A method of hard X‐ray phase‐shifting digital holography

A new method of phase‐shifting digital holography is demonstrated in the hard X‐ray region. An in‐line‐type phase‐shifting holography setup was installed in a 6.80 keV hard X‐ray synchrotron beamline. By placing a phase plate consisting of a hole and a band at the focusing point of a Fresnel lens, the relative phase of the reference and objective beams could be successfully shifted for use with a three‐step phase‐shift algorithm. The system was verified by measuring the shape of a gold test pattern and a silica sphere.     

Spectroscopic analysis of L-histidine adsorbed on gold and silver nanoparticle surfaces investigated by surface-enhanced Raman scattering

The adsorption of l-histidine on gold (Au) and silver (Ag) nanoparticle surfaces has been comparatively analyzed by means of surface-enhanced Raman scattering (SERS). The SERS spectra of l-histidine on Ag were found to be quite different from those on Au, indicating dissimilar adsorption structures depending on metal substrates. Most peaks of l-histidine on Ag appeared to be due to coordination via the carboxylate (COO(-)) group with an imidazole ring of fairly upright geometry, whereas on Au it was assumed to adsorb with a rather flat geometry. A density functional theory (DFT) calculation was performed at the level of B3LYP/LANL2DZ to estimate the energetic stability of the binding of the imidazole ring and the carboxylate group of l-histidine with the Ag and Au atoms, respectively. Based on the DFT calculation, the carboxylate group of l-histidine was predicted to bind more favorably to Ag than to Au, and this was in line with our SERS spectral analysis.     

Fabrication of microfluidic chip using micro‐hot embossing with micro electrical discharge machining mold

This study develops an improved method for generating aluminum mold inserts used in the replication of polymer‐based microfluidic chip. Since molding masters that are suitable for microfluidic chip replication must have features whose dimensions are of the order of tens to hundreds of microns, micro electrical discharge machining is employed herein to fabricate an aluminum mold insert of a microfluidic chip. The width and depth of the aluminum mold insert for the microfluidic chip are 61.50 and 49.61 µm, respectively. The surface roughness values of the microchannel and the sample reservoir in aluminum mold insert for the microfluidic chip are 53.9 and 34.3 nm, respectively. PMMA material is adopted as the molded microfluidic chip that is produced by micro‐hot embossing molding. The PMMA material can replicate the microchannel and sample reservoir very well when the aluminum mold insert is used in micro‐hot embossing molding. The results indicate that the most important parameter in the replication of molded microfluidic chip is the embossing pressure, which is also the most important parameter in determining the surface roughness of the molded microfluidic chip. Copyright © 2010 John Wiley & Sons, Ltd.     

A facile approach for the delivery of inorganic nanoparticles into the brain by passing through the blood-brain barrier (BBB)

This study provides an easy and simple method to obtain inorganic nanoparticles that can penetrate the blood-brain barrier, the heavily guarded system in the brain, via cross-linked serum albumin surface coatings. Their intact BBB permeability was confirmed in both in vitro and in vivo tests.     

Macroporous polymer thin film prepared from temporarily stabilized water-in-oil emulsion

We report a simple and convenient method for fabricating ordered porous structure in a polymeric thin film. A temporarily stabilized water-in-oil emulsion, where aqueous droplets were dispersed in the medium of polymer-organic solvent solution, was utilized for the preparation of porous structure. The water-in-oil emulsion was simply prepared by sonicating the mixture of water and polymer-organic solvent solution without any colloid stabilizer. The growth of aqueous droplets was profoundly retarded by dissolving a small amount of sucrose, selectively soluble in the dispersed phase. The prepared emulsion was recovered onto a substrate through dip-coating and subsequently air-dried to get a well-ordered porous polymer film. The polymer content in the polymer solution phase and the compositional ratio of the aqueous phase to the polymer solution phase was optimized to fabricate well-ordered structures.     

Competitive consecutive electron transfer in determination of ionization potentials: ketene derivatives

Kinetics of competitive consecutive electron transfer was used to determine ionization potentials of transient species. Kinetics of two-stage electron transfer reactions in aprotic solvent was studied using 355 nm laser flash photolysis. The concentrations of transients produced by the laser flash photolysis were monitored by their light absorption. Triplet-excited tetrachloro-p-benzo-quinone (p-chloranil) generated by a 355 nm laser flash oxidized diethyl ketene, diphenyl ketene, or phenyl ethyl ketene to form radical cations. The ketene radical cations, in turn, oxidized tertiary amine, forming ground state ketene and ammonium radical cation. The kinetics of the disappearance of ketene radical cations (and/or appearance of ammonium radical cations) due to consecutive, competitive electron transfer to ketene and p-chloranil radical cations was monitored. By monitoring kinetics in the presence of tertiary amines with different oxidation potentials, it was established that in acetonitrile the oxidation potential of diethyl ketene was 5.4 eV; for phenyl ethyl ketene, it was approximately 4.8 eV; and for diphenyl ketene, it was 4.6 eV. The results were in agreement with the oxidation potentials of ketenes computed using published data.