Systematical changes in diffraction efficiencies through Ag-photodoping into amorphous GeSe thin films

It is well known that the phenomenon of Ag-photodoping into amorphous (a-) chalcogenide film depends on film thickness (d). Herein, we report that the effects of Ag-photodoping into a-GeSe thin films exhibit a systematical change dependent on d using a holographic exposure (HeCd laser) and the measurement of diffraction efficiency (η) in real time. The η-kinetics of Ag-photodoping in the sample structure of an a-GeSe/Ag/p-type Si substrate is divided into two steps. A photodarkening-dominant process related to the generation of valence-alternation pairs (VAPs) in the chalcogenide explains the first step while a doping-dominant process accounts for the second step. In particular, we confirmed that the d-dependencies of the η-kinetics are classified into 3 groups: (A) d < 2d_P; (B) 2d_P ? d < 4d_P; (C) d > 4d_P, where d_P indicates the penetration depth of the HeCd laser. In group A, the Ag-doping process occurs simultaneously with the darkening process. In group C, the η-kinetics results from the darkening process only. Contrarily, in group B, the η-kinetics exhibits a sharp distinction between the photodarkening process and the Ag-doping process, and in particular, η_M increases almost linearly with an increase in d.     

Solid phase synthesis of benzamidine and butylamine-derived hydantoin libraries

We have constructed a number of benzamidine- and butylamine-based hydantoin compounds by means of an efficient route using solid phase synthesis in which neat diisopropylamine was employed for a novel cyclization/traceless cleavage step. All library compounds were obtained in excellent yield and high purity. This revised version was published online in August 2006 with corrections to the Cover Date.     

Effective method for preparation of oxide-free Ge2Sb2Te5 surface: An X-ray photoelectron spectroscopy study

Cleaning the surfaces of the as-deposited Ge₂Sb₂Te₅ was studied by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and X-ray diffraction (XRD). The mixed native oxides on the as-deposited Ge₂Sb₂Te₅ surface can be easily removed by dipping Ge₂Sb₂Te₅ in de-ionized water for 1 min, while the surface morphology remains unchanged after cleaning. Native oxides only re-grow after exposure to air for more than 4 min. Although dipping in water leads to a surface layer deficient in Ge and Sb, the surface composition of Ge₂Sb₂Te₅ can recover to its stoichiometric value after annealing at 200 °C in vacuum. The phase remains amorphous at room temperature after dipping in water, and changes to fcc and hcp after annealing at 100 and 220 °C, respectively.     

Effectively controlled microfluidic trap for spatiotemporal analysis of the electrotaxis of Caenorhabditis elegans

C. elegans is a popular model organism with a well‐developed neural network. Approximately 60% of the genes in C. elegans have genomic counterparts in humans, including those involved in building neural circuits. Therefore, we can extend the study of human neural network mechanisms to C. elegans which is easy to genetically manipulate. C. elegans shows behavioural responses to various external physical and chemical stimuli. Electrotaxis is one of its distinct behavioural responses, which is defined as movement towards the cathode in an electric field. In this study, we developed an effective microfluidic trap system for analysing electrotaxis in C. elegans. In addition, two mutant strains (unc‐54(s74) and unc‐6(e78)) from wild‐type (N2) worms were screened using the system. Wild‐type (N2) worms and the two mutant strains clearly showed different behavioural responses to the applied electric field, thus enabling the effective screening of the mutant worms from the wild type (N2). This microfluidic system can be utilized as a platform for the study of behavioural responses, and for the sorting and mutant screening of C. elegans.     

Tm:Ho co-doped single mode optical fibre laser pumped by a 1600 nm Er fibre laser

An all-fibre Tm:Ho laser system is reported, using a 1600 nm Er fibre pump laser and 0.3 m length of the fibre through a two-stage optimization of both the pump source and laser configuration to achieve a low threshold operation. As a result a low threshold power of 33 mW and a slope efficiency of 0.6% have been achieved, in laser operation at a wavelength of 1870 nm and a cross-comparison with 785 nm laser diode pumping has been made.     

Concurrent correction of geometric distortion and motion using the map-slice-to-volume method in echo-planar imaging

The accuracy of measuring voxel intensity changes between stimulus and rest images in fMRI echo-planar imaging (EPI) data is severely degraded in the presence of head motion. In addition, EPI is sensitive to susceptibility-induced geometric distortions. Head motion causes image shifts and associated field map changes that induce different geometric distortion at different time points. Conventionally, geometric distortion is "corrected" with a static field map independently of image registration. That approach ignores all field map changes induced by head motion. This work evaluates the improved motion correction capability of mapping slice to volume with concurrent iterative field corrected reconstruction using updated field maps derived from an initial static field map that has been spatially transformed and resampled. It accounts for motion-induced field map changes for translational and in-plane rotation motion. The results from simulated EPI time series data, in which motion, image intensity and activation ground truths are available, show improved accuracy in image registration, field corrected image reconstruction and activation detection.     

Recent advances in understanding mechanisms for the electrochemical reduction of carbon dioxide

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Hydrophobic‐Force‐Driven Removal of Organic Compounds from Water by Reduced Graphene Oxides Generated in Agarose Hydrogels

Hydrophobic reduced graphene oxides (rGOs) were generated in agarose hydrogel beads (AgarBs) by NaBH₄ reduction of graphene oxides (GOs) initially loaded in the AgarBs. The resulting rGO‐loaded AgarBs were able to effectively adsorb organic compounds in water as a result of the attractive hydrophobic force between the rGOs in the AgarBs and the organic compounds dissolved in aqueous media. The adsorption capacity of the rGOs was fairly high even toward reasonably water‐soluble organic compounds such as rhodamine B (321.7 mg g^?1) and aspirin (196.4 mg g^?1). Yet they exhibited salinity‐enhanced adsorption capacity and preferential adsorption of organic compounds with lower solubility in water. Such peculiar adsorption behavior highlights the exciting possibility for adopting an adsorption strategy, driven by hydrophobic forces, in practical wastewater treatment processes.     

Towards chemical analysis of nanostructures in biofilms II: tip-enhanced Raman spectroscopy of alginates

This study examines the feasibility of using tip-enhanced Raman spectroscopy (TERS) for label-free chemical characterization of nanostructures in biological systems. For this purpose, a well-defined model system consisting of calcium alginate fibers is studied. In a companion paper, calcium alginate fibers and their network structures were shown to be a good model for the extracellular polysaccharides of biofilms at the nanoscale. TERS analysis of biological macromolecules, such as alginates, is complicated by heterogeneity in their sequence, molecular weight, and conformations, their small Raman cross-section, and the large number of functional groups, which can chemically interact with the silver surface of the tip and cause significant band shifts. Due to these effects, Raman frequencies in TERS spectra of biopolymers do not necessarily resemble band positions in the normal Raman spectrum of the bulk material, as is the case for less complex samples (e.g., dye molecules) studied so far. Additionally, analyte decomposition due to laser heating can have a significant influence, and carbon contamination signals can sometimes even overwhelm the weak analyte signals. Based on the investigation of alginates, strategies for spectra correction, choice of appropriate reference samples, and data interpretation are presented. With this approach, characteristic frequency ranges and specific marker bands can be found for biological macromolecules that can be employed for their identification in complex environments. Figure TERS spectrum of a calcium alginate fiber bundle