Highly conjugated porphyrin derivatives, H2TP and ZnTP, are synthesized. J-aggregations of the H-aggregated dimeric porphyrin pairs are clearly observed by their single crystal structures that facilitate slip-stacked charge transport phenomenon. In particular, their SC-FETs show the highest field-effect mobilities of 0.85–2.90 cm2 V−1s−1. Furthermore, the ZnTP-based OPT displays a dramatic photoinduced current enhancement with a high photoresponsivity of 22 000 A W−1 under a very low light intensity (5.6 m W cm−2). Recently, the charge-transport phenomena of organic conjugated materials have been intensively investigated because of the potential applications of these materials in electronics and optoelectronics. Among these applications, organic field-effect transistors (OFETs) fabricated from either thin films or well-defined single crystals (SCs) as charge-transporting layers are the most promising electronic devices.1-5 In particular, the unique anisotropic arrangement of organic semiconducting molecules owing to their strong intermolecular interactions is expected to have a significant influence on the OFET performance, because the larger overlap of π-orbitals between neighboring molecules may increase the bandwidth and facilitate charge transport.6 In this regard, there has been considerable interest in the design and synthesis of planar π−conjugated molecules such as pentacene, oligothiophene, arylacetylene, indolo-[3,2-b]-carbazole, perylene, and tetrathiafulvalene for use in the fabrication of organic thin-film transistors (OTFTs).7 The molecular packing behaviors of these organic molecules are dominated by π−π interactions, leading to the formation of highly ordered polycrystalline films with good charge-transport properties. Porphyrins are one of the most important π-conjugated planar molecules in the field of electronics and optoelectronics, and they have often been employed in OFETs,8 organic phototransistors (OPTs),9 and organic photovoltaics (OPVs).10 Because of their unique structure, porphyrins may provide multiple interactions such as hydrogen bonding, π–π stacking, electrostatic interactions, and metal–ligand coordination. However, the performances of recently developed porphyrin-based OFET devices show relatively low carrier mobilities in the range of 10−6 to 10−1 cm2 V−1 s−1.8 A deeper understanding of such systems has hardly been achieved because of the lack of information on the molecular packing and intermolecular arrangement (which are closely related to the OFET performance),11 since most porphyrin-based OFET devices are based on thin films or polycrystalline objects prepared by spin-coating or vacuum-deposition processes. Although porphyrin-based single-crystalline OFETs have been reported recently along with molecular arrangement studies, relatively poor device performances have been observed because of the restricted use of π-orbital conjugation.8 For a high degree of crystallinity with an excellent determinacy as well as a high corresponding device performance to be obtained, the extension of π-conjugation and the location of conjugative substituents on the porphyrin core may play major roles in terms of the molecular electronic energies and molecular arrangements during the formation of well-defined polycrystalline films or single crystals. Therefore, herein we report the new π-extended porphyrin derivatives H2TP and ZnTP, consisting of a porphyrin core and four 2-ethynyl-5-hexylthiophene peripheral arms. We expected that such molecules would enable the best extension of π-conjugation and provide strong intermolecular π–π interactions. H2TP was readily obtained from a condensation reaction between 3-(5-hexylthiophen-2-yl)propiolaldehyde and pyrrole in dichloromethane (DCM) with 14% yield. ZnTP was further obtained by metalation of H2TP with Zn(OAc)2 in quantitative yield (see the Supporting Information for detailed synthetic procedures (Scheme S1)). These materials were found to have good film-forming properties and high solubilities in various solvents such as chloroform, DCM, tetrahydrofuran (THF), and chlorobenzene at room temperature. In particular, density functional theory (DFT) calculations revealed that the planarity of the two-dimensionally conjugated unit was sustained, with a small degree of disorder around the hexyl substituents. Using simple slow diffusion of a solution of porphyrin in toluene