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Polyimide (PI) films are well recognized for their outstanding chemical resistance, radiation resistance, thermal properties, and mechanical strength, rendering them highly valuable in advanced fields such as aerospace, sophisticated electronic components, and semiconductors. However, improving their optical transparency while maintaining excellent thermal properties remains a significant challenge. This review systematically checks over recent advancements in enhancing the optical and thermal performance of PI films, focusing on various strategies through molecular design. These strategies include optimizing the main chain, side chain, non-coplanar structures, and endcap groups. Rigid and flexible structural characteristics in the proper combination can contribute to the balance thermal stability and optical transparency. Introducing fluorinated substituents and bulky side groups significantly reduces the formation of charge transfer complexes, enhancing both transparency and thermal properties. Non-coplanar structures, such as spiro and cardo configurations, further improve the optical properties while maintaining thermal stability. Future research trends include nanoparticle doping, intrinsic microporous PI polymers, photosensitive polyimides, machine learning-assisted molecular design, and metal coating techniques, which are expected to further enhance the comprehensive optical and thermal performance of PI films and expand their applications in flexible displays, solar cells, and high-performance electronic devices. Overall, systematic molecular design and optimization have significantly improved the optical and thermal performance of PI films, showing broad application prospects. This review aims to provide researchers with valuable references, stimulate more innovative research and applications, and promote the deep integration of PI films into modern technology and industry. [ABSTRACT FROM AUTHOR]

Resin composites have become the preferred choice for chairside provisional dental restorations. However, these materials may undergo discoloration, changes in surface roughness, and mechanical properties with aging in the oral cavity, compromising the aesthetics, functionality, and success of dental restorations. To investigate the color and mechanical stability of chairside provisional composite resins, this study evaluated the optical, surface, and mechanical properties of four temporary restoration resin materials before and after aging, stimulated by thermal cycling in double-distilled water. Measurements, including CIE LAB color analysis, three-point bending test, nanoindentation, scanning electron microscopy (SEM), and atomic force microscopy (AFM), were conducted (n = 15). Results showed significant differences among the materials in terms of optical, surface, and mechanical properties. Revotek LC (urethane dimethacrylate) demonstrated excellent color stability (ΔE00 = 0.53-Black/0.32-White), while Artificial Teeth Resin (polymethyl methacrylate) exhibited increased mechanical strength with aging (p < 0.05, FS = 68.40 MPa-non aging/87.21 MPa-aging). Structur 2 SC (Bis-acrylic) and Luxatemp automix plus (methyl methacrylate bis-acrylate) demonstrated moderate stability in optical and mechanical properties (Structur 2 SC: ΔE00 = 1.97-Black/1.38-White FS = 63.20 MPa-non aging/50.07 MPa-aging) (Luxatemp automix plus: ΔE00 = 2.49-Black/1.77-White FS = 87.72 MPa-non aging/83.93 MPa-aging). These results provide important practical guidance for clinical practitioners, as well as significant theoretical and experimental bases for the selection of restorative composite resins. [ABSTRACT FROM AUTHOR]

In stealth applications, there is a growing emphasis on the development of radar-absorbing structures that are efficient, flexible, and optically transparent. This study proposes a screen-printed metamaterial absorber (MMA) on polyethylene terephthalate (PET) substrates using indium tin oxide (ITO) as the grounding layer, which achieves both optical transparency and flexibility. These materials and methods enhance the overall flexibility and transparency of MMA. To address the limited transparency caused by the silver nanoparticle ink for the top pattern, a metal mesh was incorporated to reduce the area ratio of the printed patterns, thereby enhancing transparency. By incrementing the fractal order of the structure, we optimized the operating frequency to target the X-band, which is most commonly used in radar detection. The proposed MMA demonstrates remarkable performance, with a measured absorption of 91.99% at 8.85 GHz and an average optical transmittance of 46.70% across the visible light spectrum (450 to 700 nm), indicating its potential for applications in transparent windows or drone stealth. [ABSTRACT FROM AUTHOR]

