RESUMO
Intramolecular rotation of molecules contained in a two-dimensional monolayer or a three-dimensional collapsed film at an air-water interface was investigated by in situ fluorescence spectroscopy of twisted intramolecular charge transfer (TICT) type 9-(2-carboxy-2-cyanovinyl)julolidine (CCVJ) derivatives. The TICT type molecules, CCVJ-C12 and CCVJ-Chol, that contain a linear alkyl dodecyl chain or a cholesteryl group, respectively, as their hydrophobic group, were designed and synthesized to manipulate them at the air-water interface. These lipophilized molecular rotors showed the general properties of TICT molecules in solutions that the fluorescence intensity increases with increasing viscosity of the solvent, which is induced by inhibition of internal molecular rotations. The molecular rotors CCVJ-C12 and CCVJ-Chol formed monolayers at the air-water interface and in situ fluorescence spectroscopy was performed during the in-plane compression of the monolayers. It was revealed that the monomer emissions were suppressed and only after the collapse of monolayers, excimer emission from both layers consisting of CCVJ-C12 or CCVJ-Chol was observed. Suppressed monomer emission from monolayers suggests that intramolecular rotation is not inhibited in dense ordered monolayers. Furthermore, fluorescence spectroscopy of Langmuir-Blodgett (LB) films indicated that molecular rotations are not inhibited in the monolayer transferred on the solid substrates.
RESUMO
Two-dimensional (2D) carbon nanomaterials possessing promising physical and chemical properties find applications in high-performance energy storage devices and catalysts. However, large-scale fabrication of 2D carbon nanostructures is based on a few specific carbon templates or precursors and poses a formidable challenge. Now a new bottom-up method for carbon nanosheet fabrication using a newly designed anisotropic carbon nanoring molecule, CPPhen, is presented. CPPhen was self-assembled at a dynamic air-water interface with a vortex motion to afford molecular nanosheets, which were then carbonized under inert gas flow. Their nanosheet morphologies were retained after carbonization, which has never been seen for low-molecular weight compounds. Furthermore, adding pyridine as a nitrogen dopant in the self-assembly step successfully afforded nitrogen-doped carbon nanosheets containing mainly pyridinic nitrogen species.
RESUMO
We discuss a "soft" liquid-phase adsorption (SLPA) technique for the fabrication of organic films on wettability-patterned templates by using methanol/hexane and toluene/water emulsions. The emulsions are stable for several hours at room temperature, and the diameters of the dispersed phase are estimated to be several micrometers using dynamic light scattering. The templates are fabricated by exposing self-assembled monolayers to an ultraviolet/ozone atmosphere through a shadow mask. Fluorescent dye and semiconductor polymer films are formed selectively on the hydrophilic region of the substrates and the hydrophobic region of the self-assembled monolayer, respectively. The thickness is significantly larger than those of the films fabricated by conventional film-forming techniques such as spin-coating and dip-coating, respectively. These patterned films serve as photoluminescent films. These results demonstrate that the SLPA technique allows for the fabrication of organic films on wettability-patterned templates using solution-processable materials. This technique will find application to the fabrication of electronic and photonic devices with small material consumption and few film-forming processes.
RESUMO
We discuss the micromolding in capillaries technique for the direct fabrication of calcination-free rare earth ion-doped (RE) phosphor films consisting of RE nanoparticles on plastic sheets. We synthesized two types of RE nanoparticles consisting of Y2O3 matrix doped with Er and Yb ions. Green upconversion luminescence, red upconversion luminescence, and near-infrared fluorescence appeared from the RE nanoparticles under excitation of near-infrared light. Adjusting the channel width and depth of polydimethylsiloxane molds led to control of the density of nanoparticles in the patterned RE nanoparticle films. Adjusting concentration of the RE nanoparticle dispersion and size of the RE nanoparticles allowed for the control of the density of nanoparticles in the patterned RE nanoparticle films. The density of nanoparticles in the patterned RE films on plastic sheets increased with an increase in the number of injection and drying of the RE nanoparticle dispersion. These results demonstrate that this technique enables us to directly fabricate the patterned RE phosphor films on plastic sheets, leading to the fabrication of inorganic flexible devices with small fabrication steps and material consumptions.