over n-hexane, we were able to obtain microscopic crystalline objects. Optical microscopy analysis revealed these crystalline objects to be collections of fairly uniform needles with very high aspect ratios for both H2TP and ZnTP; the widths ranged from several micrometers to tens of micrometers (Figure 1a,b). Optical microscopy images of needle crystals obtained from H2TP (a) and ZnTP (b). Crystal structures (c and d), crystal packing diagrams (e and f), and co-facial packings (g and h) in the adjacent molecules (showing clear J-aggregation of H-aggregated molecular dimeric porphyrin pairs through π–π interaction) of H2TP and ZnTP, respectively (hexyl groups in packing diagrams are omitted for clarity). SAED patterns and the corresponding TEM images of H2TP (i and j) and ZnTP (k and l). The single-crystal X-ray crystallographic structures of H2TP and ZnTP are shown in Figure 1c and 1d, respectively. As expected, the porphyrin cores in both H2TP and ZnTP are nearly planar. Three thiophene rings are slightly tilted with respect to the N1/N2/N3/N4 porphyrin core plane (6.3(2)–10.7(2)° for H2TP and 7.0(2)–12.2(2)° for ZnTP), and the fourth tethered thiophene rings are titled significantly from the porphyrin plane (23.3(2)° for H2TP and 22.8(2)° for ZnTP). Great similarities are found in the crystal structures (Table S2, Supporting Information) and crystal packing diagrams of these systems. In the packing diagram representations, two molecules act remarkably as a dimeric pair of porphyrins with a closest atom–atom distance of 3.29(5) Å for H2TP (Figure 1e) and an even shorter one (3.06(3) Å) for ZnTP (Figure 1f). These porphyrin pairs are stacked in a dramatic staircase fashion through π–π interactions, with closest atom–atom distances of 3.37(3) Å for H2TP and 3.34(3) Å for ZnTP. It should be pointed out that the H-aggregated dimeric pairs were aligned in a J-aggregation manner, which is capable of facilitating intermolecular carrier hopping and has slip-stacked carrier transport properties (Figure 1g, h). Furthermore, the distance between the porphyrins in these dimeric pairs is the shortest ever reported, and is comparable to that in a graphite layer (d = 3.335 Å). Transmission electron microscopy (TEM) images and the corresponding selected-area electron diffraction (SAED) patterns of the H2TP and ZnTP crystals were indexed based on triclinic cells, and the results agreed with the simulated powder patterns for the single crystals (Figure 1i, k). The SAED patterns were consistent throughout the whole crystal, indicating the single-crystalline nature of the needles. The UV-vis absorption spectra of the solution, film, and crystal samples of H2TP and ZnTP are shown in Figure 2. The solution samples were prepared in chloroform with a concentration of 1 × 10−6M and the thin-film samples were fabricated by spin-coating the chloroform solutions of these molecules. The crystal samples were fabricated by spreading the crystals obtained from the slow diffusion of toluene solutions over n-hexane. A drastic spectral change was observed in the film and crystal states of these samples, which is attributed to the high degree of intermolecular interaction between the porphyrins. In particular, the absorption spectrum of the ZnTP crystal is significantly broadened and red-shifted, which is unequivocal evidence of the mixed formation of H-aggregated dimers and the J-aggregated set of molecules with the closest limited distances, supporting the above single-crystal results. The optical properties and energy levels are shown in Table S1, Supporting Information. UV-Vis absorption spectra of solution (i), film (ii), and needle crystals (iii) of H2TP (a) and ZnTP (b). To examine their electrical characteristics, we investigated the charge-transport properties of H2TP and ZnTP. OFETs (bottom-gate, top-contact) were fabricated on n-octyltrichlorosilane (OTS)-SiO2/Si substrates, with N-doped polycrystalline silicon as the gate electrode, an OTS-treated SiO2 surface layer as the dielectric gate insulator, and gold electrodes deposited using a shadow mask. The film devices were prepared by spin-coating chloroform solutions of the porphyrins, and the needle-crystal devices were prepared by the slow diffusion of toluene solutions over n-hexane. The devices were dried under vacuum at room temperature for 24 h before testing at room temperature in air. The insets in