A sol–gel deposition approach was applied for obtaining nanostructured Li-doped ZnO thin films. ZnO:Li films were successfully spin-coated on quartz and silicon substrates. The evolution of their structural, vibrational, and optical properties with annealing temperature (300–600 °C) was studied by X-ray diffraction (XRD), Fourier Transform Infrared (FTIR), UV-VIS spectroscopic, and field emission scanning electron microscopic (FESEM) characterization techniques. It was found that lithium doping maintains the wurtzite arrangement of ZnO, with increasing crystallite sizes when increasing the annealing temperature. Analysis of the FTIR spectra revealed a broad main absorption band (around 404 cm−1) for Li-doped films, implying the inclusion of Li into the ZnO lattice. The ZnO:Li films were transparent, with slightly decreased transmittance after the use of higher annealing temperatures. The porous network of undoped ZnO films was transformed to a denser, grained, packed structure, induced by lithium doping. [ABSTRACT FROM AUTHOR]

In this paper, novel colorless polyimides (PIs) derived from 5,5′-bis(2,3-norbornanedicarboxylic anhydride) (BNBDA) were presented. The results of single-crystal X-ray structural analysis using a BNBDA-based model compound suggested that it had a unique steric structure with high structural linearity. Therefore, BNBDA is expected to afford new colorless PI films with an extremely high glass transition temperature (Tg) and a low linear coefficient of thermal expansion (CTE) when combined with aromatic diamines with rigid and linear structures (typically, 2,2′-bis(trifluoromethyl)benzidine (TFMB)). However, the polyaddition of BNBDA and TFMB did not form a PI precursor with a sufficiently high molecular weight; consequently, the formation of a flexible, free-standing PI film via the two-step process was inhibited because of its brittleness. One-pot polycondensation was also unsuccessful in this system because of precipitation during the reaction, probably owing to the poor solubility of the initially yielded BNBDA/TFMB imide oligomers. The combinations of (1) the structural modification of the BNBDA/TFMB system, (2) the application of a modified one-pot process, in which the conditions of the temperature-rising profile, solvents, azeotropic agent, catalysts, and reactor were refined, and (3) the optimization of the film preparation conditions overcame the trade-off between low CTE and high film toughness and afforded unprecedented PI films with well-balanced properties, simultaneously achieving excellent optical transparency, extremely high Tg, sufficiently high thermal stability, low CTE, high toughness, relatively low water uptake, and excellent solution processability. [ABSTRACT FROM AUTHOR]

Polymeric optical films with light colors, good optical transparency and high thermal resistance have gained increasing attention in advanced optoelectronic areas in recent years. However, it is somewhat inter-conflicting for achieving the good optical properties to the conventional thermal resistant polymers, such as the standard aromatic polyimide (PI) films, which are well known for the excellent combined properties and also the deep colors. In this work, a series of wholly aromatic PI films were prepared via the polycondensation chemistry of one fluorene-containing dianhydride, 9,9-bis(3,4-dicarboxyphenyl)fluorene dianhydride (FDAn) and several aromatic diamines with amide linkages in the main chain, including 9,9-bis [4-(4-aminobenzamide)phenyl]fluorene (FDAADA), 2,2′-bis(trifluoromethyl)-4,4′-bis[4-(4-aminobenzamide)] biphenyl (ABTFMB), and 2,2′-bis(trifluoromethyl)-4,4′-bis[4-(4-amino-3-methyl)benzamide] biphenyl (MABTFMB). The derived FLPI-1 (FDAn-FDAADA), FLPI-2 (FDAn-ABTFMB) and FLPI-3 (FDAn-MABTFMB) resins showed good solubility in the polar aprotic solvents, such as N-methyl-2-pyrrolidone (NMP), N,N-dimethylacetamide (DMAc) and dimethyl sulfoxide (DMSO). The solution-processing FDAn-PI films exhibited good optical transmittance over 80.0% at a wavelength of 500 nm (T500), yellow indices (b*) in the range of 1.01–5.20, and haze values lower than 1.0%. In addition, the FDAn-PI films showed low optical retardance with optical retardation (Rth) values in the range of 31.7–390.6 nm. At the same time, the FDAn-PI films exhibited extremely high glass transition temperatures (Tg) over 420 °C according to dynamic mechanical analysis (DMA) tests. The FDAn-PI films showed good dimensional stability at elevated temperatures with linear coefficients of thermal expansion (CTE) in the range of (31.8–45.8) × 10−6/K. [ABSTRACT FROM AUTHOR]

