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In this paper, we demonstrate the use of polymer dispersed liquid crystal (PDLC) imprinted with a microlens array (MLA) via solution process to improve the outcoupling efficiency of organic light emitting diodes (OLEDs). The PDLC, well known for its scattering effect, is an excellent technology for improving the outcoupling efficiency of OLEDs. Additionally, we introduce a simple spin-coating process to fabricate PDLC which is adaptable for future solution-processed OLEDs. The MLA-imprinted PDLC applied OLED shows an enhancement factor of 1.22 in outcoupling efficiency which is a 37.5% increase compared to the existing PDLC techniques without changing the electrical properties of the OLED. Through this approach, we can expect the roll-to-roll based extremely flexible OLED, and with further research on pattering PDLC by various templates, higher outcoupling efficiency is achievable through a simple UV irradiation process.
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Random Al2O3 nanoparticle-based polymer composite films are investigated as external scattering layers to enhance light extraction from flexible organic light-emitting diodes (OLEDs). We found that the size and concentration of the nanoparticles (NPs) in the polymer film play a crucial role in improving light extraction. It turned out that their increase has a favorable impact on the light output of the devices, as the high concentration of the NPs leads to the formation of large nanoparticle clusters, which, in turn, yield pore-containing films. As a result, light extraction efficiency of the flexible OLEDs on PEN substrates was enhanced by a factor of 1.65 by the incorporation of the scattering layer, with the highest Al2O3 NP concentration of 99 wt%. This outcome is attributed to the reduction of the waveguide mode and total internal reflection at the substrate/air interface induced by the randomly distributed NPs in the flexible scattering layer. Our work demonstrates an efficient, solution-processable, and low-cost light-outcoupling structure for large-area and flexible OLED applications.
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We have investigated an effective and a single-step chemical vapor deposition (CVD) method to achieve conformal visible poly-dichloro-para-xylylene (parylene C) film for light extraction enhancement in bottom-emitting organic light-emitting diodes (OLEDs) at room temperature. We report that sublimed parylene dimers pyrolyzed between 400 °C and 500 °C resulted in visible parylene films with tunable transmittance and haze, exhibiting light scattering properties due to the formation of uniformly distributed dimer crystals. We achieved a novel conformal visible parylene film with total transmittance and high haze of 79.5% and 93.6%, respectively. It is observed that the outcoupling efficiency of the OLEDs employing the visible parylene film is enhanced up to 45.8%. Additionally, the OLED with the visible parylene light extraction film shows limited angle-dependency of emission spectrum over viewing angles. The single-step room temperature fabrication process of this conformal outcoupling film paves the way to achieving commercial high-performance OLEDs.
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We proposed and analyzed an optically isotropic nano-droplet liquid crystal (LC) doped with high k nanoparticles (NPs), exhibiting enhanced Kerr effects, which could be operated with reduced driving voltages. For enhancing the contrast ratio together with the light efficiencies, the LC droplet sizes were adjusted to be shorter than the wavelength of visible light to reduce depolarization effects by optical scattering of the LC droplets. Based on the optical analysis of the depolarization effects, the influence of the relationship between the LC droplet size and the NP doping ratio on the Kerr effect change was investigated.
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Nanoparticle scattering layer based on polymer-metal oxide composite is successfully introduced to enhance the light extraction efficiency of organic light emitting diodes (OLEDs). We find that the density and the distribution of nanoparticles is the key factor to maximize the light extraction efficiency of pristine OLEDs by out-coupling the unusable light with the scattering film. In our experiment, 71 wt% of Al(2)O(3) mixed with polymer matrix shows the increase of light extraction efficiency of 40%. This method is expected to play a critical role to create the low-power OLED application such as OLED lightings with simple fabrication process and low cost.
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Based on several nano-scale groove models, we propose a new technique to simultaneously determine the azimuthal and polar surface anchoring strengths of nematic liquid crystal (LC). The optical analysis of LCs on a grooved surface made by nanoimprinting lithography was performed on special alignment material, using a typical rubbing process. In our approach, using a polarizing microscope, we can determine the LC alignment exactly as it is in a parallel state, rather than a twisted state. This simple proposed method gives an accurate value of the surface LC anchoring of various surfaces, as well as simultaneously measuring the azimuthal and polar anchoring energy.
