14.7% Efficiency Organic Photovoltaic Cells Enabled by Active Materials with a Large Electrostatic Potential Difference.

Although significant improvements have been achieved for organic photovoltaic cells (OPVs), the top-performing devices still show power conversion efficiencies far behind those of commercialized solar cells. One of the main reasons is the large driving force required for separating electron-hole pairs. Here, we demonstrate an efficiency of 14.7% in the single-junction OPV by using a new polymer donor PTO2 and a nonfullerene acceptor IT-4F. The device possesses an efficient charge generation at a low driving force. Ultrafast transient absorption measurements probe the formation of loosely bound charge pairs with extended lifetime that impedes the recombination of charge carriers in the blend. The theoretical studies reveal that the molecular electrostatic potential (ESP) between PTO2 and IT-4F is large, and the induced intermolecular electric field may assist the charge generation. The results suggest OPVs have the potential for further improvement by judicious modulation of ESP.

Design rules for minimizing voltage losses in high-efficiency organic solar cells.

The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend. Following these rules, we present a range of existing and new donor-acceptor systems that combine efficient photocurrent generation with electroluminescence yield up to 0.03%, leading to non-radiative voltage losses as small as 0.21 V. This study provides a rationale to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.

Fine-Tuned Photoactive and Interconnection Layers for Achieving over 13% Efficiency in a Fullerene-Free Tandem Organic Solar Cell.

Fabricating organic solar cells (OSCs) with a tandem structure has been considered an effective method to overcome the limited light absorption spectra of organic photovoltaic materials. Currently, the most efficient tandem OSCs are fabricated by adopting fullerene derivatives as acceptors. In this work, we designed a new non-fullerene acceptor with an optical band gap (Egopt) of 1.68 eV for the front subcells and optimized the phase-separation morphology of a fullerene-free active layer with an Egopt of 1.36 eV to fabricate the rear subcell. The two subcells show a low energy loss and high external quantum efficiency, and their photoresponse spectra are complementary. In addition, an interconnection layer (ICL) composed of ZnO and a pH-neutral self-doped conductive polymer, PCP-Na, with high light transmittance in the near-IR range was developed. From the highly optimized subcells and ICL, solution-processed fullerene-free tandem OSCs with an average power conversion efficiency (PCE) greater than 13% were obtained.

Demonstration of a microwave photonic synthetic aperture radar based on photonic-assisted signal generation and stretch processing.

A microwave photonic synthetic aperture radar (MWP SAR) is developed and experimentally demonstrated. In the transmitter, microwave photonic frequency doubling is used to generate a linearly-frequency-modulated (LFM) radar signal; while in the receiver, photonic stretch processing is employed to receive the reflection signal. The presented MWP SAR operates in Ku band with a bandwidth of 600MHz, and is evaluated through a series of inverse SAR imaging tests both in a microwave anechoic chamber and in a field trial. Its imaging performance verifies that the proposed MWP SAR works perfect and shows the potential of overcoming the conventional radar bandwidth bottleneck.

Design, Synthesis, and Photovoltaic Characterization of a Small Molecular Acceptor with an Ultra-Narrow Band Gap.

The design of narrow band gap (NBG) donors or acceptors and their application in organic solar cells (OSCs) are of great importance in the conversion of solar photons to electrons. Limited by the inevitable energy loss from the optical band gap of the photovoltaic material to the open-circuit voltage of the OSC device, the improvement of the power conversion efficiency (PCE) of NBG-based OSCs faces great challenges. A novel acceptor-donor-acceptor structured non-fullerene acceptor is reported with an ultra-narrow band gap of 1.24 eV, which was achieved by an enhanced intramolecular charge transfer (ICT) effect. In the OSC device, despite a low energy loss of 0.509 eV, an impressive short-circuit current density of 25.3 mA cm-2 is still recorded, which is the highest value for all OSC devices. The high 10.9 % PCE of the NBG-based OSC demonstrates that the design and application of ultra-narrow materials have the potential to further improve the PCE of OSC devices.

Organic photovoltaic cell with 17% efficiency and superior processability.

The development of organic photoactive materials, especially the newly emerging non-fullerene electron acceptors (NFAs), has enabled rapid progress in organic photovoltaic (OPV) cells in recent years. Although the power conversion efficiencies (PCEs) of the top-performance OPV cells have surpassed 16%, the devices are usually fabricated via a spin-coating method and are not suitable for large-area production. Here, we demonstrate that the fine-modification of the flexible side chains of NFAs can yield 17% PCE for OPV cells. More crucially, as the optimal NFA has a suitable solubility and thus a desirable morphology, the high efficiencies of spin-coated devices can be maintained when using scalable blade-coating processing technology. Our results suggest that optimization of the chemical structures of the OPV materials can improve device performance. This has great significance in larger-area production technologies that provide important scientific insights for the commercialization of OPV cells.

Investigating the Trade-Off between Device Performance and Energy Loss in Nonfullerene Organic Solar Cells.

The large energy loss (Eloss) in organic solar cells (OSCs) relative to those of silicon or inorganic/organic hybrid perovskite solar cells is one of the major factors limiting the power conversion efficiency (PCE) of OSCs. Recently, OSCs based on nonfullerene acceptors (NFAs) have achieved high PCEs at decreased Eloss values. Therefore, the present study investigates the relationship between Eloss and the device performance of NFA-based OSCs. Here, we select two polymer donors (PBDB-T and its fluorinated derivative PBDB-TF) and blend each polymer donor with each of three NFAs (indaceno[1,2-b:5,6-b']dithiophene and 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile (IEIC) and its respective fluorinated and chlorinated derivatives IE-4F and IE-4Cl), which provide varied energy-level alignments. The six blends exhibit similar morphologies and charge transport properties but varied Eloss values in OSCs. The results indicate that the charge generation and PCE of the OSCs increase with the increasing Eloss. Accordingly, the PBDB-T:IE-4Cl-based device yields the highest PCE of 11.1% with an Eloss of 0.64 eV, while the PBDB-TF:IEIC-based device provides a significantly decreased PCE of 3.8% with a diminished Eloss of 0.52 eV. These results demonstrate the great importance of finely tuning the energy-level alignments of these types of donor/acceptor systems to achieve the best device performance.