RESUMO
In this article, we propose a novel methodology for the formation of monodisperse regularly sized disks of several nanometer thickness and with diameters of less than 100 nm using Langmuir monolayers as fabrication media. An amphiphilic triimide, tri-n-dodecylmellitic triimide (1), was spread as a monolayer at the air-water interface with a water-soluble macrocyclic oligoamine, 1,4,7,10-tetraazacyclododecane (cyclen), in the subphase. The imide moieties of 1 act as hydrogen bond acceptors and can interact weakly with the secondary amine moieties of cyclen as hydrogen bond donors. The monolayer behavior of 1 was investigated through π-A isotherm measurements and Brewster angle microscopy (BAM). The presence of cyclen in the subphase significantly shifted isotherms and induced the formation of starfish-like microstructures. Transferred monolayers on solid supports were analyzed by reflection absorption FT-IR (FT-IR-RAS) spectroscopy and atomic force microscopy (AFM). The Langmuir monolayer transferred onto freshly cleaved mica by a surface touching (i.e., Langmuir-Schaefer) method contained disk-shaped objects with a defined height of ca. 3 nm and tunable diameter in the tens of nanometers range. Several structural parameters such as the disk height, molecular aggregation numbers in disk units, and 2D disk density per unit surface area are further discussed on the basis of AFM observations together with aggregate structure estimation and thermodynamic calculations. It should be emphasized that these well-defined structures are produced through simple routine procedures such as solution spreading, mechanical compression, and touching a substrate at the surface. The controlled formation of defined nanostructures through easy macroscopic processes should lead to unique approaches for economical, energy-efficient nanofabrication.
RESUMO
Donor and acceptor spatial distributions were directly formed in a surface relief grating of structured bulk heterojunction (BHJ) photovoltaic devices by simple periodic photopolymerization. Enhanced photocurrents were observed in the structured BHJ photovoltaic devices and formation of the D/A spatial distribution was confirmed by Kelvin probe force microscopy. This technique enables the fabrication of structured BHJ photovoltaic devices with solution-processable organic semiconductors, and has tremendous potential for controlling D/A spatial distribution in organic optoelectronics devices.
Assuntos
Carbazóis/química , Elétrons , Fulerenos/química , Processos Fotoquímicos/efeitos da radiação , Polimerização/efeitos da radiação , Eletroquímica/instrumentação , Eletrodos , Estrutura Molecular , Semicondutores/instrumentação , Propriedades de Superfície , Compostos de Estanho/químicaRESUMO
Techniques for patterning hydrogels are important for fabrication of cell culture, analytical, and actuator devices at the micro- and nanometer length scales. In this study, we fabricated alginate hydrogels cross-linked by divalent cations on wettability-patterned substrates by alternate soaking of precursor solutions of sodium alginate and divalent cations. The wettability-patterned substrates were fabricated on hydrophilic glass plates modified with hydrophobic self-assembled monolayers of hexamethyldisilazane followed by exposure to an ultraviolet/ozone atmosphere through a metal mask. The film thickness of alginate gels with a width and length of 0.1 and 4 mm were tuned stepwise from 30 nm to 200 nm by adjusting the precursor conditions, including the pH, type of divalent metal ions, and sodium alginate concentration, and the alternate soaking conditions, including the dipping/withdrawal speed and number of alternate soaking cycles. This technique can be applied to other functional gels and will contribute to fabrication of hydrogel devices at the micro- and nanometer scales in the future.
Assuntos
Alginatos/química , Hidrogéis/química , Cátions Bivalentes/química , Vidro/química , Hidrogéis/síntese química , Concentração de Íons de Hidrogênio , Interações Hidrofóbicas e Hidrofílicas , Metais Alcalinoterrosos/química , MolhabilidadeRESUMO
Phase separation often occurs in mixed Langmuir-Blodgett (LB) films. Usually circular domains at the micrometer length scale form in the LB films. The size and shape of the domains are governed by a compromise between two competing interactions of line tension and dipole-dipole interaction. An attempt was made to control the line tension by varying systematically the hydrophobic moieties of the film-forming molecules. Phase-separated structures of two-component mixed LB films of fatty acid [C(k)H(2k+1)COOH (HkA)] and hybrid carboxylic acid [C(m)F(2m+1)C(n)H(2n)COOH (FmHnA)] were investigated. IR spectra of the mixed LB films of H17A and F8H10A revealed that the alkyl chains were in an all-trans conformation and that the molecular orientation remained unchanged when the two components were mixed. Nanowires formed in the mixed LB films of HkA and F8H10A. The width of the nanowires increased with an increase in k. Domain size and shape in the mixed LB films of H17A and FmHnA depended strongly on the values of m and n. Circular domains at the micrometer length scale formed in the region m + n < 16. In contrast, domains at the nanometer length scale formed in the region m + n > or = 16 except for F6H10A. These results were explained by using a lattice model that considers the effect of the hydrophobic moieties of fatty acid and hybrid carboxylic acid on the line tension.