Assuntos
Cristais Líquidos/química , Teste de Materiais/métodos , Nanotecnologia/instrumentação , Refratometria/instrumentação , Desenho de Equipamento , Análise de Falha de Equipamento , Cristais Líquidos/análise , Propriedades de Superfície , Resistência à TraçãoRESUMO
We report on the thermal stability of nonvolatile memory characteristics in an organic ferroelectric field-effect transistor (OFeFET) with a ferroelectric polymer of poly(vinylidene fluoride-trifluoroethylene)[P(VDF-TrFE)]. Pentacene-based OFeFETs are thermally annealed to understand how the thermal treatment affects nonvolatile memory characteristics. As increasing the annealing temperature up to 80 degrees C, both the memory window and the memory on-off ratio show no significant difference, while the memory properties results in rather monotonic reduction for beyond 80 degrees C which corresponds to the phase transition temperature of P(VDF-TrFE) molecules. It was found that the phase transition of the P(VDF-TrFE) from ferroelectric beta-phase to paraelectric gamma-phase at Curie's temperature plays a critical role for tailoring the electric characteristics in OFeFETs.
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A convertible lenticular liquid crystal (LC) lens architecture is demonstrated using an index-matched planarization layer on a periodically undulated electrode for the homogeneous alignment of an LC. It is found that the in-plane component of the electric field by the undulated electrode plays a primary role in the flat-to-lens effect while the out-of-plane component contributes to the anchoring enhancement of the LC molecules in the surface layer. Our LC device having an index-matched planarization layer on the undulated electrode is capable of achieving the electrical tunability from the flat surface to the lenticular lens suitable for 2D/3D convertible displays.
Assuntos
Eletrodos , Imageamento Tridimensional/instrumentação , Lentes , Cristais Líquidos , Dispositivos Ópticos , Campos Eletromagnéticos , Microscopia Eletrônica de Varredura , Oscilometria/instrumentação , PeriodicidadeRESUMO
In this study, we propose a solution process for realizing colored glass for building integrated photovoltaic (BIPV) systems by spin coating a color solution composed of pearlescent pigments mixed in a Norland Optical Adhesive (NOA) matrix. Color solutions are made from mixing pearlescent pigments in NOA63. Compared to a physical vapor deposition process, color coatings are achieved by spin coating in a relatively simple and inexpensive process at room temperature. The optical properties can be easily controlled by adjusting the spin coating speed and the concentration of the pearlescent pigments. The produced colored glass achieved a high transmittance of 85% or more in the visible wavelength range, except for the wavelength spectrum exhibiting the maximum reflectance. In addition, we propose a one-step lamination process of colored glass on a solar cell by leveraging on the adhesive property of the NOA matrix. This eliminates the cost and process of additional ethylene vinyl acetate (EVA) layer or other materials used in the conventional lamination process. The colored glass produced through this study has stability that does not change its properties over time. Therefore, it is expected to be applied to the BIPV solar module market where aesthetics and energy efficiency are required.
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In this paper, we propose a single-layer thin-film color glass manufacturing process for building-integrated photovoltaics (BIPV) with excellent aesthetics and high transmittance, through a solution process using pearlescent pigments. As a matrix for the color solution, ethylene vinyl acetate (EVA), which serves as an encapsulant and adhesive for the photovoltaic module (PV), was dissolved and used as a matrix for the color solution. The color glass produced is excellent in securing the aesthetics of buildings, has a high transmittance of 90% or more, outputs a maximum solar power generation efficiency of 91% from a solar cell, and can minimize the deterioration of power generation efficiency. In addition, the characteristics do not change over time, so it is suitable as color glass for BIPV. Through this study, the solution-based color glass manufacturing process for BIPV using dissolved EVA as a matrix forms a single-layer thin film with good color extensions. The choice of EVA as a matrix makes it possible for color glass to be easily attached to a solar panel using a heat press method. This proposed technique makes it easier and simpler to manufacture color glass as compared to the physical vapor deposition process. The adoption of this solution process technique to fabricate pearlescent pigment-based color glass can effectively reduce the time and cost of the process, so it is expected to be applied to the low-cost BIPV market with excellent aesthetics and high transmittance.
