We report a simple, compact electronic speckle-pattern interferometer (ESPI) incorporating holographic optical elements (HOEs) for the study of out-of-plane vibration. Reflection and transmission HOEs provide reference and object beams in the interferometer. The alignment difficulties with conventional ESPI systems are minimized using HOEs. The time-average ESPI subtraction method is used to generate the fringe pattern and remove background speckle noise by introducing a phase shift between consecutive images. The amplitude and phase maps are obtained using path-difference modulation. 相似文献
We report on experiments performed with a cladding-pumped single-mode Er:Yb-codoped single-frequency fiber amplifier simultaneously seeded by a distributed-feedback diode at 1556 nm and a tunable external-cavity diode laser emitting at a wavelength of about 1 μm wavelength. The influence of the output wavelength of the external-cavity laser on amplification and reabsorption behavior of the Yb emission as well as the amplifier performance at a wavelength of 1556 nm is examined experimentally. 相似文献
Both the formation energy and the diffusive activation energy of a single vacancy migrating in the first four atomic layers intra- and inter-layer near Cu Σ = 9 [110] twist GB have been investigated by using the MAEAM. The formation of the vacancy is favorable on the first layer (1L) near the GB plane and is spontaneous on sites ‘2’–‘5’ especially ‘2’ and ‘4’. The effects of the GB on the intra- as well as inter-layer migration are mainly for 1L–1L as well as for 1L–1L′, 2L–1L and 3L–1L related to the 1L, respectively. Furthermore, the vacancy in 1L is favorable to migrate in 1L (intra-layer) or through GB plane to 1L′, the one in either 2L or 3L is favorable to migrate to 1L. So the vacancy tends to converge to the first layer near the GB plane. 相似文献
The true ground state of 1 is a matter of debate, but for clarity and convenience the allene resonance form 1 a , is the most appropriate. The arguments for aromaticity made by Christl and Engels are shown to be incorrect.
Alcohol oxidation and self‐assembly: the in situ oxidation of hydroxyl functional groups to quinone groups promotes the formation of enhanced hydrogen bonds and allows reorganization of the resulting supramolecular self‐assemblies, which evolve from a weakly bound dense phase to a strongly bound nanoporous open structure (see picture).
A new receptor, the bisTTF-calix[2]thiophene[2]pyrrole derivative 3, has been prepared from the Lewis acid-catalyzed condensation of 2,5-bis(1-hydroxymethylethyl)thiopheno-TTF and pyrrole.
This new system is found to form complexes with the electron-deficient guests, trinitrobenzene (TNB) and picric acid (PA),
which serve as models for nitroaromatic explosives. The binding phenomenon, which has been studied in organic solution using
proton nuclear magnetic resonance and absorption spectroscopies, results in an easy-to-visualize color change in chloroform
that is independent of the presence of chloride anion, a known interferant for an earlier tetrakisTTF-calix[4]pyrrole TNB
chemosensor. Support for the proposed binding mode comes from a preliminary solid state structure of the complex formed from
TNB, namely TNB⊂3. A color change is also observed when dichloromethane solutions of chemosensor 3 are added to solvent-free samples of TNB, PA, and 2,4,6-trinitrotoluene supported on silica gel.
Figure A new bis-tetrathiafulvalene calix[2]thiophene[2]pyrrole derivative has been prepared that gives rise to an easy-to-visualize
color change in the presence of the model nitroaromatic explosives trinitrobenzene and picric acid.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.
The asymptotic behavior of a subcritical Branching Process in Random Environment (BPRE) starting with several particles depends on whether the BPRE is strongly subcritical (SS), intermediate subcritical (IS) or weakly subcritical (WS). In the (SS+IS) case, the asymptotic probability of survival is proportional to the initial number of particles, and conditionally on the survival of the population, only one initial particle survives a.s. These two properties do not hold in the (WS) case and different asymptotics are established, which require new results on random walks with negative drift. We provide an interpretation of these results by characterizing the sequence of environments selected when we condition on the survival of particles. This also raises the problem of the dependence of the Yaglom quasistationary distributions on the initial number of particles and the asymptotic behavior of the Q-process associated with a subcritical BPRE. 相似文献
The chemical and electrostatic interactions at mineral-water interfaces are of fundamental importance in many geochemical, materials science, and technological processes; however, the effects of particle size at the nanoscale on these interactions are poorly known. Therefore, comprehensive experimental and characterization studies were completed, to begin to assess the effects of particle size on the surface reactivity and charging of metal-oxide nanoparticles in aqueous solutions. Commercially available crystalline anatase (TiO2) particles were characterized using neutron and X-ray small-angle scattering, electron microscopy, and laser diffraction techniques. The 4 nm primary nanoparticles were found to exist almost exclusively in a hierarchy of agglomerated structures. Potentiometric and electrophoretic mobility titrations were completed in NaCl media at ionic strengths from (0.005 to 0.3) mol/kg, and 25 degrees C, with these two experimental techniques matched as closely as the different procedures permitted. The pH of zero net proton charge (pHznpc, from potentiometric titration) and isoelectric point pH value (pHiep, from electrophoretic mobility titrations) were both in near perfect agreement (6.85 +/- 0.02). At high ionic strengths the apparent pHznpc value was offset slightly toward lower pH values, which suggests some specific adsorption of the Na+ electrolyte ions. Proton-induced surface charge curves of nanocrystalline anatase were very similar to those of larger rutile crystallites when expressed relative to their respective pHznpc values, indicating that the development of positive and negative surface charge away from the pHznpc for nanocrystalline anatase is similar to that of larger TiO2 crystallites. 相似文献
Layer-by-layer (LBL) polyelectrolyte films were constructed from poly(L-glutamic acid) (PGA) and poly(L-aspartic acid) (PAA) as polyanions, and from poly(L-lysine) (PLL) as the polycation. The terminating layer of the films was always PLL. According to attenuated total reflection Fourier transform infrared measurements, the PGA/PLL and PAA/PLL films, despite their chemical similarity, had largely different secondary structures. Extended beta-sheets dominated the PGA/PLL films, while alpha-helices and intramolecular beta-sheets dominated the PAA/PLL films. The secondary structure of the polyelectrolyte film affected the adsorption of human serum albumin (HSA) as well. HSA preserved its native secondary structure on the PGA/PLL film, but it became largely deformed on PAA/PLL films. Both PGA and PAA were able to extrude to a certain extent the other polyanion from the films, but the structural consequences were different. Adding PAA to a (PGA/PLL)5-PGA film resulted in a simple exchange and incorporation: PGA/PLL and PAA/PLL complexes coexisted with their unaltered secondary structures in the mixed film. The incorporation of PGA into a (PAA/PLL)5-PAA film was up to 50% and caused additional beta-structure increase in the secondary structure of the film. The proportions of the two polyanions were roughly the same on the surfaces and in the interiors of the films, indicating practically free diffusion for both polyanions. The abundance of PAA/PLL and PGA/PLL domains on the film surfaces was monitored by the analysis of the amide I region of the infrared spectrum of a reporter molecule, HSA, adsorbed onto the three-component polyelectrolyte films. 相似文献