Sol compositions for transparent TiO2 and ZnO photocatalytic thin film deposition are of interest for the wet-chemical fabrication of self-cleaning coatings. The choice of stabilizing agent is crucial for the sol film-forming properties, with acetylacetone and monoethanolamine conventionally employed for TiO2 and ZnO deposition sols, respectively. Salicylic acid (SA), capable of chelating both Ti(IV) and Zn(II) precursors, remains underexplored. This study presents novel SA-based sol formulations for the deposition of both TiO2 and ZnO films, based on titanium tetraisopropoxide (TTIP) and zinc acetate dihydrate (ZAD) precursors, in a fixed 1:3 (TTIP:SA) and 1:2 (ZAD:SA) ratio, and isopropanol solvent, varied across the 1:10 to 1:20 precursor-to-solvent ratio range. Fourier-Transform Infrared Spectroscopy analysis and Density Functional Theory computations confirmed the formation of H2Ti[SA]3 and Zn[SA]2·2H2O complexes. Scanning Electron Microscopy, X-ray diffraction, and Ultraviolet-Visible spectroscopy were employed to study the structural and optical properties of the dip-coated films, revealing dense TiO2 (86–205 nm) and ZnO (35–90 nm) layers of thickness proportional to the salicylate concentration and transmittance in the 70–90% range. Liquid-phase Methylene blue (MB) photooxidation experiments revealed that all films exhibit photocatalytic activity, with ZnO films being superior to TiO2, with 2.288 vs. 0.366 nm h−1 cm−2 MB removal rates. [ABSTRACT FROM AUTHOR]

CoFe-based alloys and rare earth (RE) elements are among the most studied materials in applying magnetic devices to improve soft magnetic characteristics. A series of Co40Fe40Sm20 films are deposited on a glass substrate via the sputtering technique, followed by an annealing process to investigate their effect on microstructural and optical properties of Co40Fe40Sm20 films. In this study, the increase in the thickness of Co40Fe40Sm20 films and annealing temperatures resulted in a smoother surface morphology. The 40 nm Co40Fe40Sm20 films annealed 300 °C are expected to have good wear resistance and adhesive properties due to their high values of H/E ratio and surface energy. Optical transparency also increased due to the smoother surface of the Co40Fe40Sm20 films. [ABSTRACT FROM AUTHOR]

Light-colored and transparent polyimide (PI) films with good high-temperature dimensional stability are highly desired for advanced optoelectronic applications. However, in practice, the simultaneous achievement of good optical and thermal properties in one PI film is usually difficult due to the inter-conflicting molecular design of the polymers. In the present work, a series of PI-SiO2 nanocomposite films (ABTFCPI) were developed based on the PI matrix derived from hydrogenated pyromellitic anhydride (HPMDA) and an aromatic diamine containing benzanilide and trifluoromethyl substituents in the structure, 2,2′-bis(trifluoromethyl)-4,4′-bis [4-(4-aminobenzamide)]biphenyl (ABTFMB). The inorganic SiO2 fillers were incorporated into the nanocomposite films in the form of colloidal nanoparticles dispersed in the good solvent of N,N-dimethylacetamide (DMAc) for the PI matrix. The derived ABTFCPI nanocomposite films showed good film-forming ability, flexible and tough nature, good optical transparency, and good thermal properties with loading amounts of SiO2 up to 30 wt% in the system. The ABTFCPI-30 film with a SiO2 content of 30 wt% in the film showed an optical transmittance of 79.6% at the wavelength of 400 nm (T400) with a thickness of 25 μm, yellow index (b*) of 2.15, and 5% weight loss temperatures (T5%) of 491 °C, which are all comparable to those the pristine ABTFCPI-0 matrix without filler (T400 = 81.8%; b* = 1.77; T5% = 492 °C). Meanwhile, the ABTFCPI-30 film exhibited obviously enhanced high-temperature dimensional stability with linear coefficients of thermal expansion (CTE) of 25.4 × 10−6/K in the temperature range of 50 to 250 °C, which is much lower than that of the AMTFCPI-0 film (CTE = 32.7 × 10−6/K). [ABSTRACT FROM AUTHOR]

In this paper, we present a study on a broadband transparent tapered slot antenna. In general, the objective of achieving optical transparency is to enable antennas to seamlessly integrate into windows, offering an aesthetically pleasing and inconspicuous appearance. The aim of our research is to develop antennas that possess the ability to adjust horizontal plane beams across a wide frequency range, from 24 to 28 GHz, for 5G applications. This structure combines three antennas into a single unit, providing an advantage in terms of saving space. Furthermore, this structure offers the possibility of choosing between using a single antenna to obtain a directional beam in the −90°, 0°, or +90° directions (depending on the activated antenna) corresponding to three states, or the combination between two states to obtain another three additional states. The combination of the three states also allows for the acquisition of another state. At this point, the total number of states is 23 − 1. Only three PIN diodes are employed to switch between all states. Additionally, by adjusting the bias values of the PIN diodes, which function as variable resistors, the antenna beamwidth can be adjusted in order to achieve a coverage of 300°, offering more radiation pattern reconfigurability. The proposed method offers several advantages, including simplicity and feasibility in controlling the beamwidth and the beam direction electronically. This structure can be easily integrated into the development of fifth-generation communication systems. [ABSTRACT FROM AUTHOR]

