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71.
Siew Leng Lim Yiliang LiuJing Li En-Tang KangChong Kim Ong 《Applied Surface Science》2011,257(15):6612-6617
Transparent TiO2 nanotube arrays of micrometer lengths were prepared by anodization of titanium thin film RF sputtered on indium tin oxide (ITO) which was coated on glass substrate. The sputtering process took place at elevated temperature of 500 °C. The structures of the films were studied using scanning electron microscopy (SEM) and X-ray diffraction (XRD) while the optical properties of the films were investigated using UV-visible spectroscopy. Two types of electrolytes were used in this work: an aqueous mixture of acetic acid and HF solution and a mixture of NH4F and water dissolved in ethylene glycol. The concentration of NH4F, voltage and the thickness of the sputtered titanium film were varied to study their effect on the formation of TiO2 nanotube arrays. It is demonstrated in this work that the nanoporous layer is formed on top of the ordered array of TiO2 nanotubes. Furthermore, the optical transmittance of TiO2 nanotubes annealed at 450 °C is much lower than the non annealed TiO2 nanotubes in the visible wavelength region. 相似文献
72.
Wee Ong Siew Seong Shan Yap Cécile Ladam Øystein Dahl Turid Worren Reenaas Teck Yong Tou 《Applied Physics A: Materials Science & Processing》2011,104(3):877-881
Nanosecond-pulsed KrF (248 nm, 25 ns) and Nd:YAG (1064 nm, 532 nm, 355 nm, 5 ns) lasers were used to ablate a polycrystalline
Si target in a background pressure of <10−4 Pa. Si films were deposited on Si and GaAs substrates at room temperature. The surface morphology of the films was characterized
using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Round droplets from 20 nm to 5 μm were detected
on the deposited films. Raman Spectroscopy indicated that the micron-sized droplets were crystalline and the films were amorphous.
The dependence of the properties of the films on laser wavelengths and fluence is discussed. 相似文献
73.
74.
Ong QK Lin XM Wei A 《The journal of physical chemistry. C, Nanomaterials and interfaces》2011,115(6):2665-2672
Core-shell Fe@Fe(3)O(4) nanoparticles exhibit substantial exchange bias at low temperatures, mediated by unidirectionally aligned moments at the core-shell interface. These spins are frozen into magnetic alignment with field cooling, and are depinned in a temperature-dependent manner. The population of such frozen spins has a direct impact on both coercivity (H(C)) and the exchange-bias field (H(E)), which are modulated by external physical parameters such as the strength of the applied cooling field and the cycling history of magnetic field sweeps (training effect). Aging of the core-shell nanoparticles under ambient conditions results in a gradual decrease in magnetization but overall retention of H(C) and H(E), as well as a large increase in the population of frozen spins. These changes are accompanied by a structural evolution from well-defined core-shell structures to particles containing multiple voids, attributable to the Kirkendall effect. Energy-filtered and high-resolution transmission electron microscopy both indicate further oxidation of the shell layer, but the Fe core is remarkably well preserved. The increase in frozen spin population with age is responsible for the overall retention of exchange bias, despite void formation and other oxidation-dependent changes. The exchange-bias field becomes negligible upon deliberate oxidation of Fe@Fe(3)O(4) nanoparticles into yolk-shell particles, with a nearly complete physical separation of core and shell. 相似文献
75.
Yaoyu Feng Say‐Leong Ong Jiangyong Hu Wun‐Jern Ng 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(1):m34-m35
Reaction of 1,10‐phenanthroline (phen) with iron trichloride in the presence of sodium nitrilotriacetate (NTA) resulted in the formation of red crystals of the title complex, [Fe(C6H6NO6)(C12H8N2)(H2O)]·H2O. The Fe atom has a distorted capped trigonal prismatic coordination comprised of one tetradentate NTA, one bidentate phen molecule and a water molecule. Intermolecular O—H?O hydrogen bonds link the molecules into infinite chains. The chains are crosslinked by hydrogen bonds involving the solvent water molecule, leading to an infinite ladder packing mode. 相似文献
76.
