Efficient Non-Fullerene Organic Solar Cells Based on a Wide-Bandgap Polymer Donor Containing an Alkylthiophenyl-Substituted Benzodithiophene Moiety.

Two wide-bandgap polymer donors containing an alkylthiophenyl substituted benzo[1,2-b : 4,5-b']dithiophene moiety, namely PTZPO and PTZPS, were designed and synthesized. Both polymers exhibit relatively wide optical bandgap of 1.95 V with similar absorption profiles. The polymer PTZPS with alkylthiophenyl substituted benzo[1,2-b : 4,5-b']dithiophene units showed enhanced light-harvesting capabilities, leading to improved short-circuit current densities. The PTZPS : ITIC film shows more appreciable film morphology and phase separation than the film composed of a blend of ITIC with alkoxyl substitutions containing copolymer PTZPO, which facilitates exciton dissociation and charge transport. The PTZPS : ITIC-based non-fullerene organic solar cells show clearly improved short-circuit current density and an impressively high power conversion efficiency of more than 11 %. These observations demonstrate the great promise of using PTZPS as electron-donating materials for high-performance non-fullerene organic solar cells.

High-Performance Ternary Organic Solar Cell Enabled by a Thick Active Layer Containing a Liquid Crystalline Small Molecule Donor.

Ternary organic solar cells (OSCs) have attracted much research attention in the past few years, as ternary organic blends can broaden the absorption range of OSCs without the use of complicated tandem cell structures. Despite their broadened absorption range, the light harvesting capability of ternary OSCs is still limited because most ternary OSCs use thin active layers of about 100 nm in thickness, which is not sufficient to absorb all photons in their spectral range and may also cause problems for future roll-to-roll mass production that requires thick active layers. In this paper, we report a highly efficient ternary OSC (11.40%) obtained by incorporating a nematic liquid crystalline small molecule (named benzodithiophene terthiophene rhodanine (BTR)) into a state-of-the-art PTB7-Th:PC71BM binary system. The addition of BTR into PTB7-Th:PC71BM was found to improve the morphology of the blend film with decreased π-π stacking distance, enlarged coherence length, and enhanced domain purity. This resulted in more efficient charge separation, faster charge transport, and less bimolecular recombination, which, when combined, led to better device performance even with thick active layers. Our results show that the introduction of highly crystalline small molecule donors into ternary OSCs is an effective means to enhance the charge transport and thus increase the active layer thickness of ternary OSCs to make them more suitable for roll-to-roll production than previous thinner devices.

Direct arylation polycondensation towards water/alcohol-soluble conjugated polymers as the electron transporting layers for organic solar cells.

Two water/alcohol soluble conjugated polymers (WSCPs), based on naphthalenediimide and amino-functionalized 3,4-(propylenedioxy)thiophene, were synthesized via direct arylation polycondensation (DArP). The polymers worked well as electron transporting layers (ETLs) for fullerene-based and fullerene-free organic solar cells (OSCs), presenting an enhancement by above 40% compared to the control devices, respectively. The doping properties and high electron mobilities of these WSCPs endow them with high performance. The research study developed an effective method to synthesize ETLs for highly efficient OSCs, which was rarely reported.

Truxene Functionalized Star-Shaped Non-fullerene Acceptor With Selenium-Annulated Perylene Diimides for Efficient Organic Solar Cells.

An electron acceptor with a truxene core and ring-fusion perylene diimide (PDI) tripolymer annulated by selenium (Se) branch, named as FTr-3PDI-Se, is designed and synthesized. FTr-3PDI-Se exhibits large conjugated planar conformation, strong absorption spectra in the regions of 300-400 and 450-550 nm, the deep HOMO energy level of 6.10 eV, and high decomposition temperature above 400°C. The FTr-3PDI-Se: PBDB-T-2Cl based device achieved a disappointing power conversion efficiency (PCE) of 1.6% together with a high V oc of 1.12 V. The low PCE was due to the large aggregates of blend film, the imbalanced hole/electron transport and low PL quenching efficiencies. The high V oc can be attributed to the high-lying LUMO level of FTr-3PDI-Se and the low-lying HOMO level of PBDB-T-2Cl. Our research presents an interesting and effective molecule-designing method to develop non-fullerene acceptor.