A cycloaliphatic tetracarboxylic dianhydride, octahydro-2,3,6,7-anthracenetetracarboxylic dianhydride (OHADA) was synthesized to obtain novel colorless polyimides (PIs). Herein, approaches for decolorizing an OHADA prototype and simplifying the entire process are described, and a plausible steric structure for OHADA is proposed. The polyaddition of OHADA and 2,2′-bis(trifluoromethyl)benzidine (TFMB) was unsuccessful; specifically, the reaction mixture remained inhomogeneous even after prolonged stirring. However, the modified one-pot process was applicable to the OHADA/TFMB system. The isolated PI powder form, as well as those for the other OHADA-based PIs, was highly soluble in numerous solvents and afforded a homogeneous and stable solution with a high solid content (20–30 wt%). Solution casting produced a colorless and ductile PI film with a very high glass transition temperature (Tg~300 °C). Furthermore, the OHADA/TFMB system exhibited remarkable thermal stability compared with those of the other related TFMB-derived semi-cycloaliphatic PIs. However, contrary to our expectations, this PI film did not exhibit a low linear coefficient of thermal expansion (CTE). This PI film also possessed excellent thermoplasticity, probably reflecting its peculiar steric structure. The use of an amide-containing diamine significantly enhanced the Tg (355 °C) and somewhat reduced the CTE (41.5 ppm K−1) while maintaining high optical transparency and excellent solubility. [ABSTRACT FROM AUTHOR]

Organic phase change materials, e.g., paraffins, are attracting increasing attention in thermal energy storage (TES) and thermal management applications. However, they also manifest interesting optical properties such as thermotropism, as they can switch from optically opaque to transparent reversibly and promptly at the melting temperature. This work aims at exploiting this feature to produce flexible silicone-based blends with thermotropic properties for applications in glazed windows or thermal sensors. Blends are produced by adding paraffin (Tm = 44 °C, up to 10 phr) to a silicone bicomponent mixture, and, for the first time, cetyltrimethylammonium bromide (CTAB) is also added to promote paraffin dispersion and avoid its exudation. CTAB is proven effective in preventing paraffin exudation both in the solid and in the liquid state when added in a fraction above 3 phr with respect to paraffin. Rheological results show that paraffin decreases the complex viscosity, but neither paraffin nor CTAB modifies the curing behavior of silicone, which indicates uniform processability across the investigated compositions. On the other hand, paraffin causes a decrease in the stress and strain at break at 60 °C, and this effect is amplified by CTAB, which acts as a defect and stress concentrator. Conversely, at room temperature, solid paraffin only slightly impairs the mechanical properties, while CTAB increases both the elastic modulus and tensile strength, as also highlighted with ANOVA. Finally, optical transmittance results suggest that the maximum transmittance difference below and above the melting temperature (65–70 percentage points) is reached for paraffin amounts of 3 to 5 phr and a CTAB amount of max. 0.15 phr. [ABSTRACT FROM AUTHOR]

