- 标题
- 摘要
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- 实验方案
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12.1: <i>Invited Paper:</i> Polarization control and optical efficiency improvement of light emitted from OLED using liquid crystalline luminophores
摘要： Highly circularly polarized (CP) light is generated by using a twisted conjugated polymer structure with a small amount of chiral molecules as the light emitting layer of the OLED. It is confirmed that the luminous efficiency is increased by 60% compared to the conventional OLED structure.
关键词： organic light emitting diodes,conjugated polymer,polarized emission,chiral dopant,Circular polarization
更新于2025-09-11 14:15:04
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MEH-PPV/Carbon Nanopearls Nanocomposites for Enhanced Organic Solar Cells Efficiencies
摘要： An organic nanocomposites, based on a conjugated polymer (MEH-PPV) as electron donor material and carbon nanopearls (CNPs) as electron acceptor material, have been elaborated and optoelectronically studied. The effect of CNPs concentration on the electric and photoelectric properties in these blends has been investigated. Dielectric measurements demonstrate that the blend conductivity displays a dramatic increase, reaching 0.6 S/m for a CNPs concentration about 1 wt.%. The elaborated organic nanocomposites were used as photoactive materials in organic solar cells.
关键词： organic nanocomposites,conjugated polymer,carbon nanopearls,photovoltaic response,organic solar cells,electric properties
更新于2025-09-11 14:15:04
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1,5-Naphthyridine-based conjugated polymers as co-sensitizers for dye-sensitized solar cells
摘要： 1,5-naphthyridine-based conjugated polymers (P1 and P2) were synthesized and extensively characterized by 1H NMR, thermogravimetric analysis (TGA), FT-IR. These polymers were employed as co-sensitizers in DSSCs sensitized with Ru (II) based N3 dye. In comparison to the N3 sensitized device, the P1 and P2 co-sensitized solar cells demonstrated enhanced open circuit voltage, (VOC) of 825 and 788 mV and better ?ll factor (FF) of 59 and 58%, respectively. The co-sensitization of P1 and P2 with N3 increased the overall e?ciencies to 5.88% and 6.21%, respectively, as compared to 5.58% for N3 sensitizer alone. The fabricated device based on N3 co-sensitized with P2 displayed higher charge recombination resistances as compared to the devices based on N3 alone or N3 co-sensitized with P1. The conjugated polymers are believed to enhance light harvesting ability and reduce the charged recombination in the co-sensitized solar cells.
关键词： 1,5-Naphthyridine-based conjugated polymers,Solar cell,Co-sensitization,N3 dye
更新于2025-09-11 14:15:04
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Polymeric, Cost-Effective, Dopant-Free, Hole Transport Materials for Efficient and Stable Perovskite Solar Cells
摘要： Perovskite solar cells (PSCs) have skyrocketed in the last decade to an unprecedented level due to its outstanding photoelectric properties and facile processability. However, the utilization of expensive hole transport materials (HTMs) and the inevitable instability instigated by the deliquescent dopants represent major concerns hindering further commercialization. Here, a series of low cost, conjugated polymers are designed and applied as dopant free HTMs in PSCs, featuring tuned energy levels, good temperature and humidity resistivity, and excellent photoelectric properties. Further studies highlight the critical and multifaceted roles of the polymers with respect to facilitating charge separation, passivating the surface trap sites of perovskite materials, and guaranteeing long-term stability of the devices. A stabilized power conversion efficiency (PCE) of 20.3% and remarkably enhanced device longevity are achieved using the dopant free P3 with a low concentration of 5 mg/mL, qualifying the devices as one of the best PSC systems constructed based on dopant-free HTMs so far. In addition, the flexible PSCs made based on P3 also exhibit a PCE of 16.2%. This work demonstrates a promising route towards commercially viable, stable and efficient PSCs.
关键词： perovskite solar cell,good stability,conjugated polymer,dopant free,hole transport material
更新于2025-09-11 14:15:04
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Intrinsically distinct hole and electron transport in conjugated polymers controlled by intra and intermolecular interactions
摘要： It is still a matter of controversy whether the relative difference in hole and electron transport in solution-processed organic semiconductors is either due to intrinsic properties linked to chemical and solid-state structure or to extrinsic factors, as device architecture. We here isolate the intrinsic factors affecting either electron or hole transport within the same film microstructure of a model copolymer semiconductor. Relatively, holes predominantly bleach inter-chain interactions with H-type electronic coupling character, while electrons’ relaxation more strongly involves intra-chain interactions with J-type character. Holes and electrons mobility correlates with the presence of a charge transfer state, while their ratio is a function of the relative content of intra- and inter-molecular interactions. Such fundamental observation, revealing the specific role of the ground-state intra- and inter-molecular coupling in selectively assisting charge transport, allows predicting a more favorable hole or electron transport already from screening the polymer film ground state optical properties.
关键词： electron transport,organic semiconductors,conjugated polymers,charge transfer state,hole transport
更新于2025-09-11 14:15:04
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Effect of Hot-Electron Injection on the Excited-State Dynamics of a Hybrid Plasmonic System Containing Poly(3-hexylthiophene)-Coated Gold Nanoparticles
摘要： We investigated the photophysical interaction between a conjugated polymer (CP) and a plasmonic gold nanoparticle (Au NP) using transient absorption spectroscopy. We prepared a hybrid system containing CP-stabilized Au NPs by reducing a Au precursor directly with a thiol-terminated poly(3-hexylthiophene) surfactant (P3HT-SH), with the unreacted P3HT-SH chains used as an organic matrix. The P3HT attached to the Au NPs plays two critical roles in our hybrid system: it suppresses exciton quenching from the P3HT matrix to Au NPs (the spacer role) and relays hot electrons induced by surface plasmon resonance of Au NPs to P3HT (the bridge role). Thus, singlet excitons are more slowly relaxed in our hybrid system than those in a neat P3HT film. Our findings may provide important information for development of the high-efficiency hybrid optoelectronic devices.
