A high performance polymer solar cells (PSCs) based on polymer donor PM6 containing fluorinated thienyl benzodithiophene unit and n -type organic semiconductor acceptor IT-4F containing fluorinated end-groups were developed. In addition to complementary absorption spectra ( 300–830 nm) with IT-4F, the PM6 also has a deep HOMO (the highest occupied molecular) level (−5.50 eV), which will lower the open-circuit voltage ( V oc) sacrifice and reduce the E loss of the IT-4F-based PSCs. Moreover, the strong crystallinity of PM6 is beneficial to form favorable blend morphology and hence to suppress recombination. As a result, in comparison with the PSCs based on a non-fluorinated D/A pair of PBDB-T:ITIC with a medium PCE of 11.2%, the PM6:IT-4F-based PSCs yielded an impressive PCE of 13.5% due to the synergistic effect of fluorination on both donor and acceptor, which is among the highest values recorded in the literatures for PSCs to date. Furthermore, a PCE of 12.2% was remained with the active layer thickness of up to 285 nm and a high PCE of 11.4% was also obtained with a large device area of 1 cm2. In addition, the devices also showed good storage, thermal and illumination stabilities with respect to the efficiency. These results indicate that fluorination is an effective strategy to improve the photovoltaic performance of materials, as well as the both fluorinated donor and acceptor pair-PM6:IT-4F is an ideal candidate for the large scale roll-to-roll production of efficient PSCs in the future.

Synergistic effect of fluorination on both donor and acceptor materials for high performance non-fullerene polymer solar cells with 13.5% efficiency

Non-fullerene fused-ring electron acceptors boost the power conversion efficiency of organic solar cells, but they suffer from high synthetic cost and low yield. Here, we show a series of low-cost noncovalently fused-ring electron acceptors, which consist of a ladder-like core locked by noncovalent sulfur–oxygen interactions and flanked by two dicyanoindanone electron-withdrawing groups. Compared with that of similar but unfused acceptor, the presence of ladder-like structure markedly broadens the absorption to the near-infrared region. In addition, the use of intramolecular noncovalent interactions avoids the tedious synthesis of covalently fused-ring structures and markedly lowers the synthetic cost. The optimized solar cells displayed an outstanding efficiency of 13.24%. More importantly, solar cells based on these acceptors demonstrate very low non-radiative energy losses. This research demonstrates that low-cost noncovalently fused-ring electron acceptors are promising to achieve high-efficiency organic solar cells. Recently, the non-fullerene acceptors with fused rings enable high-efficiency organic solar cells but they are not ideal in terms of synthetic cost and yield. Here, Huang et al. report ‘less fused’ acceptors with non-covalent S⋅⋅⋅O interactions and solar cell efficiency of up to 13%.

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Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells.

Despite the recent breakthroughs of polymer solar cells (PSCs) exhibiting a power conversion efficiency of over 17%, toxic and hazardous organic solvents such as chloroform and chlorobenzene are still commonly used in their fabrication, which impedes the practical application of PSCs. Thus, the development of eco-friendly processing methods suitable for industrial-scale production is now considered an imperative research focus. This Review provides a roadmap for the design of efficient photoactive materials that are compatible with non-halogenated green solvents (e.g., xylenes, toluene, and tetrahydrofuran). We summarize the recent development of green processing solvents and the processing methods to match with the efficient photoactive materials used in non-fullerene solar cells. We further review progress in the use of more eco-friendly solvents (i.e., water or alcohol) for achieving truly sustainable and eco-friendly PSC fabrication. For example, the concept of water- or alcohol-dispersed nanoparticles made of conjugated materials is introduced. Also, recent important progress and strategies to develop water/alcohol-soluble photoactive materials that completely eliminate the use of conventional toxic solvents are discussed. Finally, we provide our perspectives on the challenges facing the current green processing methods and materials, such as large-area coating techniques and long-term stability. We believe this Review will inform the development of PSCs that are truly clean and renewable energy sources.

Eco-Friendly Polymer Solar Cells: Advances in Green-Solvent Processing and Material Design.

Polymer electron acceptors are the key materials in all-polymer solar cells (all-PSCs). In this review, we focused on introducing the principle of boron-nitrogen coordination bond (B←N), and summarizing our recent research on polymer electron acceptors containing B←N unit for efficient all-PSC devices. Two approaches have been reported to design polymer electron acceptors using B←N unit. One is to replace a C–C unit by a B ← N unit in conjugated polymers to transform a polymer electron donor to a polymer electron acceptor. The other approach is to construct novel electron-deficient building block based on B←N unit for polymer electron acceptors. The polymer electron acceptors containing B←N unit showed tunable lowest unoccupied molecular orbital (LUMO) energy levels and exhibited excellent all-PSC device performance with power conversion efficiency of exceeding 6%. These results indicate that organic boron chemistry is a new toolbox to develop functional polymer materials for optoelectronic device applications.