Negative photosensitive polyimides (PSPIs) with the photo-patterned ability via the photocrosslinking reactions induced by the i-line (365 nm) and h-line (426 nm) emitting wavelengths in high-pressure mercury lamps have been paid increasing attention in semiconductor fabrication, optical fiber communications, and other advanced optoelectronic areas. In the current work, in view of the optical and thermo-mechanical disadvantages of the currently used negative PSPIs, such as the intrinsically photosensitive or auto-photosensitive systems derived from 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTDA) and the ortho-alkyl- substituted aromatic diamines, a series of modified negative PSPIs with the enhanced optical transparency in the wavelength of 365~436 nm and apparently reduced coefficients of linear thermal expansion (CTE) were developed. For this purpose, a specific aromatic diamine with both of trifluoromethyl and benzanilide units in the molecular structures, 2,2'-bis(trifluoromethyl)-4,4'-bis[4-(4-amino-3-methyl)benzamide]biphenyl (MABTFMB) was copolymerized with BTDA and the standard 3,3',5,5'-tetramethyl-4,4'-diaminodiphenylmethane (TMMDA) diamine via a two-step chemical imidization procedure. As compared with the pristine PI-1 (BTDA-TMMDA) system, the new-developed fluoro-containing PSPI systems (FPI-2~FPI-7) exhibited the same-level solubility in polar aprotic solvents, including N-methyl-2-pyrrolidone (NMP) and N,N- dimethylacetamide (DMAc). The FPI films cast from the corresponding FPI solutions in NMP showed the optical transmittances of 78.3–81.3% at the wavelength of 436 nm (T436, h-line), which were much higher than that of the PI-1 (T436 = 60.9%). The FPI films showed the CTE values in the range of 40.7 × 10−6/K to 54.0 × 10−6/K in the temperature range of 50 to 250 °C, which were obviously lower than that of PI-1 (CTE = 56.5 × 10−6/K). At last, the photosensitivity of the FPI systems was maintained and the micro-pattern with the line width of 10 μm could be clearly obtained via the standard photolithography process of FPI-7 with the molar ratio of 50% for MABTFMB in the diamine moiety. [ABSTRACT FROM AUTHOR]

In this study, practically useful colorless polyimides (PIs) with low coefficients of thermal expansion (CTEs) and other desirable properties were prepared from hydrogenated pyromellitic dianhydride (1-exo,2-exo,4-exo,5-exo-cyclohexanetetracarboxylic dianhydride, H-PMDA). A modified one-pot polymerization method afforded a high-molecular-weight PI with sufficient film-forming ability from 2,2′-bis(trifluoromethyl)benzidine (TFMB) with a rod-like structure and H-PMDA. However, the PI film cast from its homogeneous solution did not have low CTEs, similar to the analogous system using meta-tolidine. To solve this problem, a series of amide- and amide-imide-containing diamines were designed and synthesized. The modified one-pot polymerization of H-PMDA and the diamines in γ-butyrolactone produced homogeneous, viscous, and stable solutions of high-molecular-weight PIs with high solid contents. The cast films of certain systems examined in this study simultaneously achieved low CTEs, high optical transparency, considerably high glass transition temperatures (Tgs), and sufficient ductility. A possible mechanism for the generation of low CTEs, which is closely related to the spontaneous in-plane orientation behavior during solution casting, was proposed. Certain H-PMDA-based PIs developed in this study are promising colorless heat-resistant plastic substrates for use in image display devices and other optical applications. [ABSTRACT FROM AUTHOR]

We use indium tin oxide (ITO), one of the representative resistive materials, for the implementation of a metamaterial electromagnetic (EM) absorber with a high absorbance in a wide frequency range. Highly symmetrical split ring resonators made of ITO film are deposited on the polyethylene terephthalate with transparent and flexible features, and such a configuration causes the proposed absorber to be insensitive to polarization and incidence angles. The proposed absorber, with a profile of only 0.171 λ , exhibits a wideband absorbance of 7.2 GHz to 27 GHz, with a 90% absorption criterion. A prototype is built, and all the computed expectations from the full-wave EM simulations in this work are verified experimentally. [ABSTRACT FROM AUTHOR]

Optically Transparent Microwave Metamaterial Absorber (OTMMA) is of significant use in both civil and military field. In this paper, equivalent circuit model is adopted as springboard to navigate the design of OTMMA. The physical model and absorption mechanisms of ideal lightweight ultrathin OTMMA are comprehensively researched. Both the theoretical value of equivalent resistance and the quantitative relation between the equivalent inductance and equivalent capacitance are derived for design. Frequency-dependent characteristics of theoretical equivalent resistance are also investigated. Based on these theoretical works, an effective and controllable design approach is proposed. To validate the approach, a wideband OTMMA is designed, fabricated, analyzed and tested. The results reveal that high absorption more than 90% can be achieved in the whole 6~18 GHz band. The fabricated OTMMA also has an optical transparency up to 78% at 600 nm and is much thinner and lighter than its counterparts. [ABSTRACT FROM AUTHOR]

