polymer: [C6O]PCBM cells with similar optical properties but with a reduced voltage loss at the interface, leading to enhanced open circuit Voltage of 1.0 V (compared to 0.62 V for P3HT:[C6O]PCBM devices). The polymer is an alternating copolymer with fluorence and benzothiadiazole units (PFTBT). Well-characterised devices yield already an AM 1.5 efficiency of 4%, thus competing with state-of-the-art P3HT:PCBM devices.

Hybrid ZnO:polymer bulk heterojunction solar cells from a ZnO precursor

We describe a simple and new method to create hybrid bulk heterojunction solar cells consisting of ZnO and conjugated polymers. A gel-forming ZnO precursor, blended with conjugated polymers, is converted into crystalline ZnO at temperatures as low as 110 °C. In-situ formation of ZnO in MDMO-PPV leads to a quenching of the polymer photoluminescence. Positive charges on the MDMO-PPV are formed after photoexcitation, indicating electron transfer from the polymer to ZnO. Results without full optimization already give photovoltaic cells with an estimated performance over 1% under AM1.5 illumination. The large effect of the processing conditions on the photovoltaic effect of the solar cells, indicate that there are several parameters that require control. The choice of solvent, type of atmosphere, and the relative humidity during spin coating, are important for optimization of the photovoltaic effect. These solar cells are made from cheap materials, and via simple processing and can be regarded as promising for further research.

Exploring the limits of hybrid TiO/2/conjugated polymer photovoltaic cells

In hybrid polymer photovoltaics, conjugated polymers are combined with wide bandgap metal oxide semiconductors like TiO2 or ZnO. Reported maximum power conversion efficiencies (PCE) at AM1.5G conditions for a hybrid polymer bulkheterojunction device are up to 1.6 %. In this paper we report on the current-voltage characteristics of bi-layer devices consisting of TiO2 and a conjugated polymer. Several polymers with different optical bandgap were studied. The maximum External Quantum Efficiency (EQE) of the devices is comparable, but the PCE differs considerably (0.2-0.5%). The differences can for a large part be explained by the differences in optical bandgap of the polymers. It is shown that a low band gap is beneficial for the short circuit current, but does not automatically result in a high PCE as relative shifts of the highest occupied molecular orbital (HOMO) energy levels of the polymers reduce the open circuit voltage (Voc). The calculations show that a PCE up to ~ 19 % can be achieved using the maximum possible Voc and a fill factor of 80%. Judicious engineering of material combinations is required to achieve such a power output, and it expresses the need for a continuing search on potentially low cost, efficient metal oxide/polymer BHJ structures.