Figure 3b and d show the SEM images of each of the crystal FETs of H2TP and ZnTP, where the channel lengths (widths) were 43.0 (1.5) and 89.0 (0.9) μm, respectively. The output characteristics showed very good saturation behaviors and clear saturation currents (see Figures S3–6, Supporting Information). The mobility values were obtained by measuring more than 20 different devices. According to the transfer characteristics (Figure 3), the film devices made of H2TP and ZnTP provided unusually high field-effect mobilities of 0.014 and 1.20 cm2 V−1 s−1, respectively, together with high on/off current ratios (Ion/off = 5.0 × 104 and 1.5 × 108, respectively) and low threshold voltages (Vth ≈ –5.0 and –10.0 V, respectively). The crystalline-needle FETs made of H2TP and ZnTP provided field-effect mobilities of 0.85 and 2.90 cm2 V−1 s−1, respectively, together with high on/off current ratios (Ion/off = 1.0 × 104 and 6.0 × 103, respectively) and threshold voltages (Vth ≈ 5.0 and 2.0 V, respectively). To the best of our knowledge, these values are the highest yet reported for porphyrin-based OFET devices. The mobilities of these devices were well maintained (over 80–90% mobility compared with freshly prepared devices) even after three months' storage in air, showing that the devices have very good stabilities. Remarkably, the mobility of the H2TP single-crystal device was 60 times higher than that of the film-state one, while the mobility of the ZnTP single-crystal device was 2.5 times higher than that of the film-state one. The dramatic increase in the mobility of the H2TP single-crystal devices is presumably due to the denser molecular confinement, while the slight increase in mobility for the ZnTP single-crystal devices indicates that a highly and densely packed arrangement of polycrystallites has already been achieved in the solid film state (Figure 3). Electrical characterization of OFET devices. Transfer curves of thin film devices (a and c) and single crystal devices (b and d) made of H2TP and ZnTP, respectively. (Inset: AFM images of TFT devices (a and c); SEM images of FET devices (b and d). Furthermore, FETs made of H2TP and ZnTP displayed photoinduced enhancement of the source–drain current (IDS). OPT devices of H2TP (Figure S7a, Supporting Information) and ZnTP (Figure 4a) showed a dramatic increase in IDS when illuminated with incident light. It should be emphasized that the drastic increase in IDS was induced by the illumination of light in a broad range from 365 (UV) to 850 nm (near-IR) with a very low intensity (5.6 μW cm−2). The large increase in drain current is ascribed to the trapped photogenerated electrons in the semiconducting organic layer, which is close to the interface with the dielectric gate insulator. These trapped electrons have led to the injection and accumulation of additional holes in the active layer, thereby increasing the drain current.4 a) Transfer characteristics of ZnTP based-OPT in the dark and under monochromatic light irradiation (I = 5.6 μW cm−2) with different wavelengths; b) Variation of IDS with gate voltage (VG); 1) light-on, 2) light-off, 3) VG = –10 V, 4) VG = –20 V, 5) VG = –30 V, 6) VG = –40 V, 7) VG = –50 V, 8) VG = –60 V, 9) VG = –70 V, 10) VG = –80 V, 11) VG = –90 V, 12) VG = –100 V; c) IDS characteristics of photo-controlled optical memory operation, single-stage on–off memory under monochromatic light irradiation at 5.6 μW cm−2; 1) light-on (writing), 2) light-off (reading), and 3) VG = –100 V (erasing). From the modulation of the transfer curve, we calculated the photoresponsivity (R) of the OPT device, defined as ΔIDS/Pinc, where ΔIDS is IDS,light– IDS,dark and Pinc is the incident light intensity. The photoswitching ratio (P) was obtained from (IDS,light–IDS,dark)/IDS,dark. The P and R values were determined near the crossing point of the two curves with VDS = –100 V, I = 5.6 μW cm−2, and λ = 474 nm, and are plotted in Figure S8, Supporting Information. The OPT devices showed maximum P values of 4.4 × 104 (VG = –10.0 V) for H2TP and 4.6 × 106 (VG = –6.0 V) for ZnTP, and exhibited a short response time on the application of both gate bias and incident light. The average R values of OPT devices were found to be 6.6 × 102 AW−1 (VG = –2.0 V) for H2TP and 2.2 × 104 AW−1 (VG = 2.0 V) for ZnTP. The measured R values are significantly higher than those of inorganic single-crystal silicon FETs (300 AW−1, I = 30 μW cm−2).3 It should be pointed out that the monochromatic light intensity employed in this study was very low compared to those reported in the literature (≈ 30 to 1 mW cm−2).2-4 To the best of our knowledge, the R and P values obtained from this study are among the best yet found for OPT devices under such a low light intensity. Once the photocurrent was generated, the IDS levels could be steered by manipulating the gate voltage VG during the light-off condition (Figure S7b for H2TP and Figure 4b for ZnTP). When applying a negative VG, an abrupt increase in IDS was observed, indicating that photoinduced holes were accumulated at the interface between the insulator and the organic semiconductor. After the applied negative VG was turned off, the photoinduced currents decreased rapidly to a certain level. As the absolute value of VG increased, the resulting IDS levels decreased because of the respective diminishing of the remnant photoinduced current. This observation motivated the application of these molecules in multi-stage photocontrolled memory. Remarkably, OPTs made from these porphyrin molecules showed reproducible memory operations (Figure S7c for H2TP and Figure 4c for ZnTP). The striking single-stage memory operation with gate bias is mainly due to the slow relaxation and trapping mechanism of the photoinduced charges. First, irradiation with low-intensity light (I = 5.6 μW cm−2, λ = 474 nm) was used for the writing process (step (1)). The first on-state currents were measured (IDS = 2.4 × 10−9 A for H2TP and 1.06 × 10−8 A for ZnTP) in terms of the remnant photoinduced currents after the excitation light was turned off (step (2)). Secondly, erasing processes (step (3), VG = –100 V) in the memory-effect curves were performed through a charge-trapping mechanism at the interface between the active and gate dielectric layers. Relatively high on/off current ratios were obtained (2.2 × 102 for H2TP and 1.8 × 102 for ZnTP at VG = 0 V) under initial light illumination. In conclusion, we have demonstrated that the highly soluble new porphyrin derivatives H2TP and ZnTP can be used to fabricate high-performance OFET and OPT devices from both thin films and single-crystalline needles, which can be obtained by scalable, low-cost solution processes. In particular, OFETs made from ZnTP displayed charge mobilities of up to 1.20 cm2 V−1 s−1 in the pristine films and 2.90 cm2 V−1 s−1 in single-crystal micro-objects with high on/off current ratios having the best values yet reported in the literature for metalloporphyrin-based materials. This high performance of the FETs is mainly due to the very intriguing J-aggregation of H-aggregated dimeric porphyrin pairs in the crystalline structures, resulting in stronger intermolecular π–π interactions incorporating unusually short layer distances, which enhance the charge-transport efficiency. Furthermore, the OPT devices of these molecules showed high photoresponsivities in a broad wavelength range from 365 (UV) to 850 nm (near-IR) under very low light intensity (5.6 μW cm−2), making them potentially applicable for sensitive optoelectronic integrated devices. The results obtained in this work demonstrate unambiguously the great potential of metalloporphyrins as candidates for future organic semiconducting materials. Crystal Data for H2TP: C68H70N4S4, MW = 1071.52, Triclinic (P-1), a = 12.583(3) Å, b = 15.696(3) Å, c = 16.681(3) Å, α = 71.26(3)°, β = 85.87(3)°, γ = 68.04(3)°, V = 2889.2(10) Å3, Z = 2, (Mo Kα) = 0.210 mm−1, 16 119 reflections measured, 11 067 unique (Rint = 0.0551) which were used in all calculations, final R = 0.0699 (Rw = 0.1523) with reflections having intensities greater than 2σ, GOF (F2) = 0.974. CCDC reference number: 868812. Crystal Data for ZnTP: C68H68N4S4Zn, MW = 1134.87, Triclinic (P-1), a = 12.528(3) Å, b = 15.494(3) Å, c = 16.701(3) Å, α = 72.16(3)°, β = 86.59(3)°, γ = 68.50(3)°, V = 2866.1(10) Å3, Z = 2, (Mo Kα) = 0.620 mm−1, 16 138 reflections measured, 10 998 unique (Rint = 0.0564) which were used in all calculations, final R = 0.0666 (Rw = 0.1363) with reflections having intensities greater than 2σ, GOF (F2) = 0.994. CCDC reference number: 868813. Device Characterization: To characterize the FET performance, a bottom-gate top-contact device geometry was employed. H2TP and ZnTP were dissolved in toluene and slow diffusion over n-hexane was employed to grow