Assuntos
Ácidos Carboxílicos/química , Ácidos Graxos/química , Nanofios/química , Algoritmos , Microscopia de Força Atômica , Espectrofotometria InfravermelhoRESUMO
Rapid large-area printing techniques are required to fabricate superhydrophobic surfaces of polymer films on solid substrates. Here, we report a double-spray technique for fabrication of mixed phase-separated films of polystyrene (PS), poly(methyl methacrylate) (PMMA), and PS-b-PMMA. The surface wettability of the films changes to superhydrophobic by immersing the samples in cyclohexane, which is a good solvent for only PS. The rinsing process forms nanostructures in the remaining PMMA films that have flat surfaces before the rinsing treatment. The highest contact angle is about 150° on the film with a PMMA ratio of 0.2. X-ray photoelectron spectroscopy shows that a small amount of PS remains on the surface of the PMMA films, making the films superhydrophobic. Addition of PS-b-PMMA to the PS/PMMA films forms smaller phase-separated structures than those in the original PS/PMMA films because of an increase in the compatibility between PS and PMMA. The contact angle hysteresis in the films decreases with increasing PS-b-PMMA ratio, indicating an increase in the homogeneity of the phase-separated structures.
Assuntos
Interações Hidrofóbicas e Hidrofílicas , Nanoestruturas , Nanotecnologia/métodos , Polimetil Metacrilato/química , Poliestirenos/química , Propriedades de Superfície , Cicloexanos , Transição de Fase , Solventes , MolhabilidadeRESUMO
We discuss an alternate spray-coating technique for the direct fabrication of hydroxyapatite films using metal masks, suction-type spray nozzles and two calcification solutions of calcium hydroxide and phosphoric acid aqueous solutions. Hydroxyapatite films were formed only on the hydrophobic surface of the substrates. Scanning electron microscopy and energy dispersive X-ray spectroscopy showed that the spray-coated films consisted of hydroxyapatite nanoparticles. The Ca/P ratio was estimated to be about 1.26. X-ray diffraction patterns of the spray-coated films almost coincided with those of the hydroxyapatite powders, showing that the spray-coated films consisted of hydroxyapatite nanoparticles. Dot arrays of hydroxyapatite films at a diameter of 100 µm were formed by tuning the concentrations of calcium hydroxide and phosphoric acid aqueous solutions. This technique allows for the direct fabrication of the hydroxyapatite films without crystal growth process in hydroxyapatite precursors, the scaffolds of crystal growth such as biocompatibility SiO2-CaO glasses, or electrophoresis processes. By using this technique, large-area ceramic films with biocompatibility will be micropatterned with minimized material consumption, short fabrication time, and reduced equipment investments.
Assuntos
Durapatita/síntese química , Hidróxido de Cálcio/química , Cristalização , Durapatita/química , Nanopartículas , Ácidos Fosfóricos/químicaRESUMO
In this study, we investigated the drug-releasing behavior of a calcium carbonate (CaCO3 )-gelatin hybrid nanocarrier, fabricated through a single process using biomimetic mineralization. The organic scaffold (gelatin) of the fabricated nanocarrier is responsible for its capacity to load anionic drugs and for controlling the morphology of the inorganic matrix (CaCO3 ). We studied the drug-releasing properties of the nanocarrier by investigating the response of the CaCO3 matrix to acidic conditions. We found that under neutral conditions, drug release from the nanocarrier was inhibited, whereas under acidic conditions, the drug was efficiently released. Therefore, drug release from the nanocarrier is largely dependent on the surrounding pH.
Assuntos
Carbonato de Cálcio/química , Portadores de Fármacos/química , Gelatina/química , Nanopartículas/química , Preparações Farmacêuticas/química , Ânions/química , Liberação Controlada de Fármacos , Concentração de Íons de Hidrogênio , Microscopia de Força Atômica , Preparações Farmacêuticas/metabolismo , Espectroscopia de Infravermelho com Transformada de Fourier , Temperatura , TermogravimetriaRESUMO
MicroRNAs (miRNAs) are attracting considerable attention as potential biomarkers for the early diagnosis of cancer. We have been developing a detection method for miRNAs on a microfluidic chip with external-power-free fluid pumping and enzyme-free amplification. The assay is completed within 20 min. Here, we describe the specificity of this miRNA detection method. First, the specificity against mismatched sequences was investigated. The nonspecific detection of a 2-nucleotide mismatched sequence was negligible, while that of a 1-nucleotide mismatched sequence was observed to a reasonable extent. Next, the disturbance in mature miRNA detection by existence of its precursor miRNA was evaluated. One precursor miRNA out of four tested showed significant nonspecific responses at 1 nM or higher concentrations. However, those responses were much lower than that of the target mature miRNA at 0.1 nM. Finally, we tried to detect three endogenous miRNAs, which are known to be potential cancer biomarkers, in human leucocyte total RNA. The measured concentraions of these miRNAs agreed well with those obtained by quantitative reverse transcription polymerase chain reaction. These results indicate that the on-chip miRNA detection method has good specificity, which is promising for applications to real biological samples.