Self-filtering narrowband high performance organic photodetectors enabled by manipulating localized Frenkel exciton dissociation.

The high binding energy and low diffusion length of photogenerated Frenkel excitons have long been viewed as major drawbacks of organic semiconductors. Therefore, bulk heterojunction structure has been widely adopted to assist exciton dissociation in organic photon-electron conversion devices. Here, we demonstrate that these intrinsically "poor" properties of Frenkel excitons, in fact, offer great opportunities to achieve self-filtering narrowband organic photodetectors with the help of a hierarchical device structure to intentionally manipulate the dissociation of Frenkel excitons. With this strategy, filter-free narrowband organic photodetector centered at 860 nm with full-width-at-half-maximum of around 50 nm, peak external quantum efficiency around 65% and peak specific detectivity over 1013 Jones are obtained, which is one the best performed no-gain type narrowband organic photodetectors ever reported and comparable to commercialized silicon photodetectors. This novel device structure along with its design concept may help create low cost and reliable narrowband organic photodetectors for practical applications.

High-Performance Ternary Nonfullerene Polymer Solar Cells with Both Improved Photon Harvesting and Device Stability.

Efficiency and stability of polymer solar cells (PSCs) are the two most significant decisive factors for the purpose of actual applications. Here, highly efficient and stable ternary PSCs were fabricated by incorporating two well-compatible polymer donors (poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2- b;4,5- b0]dithiophene-2,6-diyl- alt-(4-(2-ethylhexyl)-3-fluorothieno[3,4- b]thiophene-)-2-carboxylate-2-6-diyl] and poly[[9-(1-octylnonyl)-9 H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5-thiophenediyl]) with one narrow band gap nonfullerene acceptor (3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone)-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3- d:2',3'- d']- s-indaceno[1,2- b:5,6- b']dithiophene)). It is found that Förster resonance energy transfer acts as an efficient pathway to further strengthen photon harvesting in this ternary system, which results in a significant improvement in current density ( JSC) without sacrificing the strong absorption of binary blends in the near-infrared region. Meanwhile, both of the inverted and conventional ternary PSCs exhibit better stability compared with the related binary PSCs in air condition because of the interlocked morphology in ternary films. The optimized ternary PSCs exhibit an outstanding power conversion efficiency (PCE) of 9.53% resulting from the synchronous improvements in JSC and fill factor. Moreover, this ternary strategy can be further confirmed by the use of an ultranarrow-band gap nonfullerene acceptor IEICO-4F, and the champion PCE of ternary PSCs reaches to 12.15%.

Electron Acceptors With a Truxene Core and Perylene Diimide Branches for Organic Solar Cells: The Effect of Ring-Fusion.

In this work, a star-shaped planar acceptor named FTr-3PDI was synthesized via ring-fusion between truxene core and three bay-linked perylene diimide (PDI) branches. Compared to the unfused non-planar acceptor Tr-3PDI, FTr-3PDI exhibits better structural rigidity and planarity, as well as more effective conjugation between truxene core and PDI branches. As a result, FTr-3PDI shows up-shifted energy levels, enhanced light absorption coefficient, increased electron mobility, and more favorable phase separation morphology in bulk-heterojunction (BHJ) blend films as compared to Tr-3PDI. Consequently, FTr-3PDI afforded higher power conversion efficiency (PCE) in BHJ solar cells when blended with a polymer donor PTB7-Th. This work demonstrates that ring-fusion is a promising molecular design strategy to combine the merits of truxene and PDI for non-fullerene acceptors used in organic solar cells.