This paper reviews the development of new high-temperature polymeric materials applicable to plastic substrates in image display devices with a focus on our previous results. Novel solution-processable colorless polyimides (PIs) with ultra-low linear coefficients of thermal expansion (CTE) are proposed in this paper. First, the principles of the coloration of PI films are briefly discussed, including the influence of the processing conditions on the film coloration, as well as the chemical and physical factors dominating the low CTE characteristics of the resultant PI films to clarify the challenges in simultaneously achieving excellent optical transparency, a very high Tg, a very low CTE, and excellent film toughness. A possible approach of achieving these target properties is to use semi-cycloaliphatic PI systems consisting of linear chain structures. However, semi-cycloaliphatic PIs obtained using cycloaliphatic diamines suffer various problems during precursor polymerization, cyclodehydration (imidization), and film preparation. In particular, when using trans-1,4-cyclohexanediamine (t-CHDA) as the cycloaliphatic diamine, a serious problem emerges: salt formation in the initial stages of the precursor polymerization, which terminates the polymerization in some cases or significantly extends the reaction period. The system derived from 3,3',4,4'-biphenyltetracarboxylic dianhydride (s-BPDA) and t-CHDA can be polymerized by a controlled heating method and leads to a PI film with relatively good properties, i.e., excellent light transmittance at 400 nm (T400 = ~80%), a high Tg (>300 °C), and a very low CTE (10 ppm⋅K-1). However, this PI film is somewhat brittle (the maximum elongation at break, εb max is about 10%). On the other hand, the combination of cycloaliphatic tetracarboxylic dianhydrides and aromatic diamines does not result in salt formation. The steric structures of cycloaliphatic tetracarboxylic dianhydrides significantly influence the polymerizability with aromatic diamines and the CTE values of the resultant PI films. For three isomers of hydrogenated pyromellitic dianhydride, the steric structure effect on the polymerizability and the properties of the PI films is discussed. 1,2,3,4-Cyclobutanetetracarboxylic dianhydride (CBDA) is a very unusual cycloaliphatic tetracarboxylic dianhydride that is suitable for reducing the CTE. For example, the PI system derived from CBDA and 2,2'-bis(trifluoromethyl)benzidine (TFMB) yields a colorless PI film with a relatively low CTE (21 ppm⋅K-1). However, this PI is insoluble in common organic solvents, which means that it is neither solution-processable nor compatible with the chemical imidization process; furthermore, the film is somewhat brittle (εb < 10%). In addition, the effect of the film preparation route on the film properties is shown to be significant. Films prepared via chemical imidization always have higher optical transparency and lower CTE values than those prepared via the conventional two-step process (i.e., precursor casting and successive thermal imidization). These results suggest that compatibility with the chemical imidization process is the key for achieving our goal. To dramatically improve the solubility in the CBDA-based PI systems, a novel amide-containing aromatic diamine (AB-TFMB), which possesses the structural features of TFMB and 4,4'-diaminobenzanilide (DABA), is proposed. The CBDA(70);6FDA(30)/AB-TFMB copolymer has an ultra-low CTE (7.3 ppm⋅K-1), excellent optical transparency (T400 = 80.6%, yellowness index (YI) = 2.5, and haze = 1.5%), a very high Tg (329 °C), sufficient ductility (εb max > 30%), and good solution-processability. Therefore, this copolymer is a promising candidate for use as a novel coating-type plastic substrate material. This paper also discusses how the target properties can be achieved without the help of cycloaliphatic monomers. Thus, elaborate molecular design allows the preparation of highly transparent and low-CTE aromatic poly(amide imide) and poly(ester imide) systems. [ABSTRACT FROM AUTHOR]

Acquiring an optically transparent feature on the wideband frequency selective surface (FSS), particularly for smart city applications (building window and transportation services) and vehicle windows, is a challenging task. Hence, this study assessed the performance of optically transparent mosaic frequency selective surfaces (MFSS) with a conductive metallic element unit cell that integrated Koch fractal and double hexagonal loop fabricated on a polycarbonate substrate. The opaque and transparent features of the MFSS were studied. While the study on opaque MFSS revealed the advantage of having wideband responses, the study on transparent MFSS was performed to determine the optical transparency application with wideband feature. To comprehend the MFSS design, the evolutionary influence of the unit cell on the performance of MFSS was investigated and discussed thoroughly in this paper. Both the opaque and transparent MFSS yielded wideband bandstop and bandpass responses with low cross-polarisation (-37 dB), whereas the angular stability was limited to only 25°. The transparent MFSS displayed high-level transparency exceeding 70%. Both the simulated and measured performance comparison exhibited good correlation for both opaque and transparent MFSS. The proposed transparent MFSS with wideband frequency response and low cross-polarisation features signified a promising filtering potential in multiple applications.

