Fast-Growth Polymer: Fullerene Bulk-Heterojunction Thin Films for Efficient Organic Photovoltaics.

The bulk-heterojunction (BHJ) system that uses a π-conjugated polymer as an electron donor, and a fullerene derivative as an electron acceptor, is widely used in organic solar cells (OSCs) to facilitate efficient charge separation and extraction. However, the conventional BHJ system still suffers from unwanted phase segregation caused by the existence of significant differences in surface energy between the two BHJ components and the charge extraction layer during film formation. In the present work, we demonstrate a sophisticated control of fast film-growth kinetics that can be used to achieve a uniform distribution of donor and acceptor materials in the BHJ layer of OSCs without undesirable phase separation. Our approach involves depositing the BHJ solution onto a spinning substrate, thus inducing rapid evaporation of the solvent during BHJ film formation. The fast-growth process prevents the fullerene derivative from migrating toward the charge extraction layer, thereby enabling a homogeneous distribution of the fullerene derivative within the BHJ film. The OSCs based on the fast-growth BHJ thin film are found to exhibit substantial increases in JSC, fill factor, and a PCE up to 11.27 mA/cm2, 66%, and 4.68%, respectively; this last value represents a remarkable 17% increase in PCE compared to that of conventional OSCs.

Impact of solvents on doctor blade coatings and bathocuproine cathode interlayer for large-area organic solar cell modules.

Efforts to commercialize organic solar cells (OSCs) by developing roll-to-roll compatible modules have encountered challenges in optimizing printing processes to attain laboratory-level performance in fully printable OSC architectures. In this study, we present efficient OSC modules fabricated solely through printing methods. We systematically evaluated the impact of processing solvents on the morphology of crucial layers, such as the hole transport, photoactive, and electron transport layers, applied using the doctor blade coating method, with a particular focus on processability. Notably, deposition of charge transport layer using printing techniques is still a challenging task, mainly due to the hydrophobic characteristic of the organic photoactive layer. To overcome this issue, we investigated the solvent effect of a well-studied cathode interlayer, bathocuproine (BCP). We were able to form a uniform thin BCP film (∼10 nm) on a non-fullerene based organic photoactive layer using the doctor bladed coating method. Our results showed that the use of volatile alcohols in the BCP processing required a delicate balance between wettability and vaporization, which contrasted with the results for spin-coated films. These findings provide important insights into improving the efficiency of printing techniques for depositing charge transport layers. The fully printed OSC modules, featuring uniform and continuous BCP layer formation, achieved an impressive power conversion efficiency of 10.8% with a total area of 10.0 cm2 and a geometrical fill factor of 86.5%.

Direct Observation of Confinement Effects of Semiconducting Polymers in Polymer Blend Electronic Systems.

The advent of special types of polymeric semiconductors, known as "polymer blends," presents new opportunities for the development of next-generation electronics based on these semiconductors' versatile functionalities in device applications. Although these polymer blends contain semiconducting polymers (SPs) mixed with a considerably high content of insulating polymers, few of these blends unexpectedly yield much higher charge carrier mobilities than those of pure SPs. However, the origin of such an enhancement has remained unclear owing to a lack of cases exhibiting definite improvements in charge carrier mobility, and the limited knowledge concerning the underlying mechanism thereof. In this study, the morphological changes and internal nanostructures of polymer blends based on various SP types with different intermolecular interactions in an insulating polystyrene matrix are investigated. Through this investigation, the physical confinement of donor-acceptor type SP chains in a continuous nanoscale network structure surrounded by polystyrenes is shown to induce structural ordering with more straight edge-on stacked SP chains. Hereby, high-performance and transparent organic field-effect transistors with a hole mobility of ≈5.4 cm2 V-1 s-1 and an average transmittance exceeding 72% in the visible range are achieved.

Simultaneously Passivating Cation and Anion Defects in Metal Halide Perovskite Solar Cells Using a Zwitterionic Amino Acid Additive.

