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Robust metal ion-chelated polymer interfacial layer for ultraflexible non-fullerene organic solar cells.

ABSTRACT: Achieving high power conversion efficiency and good mechanical robustness is still challenging for the ultraflexible organic solar cells. Interlayers simultaneously having good mechanical robustness and good chemical compatibility with the active layer are highly desirable. In this work, we present an interlayer of Zn²⁺-chelated polyethylenimine (denoted as PEI-Zn), which can endure a maximum bending strain over twice as high as that of ZnO and is chemically compatible with the recently emerging efficient nonfullerene active layers. On 1.3 μm polyethylene naphthalate substrates, ultraflexible nonfullerene solar cells with the PEI-Zn interlayer display a power conversion efficiency of 12.3% on PEDOT:PSS electrodes and 15.0% on AgNWs electrodes. Furthermore, the ultraflexible cells show nearly unchanged power conversion efficiency during 100 continuous compression-flat deformation cycles with a compression ratio of 45%. At the end, the ultraflexible cell is demonstrated to be attached onto the finger joint and displays reversible current output during the finger bending-spreading.

SUBMITTER: Qin F

PROVIDER: S-EPMC7481191 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Stabilizing Non-Fullerene Organic Photodiodes through Interface Engineering Enabled by a Tin Ion-Chelated Polymer.

Project description:The recent emergence of non-fullerene acceptors (NFAs) has energized the field of organic photodiodes (OPDs) and made major breakthroughs in their critical photoelectric characteristics. Yet, stabilizing inverted NF-OPDs remains challenging because of the intrinsic degradation induced by improper interfaces. Herein, a tin ion-chelated polyethyleneimine ethoxylated (denoted as PEIE-Sn) is proposed as a generic cathode interfacial layer (CIL) of NF-OPDs. The chelation between tin ions and nitrogen/oxygen atoms in PEIE-Sn contributes to the interface compatibility with efficient NFAs. The PEIE-Sn can effectively endow the devices with optimized cascade alignment and reduced interface defects. Consequently, the PEIE-Sn-OPD exhibits properties of anti-environmental interference, suppressed dark current, and accelerated interfacial electron extraction and transmission. As a result, the unencapsulated PEIE-Sn-OPD delivers high specific detection and fast response speed and shows only slight attenuation in photoelectric performance after exposure to air, light, and heat. Its superior performance outperforms the incumbent typical counterparts (ZnO, SnO2 , and PEIE as the CILs) from metrics of both stability and photoelectric characteristics. This finding suggests a promising strategy for stabilizing NF-OPDs by designing appropriate interface layers.

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Air-Stable Ultrabright Inverted Organic Light-Emitting Devices with Metal Ion-Chelated Polymer Injection Layer.

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| S-EPMC8648931 | biostudies-literature

Donor polymer design enables efficient non-fullerene organic solar cells.

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Layer-by-Layer Organic Photovoltaic Solar Cells Using a Solution-Processed Silicon Phthalocyanine Non-Fullerene Acceptor.

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| S-EPMC8908506 | biostudies-literature

A zwitterionic polymer as an interfacial layer for efficient and stable perovskite solar cells.

Project description:Perovskite solar cells have been rapidly developed in the past ten years. It was demonstrated that the interfacial layer plays an important role in device performance of perovskite solar cells. In this study, we report utilization of a photoinitiation-crosslinked zwitterionic polymer, namely dextran with carboxybetaine modified by methacrylate (Dex-CB-MA), as an interfacial layer to improve the film morphology of the CH3NH3PbI3 photoactive layer and the interfacial contact between the poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) hole extraction layer and CH3NH3PbI3 photoactive layer. It is found that the Dex-CB-MA thin layer forms a better band alignment between the PEDOT:PSS hole extraction layer and CH3NH3PbI3 photoactive layer, and improves the crystallization of the CH3NH3PbI3 photoactive layer, resulting in efficient charge carrier transport. As a result, perovskite solar cells with the PEDOT:PSS/Dex-CB-MA hole extraction layer exhibit more than 30% enhancement in efficiency and dramatically boosted stability as compared with that with the PEDOT:PSS hole extraction layer. Our studies provide an effective and facile way to fabricate stable perovskite solar cells with high power conversion efficiency.