high quality crystalline needles on the surface of an OTS-treated SiO2 insulator. The source and drain electrodes were then thermally evaporated (120 nm in thickness). All field effect mobilities were extracted in the saturation regime. The device performance was evaluated in air using a 4200-SCS semiconductor characterization system in ambient conditions. For the light source, a xenon lamp (Thermo Oriel) equipped with an optical fiber and high-speed monochromator (Oriel Cornerstone130 1/8 m Monochromator) were employed. The light illumination power was measured by using a Newport 2385-C Si photodetector with a calibration module. Supporting Information is available from the Wiley Online Library or from the author. CCDC 868812 for H2TP and 868813 for ZnTP contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. Support from the National Research Foundation of Korea (NRF20120002285 and 2012R1A2A1A01008797) and by Priority Research Centers Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF20120005860). Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Abstract The polyurethane composites were prepared by a one‐pot free‐rising method with Melamine cyanurate (MC) and Cloisite 20A additives. Flame‐retardant and mechanical properties of the foams were investigated. The vertical burning test showed that PUF composite loading 15 wt% MC was reached V0 classification of V‐rating. Limiting oxygen index (LOI) test revealed that the PU foam changed from an especially flammable material (LOI = 18.4 %) to a flame‐resistant material (LOI = 24.1 %) upon adding 25 wt% MC. However, the presence of MC reduced the compressive strength of the foam. In this report, we demonstrated the incorporation of organoclay and MC into PUF could improve the flame retardancy and the compressive strength of polyurethane foam.
Abstract Controlled polymer techniques have significantly advanced thanks to using the energy of light to control radical polymerizations. Although many photocatalysts (e.g. metal catalysts, organocatalysts, semiconductor materials, etc.) have been reported, most of these catalysts are still expensive synthetic, trace oxygen-sensitive, and often use UV source light to create the activator to the polymerization. Metal-organic frameworks (MOFs), consisting of metal clusters coordinated to organic ligands, are rising stars as heterogeneous photocatalysis for living radical polymerization techniques because they have many advantages such as facile operation, low-toxic, air stability, and sustainability. Herein, we reported a robust and versatile Fe(III)-MOF, MIL-100(Fe), as a heterogeneous photocatalyst for controlled atom transfer radical polymerization (ATRP) under visible light and natural sunlight without any additives. Moreover, controlled polymerization was also achieved in the presence of oxygen. Many polymer compositions including homopolymers, random copolymers, and diblock copolymers were successfully prepared with well-defined molecular weights and narrow dispersity index values (Đ < 1.5). Most importantly, the heterogeneous Fe(III)-MOF catalyst was allowed easily separated and can be reused again for ATRP reaction for ten cycles that remains the high photocatalytic efficiency. This method provides a new avenue for exploring MIL-100(Fe) as a low-cost, high-performance, and sustainable catalyst for photo-ATRP.
Abstract The flame‐retardant low‐density polyethylene (LDPE) composites loading aluminum hydroxide (ATH), red phosphorus (RP), and expandable graphite (EG) were successfully prepared. The flame retardancy, the thermo‐oxidative stability, and the mechanical property of the composites were investigated. The synergistic effect of ATH, RP, and EG on the flame‐retardant property and thermal behavior of LDPE were observed. The limiting oxygen index value of LDPE significantly increased from 17.1% to 25.4% upon the incorporation of 15 wt.% of the mixture of three fillers with ATH:RP:EG mass ratio of 1:1:1; and this composite achieved the V‐0 classification of the UL94 vertical burning test. The thermogravimetric analysis of this composite under air atmosphere revealed that its residue weight remained 27.89% at 900°C. Furthermore, the results of tension tests indicated that the surface modification of ATH by magnesium stearate and RP by poly(methylhydrosiloxane) noticeably improved the tensile strength and the elongation of the composite.
