Enhancement of All-Polymer Solar Cells by Addition of a Chlorinated Polymer and Formation of an Energy Cascade in a Nonhalogenated Solvent.

Ternary organic solar cells (OSCs) containing a three-component photoactive layer with cascading energy alignments could benefit the charge transfer and improve the open-circuit voltage and power conversion efficiency. Herein, we report the incorporation of a derived chlorinated polymer, J52-Cl, as a guest donor into the donor J52 and acceptor N2200 blend film. The lowest unoccupied molecular orbital and the highest occupied molecular orbital levels of J52-Cl are between the corresponding energy levels of J52 and N2200, and this leads to generation of a cascade of energy levels. Photoluminescence measurements and the J-V of devices containing the donors indicated that this incorporation of J52-Cl could promote the charge transfer of the solar cells. The contribution from J52-Cl reduced the energy loss of J52-based binary devices significantly from 0.932 to 0.797 eV and the nonradiative energy loss from 0.399 to 0.269 eV, leading to an enhancement of Voc from 0.79 to 0.93 V. This introduction of chlorinated polymers also improves the intermolecular interactions and leads to a favorable morphology with appropriate phase separation and interpenetrating networks. As expected, the power conversion efficiency of ternary all-polymer solar cells (all-PSCs) processed in o-xylene solvent was increased from 8.55 to 11.02%. These results indicate that the ternary devices with the appropriate cascade of energy levels can fine tune the device's open-circuit voltage and finally improve the photovoltaic performance of OSCs.

Employing a Narrow-Band-Gap Mediator in Ternary Solar Cells for Enhanced Photovoltaic Performance.

Ternary organic solar cells (OSCs) provide a convenient and effective means to further improve the power conversion efficiency (PCE) of binary ones via composition control. However, the role of the third component remains to be explored in specific binary systems. Herein, we report ternary blend solar cells by adding the narrow-band-gap donor PCE10 as the mediator into the PBDB-T:IDTT-T binary blend system. The extended absorption, efficient fluorescence resonance energy transfer, enhanced charge dissociation, and induced tighter molecular packing of the ternary blend films enhance the photovoltaic properties of devices and deliver a champion PCE of 10.73% with an impressively high open-circuit voltage (VOC) of 1.03 V. Good miscibility and similar molecular packing behavior of the components guarantee the desired morphology in the ternary blend films, leading to solar cell devices with over 10% PCEs at a range of compositions. Our results suggest that ternary systems with properly aligned energy levels and overlapping absorption among the components hold great promises to further enhance the performance of corresponding binary ones.

Highly Efficient and Photostable Ternary Organic Solar Cells Enabled by the Combination of Non-Fullerene and Fullerene Acceptors with Thienopyrrolodione-based Polymer Donors.

Two polymer donors, PFBDT-8ttTPD and PClBDT-8ttTPD, consisting of halogenated thiophene-substituted benzo[1,2-b:4,5-b']dithiophene and alkyl-substituted thieno[3,2-b]thiophene linked thieno[3,4-c]pyrrole-4,6(5H)-dione, were designed and synthesized for the evaluation of photovoltaic performances. The fabricated IT-4F-based organic solar cells (OSCs) exhibited maximum power conversion efficiency (PCE) values of 12.81 and 11.12% for PFBDT-8ttTPD and PClBDT-8ttTPD, respectively. Furthermore, PFBDT-8ttTPD:Y6 showed significantly improved PCE (15.05%) due to the extended light harvesting in the broad solar spectrum, whereas the PClBDT-8ttTPD:Y6 displayed relatively low PCE (10.02%). A ternary system incorporating PC71BM as the third component into bulk-heterojuction composites (PFBDT-8ttPTD:non-fullerene) was investigated with the aim of utilizing the advantages of PC71BM. As a result, PFBDT-8ttTPD:IT-4F:PC71BM exhibited an improved PCE (13.67%) compared to that of the corresponding binary OSC. In particular, ternary OSC of PFBDT-8ttTPD:Y6:PC71BM showed outstanding photovoltaic performance (PCE = 16.43%) as well as photostability, retaining approximately 80% of the initial PCE after 500 h under continuous illumination. The introduction of a small amount of PC71BM resulted in favorable and dense molecular packing with improved crystallinity as well as enhanced charge carrier mobility for efficient OSC.

Highly Crystalline Near-Infrared Acceptor Enabling Simultaneous Efficiency and Photostability Boosting in High-Performance Ternary Organic Solar Cells.

The near-infrared (NIR) absorbing fused-ring electron acceptor, COi8DFIC, has demonstrated very good photovoltaic performance when combined with PTB7-Th as a donor in binary organic solar cells (OSCs). In this work, the NIR acceptor was added to state-of-the-art PBDBT-2F:IT4F-based solar cells as a third component, leading to (i) an efficiency increase of the ternary devices compared to the binary solar cells in the presence of the highly crystalline COi8DFIC acceptor and (ii) much-improved photostability under 1-sun illumination. The electron transport properties were investigated and revealed the origin of the enhanced device performance. Compared to the binary cells, the optimized ternary PBDBT-2F:COi8DFIC:IT4F blends exhibit improved electron transport properties in the presence of 10% COi8DFIC, which is attributed to improved COi8DFIC molecular packing. Furthermore, transient absorption spectroscopy revealed a slow recombination of charge carriers in the ternary blend. The improved electron transport properties were preserved in the ternary OSC upon aging, while in the binary devices they seriously deteriorated after simulated 1-sun illumination of 240 h. Our work demonstrates a simple approach to enhance both OSC efficiency and photostability.

Porphyrin-Containing Polymer as a Superior Blue Light-Absorbing Additive To Afford High- Jsc Ternary Solar Cells.

Integrating an additional component featuring complementary light absorption into binary polymer solar cells is a superior tactic to ameliorate solar cell efficiency and stability. An appropriate additive not only extends the absorption range but may also facilitate charge separation and transport processes. In this work, we elucidate the effects of incorporating a porphyrin-containing conjugated polymer (PPor-1), which displays absorption in 350-500 nm, into binary PTB7-Th:4TIC and PTB7-Th:ITIC blends, affording devices with an average power conversion efficiency approaching 9%. We successfully demonstrate that PPor-1 can be incorporated as an additive to impart improved Jsc (up to 19.1 mA cm-2).