Layer-by-Layer-Processed Ternary Organic Solar Cells Using Perylene Bisimide as a Morphology-Inducing Component.

A perylene bisimide (PBI-C4) with strong self-aggregation ability was used with polythieno[3,4-b]-thiophene/benzodithiophene (PTB7) to form an underlying morphology-inducing layer in organic solar cells. The PTB7:PC71BM ([6,6]-phenyl C71 butyric acid methyl ester) spin-coated atop the preprocessed morphology-inducing thin layer showed an enhanced domain size with better phase separation compared with the conventional spin-coating of PTB7:PC71BM on ZnO directly. Proper aggregation morphology of the active layer shows higher electrical properties resulting in a 14% improvement in the power conversion efficiency (PCE) (8.96% vs 7.85%). After replacing the ZnO cathode interlayer with a photoconductive interlayer (ZnO:PBI-H), a maximum PCE of 9.47% is obtained, which is among the best device performance based on PTB7:PC71BM systems.

Cross-Linkable and Dual Functional Hybrid Polymeric Electron Transporting Layer for High-Performance Inverted Polymer Solar Cells.

A cross-linkable dual functional polymer hybrid electron transport layer (ETL) is developed by simply adding an amino-functionalized polymer dopant (PN4N) and a light crosslinker into a commercialized n-type semiconductor (N2200) matrix. It is found that the resulting hybrid ETL not only has a good solvent resistance, facilitating multilayers device fabrication but also exhibits much improved electron transporting/extraction properties due to the doping between PN4N and N2200. As a result, by using PTB7-Th:PC71 BM blend as an active layer, the inverted device based on the hybrid ETL can yield a prominent power conversion efficiency of around 10.07%. More interestingly, photovoltaic property studies of bilayer devices suggest that the absorption of the hybrid ETL contributes to photocurrent and hence the hybrid ETL simultaneously acts as both cathode interlayer material and an electron acceptor. The resulting inverted polymer solar cells function like a novel device architectures with a combination of a bulk heterojunction device and miniature bilayer devices. This work provides new insights on function of ETLs and may be open up a new direction for the design of new ETL materials and novel device architectures to further improve device performance.

Naphthalene Diimide Based n-Type Conjugated Polymers as Efficient Cathode Interfacial Materials for Polymer and Perovskite Solar Cells.

A series of naphthalene diimide (NDI) based n-type conjugated polymers with amino-functionalized side groups and backbones were synthesized and used as cathode interlayers (CILs) in polymer and perovskite solar cells. Because of controllable amine side groups, all the resulting polymers exhibited distinct electronic properties such as oxidation potential of side chains, charge carrier mobilities, self-doping behaviors, and interfacial dipoles. The influences of the chemical variation of amine groups on the cathode interfacial effects were further investigated in both polymer and perovskite solar cells. We found that the decreased electron-donating property and enhanced steric hindrance of amine side groups substantially weaken the capacities of altering the work function of the cathode and trap passivation of the perovskite film, which induced ineffective interfacial modifications and declining device performance. Moreover, with further improvement of the backbone design through the incorporation of a rigid acetylene spacer, the resulting polymers substantially exhibited an enhanced electron-transporting property. Upon use as CILs, high power conversion efficiencies (PCEs) of 10.1% and 15.2% were, respectively, achieved in polymer and perovskite solar cells. Importantly, these newly developed n-type polymers were allowed to be processed over a broad thickness range of CILs in photovoltaic devices, and a prominent PCE of over 8% for polymer solar cells and 13.5% for perovskite solar cells can be achieved with the thick interlayers over 100 nm, which is beneficial for roll-to-roll coating processes. Our findings contribute toward a better understanding of the structure-performance relationship between CIL material design and solar cell performance, and provide important insights and guidelines for the design of high-performance n-type CIL materials for organic and perovskite optoelectronic devices.