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With the aim of developing high‐performance flexible polymer solar cells, the preparation of flexible transparent electrodes (FTEs) via a high‐throughput gravure printing process is reported. By varying the blend ratio of the mixture solvent and the concentration of the silver nanowire (AgNW) inks, the surface tension, volatilization rate, and viscosity of the AgNW ink can be tuned to meet the requirements of gravure printing process. Following this method, uniformly printed AgNW films are prepared. Highly conductive FTEs with a sheet resistance of 10.8 Ω sq−1 and a high transparency of 95.4% (excluded substrate) are achieved, which are comparable to those of indium tin oxide electrode. In comparison with the spin‐coating process, the gravure printing process exhibits advantages of the ease of large‐area fabrication and improved uniformity, which are attributed to better ink droplet distribution over the substrate. 0.04 cm2 polymer solar cells based on gravure‐printed AgNW electrodes with PM6:Y6 as the photoactive layer show the highest power conversion efficiency (PCE) of 15.28% with an average PCE of 14.75 ± 0.35%. Owing to the good uniformity of the gravure‐printed AgNW electrode, the highest PCE of 13.61% is achieved for 1 cm2 polymer solar cells based on the gravure‐printed FTEs.

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Owing to the sensitivity of the perovskite thin film to solvent, preparation of metal top electrode by solution process is of great challenging. This is the key technology for the realization of fully solution processed perovskite solar cells. In this paper, we report the preparation of transparent silver nanowires (AgNW) top electrode for perovskite solar cells using inkjet printing process. Experiment results demonstrate that low device performance with low fill factor was obtained when the AgNW is directly printed onto the PC61BM layer. This is ascribed to the mismatched work functions of the AgNW electrode and PC61BM layer, and the solvent assisted chemical corrosion of the AgNW electrode by halogen anions. By inserting a thin layer of polyethylenimine (PEI), the charge injection barrier between PC61BM and AgNW electrode was minimized. More importantly, such a thin PEI layer suppresses the chemical corrosion of AgNW electrode during printing, yielding a condensed and uniform AgNW networks. The introduction of a thin PEI layer greatly improves the device performance and stability. A high power conversion efficiency of 14.17% with an averaged light transmittance of 21.2% was achieved for the PEI/AgNW cells. In addition, improved performance stability was measured for the PEI/AgNW cells.

In the aim to realize high performance semitransparent fully coated organic solar cells, printable electrode buffer layers and top electrodes are two important key technologies. An ideal ink for the preparation of the electrode buffer layer for printed top electrodes should have good wettability and negligible solvent corrosion to the underlying layer. This work reports a novel organic-inorganic composite of phosphomolybdic acid (PMA) and PEDOT:PSS that features excellent wettability with the active layer and printed top Ag nanowires and high resistibility to solvent corrosion. This composite buffer layer can be easily deposited on a polymer surface to form a smooth, homogeneous film via spin-coating or doctor-blade coating. Through the use of this composite anode buffer layer, fully coated semitransparent devices with doctor-blade-coated functional layers and spray-coated Ag nanowire top electrodes showed the highest power conversion efficiency (PCE) of 5.01% with an excellent average visible-light transmittance (AVT) of 50.3%, demonstrating superior overall characteristics with a comparable performance to and a much higher AVT than cells based on a thermally evaporated MoO/Ag/MoO thin film electrode (with a PCE of 5.77% and AVT of 19.5%). The current work reports the fabrication of fully coated inverted organic solar cells by combining doctor-blade coating and spray coating and, more importantly, demonstrates that a nanocomposite of a polyoxometalate and conjugated polymer could be an excellent anode buffer layer for the fully coated polymer solar cells with favorable interfacial contact, hole extraction efficiency, and high comparability with full printing.

The Ag grid electrode is a candidate for use as a transparent conductive electrode in large‐area flexible thin‐film photovoltaics due to its high conductivity and high optical transparency. But the device performance and stability are greatly inhibited due to the corrosion of Ag electrode by perovskite. The PH1000 (highly conductive PEDOT:PSS)‐involved electrochemical corrosion of the Ag electrode is found to be a major reason of the low device performance for flexible Ag grid electrode‐based perovskite solar cells. This redox reaction occurred via the reduction of PH1000 (a kind of highly conductive PEDOT:PSS) layer and the oxidation of Ag electrode, and finally caused a rapid reaction between the Ag electrode and perovskite precursor solution. Such corrosion is suppressed by introduction of an ammonia: polyethylenimine modified PH1000 (PH1000:ammonia:PEI) layer, possibly because PH1000 is reduced by PEI in the composite layer prior to Ag. High‐performance flexible perovskite solar cells with power conversion efficiencies (PCEs) of 14.52% are fabricated on PET/Ag‐grid/modified highly conductive PEDOT:PSS (PH1000) flexible composite transparent electrodes via a facile one‐step anti‐solvent‐assisted fast crystallization route. Flexible perovskite solar cells using this composite electrode exhibited excellent robustness and durability, maintaining more than 86% of the initial performance after 5000 full bending cycles.

Our data indicate that miR-761 acts as an oncogene in TNBC. This mode of action can, at least partially, be ascribed to the down-regulation of its target TRIM29. We suggest that miR-761 may serve as a promising therapeutic target for TNBC.

We have demonstrated in this article that both power conversion efficiency (PCE) and performance stability of inverted planar heterojunction perovskite solar cells can be improved by using a ZnO:PFN nanocomposite (PFN: poly[(9,9-bis(3'-(N,N-dimethylamion)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctyl)-fluorene]) as the cathode buffer layer (CBL). This nanocomposite could form a compact and defect-less CBL film on the perovskite/PC61BM surface (PC61BM: phenyl-C61-butyric acid methyl ester). In addition, the high conductivity of the nanocomposite layer makes it works well at a layer thickness of 150 nm. Both advantages of the composite layer are helpful in reducing interface charge recombination and improving device performance. The power conversion efficiency (PCE) of the best ZnO:PFN CBL based device was measured to be 12.76%, which is higher than that of device without CBL (9.00%), or device with ZnO (7.93%) or PFN (11.30%) as the cathode buffer layer. In addition, the long-term stability is improved by using ZnO:PFN composite cathode buffer layer when compare to that of the reference cells. Almost no degradation of open circuit voltage (VOC) and fill factor (FF) was found for the device having ZnO:PFN, suggesting that ZnO:PFN is able to stabilize the interface property and consequently improve the solar cell performance stability.