Ionic defects (e.g., organic cations and halide anions), preferably residing along grain boundaries (GBs) and on perovskite film surfaces, are known to be a major source of the notorious environmental instability of perovskite solar cells (PeSCs). Although passivating ionic defects is desirable, previous approaches using Lewis base or acid molecules as additives suppress only the negatively or positively charged defects, thus leaving oppositely charged defects. In this work, both the cationic and anionic defects inside methyl ammonium lead tri-iodide (MAPbI3 ) are simultaneously passivated by introducing a zwitterionic form of the amino acid, L-alanine, into the precursor solution as an additive. L-alanine has both positive (NH3+ ) and negative (COO- ) functional groups at a specific solvent pH, thereby passivating both the cation and anion defects in MAPbI3 . The addition of L-alanine increases the grain size of the perovskite crystals and lengthens the charge carrier lifetime (τ > 1 µs), leading to improved power conversion efficiencies (PCEs) of 20.3% (from 18.3% without an additive) for small-area (4.64 mm2 ) devices and 15.6% (from 13.5%) for large-area submodules (9.06 cm2 ). More importantly, the authors' approach also significantly enhances the shelf storage and photoirradiation stabilities of PeSCs.

Large-Area Nonfullerene Organic Solar Cell Modules Fabricated by a Temperature-Independent Printing Method.

Despite recent breakthroughs in the fabrication of spin-coated small-area devices (≤0.1 cm2) with power conversion efficiencies (PCEs) of more than 17%, printed large-area organic solar cells (OSCs) are significantly less efficient because of the intrinsic differences between the coating dynamics of the two types of OSCs. The PCEs of printed large-area (∼100 cm2) OSCs have typically been decreased compared with those of small-area spin-coated devices. In this work, an efficient low-temperature printing method to fabricate high-efficiency large-area nonfullerene-based OSC modules is successfully demonstrated. A systematic study of the relationship between the concentration of the photoactive solution and the resulting film properties reveals that the large-area modules (85 cm2) produced in this work deliver excellent performance, yielding PCEs of up to 8.18% with a geometric fill factor of 85%. These novel OSC modules are ∼87% as efficient as small-area printed single cells (cell PCE ∼9.43% with 1 cm2).

High-efficiency large-area perovskite photovoltaic modules achieved via electrochemically assembled metal-filamentary nanoelectrodes.

Realizing industrial-scale, large-area photovoltaic modules without any considerable performance losses compared with the performance of laboratory-scale, small-area perovskite solar cells (PSCs) has been a challenge for practical applications of PSCs. Highly sophisticated patterning processes for achieving series connections, typically fabricated using printing or laser-scribing techniques, cause unexpected efficiency drops and require complicated manufacturing processes. We successfully fabricated high-efficiency, large-area PSC modules using a new electrochemical patterning process. The intrinsic ion-conducting features of perovskites enabled us to create metal-filamentary nanoelectrodes to facilitate the monolithic serial interconnections of PSC modules. By fabricating planar-type PSC modules through low-temperature annealing and all-solution processing, we demonstrated a notably high module efficiency of 14.0% for a total area of 9.06 cm2 with a high geometric fill factor of 94.1%.

Highly Deformable and See-Through Polymer Light-Emitting Diodes with All-Conducting-Polymer Electrodes.

Despite the high expectation of deformable and see-through displays for future ubiquitous society, current light-emitting diodes (LEDs) fail to meet the desired mechanical and optical properties, mainly because of the fragile transparent conducting oxides and opaque metal electrodes. Here, by introducing a highly conductive nanofibrillated conducting polymer (CP) as both deformable transparent anode and cathode, ultraflexible and see-through polymer LEDs (PLEDs) are demonstrated. The CP-based PLEDs exhibit outstanding dual-side light-outcoupling performance with a high optical transmittance of 75% at a wavelength of 550 nm and with an excellent mechanical durability of 9% bending strain. Moreover, the CP-based PLEDs fabricated on 4 µm thick plastic foils with all-solution processing have extremely deformable and foldable light-emitting functionality. This approach is expected to open a new avenue for developing wearable and attachable transparent displays.

Achieving Large-Area Planar Perovskite Solar Cells by Introducing an Interfacial Compatibilizer.

Despite the recent unprecedented increase in the power conversion efficiencies (PCEs) of small-area devices (≤0.1 cm2 ), the PCEs deteriorate drastically for PSCs of larger areas because of the incomplete film coverage caused by the dewetting of the hydrophilic perovskite precursor solutions on the hydrophobic organic charge-transport layers (CTLs). Here, an innovative method of fabricating scalable PSCs on all types of organic CTLs is reported. By introducing an amphiphilic conjugated polyelectrolyte as an interfacial compatibilizer, fabricating uniform perovskite films on large-area substrates (18.4 cm2 ) and PSCs with the total active area of 6 cm2 (1 cm2 × 6 unit cells) via a single-turn solution process is successfully demonstrated. All of the unit cells exhibit highly uniform PCEs of 16.1 ± 0.9% (best PCE of 17%), which is the highest value for printable PSCs with a total active area larger than 1 cm2 .