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Poly-dichloro-para-xylylene (parylene-C) film is formed through a chemical vapor deposition process, where monomeric gases are polymerized on the target surface at room temperature and are used as transparent insulating coating films. The thin parylene-C films exhibit uniform conformal layers even when deposited on substrates or surfaces with fine cracks, structures, and bumps. However, the film is highly transparent in the visible range (transmittance > 90%); thus, it is difficult to visually identify, inspect the coating process and check for any defects when used as an insulation film. Some reports have demonstrated the deposition of visible (hazy) parylene films through the control of the vaporization or pyrolysis of the parylene-C powder and sublimed dimers, respectively. Even though these films have been applied as device substrates and light extraction layers in organic light-emitting diodes (OLEDs), their optical and electrical characteristics have not been extensively explored, especially for their applications as insulation coatings. In this study, the characteristics of visible parylene films produced by tuning the ratio of dimer to monomer gases via the adjustments of the pyrolysis temperature are analyzed with electrical and optical methods. Parylene-C films deposited within the pyrolysis temperature of 400−700 °C exhibited a haze range of 10−90%. A relative reflectance of 18.8% at 550 nm of the visible light region was achieved in the visible parylene film deposited with a pyrolysis temperature of 400 °C. Resistivity in the order of 1010 Ω cm was achieved for the visible parylene films measured with the transmission line measurement (TLM) method. The films can be applied in advanced insulation coatings for various optical systems and electronic devices.
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We demonstrated the enhancement of the retention characteristics in solution-processed ferroelectric memory transistors. For enhanced retention characteristics, solution-processed Indium Gallium Zinc Oxide (InGaZnO) semiconductor is used as an active layer in a dual-gate structure to achieve high memory on-current and low memory off-current respectively. In our dual-gate oxide ferroelectric thin-film transistor (DG Ox-FeTFT), while conventional TFT characteristic is observed during bottom-gate sweeping, large hysteresis is exhibited during top-gate sweeping with high memory on-current due to the high mobility of the InGaZnO. The voltage applied to the counter bottom-gate electrode causes variations in the turn-on voltage position, which controlled the memory on- and off-current in retention characteristics. Specifically, due to the full depletion of semiconductor by the high negative counter gate bias, the memory off-current in reading operation is dramatically reduced by 104. The application of a high negative counter field to the dual-gate solution-processed ferroelectric memory gives a high memory on- and off-current ratio useful for the production of high performance multi-bit memory devices.
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This study proposes front colored glass for building integrated photovoltaic (BIPV) systems based on multi-layered derivatives of glass/MoO3/Al2O3 with a process technology developed to realize it. Molybdenum oxide (MoO3) and aluminum oxide (Al2O3) layers are selected as suitable candidates to achieve thin multi-layer color films, owing to the large difference in their refractive indices. We first investigated from a simulation based on wave optics that the glass/MoO3/Al2O3 multi-layer type offers more color design freedom and a cheaper fabrication process when compared to the glass/Al2O3/MoO3 multi-layer type. Based on the simulation, bright blue and green were primarily fabricated on glass. It is further demonstrated that brighter colors, such as yellow and pink, can be achieved secondarily with glass/MoO3/Al2O3/MoO3 due to enhanced multi-interfacial reflections. The fabricated color glasses showed the desired optical properties with a maximum transmittance exceeding 80%. This technology exhibits promising potential in commercial BIPV system applications.
