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71.
A series of polyurethane/polyaniline/silica organic/inorganic hybrids were synthesized via the conventional polyurethane (PU) prepolymer technique. Amine-endcapped polyaniline (PANI) with low molecular weight and higher solubility was firstly synthesized. This PANI oligomer was then used together with nano-silica bearing silanol groups as chain extenders to prepare the conducting polyurethane hybrids. The polyurethane hybrids were designated as PU-xPANI-ySiO2 (x + y = 1). For comparison, the urethane-aniline block copolymer and the PU/silica hybrid were designated as PU-PANI and PU-SiO2, respectively.The structures of PU-PANI, PU-SiO2 and conducting polyurethane hybrids were confirmed by FT-IR, solid-state 13C, and 29Si NMR spectra. In nano-silica containing organic/inorganic conducting polyurethane hybrids, UV-vis spectra revealed the maximum absorption bands similar to that of PU-PANI. X-ray diffraction patterns indicated that these samples are typical of semicrystalline/amorphous materials. SEM image of PU-0.5PANI-0.5SiO2 showed that PANI was dispersed homogeneously and interconnected continuously in the insulating PU-silica matrix. TGA results of the polymer hybrids exhibited higher thermal stabilities and lower decomposition rates than that of PU-PANI both in nitrogen and air. Differential scanning calorimetry (DSC) studies indicated that the polyurethane hybrids had higher glass-transition temperatures (Tg) with the increase of PANI, but lower than that of PU-PANI. Stress-strain curves for all of the polyurethane hybrids showed the elastomeric behavior of typical polyurethanes. The surface resistivity values of all hybrids were about 108 ∼ 1010 Ω/sq. and might meet the requirement of the anti-electrostatic materials. 相似文献
72.
Molecular Engineering of Push–Pull Porphyrin Dyes for Highly Efficient Dye‐Sensitized Solar Cells: The Role of Benzene Spacers 下载免费PDF全文
Shaik M. Zakeeruddin Shu‐Nung Chang Chi‐Hung Hsieh Chen‐Yu Yeh Michael Grätzel 《Angewandte Chemie (International ed. in English)》2014,53(11):2973-2977
Porphyrins have drawn much attention as sensitizers owing to the large absorption coefficients of their Soret and Q bands in the visible region. In a donor and acceptor zinc porphyrin we applied a new strategy of introducing 2,1,3‐benzothiadiazole (BTD) as a π‐conjugated linker between the anchoring group and the porphyrin chromophore to broaden the absorption spectra to fill the valley between the Soret and Q bands. With this novel approach, we observed 12.75 % power‐conversion efficiency under simulated one‐sun illumination (AM1.5G, 100 mW cm?2). In this study, we showed the importance of introducing the phenyl group as a spacer between the BTD and the zinc porphyrin in achieving high power‐conversion efficiencies. Time‐resolved fluorescence, transient‐photocurrent‐decay, and transient‐photovoltage‐decay measurements were employed to determine the electron‐injection dynamics and the lifetime of the photogenerated charge carriers. 相似文献
73.
Chih-Chung Yang Wen-Tse Hsiao Chien-Kai Chung Hsin-Yi Tsai Jer-Liang Andrew Yeh Kuo-Cheng Huang 《Applied Physics A: Materials Science & Processing》2014,114(1):161-168
This study presents a maskless method to conduct microelectrode patterning of metal films using pulsed UV-laser-writing technology. The experimental procedures involved designing the ablation region of a glass substrate, ablation path planning, and determining detailed laser-writing parameters. The various parameters used in a UV-laser-writing system were investigated and analyzed using an optical microscope and a three-dimensional confocal laser scanning microscope. This technique was successfully applied in patterning aluminum (Al) thin film on a glass substrate for use in microheater devices. The measurements of electrical resistance and temperature distribution on the substrate demonstrated that no short circuiting occurred in the microheater, confirming the quality of the electrical isolation values. 相似文献
74.
Chih-Ping Yen Cheng-Shiuan Wong Chi-Yu Yeh Yen-Mu Chen Hsu-Hsin Chu Jiunn-Yuan Lin Jyhpyng Wang Ping-Hsun Lin Szu-yuan Chen 《Applied Physics A: Materials Science & Processing》2014,115(2):671-677
Growth of strongly textured $\mathrm{FeCO}_{3}$ thin films on substrates was achieved with ultrashort-pulsed laser deposition using 810-nm, 46-fs ablation pulses. The crystallinity and composition were verified with X-ray diffraction and Raman spectroscopy. Using Mössbauer spectroscopy, it is shown that the deposited $\mathrm{FeCO}_{3}$ thin films possess the film quality required for application in research of nuclear quantum optics. It is found that a relatively low substrate temperature is crucial for growing a strongly textured film of $\mathrm{FeCO}_{3}$ while avoiding decomposition of $\mathrm{FeCO}_{3}$ into $\mathrm{Fe}_{2}\mathrm{O}_{3}$ and $\mathrm{CO}_{2}$ . This supports the importance of the use of ultrashort-pulsed laser deposition in providing adatoms with high mobility for attaining good crystallinity. The surface morphology was characterized by surface profilometry, scanning electron microscopy and atomic force microscopy. It is found to be significantly affected by changing the ablation laser parameters, including laser fluence, pulse duration, and on-target spot size. The results show that the peak deposition flux must be below approximately 0.03 nm/pulse in order to grow a flat film. 相似文献
75.