Highly Stretchable and Highly Conductive PEDOT:PSS/Ionic Liquid Composite Transparent Electrodes for Solution-Processed Stretchable Electronics.

Stretchable conductive materials have received great attention owing to their potential for realizing next-generation stretchable electronics. However, the simultaneous achievement of excellent mechanical stretchability and high electrical conductivity as well as cost-effective fabrication has been a significant challenge. Here, we report a highly stretchable and highly conducting polymer that was obtained by incorporating an ionic liquid. When 1-ethyl-3-methylimidazolium tetracyanoborate (EMIM TCB) was added to an aqueous conducting polymer solution of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), it was found that EMIM TCB acts not only as a secondary dopant but also as a plasticizer for PEDOT:PSS, resulting in a high conductivity of >1000 S cm-1 with stable performance at tensile strains up to 50% and even up to 180% in combination with the prestrained substrate technique. Consequently, by exploiting the additional benefits of high transparency and solution-processability of PEDOT:PSS, we were able to fabricate a highly stretchable, semitransparent, and wholly solution-processed alternating current electroluminescent device with unimpaired performance at 50% strain by using PEDOT:PSS/EMIM TCB composite films as both bottom and top electrodes.

Long-Term Stable Recombination Layer for Tandem Polymer Solar Cells Using Self-Doped Conducting Polymers.

Recently, the most efficient tandem polymer solar cells (PSCs) have used poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) ( PEDOT: PSS) as a p-type component of recombination layer (RL). However, its undesirable acidic nature, originating from insulating PSS, of PEDOT: PSS drastically reduces the lifetime of PSCs. Here, we demonstrate the efficient and stable tandem PSCs by introducing acid-free self-doped conducting polymer (SCP), combined with zinc oxide nanoparticles (ZnO NPs), as RL for PEDOT: PSS-free tandem PSCs. Moreover, we introduce an innovative and versatile nanocomposite system containing photoactive and p-type conjugated polyelectrolyte (p-CPE) into the tandem fabrication of an ideal self-organized recombination layer. In our new RL, highly conductive SCP facilitates charge transport and recombination process, and p-CPE helps to achieve nearly loss-free charge collection by increasing effective work function of indium tin oxide (ITO) and SCP. Because of the synergistic effect of extremely low electrical resistance, ohmic contact, and pH neutrality, tandem devices with our novel RL performed well, exhibiting a high power conversion efficiency of 10.2% and a prolonged lifetime. These findings provide a new insight for strategic design of RLs using SCPs to achieve efficient and stable tandem PSCs and enable us to review and extend the usefulness of SCPs in various electronics research fields.

A series connection architecture for large-area organic photovoltaic modules with a 7.5% module efficiency.

The fabrication of organic photovoltaic modules via printing techniques has been the greatest challenge for their commercial manufacture. Current module architecture, which is based on a monolithic geometry consisting of serially interconnecting stripe-patterned subcells with finite widths, requires highly sophisticated patterning processes that significantly increase the complexity of printing production lines and cause serious reductions in module efficiency due to so-called aperture loss in series connection regions. Herein we demonstrate an innovative module structure that can simultaneously reduce both patterning processes and aperture loss. By using a charge recombination feature that occurs at contacts between electron- and hole-transport layers, we devise a series connection method that facilitates module fabrication without patterning the charge transport layers. With the successive deposition of component layers using slot-die and doctor-blade printing techniques, we achieve a high module efficiency reaching 7.5% with area of 4.15 cm(2).

A new architecture for printable photovoltaics overcoming conventional module limits.

A new architecture for manufacturing large-area polymer solar cells that does not produce concomitant aperture and Ohmic losses is presented. By introducing the innovative concept of metal-filamentary nanoelectrodes, which are vertically formed inside the main active layers, loss-free, widely expandable solar cells with the highest relative power conversion efficiency (ca. 90%) in organic photovoltaic systems are demonstrated.

Self-assembly of interfacial and photoactive layers via one-step solution processing for efficient inverted organic solar cells.