关键词： surface plasmon resonance,transient absorption spectroscopy,conjugated polymer,photophysical interaction,plasmonic gold nanoparticle,optoelectronic devices,hot-electron injection
更新于2025-09-11 14:15:04
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Small Band gap Boron Dipyrromethene-Based Conjugated Polymers for All-Polymer Solar Cells: The Effect of Methyl Units
摘要： Naphthalene diimide (NDI)-based conjugated polymers have been widely used as the nonfullerene electron acceptor for all-polymer solar cells (all-PSCs), but their low absorption coefficient in the near-infrared (NIR) region severely limits the light harvesting ability in solar cells and hence lowers their photovoltaic performance. In this work, two narrow band gap donor?acceptor conjugated polymers based on boron dipyrromethene (BODIPY) as the electron-deficient unit were developed as the electron donor to combine with a NDI-polymer acceptor in order to significantly improve the photoresponse in the NIR region. More importantly, we found that methyl substitution on the BODIPY segment played an important role in charge transport in these polymers. When methyl units were attached to the α-position of BODIPY, the polymer PMBBDT exhibited high-lying energy levels, improved crystallinity, and dramatically high hole mobility compared to the polymer PBBDT without methyl substitution. Consequently, the power conversion efficiencies (PCEs) could be enhanced from 0.32% for PBBDT- to 5.8% for PMBBDT-based all-PSCs, and the photoresponse covered from 300 to 900 nm. Our results demonstrate that methyl-substituted BODIPY-based conjugated polymers are promising candidates to solve the NIR absorption issue in NDI polymers and, therefore, can be potentially used to further boost the PCEs of all-PSCs similar with organic solar cells based on NIR-fused ring electron acceptors.
关键词： Boron dipyrromethene,Methyl substitution,Conjugated polymers,Near-infrared absorption,All-polymer solar cells
更新于2025-09-11 14:15:04
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[IEEE 2019 26th International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD) - Kyoto, Japan (2019.7.2-2019.7.5)] 2019 26th International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD) - Latest Development of Soluble-OLED Material and its Application to Mid- to large-sized Panel Production
摘要： We present the latest status of soluble OLED material development based on our conjugated polymer technology. The materials are highly suitable for printing OLED panel fabrication, especially for mid- to large-sized displays. We also show the fundamentals to secure the best performance of ink-jet (IJ) printed devices. Finally we discuss the expectation for IJP-OLED panel production from a viewpoint of its process, resolution & panel size, and performance as well as the comparison with WOLED.
关键词： soluble OLED material,ink-jet printed devices,conjugated polymer technology,IJP-OLED panel production,printing OLED panel fabrication
更新于2025-09-11 14:15:04
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Highly Efficient Indoor Organic Solar Cells by Voltage Losses Minimization through Fine-tuning of Polymer Structures
摘要： Herein we report a detailed study on the optoelectronic properties, photovoltaic performance, structural conformation, morphology variation, charge carrier mobility and recombination dynamics in bulk heterojunction (BHJ) solar cells comprising of a series of donor-acceptor (D-A) conjugated polymers as electron donors based on benzodithiophene (BDT) and 5,8-bis(5-bromothiophen-2-yl)-6,7-difluoro-2,3-bis(3-(octyloxy)phenyl)quinoxaline as a function of the BDT’s thienyl substitution (alkyl (WF3), alkylthio (WF3S) and fluoro (WF3F)). It is manifested the synergistic positive effects of the fluorine substituents on the minimization of the bimolecular recombination losses, the reduction of the series resistances (RS), the increment of the shunt resistances (RSh), the suppression of the trap-assisted recombination losses, the balanced charge transport, the finer nanoscale morphology and the deeper highest occupied molecular orbital (EHOMO) versus the alkyl- and alkylthio- substituents. According to these findings, WF3F:[6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) based-organic photovoltaic (OPV) device is a scarce example that feature a high power conversion efficiency (PCE) of 17.34% under 500 lx indoor LED light with a high open-circuit voltage (VOC) of 0.69 V, due to the suppression of the voltage losses and a PCE of 9.44% at 1-sun (100 mW/cm2) conditions, simultaneously.
关键词： Series and Shunt resistances,Coherence length,Conjugated polymers,Wide-angle X-ray scattering,Organic photovoltaic devices,Recombination losses,Indoor lighting conditions
更新于2025-09-11 14:15:04
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π-Conjugated small molecules enable efficient perovskite growth and charge-extraction for high-performance photovoltaic devices
摘要： A π-conjugated small molecule N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)benzidine (NPB) is introduced into a poly (bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA) hole transport layer in inverted perovskite solar cells (PSCs). The NPB doping induces better perovskite crystal growth owing to a strong π-π interaction with PTAA and cation-π interactions with CH3NH3+ (MA+). In addition, NPB doping not only improves the wettability of PTAA and regulates the perovskite crystallization to achieve a larger grain size, but also moves the valence band energy of the hole transport layer closer to the perovskite layer. Consequently, the fabricated PSCs delivered a power conversion efficiency (PCE) of 20.15%, with a short-circuit current density (JSC) of 22.60 mA/cm2 and open-circuit voltage (VOC) of 1.14 V. This outcome indicates that PTAA:NPB composite materials present great potential for fabricating high-performance PSCs.
关键词： Energy level alignment,Charge extraction,π-conjugated molecule
更新于2025-09-11 14:15:04