Photon‐Pair Generation with a 100 nm Thick Carbon Nanotube Film

Nonlinear optics based on bulk materials is the current technique of choice for quantum‐state generation and information processing. Scaling of nonlinear optical quantum devices is of significant interest to enable quantum devices with high performance. However, it is challenging to scale the nonlinear optical devices down to the nanoscale dimension due to relatively small nonlinear optical response of traditional bulk materials. Here, correlated photon pairs are generated in the nanometer scale using a nonlinear optical device for the first time. The approach uses spontaneous four‐wave mixing in a carbon nanotube film with extremely large Kerr‐nonlinearity (≈100 000 times larger than that of the widely used silica), which is achieved through careful control of the tube diameter during the carbon nanotube growth. Photon pairs with a coincidence to accidental ratio of 18 at the telecom wavelength of 1.5 µm are generated at room temperature in a ≈100 nm thick carbon nanotube film device, i.e., 1000 times thinner than the smallest existing devices. These results are promising for future integrated nonlinear quantum devices (e.g., quantum emission and processing devices).     

Quantification of metabolites from single-voxelin vivo 1H NMR data of normal human brain by means of time-domain data analysis

We present here a combination of time-domain signal analysis procedures for quantification of human brainin vivo ¹H NMR spectroscopy (MRS) data. The method is based on a separate removal of a residual water resonance followed by a frequency-selective time-domain line-shape fitting analysis of metabolite signals. Calculation of absolute metabolite concentrations was based on the internal water concentration as a reference. The estimated average metabolite concentrations acquired from six regions of normal human brain with a single-voxel spin-echo technique for theN-acetylaspartate, creatine, and choline-containing compounds were 11.4±1.0,6.5±0.5, and 1.7±0.2 mmol kg^–1 wet weight, respectively. The time-domain analyses ofin vivo ¹H MRS data from different brain regions with their specific characteristics demonstrate a case in which the use of frequency-domain methods pose serious difficulties.     

Fullerene‐based ruthenium catalysts in cinnamaldehyde hydrogenation

Ruthenium on fullerenes and ruthenium and palladium on activated carbon were compared for their catalytic activity and selectivity in cinnamaldehyde hydrogenation. The fullerene support had a marked effect on the selectivity, even though the fullerenes themselves showed no catalytic activity. This revised version was published online in July 2006 with corrections to the Cover Date.     

Detection of copper in water using on-line plasma-excited atomic absorption spectroscopy (AAS)

A measurement method and apparatus was developed to measure continuously toxic metal compounds in industrial water samples. The method was demonstrated by using copper as a sample metal. Water was injected into the sample line and subsequently into a nitrogen plasma jet, in which the samples comprising the metal compound dissolved in water were decomposed. The transmitted monochromatic light was detected and the absorbance caused by copper atoms was measured. The absorbance and metal concentration were used to calculate sensitivity and detection limits for the studied metal. The sensitivity, limit of detection, and quantification for copper were 0.45 ± 0.02, 0.25 ± 0.01, and 0.85 ± 0.04 ppm, respectively.     

Synthesis of graphene nanoribbons encapsulated in single-walled carbon nanotubes

A novel material, graphene nanoribbons encapsulated in single-walled carbon nanotubes (GNR@SWNT), was synthesized using confined polymerization and fusion of polycyclic aromatic hydrocarbon (PAH) molecules. Formation of the GNR is possible due to confinement effects provided by the one-dimensional space inside nanotubes, which helps to align coronene or perylene molecules edge to edge to achieve dimerization and oligomerization of the molecules into long nanoribbons. Almost 100% filling of SWNT with GNR is achieved while nanoribbon length is limited only by the length of the encapsulating nanotube. The PAH fusion reaction provides a very simple and easily scalable method to synthesize GNR@SWNT in macroscopic amounts. First-principle simulations indicate that encapsulation of the GNRs is energetically favorable and that the electronic structure of the encapsulated GNRs is the same as for the free-standing ones, pointing to possible applications of the GNR@SWNT structures in photonics and nanoelectronics.     

