Recent Advances in Bulk Heterojunction Polymer Solar Cells

Organic solar cells have desirable properties, including low cost of materials, high-throughput roll-to-roll production, mechanical flexibility and light weight. However, all top-performance devices are at present processed using halogenated solvents, which are environmentally hazardous and would thus require expensive mitigation to contain the hazards. Attempts to process organic solar cells from non-halogenated solvents lead to inferior performance. Overcoming this hurdle, here we present a hydrocarbon-based processing system that is not only more environmentally friendly but also yields cells with power conversion efficiencies of up to 11.7%. Our processing system incorporates the synergistic effects of a hydrocarbon solvent, a novel additive, a suitable choice of polymer side chain, and strong temperature-dependent aggregation of the donor polymer. Our results not only demonstrate a method of producing active layers of organic solar cells in an environmentally friendly way, but also provide important scientific insights that will facilitate further improvement of the morphology and performance of organic solar cells. The processing of high-performance organic solar cells usually requires environmentally hazardous solvents. Now, hydrocarbon-based processing is shown to achieve relatively high performance in a more environmentally friendly way.

Efficient organic solar cells processed from hydrocarbon solvents

A nonfullerene-based polymer solar cell (PSC) that significantly outperforms fullerene-based PSCs with respect to the power-conversion efficiency is demonstrated for the first time. An efficiency of >11%, which is among the top values in the PSC field, and excellent thermal stability is obtained using PBDB-T and ITIC as donor and acceptor, respectively.

Fullerene-Free Polymer Solar Cells with over 11% Efficiency and Excellent Thermal Stability

We thank the University of St Andrews for support. EZ-C thanks the Leverhulme Trust for financial support (RPG-2016-047). and the EPSRC (EP/P010482/1) for financial support.

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Purely Organic Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes.

ConspectusThe active layer in a solution processed organic photovoltaic device comprises a light absorbing electron donor semiconductor, typically a polymer, and an electron accepting fullerene acceptor. Although there has been huge effort targeted to optimize the absorbing, energetic, and transport properties of the donor material, fullerenes remain as the exclusive electron acceptor in all high performance devices. Very recently, some new non-fullerene acceptors have been demonstrated to outperform fullerenes in comparative devices. This Account describes this progress, discussing molecular design considerations and the structure–property relationships that are emerging.The motivation to replace fullerene acceptors stems from their synthetic inflexibility, leading to constraints in manipulating frontier energy levels, as well as poor absorption in the solar spectrum range, and an inherent tendency to undergo postfabrication crystallization, resulting in device instability. New acceptors have to address ...

Non-Fullerene Electron Acceptors for Use in Organic Solar Cells

Effects of brominated terminal groups on the performance of fused-ring electron acceptors in organic solar cells

Bulky electron donating side chain enhances the open-circuit voltage of benzodithiophene photovoltaic polymers

Liquid-crystal small molecule donor (LC-SMD) is a new type organic semiconductor, which is attractive not only for the easy synthesis and purification, well-defined chemical structures, etc., but also for the LC state that makes the crystallinity and aggregation state of molecules adjustable. Here, one new LC-SMD (a-BTR-H4) is synthesized with 1D alkoxyl and 2D thiophene-alkylthiol side-chained benzo[1,2-b:4,5-b']dithiophene core, trithiophene π-bridge, and 3-(2-ethylhexyl) rhodanine end group. a-BTR-H4 shows low LC transition temperature, 117 °C, however, counterpart material (a-BTR-H5) with the same main structure but 3-ethyl rhodanine terminal group does not show LC properties. Although a-BTR-H4/H5 show similar Ultraviolet-visible absorption spectrum and energy levels, a-BTR-H4 affords relatively high photovoltaic performances due to favorable blend morphology produced by the consistent annealing temperature of Y6-based accepters and liquid crystal temperature of donors. Preliminary results indicate that a-BTR-H4 gains a power conversion efficiency (PCE) of 11.36% for Y6-based devices, which is ascribed to better light harvest as well as balanced carrier generation and transport, while a-BTR-H5 obtains 7.57% PCE. Therefore, some materials with unique nematic LC phase have great application potential in organic electronics, and further work to utilize a-BTR-H4 for high-performance device is underway.

End Group Effect of Asymmetric Benzodithiophene-Based Donor with Liquid-Crystal State for Small-Molecule Binary Solar Cell.

Employing Symmetry-breaking Strategy to Reduce Self-aggregation of Donor in Blend Films to Control Morphology for All Small Molecular Organic Solar Cells

TiO2 films were formed on metallic titanium substrates by the anodic oxidation method in H2SO4 solution under the 80V D.C.. Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions. Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves. The result showed that the TiO2 film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface. The average water contact angle of the film was 116.4° in dark, in contrast to an angle of 42.7° under the UV illumination for 2 hours, which demonstrates good hydrophobic property. The anti-corrosion behavior of the TiO2 film was declining with the extended immersion time. Under dark conditions, however, the hydrophobic TiO2 film retarded the water infiltrating into the substrate. The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight. All of those mentioned above indicate that the TiO2 film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.

Mingliang Sun

Papers

Effects of brominated terminal groups on the performance of fused-ring electron acceptors in organic solar cells

Bulky electron donating side chain enhances the open-circuit voltage of benzodithiophene photovoltaic polymers

End Group Effect of Asymmetric Benzodithiophene-Based Donor with Liquid-Crystal State for Small-Molecule Binary Solar Cell.

Employing Symmetry-breaking Strategy to Reduce Self-aggregation of Donor in Blend Films to Control Morphology for All Small Molecular Organic Solar Cells

Corrosion behavior of anodic oxidized TiO2 film in seawater