A ternary organic solar cell with 300 nm thick active layer shows over 14% efficiency

In order to meet the requirements for making organic solar cells(OSCs) through solution printing techniques, great efforts have been devoted into developing high performance OSCs with relatively thicker active layers. In this work, a thick-film(300 nm)ternary OSC with a power conversion efficiency of 14.3% is fabricated by introducing phenyl-C_(61)-butyric-acid-methyl ester(PC_(61)BM) into a PBDB-T-2Cl:BTP-4 F host blend. The addition of PC_(61)BM is found to be helpful for improving the hole and electron mobilities, and thus facilitates charge transport as well as suppresses charge recombination in the active layers, leading to the improved efficiencies of OSCs with relatively thicker active layers. Our results demonstrate the feasibility of employing fullerene derivative PC_(61)BM to construct a high-efficiency thick-film ternary device, which would promote the development of thick layer ternary OSCs to fulfill the requirements of future roll to roll production.     

Benchmarking of Density Functionals for the Description of Optical Properties of Newly Synthesized π-Conjugated TADF Blue Emitters

Computational modeling of the optical characteristics of organic molecules with potential for thermally activated delayed fluorescence (TADF) may assist markedly the development of more efficient emitting materials for organic light-emitting diodes. Recent theoretical studies in this area employ mostly methods from density functional theory (DFT). In order to obtain accurate predictions within this approach, the choice of a proper functional is crucial. In the current study, we focus on testing the performance of a set of DFT functionals for estimation of the excitation and emission energy and the excited singlet-triplet energy gap of three newly synthesized compounds with capacity for TADF. The emitters are designed specifically to enable charge transfer by π-electron conjugation, at the same time possessing high-energy excited triplet states. The functionals chosen for testing are from various groups ranging from gradient-corrected through global hybrids to range-separated ones. The results show that the monitored optical properties are especially sensitive to how the long-range part of the exchange energy is treated within the functional. The accurate functional should also be able to provide well balanced distribution of the π-electrons among the molecular fragments. Global hybrids with moderate (less than 0.4) share of exact exchange (B3LYP, PBE0) and the meta-GGA HSE06 are outlined as the best performing methods for the systems under study. They can predict all important optical parameters correctly, both qualitatively and quantitatively.     

基于PSNR-NC函数优化和非抽样双树复小波变换的自适应多重水印算法

针对多重水印信息的有效嵌入和提取,提出了一种基于峰值信噪比-归一化相关系数函数(PSNR-NC)优化和非抽样双树复小波变换的自适应多重水印算法。该算法首先利用PSNR-NC函数来确定水印的最佳嵌入位置,其次通过非抽样双树复小波变换-奇异值分解(UDTCWT-SVD)算法将多个相互独立的水印信息嵌入到彩色宿主图像中,最后通过水印提取算法在含水印图像中提取多重水印,有效实现了多个版权信息的嵌入和提取。实验结果表明,嵌入水印图像具备良好的不可见性,所提算法对常见的图像处理攻击,特别是在抵抗JPEG压缩、噪声攻击和滤波攻击方面表现出较强的鲁棒性。     

Effects of Chemical Structure of Phenolic Resin on Damping Properties of Acrylate Rubber-Based Blends

Two types of acrylate rubber (AR)-based damping blends were prepared by using two types of phenolic resins (PF), a resole resin (RR) and a novolac resin (NR), as organic fillers. The structure and damping properties of the AR/RR and AR/NR blends obtained by hot-pressing were characterized and compared by Fourier transform infrared spectrum, scanning electron microscopy, differential scanning calorimetry, and dynamic mechanical analysis. The results showed that the chemical structures of PF and the hot-pressing process had a significant effect on the damping properties of the AR-based composites. The loss peak of AR/RR shifted to a lower temperature accompanied with a gradually reduced peak intensity with the increase of RR content. In contrast, hot-pressed AR/NR showed great improvement in damping properties, which can broaden the effective damping temperature region and an increase in the temperature of the loss peak. It was thus concluded that NR with linear structure and abundant phenolic hydroxyl groups, which can create effective hydrogen bonds with an AR matrix, even after hot-pressing, makes it a promising NR to choose as an organic additive in ARs to prepare advanced damping blends.     

Enhanced intermolecular interactions to improve twisted polymer photovoltaic performance

Science China Chemistry - In polymer solar cells (PSCs), twisted polymer donors usually have low photovoltaic efficiencies due to their poor photoactive layer morphologies. Herein, we successfully...     

Layered Thiadiazoloquinoxaline‐Containing Long Pyrene‐Fused N‐Heteroacenes

Three thiadiazoloquinoxaline‐containing long pyrene‐fused N‐heteroacenes with 8, 13, and 18 rings were designed and synthesized. They show high electron affinities (EAs) of approximately 4.1 eV, which were derived from the onset of the reduction peaks in cyclic voltammetry. Crystal structure analysis revealed in‐plane extension through close contacts between thiadiazole units as well as layered packing, enabling in‐plane and interlayer electron transport. Organic field‐effect transistor devices provided electron mobilities, which suggest a potential way to enhance the charge transport in long N‐heteroacenes.     

The Crucial Role of Chlorinated Thiophene Orientation in Conjugated Polymers for Photovoltaic Devices

Chlorinated conjugated polymers not only show great potential for the realization of highly efficient polymer solar cells (PSCs) but also have simple and high‐yield synthetic routes and low‐cost raw materials available for their preparation. However, the study of the structure–property relationship of chlorinated polymers is lagging. Now two chlorinated conjugated polymers, PCl(3)BDB‐T and PCl(4)BDB‐T are investigated. When the polymers were used to fabricate PSCs with the nonfullerene acceptor (IT‐4F), surprisingly, the PCl(3)BDB‐T:IT‐4F‐based device exhibited a negligible power conversion efficiency (PCE) of 0.18 %, while the PCl(4)BDB‐T:IT‐4F‐based device showed an outstanding PCE of 12.33 %. These results provide new insight for the rational design and synthesis of novel chlorinated polymer donors for further improving the photovoltaic efficiencies of PSCs.