1 cm2 Organic Photovoltaic Cells for Indoor Application with over 20% Efficiency.

Organic photovoltaic (OPV) technologies have the advantages of fabricating larger-area and light-weight solar panels on flexible substrates by low-cost roll-to-toll production. Recently, OPV cells have achieved many significant advances with power conversion efficiency (PCE) increasing rapidly. However, large-scale solar farms using OPV modules still face great challenges, such as device stability. Herein, the applications of OPV cells in indoor light environments are studied. Via optimizing the active layers to have a good match with the indoor light source, 1 cm2 OPV cells are fabricated and a top PCE of 22% under 1000 lux light-emitting diode (2700 K) illumination is demonstrated. In this work, the light intensities are measured carefully. Incorporated with the external quantum efficiency and photon flux spectrum, the integral current densities of the cells are calculated to confirm the reliability of the photovoltaic measurement. In addition, the devices show much better stability under continuous indoor light illumination. The results suggest that designing wide-bandgap active materials to meet the requirements for the indoor OPV cells has a great potential in achieving higher photovoltaic performance.

Eco-Compatible Solvent-Processed Organic Photovoltaic Cells with Over 16% Efficiency.

Recent advances in nonfullerene acceptors (NFAs) have enabled the rapid increase in power conversion efficiencies (PCEs) of organic photovoltaic (OPV) cells. However, this progress is achieved using highly toxic solvents, which are not suitable for the scalable large-area processing method, becoming one of the biggest factors hindering the mass production and commercial applications of OPVs. Therefore, it is of great importance to get good eco-compatible processability when designing efficient OPV materials. Here, to achieve high efficiency and good processability of the NFAs in eco-compatible solvents, the flexible alkyl chains of the highly efficient NFA BTP-4F-8 (also known as Y6) are modified and BTP-4F-12 is synthesized. Combining with the polymer donor PBDB-TF, BTP-4F-12 shows the best PCE of 16.4%. Importantly, when the polymer donor PBDB-TF is replaced by T1 with better solubility, various eco-compatible solvents can be applied to fabricate OPV cells. Finally, over 14% efficiency is obtained with tetrahydrofuran (THF) as the processing solvent for 1.07 cm2 OPV cells by the blade-coating method. These results indicate that the simple modification of the side chain can be used to tune the processability of active layer materials and thus make it more applicable for the mass production with environmentally benign solvents.

Achieving Over 15% Efficiency in Organic Photovoltaic Cells via Copolymer Design.

Ternary blending and copolymerization strategies have proven advantageous in boosting the photovoltaic performance of organic solar cells. Here, 15% efficiency solar cells using copolymerization donors are demonstrated, where the electron-withdrawing unit, ester-substituted thiophene, is incorporated into a PBDB-TF polymer to downshift the molecular energy and broaden the absorption. Copolymer-based solar cells suitable for large-area devices can be fabricated by a blade-coating method from a nonhalogen and nonaromatic solvent mixture. Although ternary solar cells can achieve comparable efficiencies, they are not suitable for environment-friendly processing conditions and show relatively low photostability compared to copolymer-based devices. These results not only demonstrate high-efficiency organic photovoltaic cells via copolymerization strategies but also provide important insights into their applications in practical production.

Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors.

To make organic solar cells (OSCs) more competitive in the diverse photovoltaic cell technologies, it is very important to demonstrate that OSCs can achieve very good efficiencies and that their cost can be reduced. Here, a pair of nonfullerene small-molecule acceptors, IT-2Cl and IT-4Cl, is designed and synthesized by introducing easy-synthesis chlorine substituents onto the indacenodithieno[3,2-b]thiophene units. The unique feature of the large dipole moment of the CCl bond enhances the intermolecular charge-transfer effect between the donor-acceptor structures, and thus expands the absorption and down shifts the molecular energy levels. Meanwhile, the introduction of CCl also causes more pronounced molecular stacking, which also helps to expand the absorption spectrum. Both of the designed OSCs devices based on two acceptors can deliver a power conversion efficiency (PCE) greater than 13% when blended with a polymer donor with a low-lying highest occupied molecular orbital level. In addition, since IT-2Cl and IT-4Cl have very good compatibility, a ternary OSC device integrating these two acceptors is also fabricated and obtains a PCE greater than 14%. Chlorination demonstrates effective ability in enhancing the device performance and facile synthesis route, which both deserve further exploitation in the modification of photovoltaic materials.

Achieving Highly Efficient Nonfullerene Organic Solar Cells with Improved Intermolecular Interaction and Open-Circuit Voltage.

A new acceptor-donor-acceptor-structured nonfullerene acceptor ITCC (3,9-bis(4-(1,1-dicyanomethylene)-3-methylene-2-oxo-cyclopenta[b]thiophen)-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d':2,3-d']-s-indaceno[1,2-b:5,6-b']-dithiophene) is designed and synthesized via simple end-group modification. ITCC shows improved electron-transport properties and a high-lying lowest unoccupied molecular orbital level. A power conversion efficiency of 11.4% with an impressive V OC of over 1 V is recorded in photovoltaic devices, suggesting that ITCC has great potential for applications in tandem organic solar cells.