Assuntos
Dispositivos Lab-On-A-Chip , Limite de Detecção , MicroRNAs/análise , Sequência de Bases , Humanos , Leucócitos/metabolismo , Técnicas de Amplificação de Ácido NucleicoRESUMO
We discuss an alternate method for calcification in microcapillaries for fabricating calcium phosphate films using silicone molds and calcifying solutions. Calcium phosphate films with a line/space of 5-50 µm were fabricated by controlling the concentrations of calcium chloride and sodium phosphate solutions. Plate-type crystals of hydroxyapatite were grown when the calcium phosphate films were immersed in hydroxyapatite precursors. In the initial stage of hydroxyapatite crystal growth, the c-plane of the crystals was grown parallel to the substrates, and subsequently the growth followed with the c-plane growing perpendicular to the substrates. In narrow capillaries, dendritic structures were formed with a tendency to grow in a direction parallel to the direction of the microcapillaries. This technique is useful in the micropatterning of biocompatible ceramics with a minimized material consumption and a short fabrication time.
Assuntos
Materiais Revestidos Biocompatíveis/síntese química , Durapatita/síntese química , Cloreto de Cálcio/química , Materiais Revestidos Biocompatíveis/química , Cristalização , Durapatita/química , Luz , Fosfatos/químicaRESUMO
We report on a detection method for methylated DNA on a microfluidic chip, which needs no external power for fluid pumping. The methylated DNA was sandwiched by immobilized probe DNA and an anti-methylcytosine antibody. The fluorescence signal was amplified by our original amplification technology. The detection method was first optimized using a 22-mer DNA sequence, then further validated using a 60-mer DNA sequence adapted from the SEPT9 gene. We were able to detect the methylated 60-mer DNA at 0.4 nM within 18 min.
Assuntos
Técnicas Biossensoriais/instrumentação , Metilação de DNA , DNA/análise , DNA/genética , Dispositivos Lab-On-A-Chip , 5-Metilcitosina/metabolismo , Sequência de Bases , Calibragem , DNA/química , Sondas de DNA/química , Humanos , Limite de Detecção , Septinas/genéticaRESUMO
We report on the use of microcrystallization in capillaries to fabricate patterned crystalline microstructures of the low-bandgap ambipolar quinoidal quaterthiophene derivative (QQT(CN)4) from a chloroform solution. Aligned needle-shaped QQT(CN)4 crystals were formed in thin film microstructures using either open- or closed- capillaries made of polydimethylsiloxane (PDMS). Their charge transport properties were evaluated in a bottom-gate top-contact transistor configuration. Hole and electron mobilities were found to be as high as 0.17 and 0.083 cm(2) V(-1) s(-1), respectively, approaching the values previously obtained in individual QQT(CN)4 single crystal microneedles. It was possible to control the size of the needle crystals and the microline arrays by adjusting the structure of the PDMS mold and the concentration of QQT(CN)4 solution. These results demonstrate that the microcrystallization in capillaries technique can be used to simultaneously pattern organic needle single crystals and control the microcrystallization processes. Such a simple and versatile method should be promising for the future development of high-performance organic electronic devices.
RESUMO
We investigate the correlation of the number of thiophene units with the structural order and carrier mobility of the films through studies on thin-film transistors (TFTs) based on alpha-quinquethiophene (5T), alpha-sexithiophene (6T), and alpha-septithiophene (7T). The X-ray diffraction (XRD) data of the nT films deposited at low substrate temperatures present obviously different structural orders depending on the parity of the number of thiophene units. Although even-numbered nT films present well-ordered structures and large carrier mobilities, odd-numbered nT films present two different crystalline polymorphs and vastly low carrier mobilities reflecting the coexistence of two crystalline polymorphs. However, the XRD data of both even- and odd-numbered nT films deposited at high substrate temperatures indicate that the nT molecules form single well-ordered structures. Those ordered TFTs exhibit large carrier mobilities accompanying an increase in the number of thiophene units, 0.05, 0.08, and 0.13 cm2 V(-1) s(-1) for 5T, 6T, and 7T, respectively. The parity of the number of thiophene units affects the structural order intrinsically in grown thin films, and affects carrier mobilities extrinsically in their TFTs.
