Composite material with enhanced recyclability as encapsulant for photovoltaic modules.

Encapsulation of photovoltaic cells was carried out using a transparent glass fiber reinforced composite with enhanced chemical recyclability based on a matrix of an epoxy resin containing cleavable functional groups. The current-voltage curves showed a decrease of 6.3% on the short-circuit current (Isc) after encapsulation of the cell, lower than the one observed for the reference non-recyclable standard epoxy composite. Its performance stability under thermal cycling, ultraviolet (UV), and damp-heat exposure was evaluated and compared with the one of the reference standard epoxy. Both resins showed good stability performance under UV exposure and thermal cycling accelerated aging. Moreover, a power loss below the 5% allowed by the photovoltaic standard was observed for the recyclable resin after 1000 h of damp-heat exposure, even the pronounced loss of 4.7% in power remains a concern. Regarding the recyclability, the composite was dissolved in acetic acid dissolution and glass fiber fabrics were successfully recovered. A new module was manufactured with these fabrics, showing this time a loss of 12% in Isc comparing with the non-encapsulated cell. Further work will consider improving the moisture barrier properties of the composite, and adjusting the recycling conditions to allow component recovery valid for new modules.

High Solar-to-Hydrogen Conversion Efficiency at pH 7 Based on a PV-EC Cell with an Oligomeric Molecular Anode.

In the urgent quest for green energy vectors, the generation of hydrogen by water splitting with sunlight occupies a preeminent standpoint. The highest solar-to-hydrogen (STH) efficiencies have been achieved with photovoltaic-electrochemical (PV-EC) systems. However, most PV-EC water-splitting devices are required to work at extreme conditions, such as in concentrated solutions of HClO4 or KOH or under highly concentrated solar illumination. In this work, a molecular catalyst-based anode is incorporated for the first time in a PV-EC configuration, achieving an impressive 21.2% STH efficiency at neutral pH. Moreover, as opposed to metal oxide-based anodes, the molecular catalyst-based anode allows us to work with extremely small catalyst loadings (<16 nmol/cm2) due to a well-defined metallic center, which is responsible for the fast catalysis of the reaction in the anodic compartment. This work paves the way for integrating molecular materials in efficient PV-EC water-splitting systems.

Hot electron injection into semiconducting polymers in polymer based-perovskite solar cells and their fate.

Metal halide perovskites are known to possess upon photoexcitation long-lived hot carriers. By using femtosecond laser transient absorption spectroscopy, we probed in the current work interfacial charge transfer, that is, hot electrons and holes in methylammonium lead iodide perovskite. The focus was, on the one hand, on titanium dioxide as an electron transporting material and, on the other hand, on several organic semiconducting materials as hole transporting materials in perovskite solar cells. An unexpected carrier loss pathway for hot electrons was found in the form of injection into the low lying LUMOs of several organic semiconducting materials. Of great importance is the fact that the final photocurrents of perovskite solar cells scale with the suppression of this newly discovered loss pathway.

Diphenylphenoxy-Thiophene-PDI Dimers as Acceptors for OPV Applications with Open Circuit Voltage Approaching 1 Volt.

Two new perylenediimides (PDIs) have been developed for use as electron acceptors in solution-processed bulk heterojunction solar cells. The compounds were designed to exhibit maximal solubility in organic solvents, and reduced aggregation in the solid state. In order to achieve this, diphenylphenoxy groups were used to functionalize a monomeric PDI core, and two PDI dimers were bridged with either one or two thiophene units. In photovoltaic devices prepared using PDI dimers and a monomer in conjunction with PTB7, it was found that the formation of crystalline domains in either the acceptor or donor was completely suppressed. Atomic force microscopy, X-ray diffraction, charge carrier mobility measurements and recombination kinetics studies all suggest that the lack of crystallinity in the active layer induces a significant drop in electron mobility. Significant surface recombination losses associated with a lack of segregation in the material were also identified as a significant loss mechanism. Finally, the monomeric PDI was found to have sub-optimum LUMO energy matching the cathode contact, thus limiting charge carrier extraction. Despite these setbacks, all PDIs produced high open circuit voltages, reaching almost 1 V in one particular case.

Charge Injection, Carriers Recombination and HOMO Energy Level Relationship in Perovskite Solar Cells.

We present a comparative study between a series of well-known semiconductor polymers, used in efficient organic solar cells as hole transport materials (HTM), and the state-of-the art material used as hole transport material in perovskite solar cells: the spiro-OMeTAD. The observed differences in solar cell efficiencies are studied in depth using advanced photoinduced spectroscopic techniques under working illumination conditions. We have observed that there is no correlation between the highest occupied molecular orbital (HOMO) energy levels of the organic semiconductors and the measured open-circuit voltage (VOC). For instance, spiro-OMeTAD and P3HT have a comparable HOMO level of ~5.2 eV vs vacuum even though a difference in VOC of around 200 mV is recorded. This difference is in good agreement with the shift observed for the charge vs voltage measurements. Moreover, hole transfer from the perovskite to the HTM, estimated qualitatively from fluorescence quenching and emission lifetime, seems less efficient for the polymeric HTMs. Finally, the recombination currents from all devices were estimated by using the measured charge (calculated using photoinduced differential charging) and the carriers' lifetime and their value resulted in accordance with the registered short-circuit currents (JSC) at 1 sun.

Increased short circuit current in an azafullerene-based organic solar cell.

We report the synthesis of a solution-processable, dodecyloxyphenyl-substituted azafullerene monoadduct (DPC59N) and its application as electron acceptor in bulk heterojunction organic solar cells (BHJ-OSCs). Due to its relatively strong absorption of visible light, DPC59N outperforms PC60BM in respect to short circuit current (JSC) and external quantum efficiency (EQE) in blends with donor P3HT.

Influence of the molecular weight and size dispersion of the electroluminescent polymer on the performance of air-stable hybrid light-emitting diodes.

The influence of the chain length and the molecular weight distribution of the electroluminescent polymer on the carrier transport properties and morphology of air stable hybrid light-emitting diodes is reported. It is found that variations between diverse as-received commercial batches play a major role in the performance of the devices, whose maximum luminance can differ up to 2 orders of magnitude. Through complementary optoelectronic, structural, and morphological characterization techniques, we provide insights into the relationship between charge dynamics and the structure of polymeric electroluminescent materials. The carrier dynamics are found to be dominated by both the polymeric chain length and the hole transport, which in turn is dependent on the concentration of trap states. Furthermore, the chain length is seen to affect the morphology of the active layer.

Small molecule-based tandem solar cells with solution-processed and vacuum-processed photoactive layers.

A tandem solar cell device whose sub-cells are fabricated exclusively from small molecules (SMs) through both solution-processed and vacuum-processed deposition techniques is described. The front sub-cell's active layer consists of a bulk heterojunction (BHJ) DPP(TBFu)2:PC70BM device while the back cell has a typical bilayer structure employing a 2,4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl] squaraine (SQ) donor and a C60 acceptor.