Clinical picture of community-acquired Chlamydia pneumoniae pneumonia requiring hospital treatment: a comparison between chlamydial and pneumococcal pneumonia

AIM: To assess potencies of tetrahydroprotoberberines (THPB) and hydrobenzyltetrahydroisoquinolines (HBTI) on DA receptors. METHODS: The receptor binding assay with calf striatum to D1 and D2 receptors, and the animal behavior tests were used. RESULTS: (+/-) 12-Chloroscoulerine (CSL) was the most potent one among the THPB and HBTI. The affinities of CSL to D1 and D2 receptors were 13 and 51 nmol.L-1, respectively. In rats, CSL showed an antagonistic effect on the stereotypy and induced catalepsy. In the 6-OHDA lesioned rats, however, CSL exerted the agonistic effect to DA receptors. CONCLUSION: CSL had dual actions to DA receptors and its effects were similar to that of (-)stepholidine.     

Fourier transform infrared measurement of solid-, liquid-, and gas-phase samples with a single photoacoustic cell

A photoacoustic detector based on the optical cantilever microphone has been built. The detector is capable of measuring solid-, liquid-, and gas-phase samples. Photoacoustic Fourier transform infrared (FT-IR) measurement with three samples in different phases was demonstrated. Example samples were polyethene, sunflower oil, and methane. The sensitivity of the cell was compared to a commercial photoacoustic FT-IR detector. With the standard carbon black sample the cantilever detector gave approximately five times higher signal-to-noise ratio than the reference detector. The sensitivity with methane was also compared to the DTGS detector of the FT-IR instrument corresponding to an absorption path of 6.3 cm. Simulation of the photoacoustic signal showed that a compromise has to be made in the cell design between sensitivity for solid- and gas-phase samples but it is possible to highly enhance the sensitivity for all types of samples by reducing cantilever dimensions.     

Organic memory using [6,6]-phenyl-C(61) butyric acid methyl ester: morphology, thickness and concentration dependence studies

We report a simple memory device in which the fullerene-derivative [6,6]-phenyl-C(61) butyric acid methyl ester (PCBM) mixed with inert polystyrene (PS) matrix is sandwiched between two aluminum (Al) electrodes. Transmission electron microscopy (TEM) images of PCBM:PS films showed well controlled morphology without forming any aggregates at low weight percentages (<10?wt%) of PCBM in PS. Energy dispersive x-ray spectroscopy (EDX) analysis of the device cross-sections indicated that the thermal evaporation of the Al electrodes did not lead to the inclusion of Al metal nanoparticles into the active PCBM:PS film. Above a threshold voltage of <3?V, independent of thickness, a consistent negative differential resistance (NDR) is observed in devices in the thickness range from 200 to 350?nm made from solutions with 4-10?wt% of PCBM in PS. We found that the threshold voltage (V(th)) for switching from the high-impedance state to the low-impedance state, the voltage at maximum current density (V(max)) and the voltage at minimum current density (V(min)) in the NDR regime are constant within this thickness range. The current density ratio at V(max) and V(min) is more than or equal to 10, increasing with thickness. Furthermore, the current density is exponentially dependent on the longest tunneling jump between two PCBM molecules, suggesting a tunneling mechanism between individual PCBM molecules. This is further supported with temperature independent NDR down to 240?K.     

Kinematic Coagulation of Charged Droplets in an Alternating Electric Field

An analytic-numerical model has been developed to study kinematic coagulation caused by the vibrational motion of charged particles in an alternating electric field. The primary aim of this study was to find out the reduction in the number concentration of fine particles of diameter 0.1 μm-1.0 μm caused by collisions with larger, supermicron particles. Three cases are considered: (1) unipolar charging, (2) fine particles are neutral, and (3) fine particles and large particles have opposite polarity. We find out that in cases 1 and 2 the rate of kinematic coagulation in negligible and in case 3 significant. The results are demonstrated with two sample calculations with total mass loadings of 2 and 20 g/m³. In the former, where the mass median diameter is 3.0 μm, we discover a 20%-50% reduction in number concentration of particles in the range 0.5–1.0 μm and less significant reduction in smaller particles. The latter (MMD = 6.0 μm) represents power plant conditions. In this case the reduction varies from 10% (0.1 μm) to 95% (1.0 μm).