Conductive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is widely used for practical applications such as energy conversion and storage devices owing to its good flexibility, processability, high electrical conductivity, and superior optical transparency, among others. However, its hygroscopic character, short durability, and poor thermoelectric performance compared to inorganic counterparts has greatly limited its high-tech applications. In this work, PEDOT:PSS/SnO2 nanocomposites have been prepared via a simple, low cost, environmentally friendly method without the use of organic solvents or compatibilizing agents. Their morphology, thermal, thermoelectrical, optical, and mechanical properties have been characterized. Electron microscopy analysis revealed a uniform dispersion of the SnO2 nanoparticles, and the Raman spectra revealed the existence of very strong SnO2-PEDOT:PSS interactions. The stiffness and strength of the matrix gradually increased with increasing SnO2 content, up to 120% and 65%, respectively. Moreover, the nanocomposites showed superior thermal stability (as far as 70 °C), improved electrical conductivity (up to 140%), and higher Seebeck coefficient (about 80% increase) than neat PEDOT:PSS. On the other hand, hardly any change in optical transparency was observed. These sustainable nanocomposites show considerably improved performance compared to commercial PEDOT:PSS, and can be highly useful for applications in energy storage, flexible electronics, thermoelectric devices, and related fields. [ABSTRACT FROM AUTHOR]

Poly (amic acid) s (PAAs) were synthesized using 4,4′-(hexafluoroisopropyl-idene) diphthalic anhydride (6FDA) and two types of diamines—bis(3-aminophenyl) sulfone (BAS) and bis(3-amino-4-hydroxyphenyl) sulfone (BAS-OH). Two series of transparent polyimide (PI) hybrid films were synthesized by solution intercalation polymerization and thermal imidization using various concentrations (from 0 to 1 wt%) of organically modified clay Cloisite 30B in PAA solution. The thermo-mechanical properties, morphology, and optical transparency of the hybrid films were observed. The transmission electronic microscopy (TEM) results showed that some of the clays were agglomerated, but most of them showed dispersed nanoscale clay. The effects of -OH groups on the properties of the two PI hybrids synthesized using BAS and BAS-OH monomers were compared. The BAS PI hybrids were superior to the BAS-OH PI hybrids in terms of thermal stability and optical transparency, but the BAS-OH PI hybrids exhibited higher glass transition temperatures (Tg) and mechanical properties. Analysis of the thermal properties and tensile strength showed that the highest critical concentration of organoclay was 0.50 wt%. [ABSTRACT FROM AUTHOR]

A series of colorless copolyimide films with high thermal stability and good solubility are synthesized from (trifluoromethyl)biphenyl-4,4'-diamine (TFMB) with different 1,2,4,5-cyclohexanetetracarboxylic dianhydride (HPMDA) to 2,2-bis(3,4-dicarboxyphenyl)-hexafluoropropane (6FDA) dianhydride mole ratios through one-pot solution polycondensation. These copolyimide films exhibit excellent optical transparency (T400 > 90% and λ0 ~305–333 nm) with a thickness of 15 μm and good solubility in most organic solvents. The excellent optical properties are mainly attributed to the low inter- and intra-molecular charge transfer interactions due to the alicyclic structure and the strong electronegative CF3 groups. The glass transition temperature increases from 332 to 352 °C with increasing HPMDA content in the copolymers, while the thermal decomposition temperature is improved with increasing 6FDA content. These results indicate that the copolyimide films can be successfully utilized in the development of novel heat-resistant plastic substrates for the optoelectronic engineering applications. [ABSTRACT FROM AUTHOR]

Optically transparent polyimides with excellent thermal stability and shape memory effect have potential applications in optoelectronic devices and aerospace industries. A series of optically transparent shape memory polyimide hybrid films are synthesized from 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) and 2,2′-bis-(trifluoromethyl)biphenyl-4,4′-diamine (TFMB) with various polyhedral oligomeric silsesquioxane (POSS) contents and then subjected to thermal imidization. The hybrid films show good optical transparency (>80% at 400 nm and >95% at 500 nm) with cutoff wavelengths ranging from 318 to 336 nm. Following the incorporation of the inorganic POSS structure, the hybrid films exhibit excellent thermal stability with glass transition temperature (Tg) ranging from 351 to 372 °C. The hybrid films possess the highest Tg compared with the previously-reported shape memory polymers. These findings show that POSS is successfully utilized to develop transparent polyimides with excellent thermal stability and shape memory effect. [ABSTRACT FROM AUTHOR]

