Synergetic Effect of Different Carrier Dynamics in Pm6:Y6:ITIC-M Ternary Cascade Energy Level System.

Although reported ternary polymer solar cells have higher power conversion efficiency than binary polymers, the mechanism of exciton separation and charge transport in this complex ternary system is still unclear. Herein, based on PM6:Y6:ITIC-M ternary solar cells, we combine the technique of luminescence spectroscopy, including electroluminescence (EL) and photoluminescence (PL) with photovoltaic measurements, to understand clearly the detailed roles of ITIC-M as the third component in the contribution of device performance. The results show that ITIC-M can form the alloy-like composite with Y6 but leave individual Y6 acceptor to conduct charge transfer with PM6 donor, which improves Voc but decreases Jsc because of poor charge transfer capacity of ITIC-M. Meanwhile, the energy transfer from PM6 to ITIC-M exists in the active layers; small IE suppresses exciton dissociation. Deteriorating performance of solar cells demonstrates that, except for complementary absorption spectrum and suitable energy levels in PM6:Y6:ITIC-M system, the synergetic effects of carrier dynamics among different organic materials play an important role in influencing the performance of ternary solar cells.

With PBDB-T as the Donor, the PCE of Non-Fullerene Organic Solar Cells Based on Small Molecule INTIC Increased by 52.4.

At present, most high-performance non-fullerene materials are centered on fused rings. With the increase in the number of fused rings, production costs and production difficulties increase. Compared with other non-fullerenes, small molecule INTIC has the advantages of easy synthesis and strong and wide infrared absorption. According to our previous report, the maximum power conversion efficiency (PCE) of an organic solar cell using PTB7-Th:INTIC as the active layer was 7.27%. In this work, other polymers, PTB7, PBDB-T and PBDB-T-2F, as the donor materials, with INTIC as the acceptor, are selected to fabricate cells with the same structure to optimize their photovoltaic performance. The experimental results show that the optimal PCE of PBDB-T:INTIC based organic solar cells is 11.08%, which, thanks to the open voltage (VOC) increases from 0.80 V to 0.84 V, the short circuit current (JSC) increases from 15.32 mA/cm2 to 19.42 mA/cm2 and the fill factor (FF) increases from 60.08% to 67.89%, then a 52.4% improvement in PCE is the result, compared with the devices based on PTB7-Th:INTIC. This is because the PBDB-T:INTIC system has better carrier dissociation and extraction, carrier transportation and higher carrier mobility.

Highly Efficient and Operational Stability Polymer Solar Cells Employing Nonhalogenated Solvents and Additives.

The power conversion efficiencies (PCEs) of potential polymer solar cells have been shown to rapidly exceed 15%. However, these high-performance devices are based on halogenated solvents that pose a significant hazard to the atmospheric environment and human beings. The use of nonhalogenated solvents makes the device less efficient because of its solubility issues. In this work, we report high-efficiency devices utilizing PffBT4T-2OD and [6,6]-phenyl C71 butyric acid methyl ester system from nonhalogenated solvents such as o-xylene ( o-XY) and 1-methylnaphthalene (Me) hydrocarbon solvent. When Me was used as the additive, the PCE of prepared devices improved from 1.83 to 10.13%, which is rather higher than that of the devices processed with traditional solvents combined with chlorobenzene and 1,8-diiodooctane (8.18%). Both atomic force microscopy and transmission electron microscopy confirmed that after nonhalogen solvents are treated, a more finely phase-separated dense morphology of active layers than after halogen solvents. At the same time, grazing incident wide-angle X-ray scattering patterns show that the combination of nonhalogenated solvents o-XY and Me ingeniously formed an ordered crystal and π-π stacking. Also, the stability of devices prepared from nonhalogenated solvents was significantly better than that of halogenated solvents under continuous illumination in the air without encapsulation.

Improving charge transport by the ultrathin QDs interlayer in polymer solar cells.

Lead sulfide (PbS) quantum dots (QDs) have been incorporated into PTB7:PC71BM BHJ active layers to fabricate polymer solar cells (PSCs) and gather on the top surface of active layers to form an ultrathin interlayer. The PbS QDs ultrathin interlayer with an appropriate thickness increases the carrier transport capacity, exciton dissociation and reduces the carrier recombination, which leads to a higher short circuit current (J sc) and fill factor (FF). Finally, the power conversion efficiency (PCE) improves from 7.03% (control devices) to 7.87% with an ultrathin interlayer by doping 5% PbS QDs, while the current density (J sc) and fill factor (FF) enhances from 13.83 mA cm-2 to 14.81 mA cm-2 and from 68.70% to 70.85%, respectively.