For the first time, barium ferrite films with in-plane orientation were prepared at 700°C by pulsed laser deposition technique (PLD) on Si(1 1 1) without any post-annealing. An amorphous Ba–Fe–O film is used as underlayer to facilitate the crystallization and improve the orientation of films. Sharp (1 1 0) and (2 2 0) peaks appeared in the XRD pattern. The surface morphologies observed by SEM are similar to the typical computer generated grain arrangements obtained by Suzuki et al. in their micromagnetics study. Furthermore, a particular kind of structure of film cross-section was identified in PLD for barium ferrite films. The grain size is about 3 μm, and the coercivity is around 1500 Oe. 相似文献
77.
We have performed Car-Parrinello molecular dynamics (CPMD) calculations of the hydrogen-bonded NH(3)-HCl dimer. Our main aim is to establish how ionic-orbital coupling in CPMD affects the vibrational dynamics in hydrogen-bonded systems by characterizing the dependence of the calculated vibrational frequencies upon the orbital mass in the adiabatic limit of Car-Parrinello calculations. We use the example of the NH(3)-HCl dimer because of interest in its vibrational spectrum, in particular the magnitude of the frequency shift of the H-Cl stretch due to the anharmonic interactions when the hydrogen bond is formed. We find that an orbital mass of about 100 a.u. or smaller is required in order for the ion-orbital coupling to be linear in orbital mass, and the results for which can be accurately extrapolated to the adiabatic limit of zero orbital mass. We argue that this is general for hydrogen-bonded systems, suggesting that typical orbital mass values used in CPMD are too high to accurately describe vibrational dynamics in hydrogen-bonded systems. Our results also show that the usual application of a scaling factor to the CPMD frequencies to correct for the effects of orbital mass is not valid. For the dynamics of the dimer, we find that the H-Cl stretch and the N-H-Cl bend are significantly coupled, suggesting that it is important to include the latter degree of freedom in quantum dynamical calculations. Results from our calculations with deuterium-substitution show that both these degrees of freedom have significant anharmonic interactions. Our calculated frequency for the H-Cl stretch using the Becke-exchange Lee-Yang-Parr correlation functional compares reasonably well with a previous second-order M?ller-Plesset calculation with anharmonic corrections, although it is low compared to the experimental value for the dimer trapped in a neon-matrix. 相似文献
78.
Kuai L Ong SE Madison JM Wang X Duvall JR Lewis TA Luce CJ Conner SD Pearlman DA Wood JL Schreiber SL Carr SA Scolnick EM Haggarty SJ 《Chemistry & biology》2011,18(7):891-906
Target identification remains challenging for the field of chemical biology. We describe an integrative chemical genomic and proteomic approach combining the use of differentially active analogs of small molecule probes with stable isotope labeling by amino acids in cell culture-mediated affinity enrichment, followed by subsequent testing of candidate targets using RNA interference-mediated gene silencing. We applied this approach to characterizing the natural product K252a and its ability to potentiate neuregulin-1 (Nrg1)/ErbB4 (v-erb-a erythroblastic leukemia viral oncogene homolog 4)-dependent neurotrophic factor signaling and neuritogenesis. We show that AAK1 (adaptor-associated kinase 1) is a relevant target of K252a, and that the loss of?AAK1?alters ErbB4 trafficking and expression levels,?providing evidence for a previously unrecognized role for AAK1 in Nrg1-mediated neurotrophic?factor signaling. Similar strategies should lead to the discovery of novel targets for therapeutic development. 相似文献
79.
Ren C Maurizot V Zhao H Shen J Zhou F Ong WQ Du Z Zhang K Su H Zeng H 《Journal of the American Chemical Society》2011,133(35):13930-13933
Described in this study is a conceptually new class of five-fold-symmetric cavity-containing planar pentameric macrocycles with their interior decorated by five convergently aligned, properly spaced carbonyl oxygen atoms. These cation-binding oxygens enclose a hydrophilic lumen of 2.85 ? in radius and thus display high-affinity binding toward alkali metal cations, and possibly many other cations, too. Arising from their high-affinity recognition of metal ions, these planar macrocycles form cation- or ion-pair-induced one-dimensional columnar aggregates, and subsequently fascinating fibrillation results. 相似文献
80.
Mir MH Ong JX Kole GK Tan GK McGlinchey MJ Wu Y Vittal JJ 《Chemical communications (Cambridge, England)》2011,47(42):11633-11635
A pair of trans,trans-muconate ligands have been successfully aligned in two novel Au(I) macrocycles by design from phosphino metal precursors that undergo photochemical cycloaddition reactions quantitatively, resulting in the formation of cyclooctadiene derivatives. 相似文献