Conjugated polymers containing B←N unit as electron acceptors for all-polymer solar cells

A new fluorinated electron acceptor (FINIC) based on 6,6,12,12-tetrakis(3-fluoro-4-hexylphenyl)-indacenobis(dithieno[3,2-b;2',3'-d]thiophene) as the electron-donating central core and 5,6-difluoro-3-(1,1-dicyanomethylene)-1-indanone as the electron-deficient end groups is rationally designed and synthesized. FINIC shows similar absorption profile in dilute solution to the nonfluorinated analogue INIC. However, compared with INIC, FINIC film shows red-shifted absorption, down-shifted frontier molecular orbital energy levels, enhanced crystallinity, and more ordered molecular packing. Single-crystal structure data show that FINIC molecules pack into closer 3D "network" motif through H-bonding and π-π interaction, while INIC molecules pack into incompact "honeycomb" motif through only π-π stacking. Theoretical calculations reveal that FINIC has stronger electronic coupling and more molecular interactions than INIC. FINIC has higher electron mobilities in both horizontal and vertical directions than INIC. Moreover, FINIC and INIC support efficient 3D exciton transport. PBD-SF/FINIC blend has a larger driving force for exciton splitting, more efficient charge transfer and photoinduced charge generation. Finally, the organic solar cells based on PBD-SF/FINIC blend yield power conversion efficiency of 14.0%, far exceeding that of the PBD-SF/INIC-based devices (5.1%).

High-Performance Fluorinated Fused-Ring Electron Acceptor with 3D Stacking and Exciton/Charge Transport.

Star-shaped electron acceptors containing a truxene core for non-fullerene solar cells

In 2018, several major breakthroughs have been achieved in organic solar cells (OSCs) with the record power conversion efficiency (PCE) reaching over 17 %. With this increased efficiency, it is time to take a step forward to consider how to convert this technology into large scale production. For this, the economic and environmental profile of OSCs should be taken seriously-simplified synthetic routes and green chemistry methods should be applied. According to previous studies, OSCs are competitive and profitable in the commercial market. However, toxic and/or hazardous chemicals are currently used in materials synthesis and device fabrication of OSCs. In this account, we will talk about contributions and efforts we have made to minimize the economic and environmental disadvantages in the production of OSCs. We will start with the background on how our projects were conceived and will specifically discuss our work on direct arylation and green solvent. Developments of direct arylation for synthesizing conjugated polymers will be illustrated along with our recent finding regarding the effect of green solvents on device performance and stability.

Towards Green Synthesis and Processing of Organic Solar Cells.

A series of novel wide bandgap small molecules (IFT-ECA, IFT-M, IFT-TH and IFT-IC) based on the A-D-A structure with indenofluorene core, thiophene bridge, and different electron-deficient end-capping groups, were synthesized and used as non-fullerene acceptors in organic solar cells. The influences of end-capping groups on the device performance were studied. The four materials exhibited different physical and chemical properties due to the variation of end-capping groups, which further affect the exciton dissociation, charge transport, morphology of the bulk-heterojunction films and device performance. Among them, IFT-IC-based device delivered the best power conversion efficiency of 7.16% due to proper nano-scale phase separation morphology and high electron mobility, while the devices based on the other acceptors achieved lower device performance (4.14% for IFT-TH, <1% for IFT-ECA and IFT-M). Our results indicate the importance of choosing suitable electron-withdrawing groups to construct high-performance non-fullerene acceptors based on A-D-A motif.

The effect of end-capping groups in A-D-A type non-fullerene acceptors on device performance of organic solar cells

Research at the University of Washington regarding organic semiconductors is reviewed, covering four major topics: electro-optics, organic light emitting diodes, organic field-effect transistors, and organic solar cells. Underlying principles of materials design are demonstrated along with efforts toward unlocking the full potential of organic semiconductors. Finally, opinions on future research directions are presented, with a focus on commercial competency, environmental sustainability, and scalability of organic-semiconductor-based devices.

Organic Semiconductors at the University of Washington: Advancements in Materials Design and Synthesis and toward Industrial Scale Production

Carrier spins in semiconductor nanocrystals are promising candidates for quantum information processing. Using a combination of time-resolved Faraday rotation and photoluminescence spectroscopies, ...

Yunping Huang

Papers

Star-shaped electron acceptors containing a truxene core for non-fullerene solar cells

Towards Green Synthesis and Processing of Organic Solar Cells.

The effect of end-capping groups in A-D-A type non-fullerene acceptors on device performance of organic solar cells

Organic Semiconductors at the University of Washington: Advancements in Materials Design and Synthesis and toward Industrial Scale Production

Coherent Spin Precession and Lifetime-Limited Spin Dephasing in CsPbBr3 Perovskite Nanocrystals.