Epitaxial VO2 films were prepared on the TiO2 (001) substrates by the excimer-laser-assisted metal–organic deposition (ELAMOD). The quality of the epitaxial films obtained
by irradiation with a KrF laser was found to be affected by the film structure obtained after preheating at 500 or 300°C.
When the films containing crystal domains, which were obtained by preheating at 500°C, were irradiated with the laser at room
temperature under a base pressure of 250 Pa, epitaxial and polycrystalline VO2 phases were simultaneously formed. In contrast, when the amorphous films containing organic components, which were obtained
by preheating at 300°C, were irradiated with the laser at room temperature in air, a single phase of epitaxial VO2 was formed. By using thermal simulations, we determined that the formation of the epitaxial phase was affected both by the
temperature distribution within the film during the laser irradiation and by the laser intensity at the interface between
the substrate and the film. The latter factor is considered to play a role in the nucleation of crystallization, causing the
epitaxial phase to form preferentially compared to the polycrystalline phase in the amorphous matrix of the films. These results
indicate that the ELAMOD process is effective for the fabrication of epitaxial VO2 films at low temperature. 相似文献
Iron man or weakling? Ligand‐field strengths are conveniently expressed by the empirical spectrochemical series. Although cyanide has been deeply entrenched as a strong‐field ligand, a couple of recent examples cast doubt toward the position of this ligand, namely the high‐spin (S=2) states of [CrII(CN)5]3? and [FeII(tpp)(CN)]?. tpp=meso‐tetraphenylporphinate.
The ins and outs of spin : Using the microporous coordination polymer {Fe(pz)[Pt(CN)4]} ( 1 , pz=pyrazine), incorporating spin‐crossover subunits, two‐directional magnetic chemo‐switching is achieved at room temperature. In situ magnetic measurements following guest vapor injection show that most guest molecules transform 1 from the low‐spin (LS) state to the high‐spin (HS) state, whereas CS2 uniquely causes the reverse HS‐to‐LS transition.
Bidirectional chemo‐switching of magnetism occurs in a microporous coordination polymer containing spin‐crossover subunits, as described by M. Ohba, J. A. Real, S. Kitagawa, and co‐workers in their Communication on page 4767 ff. In situ magnetic measurements reveal that most guest molecules transform the framework spin state from diamagnetic low spin (red) to paramagnetic high spin (yellow), whereas the guest CS2 stabilizes the low‐spin state. These induced spin states are retained as a memory effect after the release of the guest.
We report the synthesis of the novel fluorescence-labeled jasmonate glycoside 2 based on β-d-glucopyranosyl 12-hydroxyjasmonate 1, which is a leaf-closing substance of Albizzia julibrissin Durazz. The fluorescence study using 2 revealed that the target cell for 1 is a motor cell. Probe 2 bound to the motor cells of two plants belonging to genus Albizzia. This result suggested that a receptor for 2, which is common among genus Albizzia would be involved in the nyctinastic leaf movement. 相似文献
In situ x-ray diffraction measurements were carried out for investigating the liquid structure in the ultrasonic fountain jet to consider the mechanism of the "ultrasonic ethanol separation" reported by Sato et al. [J. Chem. Phys. 114, 2382 (2001)]. For pure liquids (water and ethanol), it was found that the high frequency ultrasound does not affect the liquid structure microscopically. For the 20 mol % ethanol-water mixture, the estimated ethanol mole fraction in the ultrasonic fountain jet by using the position of the main maximum in the x-ray diffraction profile coincided with that in the reservoir. This result suggests that the ethanol separation is not caused by any distorted liquid structure under the ultrasound irradiation and occurs when or after the generation of the liquid droplet mist. 相似文献
The interaction forces between poly(N-isopropylacrylamide) (PNIPAAm)-grafted surfaces and colloidal particles in an aqueous solution were investigated using an atomic force microscope. Measurements were conducted between smooth silicon wafers on which PNIPAAm was terminally grafted and silica particles hydrophobized with a silanating reagent in an aqueous electrolyte solution under controlled temperature. Below the lower critical solution temperature (LCST) of PNIPAAm, there were large repulsive forces between the surfaces, both on approach and separation of the surfaces. On the other hand, above LCST, attractive forces were observed both in approaching and in separating force curves. When surface hydrophobicity of the particles increased, the maximum attractive force tended to increase. The changes of hydration state of the grafted PNIPAAm chains depending on temperature are considered to greatly alter the interaction force properties. The role of the intermolecular interaction between the PNIPAAm chains and the hydrophobic particles in the interaction forces is discussed. 相似文献
Isocyanide-bound model hemes always adopt the (dxz, dyz)4(dxy)1 ground state, however, we have found that the replacement of porphyrin by diazaporphyrin leads to the formation of an unprecedented low-spin bis(tert-butylisocyanide) complex with the (dxy)2(dxz, dyz)3 ground state. 相似文献
Heat capacity changes of short-lived transient species in different time ranges were measured for the first time by using the thermal component of the transient grating and transient lens signals at various temperatures. This method was applied to the transient intermediates of Photoactive Yellow Protein (PYP). The temperature dependence of the enthalpy change shows that the heat capacity of the short-lived intermediate pR2 (also called I1 or PYP(L)) species is the same as that of the ground state (pG) species within our experimental accuracy, whereas that of the long-lived intermediate pB (I2 or PYP(M)) is much larger (2.7 +/- 0.4 kJ/mol K) than that of pG. The larger heat capacity is interpreted in terms of the conformational change of the pB species such as melted conformation and/or exposure of the nonpolar residues to the aqueous phase. This technique can be used for photochemical reactions in general to investigate the conformational change and the hydrophobic interaction in a time domain. 相似文献