Vertically self-assembled bilayers with an interfacial bottom layer and a photoactive top layer are demonstrated via a single coating step of a blend composed of an amine-containing nonconjugated polyelectrolyte (NPE) and an organic electron donor-acceptor bulk heterojunction composite. The self-assembled NPE layer reduces the work function of an indium tin oxide (ITO) cathode, which leads to efficient inverted organic solar cells without any additional interface engineering of the ITO.

Effect of a new beta-sitosterol analogue on plasma lipid concentrations in rats.

N-Substituted succinamic acid beta-sitosteryl ester derivatives were prepared and evaluated. Compounds 1 and 2 were prepared in 76-92% yields by the reaction of beta-sitosterol and succinic anhydride, followed by the activation of the resulting acid compound 1 by thionyl chloride or methyl chloroformate, and finally by amination with appropriate amines. Compound 2a (DANA87) was also easily obtained in one step by the direct addition of beta-sitosterol to dicyclohexylcarbodiimide (DCC) in 80% yield. Administration of the dietary compound DANA87 resulted in significant decreases in total plasma cholesterol (TC) and low-density lipoprotein (LDL) cholesterol concentrations compared with controls in a rat model. High-density lipoprotein cholesterol and plasma triglyceride levels were not affected. These findings indicate that DANA87 functions as TC and LDL cholesterol-reducing agent.

Osseointegration assessment of dental implants using a synchrotron radiation imaging technique: a preliminary study.

PURPOSE: This study tests the possibility of using synchrotron radiation (SR) x-ray micro-imaging as a new method to evaluate osseointegration. MATERIALS AND METHODS: A simple imaging setup with primarily unmonochromatic SR was used to study the interface of a dental implant in contact with bone. The samples were prepared by sectioning the undecalcified specimen of a titanium screw implanted in the tibia of a New Zealand white rabbit. Radiographs of the interface between surrounding tissues and dental titanium implant were imaged using the SR imaging system at PLS (Pohang Light Source) 5C1 beamline, a micro-computed tomography (microCT) system (SkyScan-1072), and a conventional dental x-ray system (Siemens Heliodent MD). RESULTS: The image quality of the osseointegrated titanium implant was compared among the 3 imaging systems. The SR imaging technique showed greater details than other radiographic modalities for evaluation of the healing stage of bone-implant contact. DISCUSSION: The evaluation was especially focused on the image quality of the osseous contact at the bone-to-implant interfaces. CONCLUSIONS: This SR imaging technique provides finer details and can be expected to make an impact in the clinical study of osseointegration.

Quantitative evaluation of acquisition parameters in three-dimensional imaging with multidetector computed tomography using human skull phantom.

This study evaluated the quantitative measurements of three-dimensional (3D) volume images using multidetector row computed tomography (MDCT) and one skull specimen. Twenty-one linear distances were measured five times each by vernier caliper. A dry human skull was imaged with MDCT for various acquisition parameters at slice thicknesses of 1.25, 2.50, 3.75, and 5.00 mm for the different acquisition modes of axial and spiral scan. The distance of each corresponding item displayed on 3D rendered images was measured seven times by an uninvolved observer using a 3D software tool. Data analysis was performed to determine if there were any statistically significant differences in acquisition parameters. No significant image differences were found among the scan modes for each slice thickness. For a given scan mode, acquisition slice thickness was the important factor for quantitative measurement of 3D rendered CT images.

Quantitative analysis of three-dimensional rendered imaging of the human skull acquired from multi-detector row computed tomography.

The purpose of this study was to evaluate the quantitative accuracy of three-dimensional (3D) rendered images acquired with multi-detector row computed tomography (MDCT) by means of distance measurements of a dry human skull for various slice thicknesses and acquisition modes. A radiologist directly measured the distance of line items on the skull surface to establish reference "gold standards." The skull specimen was scanned with a MDCT with various scanning parameters (slice thicknesses and acquisition modes). An observer measured the corresponding distances of the same items on 3D rendered images. The quantitative accuracy of distance measurements was statistically evaluated. There were no significant statistical differences (P value <.05) in accuracy of distance measurements among the scan modes. However, the results showed that acquisition slice thickness was the influential factor in determining the accuracy of the 3D rendered MDCT images. The quantitative analysis of distance measurement may be a useful tool evaluating the accuracy and defining optimal parameters of 3D rendered images.