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We demonstrated the effect of a buffer layer on the electrical characteristics of ferroelectric polymer capacitors and field-effect transistors. Various polymer materials with a dielectric constant between 2 and 42 were used to form buffer layers with a similar thicknesses, but with different capacitances. In order to evaluate the characteristics of the ferroelectrics with a buffer layer, the polarization-voltage characteristics of the capacitor, the transfer characteristics, and the retention characteristics of the transistors were investigated. As the capacitance of the buffer layer increased, high remnant polarization (Pr), high hysteresis, and long retention times were observed. Exceptionally, when poly(methylmethacrylate) and rigid poly(aryl ether) (poly(9,9-bis(4-hydroxyphenyl)fluorene-co-decafluorobiphenyl)) were used as the buffer layer, Pr had a value close to 0 in the dynamic measurement polarization-voltage (P-V) characteristic, but the quasi-static measurement transfer characteristic and the static measurement retention characteristic showed relatively high hysteresis and long retention times. Our study provides a scientific and technical basis for the design of ferroelectric memory and neuromorphic devices.
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A substrate coated with an achiral polyimide alignment layer was scribed bidirectionally with the stylus of an atomic force microscope to create an easy axis for liquid crystal orientation. The resulting noncentrosymmetric topography resulted in a chiral surface that manifests itself at the molecular level. To show this unambiguously, a planar-aligned negative dielectric aniostropy achiral nematic liquid crystal was placed in contact with the surface and subjected to an electric field E. The nematic director was found to undergo an azimuthal rotation approximately linear in E. This so-called "surface electroclinic effect" is a signature of surface chirality and was not observed when the polyimide was treated for a centrosymmetric topography, and therefore was nonchiral.
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We present a microlens array characterized by the electroclinic effect of chiral smectic A (SmA(*)) liquid crystals, which show the very fast dynamic switching characteristics required in high-speed optical devices. In order to easily control the intensity at the focal length of the proposed dynamic microlens structure, we adopt a solid-type liquid crystal polymer with optical anisotropy, which can split the beam intensity into two directions, depending on the vectorial portion of the polarization state of the light. The proposed microlens shows a focal intensity tunable by controlling the polarization of light at the SmA(*) liquid crystal. The lens has a very fast switching time of about 24 micros, which is several times faster than conventional microlens arrays with surface-stabilized ferroelectric liquid crystals.
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We investigate the pretilt characteristics of a nematic liquid crystal [LC] in terms of ion beam exposure conditions on the homeotropic polyimide alignment layer. The pretilt angle of LCs in the case of high-energy ion beam treatment was decreased considerably almost the same to that of the homogenous alignment layer though we used homeotropic polyimide film at first. Increasing irradiating energy, we could control the pretilt from 90° to 1° with several steps. We believe that this is because the side chain with hydrophobicity in the used polyimide is broken by ion beam exposure. To confirm it, contact angle measurement was carried out. With this result, we can easily control the LC pretilt in the pixel with appropriate exposure conditions which is critical to achieve excellent electrooptic characteristics and good image quality.
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A herringbone "easy axis" pattern is scribed into a polyimide alignment layer for liquid-crystal orientation using the stylus of an atomic force microscope. Owing to the liquid crystal's bend elasticity K33 , the nematic director is unable to follow the sharp turn in the scribed easy axis, but instead relaxes over an extrapolation length L=K33/W2φ, where W2φ is the quadratic azimuthal anchoring strength coefficient. By immersing a tapered optical fiber into the liquid crystal, illuminating the fiber with polarized light, and scanning the fiber close to the substrate, a visualization and direct measurement of L are obtained on approaching the nematic-smectic- A phase transition temperature T NA from above. L is found to exhibit a sharp pretransitional increase near T NA, consistent with a diverging bend elastic constant.
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A substrate coated with a polyimide alignment layer is scribed bidirectionally with the stylus of an atomic force microscope to create an easy axis for liquid-crystal orientation. The resulting noncentrosymmetric topography breaks two-dimensional inversion symmetry and results in a spatial amplitude modulation of an imposed twisted nematic state. This is observed optically as spatially periodic light and dark stripes. When the alignment layer is scribed unidirectionally the centrosymmetric topography maintains inversion symmetry, and no stripes are observed. The appearance of the twist modulation is consistent with a chiral term in the free energy.