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991.
Shin JH Kang JH Jin WM Park JH Cho YS Moon JH 《Langmuir : the ACS journal of surfaces and colloids》2011,27(2):856-860
Engineering of TiO(2) electrode layers is critical to guaranteeing the photoconversion efficiency of dye-sensitized solar cells (DSSCs). Recently, a novel approach has been introduced for producing TiO(2) electrodes using the inverted structures of colloidal crystals. This paper describes a facile route to producing ordered macroporous electrodes from colloidal crystal templates for DSSCs. Using concentrated colloids dispersed in a volatile medium, the colloidal crystal templates were obtained within a few minutes, and the thickness of the template was easily controlled by changing the quantity of colloidal solution deposited. Here, the effects of the structural properties of the inverse opal TiO(2) electrodes on the photovoltaic parameters of DSSCs were investigated. The photovoltaic parameters were measured as a function of pore ordering and electrode film thickness. Moreover, DSSC applications that used either liquid or viscous polymer electrolyte solutions were investigated to reveal the effects of pore size on performance of an inverse opal TiO(2) electrode. 相似文献
992.
Lim J Kwon YS Park SH Song IY Choi J Park T 《Langmuir : the ACS journal of surfaces and colloids》2011,27(23):14647-14653
TiO(2) electrodes, sensitized with the N719 dye at high immersion temperatures during the sensitization process, were found to have large fractions of weakly bound N719 on the electrode surface, which resulted in dye aggregation and decreased device longevity. These disadvantages were ameliorated using a low-temperature stearic acid (SA)-assisted anchoring method described here. The activation energy (ΔE(NS)(++)) and relative fraction of strongly bound N719 were twice as large as the respective values obtained without the use of SA. Slowing of adsorption, both by thermal means and through SA-mediated processes, effectively controlled the binding mode of N719 on the surface of TiO(2). The resulting sensitized electrodes displayed enhanced device longevity and improved generation of photoinduced electrons. 相似文献
993.
Mingshi Jin Jung-Nam Park Jeong Kuk Shon Zhenghua Li Min Young Yoon Hyun Jung Na Young-Kwon Park Ji Man Kim 《Research on Chemical Intermediates》2011,37(9):1181-1192
Highly ordered mesoporous cerium dioxide (meso-CeO2) was successfully synthesized using a facile solvent-free infiltration method from a mesoporous silica template, KIT-6. The
meso-CeO2 material, thus obtained, exhibited well-defined mesostructure and high surface area (153 m2 g−1). The physicochemical properties of meso-CeO2 material and Pd-supported on meso-CeO2 (Pd/meso-CeO2) were characterized by electron microscopy, X-ray diffraction, N2 adsorption–desorption, and temperature-programmed experiments. The Pd/meso-CeO2 catalyst exhibited excellent catalytic activity for CO oxidation compared with those of other Pd/CeO2 catalysts which were prepared using nanocrystalline CeO2 and bulk-CeO2 as the supports. Moreover, a hydrogen pretreatment of the Pd/meso-CeO2 catalyst resulted in a remarkable increase of catalytic activity (T
100 = 52 °C). 相似文献
994.
Soyoung Yun Eunok Lee Young-Kwon Park Soon-Yong Jeong Jeongsik Han Byunghun Jeong Jong-Ki Jeon 《Research on Chemical Intermediates》2011,37(9):1215-1223
In this study, in order to develop catalysts for the selective isomerization of higher paraffin, the hydroisomerization reaction of n-dodecane was performed as a model reaction. Pt/ZSM-48, Pt/HZSM-5, Pt/HY, and Pt/SAPO-11 were examined for the selective hydroisomerization of n-dodecane. The catalysts were characterized via X-ray powder diffraction, N2 adsorption, and the temperature-programmed desorption of ammonia. Among the catalysts studied, the Pt/HZSM-48 catalyst exhibited the best isomerization selectivity in the hydroisomerization reaction of n-dodecane, which is attributed to the moderate acid sites and medium-sized pores present in the HZSM-48. The highest iso-dodecane yield was obtained at a reaction temperature of 280 °C in the Pt/HZSM-48 catalyst. The optimal selectivity of the n-dodecane hydroisomerization over the Pt/SAPO-11 catalyst was obtained at approximately 300 °C, which was slightly higher than that of the Pt/HZSM-48 catalyst. 相似文献
995.
The effect of two initiators, so-called dual initiators system on atom radical transfer polymerization (ATRP), were studied with dimethyl-2,6-dibromohepanedioate (DMDBHD) and ethyl-2-bromoisobutyrate (EBIB). Cu(I)Br as catalyst and N,N,N??,N??,N??-pentamethyl-diethylenetriamine as ligand were employed for styrene ATRP. Interestingly, bimodal MWD were shown for the dual initiator system, and one of the peaks had higher molecular weight (MW) and the other had lower MW compared to a one-initiator system. The lower MW peak in bimodal peaks seemed to be mainly resulting from EBIB and the higher MW peak from DMDBHD. Furthermore, methylaluminoxane (MAO) was fed into the ATRP reaction to observe the effect of it on ATRP. As the MAO/CuBr molar ratio in feed increased from 0 to 1, the molecular weight and conversion increased without a notable change in PDI and curve shape of GPC. The conversion in the presence of MAO was also increased with the increase in MAO/CuBr molar ratio. The effect of Cp*TiCl3 on the ATRP was opposite to that of MAO. As the Cp*TiCl3/CuBr molar ratio increased from 0 to 1, the conversion of polymerization was down from 56 to 35%. Furthermore, the molecular weight was drastically decreased from 10,000 to 5,500, but their PDI did not show a significant change. These results can elucidated by the retarding effect of Cp*TiCl3 on the propagation of polymerization. 相似文献
996.