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Statistical analyses on inverted perovskite solar cells employing non-fullerene-based small molecule as a cathode interfacial layer.

Project description:In this data article, we present the influences of the solvent, concentration, and spin rates of 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) (ITIC) material on the performances of perovskite solar cells (PSCs). The device parameters such as open-circuit voltage (Voc), short circuit current (Jsc), fill factor (FF), and power conversion efficiency (PCE) were measured with Keithley 2400 source meter unit under 100 mW/cm2 (AM 1.5 G). The data in this article describe the optimization of ITIC-based PSCs and are directly related to our research article "Non-fullerene-based small molecules as an efficient n-type electron transporting layers in inverted organic-inorganic halide perovskite solar cells" (Noh et al., Submitted for publication) [1].

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Functionalized Amphiphilic Diblock Fullerene Derivatives as a Cathode Buffer Layer for Efficient Inverted Organic Solar Cells.

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Optimized active layer morphology toward efficient and polymer batch insensitive organic solar cells.

Project description:Morphology control in laboratory and industry setting remains as a major challenge for organic solar cells (OSCs) due to the difference in film-drying kinetics between spin coating and the printing process. A two-step sequential deposition method is developed to control the active layer morphology. A conjugated polymer that self-assembles into a well-defined fibril structure is used as the first layer, and then a non-fullerene acceptor is introduced into the fibril mesh as the second layer to form an optimal morphology. A benefit of the combined fibril network morphology and non-fullerene acceptor properties was that a high efficiency of 16.5% (certified as 16.1%) was achieved. The preformed fibril network layer and the sequentially deposited non-fullerene acceptor form a robust morphology that is insensitive to the polymer batches, solving a notorious issue in OSCs. Such progress demonstrates that the utilization of polymer fibril networks in a sequential deposition process is a promising approach towards the fabrication of high-efficiency OSCs.

| S-EPMC7275072 | biostudies-literature

Self-Organized Fullerene Interfacial Layer for Efficient and Low-Temperature Processed Planar Perovskite Solar Cells with High UV-Light Stability.

Project description:In this Communication, a self-organization method of [6,6]-phenyl-C61-butyric acid 2-((2-(dimethylamino)-ethyl) (methyl)amino)ethyl ester (PCBDAN) interlayer in between 6,6-phenyl C61-butyric acid methyl ester (PCBM) and indium tin oxide (ITO) has been proposed to improve the performance of N-I-P perovskite solar cells (PSCs). The introduction of self-organized PCBDAN interlayer can effectively reduce the work function of ITO and therefore eliminate the interface barrier between electron transport layer and electrode. It is beneficial for enhancing the charge extraction and decreasing the recombination loss at the interface. By employing this strategy, a highest power conversion efficiency of 18.1% has been obtained with almost free hysteresis. Furthermore, the N-I-P PSCs have excellent stability under UV-light soaking, which can maintain 85% of its original highest value after 240 h accelerated UV aging. This self-organization method for the formation of interlayer can not only simplify the fabrication process of low-cost PSCs, but also be compatible with the roll-to-roll device processing on flexible substrates.

| S-EPMC5566248 | biostudies-literature

The influence of polymer purification on the efficiency of poly(3-hexylthiophene):fullerene organic solar cells.

Project description:We report the influence of different polymer purification procedures on the photovoltaic performance of bulk heterojunction solar cells formed from binary blends of poly(3-hexylthiophene) (P3HT) and fullerenes. Selective Soxhlet extractions and metal scavenging agents were used to remove residual monomer, magnesium salt by-products and catalyst from high-weight P3HT (Mw 121?kg/mol, PDI 1.8, RR 99%) synthesised by the Grignard metathesis (GRIM) polymerization route. Using phenyl-C61-butyric acid methyl ester (PC60BM) as an electron acceptor, we observed an increase in average power conversion efficiency from 2.3 to 4.8% in going from crude to fully purified material. Using indene-C60 bisadduct (IC60BA) in place of PC60BM, we observed a further increase to an average value of 6.6% - high for a bulk heterojunction formed from a binary blend of P3HT and C60 fullerene derivatives.

| S-EPMC4814819 | biostudies-other

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