We have investigated the enhancement absorption light and luminescence properties of the blend conducting polymers using poly(N-vinylcarbazole) and poly(N-hexylthiophene). The optimized material showed a broad absorption in the region of ultra violet to near infra-red and the better of luminescence ability than the pristine conducting polymers. The remarkable improvements in photoluminescences of the blends provide useful information to the application of this material in fabrication of optical – electronic devices.
High-performance flexible multilayer transparent conducting electrodes (TCE) based on silver nanowires (AgNWs), graphene oxide (GO), and poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) materials on the flexible polyethylene terephthalate (PET) substrate were successfully fabricated by spin-coating technique. The multilayer electrodes were fabricated using different combinations of AgNWs, GO, and PEDOT:PSS materials. The morphological, physical properties, surface roughness, and durability of the fabricated electrodes were investigated. The results indicated that the five-layer structured electrode of PEDOT:PSS/GO/AgNW/GO/PEDOT:PSS possesses the best performance with a sheet resistance of 23 Ω/sq, transmittance of 85 %, and the figure of merit (FoM) value of 8.6, which is equivalent to the commercial ITO electrode. Besides, the five-layer structured electrode possessed a surface roughness of only 8 nm. The PEDOT:PSS/GO/AgNW/GO/PEDOT:PSS electrode also exhibited high durability after being exposed to the environment for 30 days. Owing to the combination of AgNWs, GO, and PEDOT: PSS materials, the five-layer electrode of PEDOT:PSS/GO/AgNW/GO/PEDOT:PSS improved the inherent disadvantages of AgNWs electrodes. In addition, the electrode possessed good conductivity, high stability, low cost, and simplicity. The electrode can be used as a promising electrode in optoelectronic devices.
Astaxanthin and kaempferol, renowned natural compounds, possess potent antioxidant properties and exhibit remarkable biological activities. However, their poor water solubility, low stability, and limited bioavailability are the primary bottlenecks that restrict their utilization in pharmaceuticals and functional foods. To overcome these drawbacks, this study aims to fabricate astaxanthin/kaempferol co-encapsulated nanoparticles and investigate their synergistic effects on reducing the risk of stress oxidation, chronic inflammation, and lipid accumulation in RAW264.7 and HepG2 cells. The synthesized astaxanthin/kaempferol nanoparticles exhibited well-defined spherical morphology with an average particle diameter ranging from 74 to 120 nm. These nanoparticles demonstrated excellent stability with the remaining astaxanthin content ranging from 82.5% to 92.1% after 6 months of storage at 4 °C. Nanoastaxanthin/kaempferol displayed high dispersibility and stability in aqueous solutions, resulting in a significant enhancement of their bioactivity. In vitro assessments on cell lines revealed that nanoastaxanthin/kaempferol enhanced the inhibition of H2O2-induced oxidative stress in HepG2 and LPS-induced NO production in RAW264.7 compared to nanoastaxanthin. Additionally, these nanoparticles reduced the expression of genes involved in inflammation (iNOS, IL-6 and TNF-α). Moreover, hepatocytes treated with nanoastaxanthin/kaempferol showed a reduction in lipid content compared to those treated with nanoastaxanthin, through enhanced regulation of lipid metabolism-related genes. Overall, these findings suggest that the successful fabrication of co-encapsulated nanoparticles containing astaxanthin and kaempferol holds promising therapeutic potential in the treatment of non-alcoholic fatty liver disease.
The charge-transport phenomena of organic conjugated materials have been intensively investigated because of the potential applications of these materials in electronics and optoelectronics. Among these applications, organic field-effect transistors (OFETs) fabricated from either thin films or well-defined single crystals as charge-transporting layers are the most promising electronic devices. In this work, the effect of molecular packing on the performance of OFETs is investigated through the fabrication and characterization of devices based on zinc(II) porphyrins TPZ and TBPZ. The field-effect mobility of the transistors is found to increase with decreasing intermolecular distance, attributable to greater overlap of π orbitals among close-packed molecules and thereby enhance the charge transport.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
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