RESUMO
We report calcination-free micromolding in capillaries for the nanopatterning of inorganic upconversion luminescent layers on flexible plastic sheets. We prepared Er(3+)- and Yb(3+)-codoped NaYF4 nanoparticles modified with a cationic polymer to improve dispersion stability of aqueous dispersion of the NaYF4 nanoparticles. We controlled the line width and density of nanoparticles in the NaYF4 nanoparticle films on flexible plastic sheets by adjusting the concentrations of the NaYF4 nanoparticle dispersion and the channel sizes of silicone stamps, resulting in the formation of nanopatterned NaYF4 nanoparticle films at the line width of the nanoparticle size (50 nm). Visible upconversion luminescence and near-infrared fluorescence appeared from the NaYF4 nanoparticle films excited with a near-infrared laser beam. These results demonstrate that calcination free micromolding in capillaries using aqueous dispersion of NaYF4 nanoparticles modified with a cationic polymer allows for the nanopatterning of inorganic upconversion luminescent layers on flexible plastic sheets.
RESUMO
We report a soft liquid-phase adsorption (SLPA) technique for the fabrication of organic semiconductor films on wettability-patterned substrates using toluene/water emulsions. Wettability-patterned substrates were obtained by the UV-ozone treatment of self-assembled monolayers of silane coupling agents on glass plates using a metal mask. Organic semiconductor polymer films were formed selectively on the hydrophobic part of the wettability-patterned substrates. The thickness of the films fabricated by the SLPA technique is significantly larger than that of the films fabricated by dip-coating and spin-coating techniques. The film thickness can be controlled by adjusting the volume ratio of toluene to water, immersion angle, immersion temperature, and immersion time. The SLPA technique allows for the direct production of organic semiconductor films on wettability-patterned substrates with minimized material consumption and reduced number of fabrication steps.
Assuntos
Química Orgânica/métodos , Membranas Artificiais , Polímeros , Semicondutores , Molhabilidade , Adsorção , Emulsões , Vidro , Metais , Ozônio , Silanos , Tolueno , Raios Ultravioleta , ÁguaRESUMO
We demonstrate a patterning technique of rare-earth-ion-doped (RE) nanoparticle films directly on wettability-patterned surfaces fabricated on plastic sheets in one step. Self-assembled monolayers consisting of silane-coupling agent with hydrophobic groups were fabricated on plastic sheets. UV-ozone treatments were performed through a metal mask to selectively remove the self-assembled monolayers in a patterned manner, resulting in the formation of wettability-patterned surfaces on plastic sheets. Using a water dispersion of Er(3+) and Yb(3+)-codoped Y2O3 nanoparticles at a diameter of 100 nm, RE-nanoparticle films were fabricated on the wettability-patterned surfaces by a dip-coating technique. By adjusting the concentration of RE-nanoparticle dispersion, withdrawal speed, and withdrawal angle, amount of RE-nanoparticles, we were able to control the structures of the RE-nanoparticle films. Fluorescence microscope observations demonstrate that visible upconversion luminescence and near-infrared fluorescence were emitted from the RE-nanoparticle films on the wettability-patterned surfaces. This technique allows for the fabrication of flexible emitting devices with long-operating life time with minimized material consumption and few fabrication steps, and for the application to sensors, emitting devices, and displays in electronics, photonics, and bionics in the future.
RESUMO
Here, we describe the formation of J-aggregates triggered by isomerization of an azobenzene derivative, N-[p-[(p-dodecylphenylazo)phenyloxy]dodecylpyridinium bromide (AzP), in mixed Langmuir-Blodgett (LB) films that contain an amphiphilic spiropyran with a methoxy group at the 5' position, MeO-SP1822. Pure LB films of MeO-SP1822 consist of multilayer domains embedded in a monolayer. UV irradiation of the films causes the isomerization of MeO-SP1822 to its merocyanine form, MeO-MC1822. Pure LB films of AzP comprise finger-like domains and granular domains. Irradiating mixed films of MeO-SP1822 and AzP with alternating UV and visible light causes J-aggregation of MeO-MC1822, with the amount of J-aggregates reaching a maximum at a 1:1 molar ratio. J-aggregation occurs in flat finger-like structures originating in the AzP-rich granular domains that are located on top of the MeO-MC1822-rich multilayer domains. J-aggregates are also present under the AzP-rich granular domains, though these domains do not serve as nucleation sites for the finger-like structures. We propose that granular domains serving as nucleation sites are partially buried in the multilayer domains, whereas those triggering the J-aggregation of MeO-MC1822 under the granular domains are situated on top of the multilayer domains.