Park JW 《Colloids and surfaces. B, Biointerfaces》2011,86(1):166-168
Phospholipid bilayers were formed through liposome fusion on surfaces with different curvatures that were defined with silica spheres deposited on silicon water. Prior to the fusion, the surfaces became hydrophobic with octadecyltrimethoxysilane solution. Using atomic force microscope, surface forces were measured on dipalmitoylphosphatidylcholine (DPPC) layers and dioleoylphosphatidylcholine (DOPC) layers upon the curvature at 25°C. The short-range repulsions were higher at 20 and 100 nm curvatures than other curvatures for the DPPC layer, while they were lower for the DOPC layer. Since it was known that the forces are related to its low mechanical stability of the lipid layer, this opposite behavior was analyzed in terms of stability upon the curvature, which appears to be eventually determined by the correlation between the lipid molecule geometry and the surface curvature. 相似文献
997.
Yu Bai Il Song Park Hyeoung Ho Park Min Ho Lee Tae Sung Bae Warwick Duncan Michael Swain 《Surface and interface analysis : SIA》2011,43(6):998-1005
Well‐ordered TiO2 nanotubes were prepared by the electrochemical anodization of titanium in an ethylene glycol electrolyte containing 1 wt% NH4F and 10 wt% H2O at 20 V for 20 min, followed by annealing. The surface morphology and crystal structure of the samples were examined as a function of the annealing temperature by field emission scanning electron microscopy (FE‐SEM) and X‐ray diffraction (XRD), respectively. Crystallization of the nanotubes to the anatase phase occurred at 450 °C, while rutile formation was observed at 600 °C. Disintegration of the nanotubes was observed at 600 °C and the structure vanished completely at 750 °C. Electrochemical corrosion studies showed that the annealed nanotubes exhibited higher corrosion resistance than the as‐formed nanotubes. The growth of hydroxyapatite on the different TiO2 nanotubes was also investigated by soaking them in simulated body fluid (SBF). The results indicated that the tubes annealed to a mixture of anatase and rutile was clearly more efficient than that in their amorphous or plain anatase state. The in vitro cell response in terms of cell morphology and proliferation was evaluated using osteoblast cells. The highest cell activity was observed on the TiO2 nanotubes annealed at 600 °C. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
998.
In this work, silver (Ag) nanoparticles were deposited on multi-walled carbon nanotubes (MWNTs) by chemical reduction while Ag-decorated MWNTs (Ag-MWNTs)/polyaniline (PANI) composites were prepared by oxidation polymerization. The effect of the Ag incorporated into the interface of the composites on the electrochemical performance of the MWNTs/PANI was investigated. It was found that highly dispersed Ag nanoparticles were deposited onto the MWNTs, and the Ag-MWNTs were successfully coated by PANI. According to cyclic voltammograms, the Ag-MWNTs/PANI exhibited significantly increased electrochemical performances compared to MWNTs/PANI and the highest specific capacitance obtained of MWNTs/PANI and 0.15 M Ag-MWNTs/PANI was 162 F/g and 205 F/g, respectively. This indicated that Ag nanoparticles that were deposited onto the MWNTs caused an enhanced electrochemical performance of the MWNTs/PANI due to their high electric conductivity, which resulted in an increase of the charge transfer between the MWNTs and PANI by a bridge effect. 相似文献
999.
Barium calcium magnesium silicate (BaCa2MgSi2O8), a compound whose space group was obtained via X-ray diffraction data, was re-investigated using neutron diffraction techniques. A combined powder X-ray and neutron Rietveld method revealed that BaCa2MgSi2O8 crystallizes in the trigonal space group P3? (Z=1, a=5.42708(5) Å, c=6.79455(7) Å, V=173.310(4) Å3; Rp/Rwp=5.52%/7.63%), instead of the previously believed space group P3?m1. The difference in the two structures arises from the displacement of the O2 atom. Blue emission from Ba0.98Eu0.02Ca2MgSi2O8 under 325-nm excitation is ascribed to the 4f65d1→4f7 transitions of Eu2+ ions at Ba sites and Ca sites. Site assignment of Eu2+ ions in the titled compound was performed by analysis of emission spectra at temperatures in the range of 4.2-300 K. 相似文献
1000.
Yoko Nunome Kenji Kodama Hyunkook Park Kozo Matsumoto Sang Chun Lee Kuniyuki Kitagawa 《Microchemical Journal》2011,99(2):470-477
A new system combining a soft plasma ionization (SPI) source with a time-of-flight mass spectrometer (TOFMS) has been successfully developed and applied to direct and on-line analysis of nanoparticles in smoke generated during combustion of mosquito coils with no sample preparation. The mass spectra of nanoparticles in smoke were examined in conjunction with the effects of species, pressure and current of the SPI discharge on fragmentation. The results indicated that a maximum mass of m/z 1576 was detectable when the following optima SPI conditions were satisfied: a He gas pressure of 1000 Pa with an air pressure of 1600 Pa and a discharge current of 110 mA. Furthermore, considering the results for emission spectra we suppose an ionization mechanism of SPI in which excitation and ionization of nitrogen molecule is promoted by the presence of He gas, leading to promote the smoke sample ionization. The mass spectrum of nanoparticles showed specific patterns of a peak interval of 74 which were assigned to triacetylene (1,3,5-hexatriyne). The most abundant peak in the mass spectrum, at m/z 452, was assigned to triacontanoic acid. 相似文献