This paper reviews the development of new high-temperature polymeric materials applicable to plastic substrates in image display devices with a focus on our previous results. Novel solution-processable colorless polyimides (PIs) with ultra-low linear coefficients of thermal expansion (CTE) are proposed in this paper. First, the principles of the coloration of PI films are briefly discussed, including the influence of the processing conditions on the film coloration, as well as the chemical and physical factors dominating the low CTE characteristics of the resultant PI films to clarify the challenges in simultaneously achieving excellent optical transparency, a very high T g , a very low CTE, and excellent film toughness. A possible approach of achieving these target properties is to use semi-cycloaliphatic PI systems consisting of linear chain structures. However, semi-cycloaliphatic PIs obtained using cycloaliphatic diamines suffer various problems during precursor polymerization, cyclodehydration (imidization), and film preparation. In particular, when using trans -1,4-cyclohexanediamine ( t -CHDA) as the cycloaliphatic diamine, a serious problem emerges: salt formation in the initial stages of the precursor polymerization, which terminates the polymerization in some cases or significantly extends the reaction period. The system derived from 3,3',4,4'-biphenyltetracarboxylic dianhydride (s-BPDA) and t -CHDA can be polymerized by a controlled heating method and leads to a PI film with relatively good properties, i.e., excellent light transmittance at 400 nm ( T 400 = ~80%), a high T g (>300 °C), and a very low CTE (10 ppm·K -1 < 10%). In addition, the effect of the film preparation route on the film properties is shown to be significant. Films prepared via chemical imidization always have higher optical transparency and lower CTE values than those prepared via the conventional two-step process (i.e., precursor casting and successive thermal imidization). These results suggest that compatibility with the chemical imidization process is the key for achieving our goal. To dramatically improve the solubility in the CBDA-based PI systems, a novel amide-containing aromatic diamine (AB-TFMB), which possesses the structural features of TFMB and 4,4'-diaminobenzanilide (DABA), is proposed. The CBDA(70);6FDA(30)/AB-TFMB copolymer has an ultra-low CTE (7.3 ppm·K ε ), excellent optical transparency ( b max is about 10%). On the other hand, the combination of cycloaliphatic tetracarboxylic dianhydrides and aromatic diamines does not result in salt formation. The steric structures of cycloaliphatic tetracarboxylic dianhydrides significantly influence the polymerizability with aromatic diamines and the CTE values of the resultant PI films. For three isomers of hydrogenated pyromellitic dianhydride, the steric structure effect on the polymerizability and the properties of the PI films is discussed. 1,2,3,4-Cyclobutanetetracarboxylic dianhydride (CBDA) is a very unusual cycloaliphatic tetracarboxylic dianhydride that is suitable for reducing the CTE. For example, the PI system derived from CBDA and 2,2'-bis(trifluoromethyl)benzidine (TFMB) yields a colorless PI film with a relatively low CTE (21 ppm·K -1 ). However, this PI is insoluble in common organic solvents, which means that it is neither solution-processable nor compatible with the chemical imidization process; furthermore, the film is somewhat brittle ( ε b < 10%). In addition, the effect of the film preparation route on the film properties is shown to be significant. Films prepared via chemical imidization always have higher optical transparency and lower CTE values than those prepared via the conventional two-step process (i.e., precursor casting and successive thermal imidization). These results suggest that compatibility with the chemical imidization process is the key for achieving our goal. To dramatically improve the solubility in the CBDA-based PI systems, a novel amide-containing aromatic diamine (AB-TFMB), which possesses the structural features of TFMB and 4,4'-diaminobenzanilide (DABA), is proposed. The CBDA(70);6FDA(30)/AB-TFMB copolymer has an ultra-low CTE (7.3 ppm·K -1 ), excellent optical transparency ( T 400 = 80.6%, yellowness index (YI) = 2.5, and haze = 1.5%), a very high T g (329 °C), sufficient ductility ( ε b max > 30%), and good solution-processability. Therefore, this copolymer is a promising candidate for use as a novel coating-type plastic substrate material. This paper also discusses how the target properties can be achieved without the help of cycloaliphatic monomers. Thus, elaborate molecular design allows the preparation of highly transparent and low-CTE aromatic poly(amide imide) and poly(ester imide) systems., Competing Interests: All authors declare no conflict of interest.