Li‐Ya Wang En‐Chiuan Chang Mou‐Yung Yeh Yu Hsuan Chung Jiann‐Jyh Huang Fung Fuh Wong 《Heteroatom Chemistry》2014,25(3):171-177
A new series of 1,3,4‐oxadiazole‐based aromatic and heterocyclic/phenylpyrazole derivatives 6a–c , 7a–d , and 8 were synthesized via sequential 1,3‐dipolar cyclization, hydrazidation, benzoylation, dehydrative cyclization, and the Suzuki coupling reaction. Among the derivatives, compounds 7a and 7c with the corresponding 2‐thienyl and 2‐benzo[b]thienyl (Ar) at the phenyl group located at the N‐1 position of pyrazole showed a better conjugation range. 相似文献
76.
77.
Bar‐Yuan Hsieh Kun‐Ming Yeh Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2005,43(21):5009-5022
New copoly(aryl ether)s ( P1 – P3 ) containing alternate 2,5‐dihexyloxy‐1,4‐di(m‐ethoxystyryl)benzene ( P1 , P2 ) or 2,5‐dihexyloxy‐1,4‐distyrylbenzene ( P3 ) chromophores and aromatic 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) segments were prepared by Horner reaction ( P1 and P2 ) or nucleophilic displacement reaction ( P3 ). They are basically amorphous materials with 5% weight‐loss temperature above 410 °C. Their absorption, photoluminescence spectra, and quantum yields are dependent on the composition of the isolated fluorophores. The emissions are exclusively dominated by 1,4‐distyrylbenzene segments via excitation energy transfer from electron‐transporting 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) chromophores. The HOMO and LUMO energy levels have been estimated from their cyclic voltammograms, and the observations confirm that oxidation and reduction start from the emitting 1,4‐distyrylbenzene and electron‐transporting segments, respectively, indicating that both carriers affinity can be enhanced simultaneously. Among the two‐layer PLED devices (ITO/PEDOT/ P1 – P3 /Al), P1 exhibits the best performance with a turn‐on field of 4 × 105 V/cm and a maximum luminance of 225 cd/m2. However, P2 emits green–yellow light (555 nm), owing to the excimer emission. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5009–5022, 2005 相似文献
78.
Siao‐Wei Yeh Tzung‐Luen Wu Kung‐Hwa Wei Ya‐Sen Sun Keng S. Liang 《Journal of Polymer Science.Polymer Physics》2005,43(10):1220-1229
Surface‐modified CdS nanoparticles selectively dispersed in hexagonally packed poly(ethylene oxide) (PEO) cylinders of poly(styrene‐b‐ethylene oxide) (PSEO) block copolymers were prepared. The photoluminescence and ultraviolet–visible characteristics of the presynthesized CdS nanoparticles in N,N‐dimethylformamide and in PEO domains of the PSEO block copolymers were determined. Because of strong interactions between the CdS nanoparticles and PEO chains, as shown by Fourier transform infrared spectroscopy, the incorporation of the CdS nanoparticles prevented the PEO cylinders from properly crystallizing; this was confirmed by differential scanning calorimetry and wide‐angle X‐ray diffraction measurements. The intercylinder distance between the swollen and reduced‐crystallinity CdS/PEO cylinders in turn increased, as confirmed by small‐angle X‐ray scattering and transmission electron microscopy. At a high CdS concentration (43 wt % or 8.3 vol % with respect to PEO), however, the hexagonally packed cylindrical nanostructure of the PSEO diblock copolymers was destroyed. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 1220–1229, 2005 相似文献
79.
Digital shifting photoelasticity with optical enlarged unwrapping technology for local stress measurement 总被引:1,自引:0,他引:1
Xue-Feng Yao Long-Hui Jian Wei Xu Guan-Chang Jin Hsien-Yang Yeh 《Optics & Laser Technology》2005,37(7):582-589
In this paper, photoelasticity combined with phase shifting technology is used to obtain stress distribution within the stress concentration zone. Both the optical enlarged unwrapping technology and the combined path shear difference technology are provided for evaluating the local stress information. By means of a phase shifting photoelastic experiment of a diametric-compressed disc, the stress components surrounding the local loading zone are determined. The results show not only a good improvement compared with conventional photoelastic analysis but also a good agreement with theoretical data. 相似文献
80.
Microporous poly(vinylidene fluoride) (PVDF) membranes with asymmetric pore structure were prepared by a wet phase inversion process. The polymer was precipitated from a casting solution when immersed in a cold water (gelation) bath. The casting solution was, in most cases, composed of polymer, solvent, and nonsolvent. In this solvent-nonsolvent system, the solvents used were triethylphosphate (TEP) and dimethylsulfoxide (DMSO), and the nonsolvents used were glycerol and ethanol. Mean pore sizes and effective porosity of the microporous membranes were calculated using the gas permeation method. They were studied as a function of evaporation time of wet nascent film, polymer molecular weight, concentration of polymer, and concentration of nonsolvent. The morphology of the membranes was examined by scanning electron microscopy (SEM). 相似文献