Probes for magnetic force microscopy (MFM) were prepared by pinning iron-filled multiwall carbon nanotubes to conventional scanning force microscopy probes. These nanotube MFM probes reveal a great potential for high spatial resolution of both topography and magnetic stray field. The ends of the high aspect ratio iron nanowires within the nanotubes can be considered as stationary effective magnetic monopole moments which opens the possibility of quantitative stray field measurements in a straightforward manner. The carbon shells around the iron nanowires provide wear resistance and oxidation protection.
Carbon nanotube reinforced copper matrix ͑CNT/Cu͒ nanocomposites were fabricated by the modified molecular-level mixing process, which produces a homogeneous dispersion of CNTs in a fine grained metal matrix. These nanocomposites, consisting of 1.5 m Cu matrix grains and 5 vol % of multiwall CNTs, show a high strengthening capability; enhancing the yield strength of unreinforced Cu by 2.3 times. The enhanced yield strength stems from the reinforcing effect of CNTs and additional hardening of the Cu matrix by grain refinement. The results reveal that the metallurgical treatment of the matrix is important for the development of high-strength CNT/metal nanocomposites.
We report on multi-wavelength arrays of master-oscillator power-amplifier quantum cascade lasers operating at wavelengths between 9.2 and 9.8 μm. All elements of the high-performance array feature longitudinal (spectral) as well as transverse single-mode emission at peak powers between 2.7 and 10 W at room temperature. The performance of two arrays that are based on different seed-section designs is thoroughly studied and compared. High output power and excellent beam quality render the arrays highly suitable for stand-off spectroscopy applications.
YBa 2 Cu 3 O 7 24 • (30 •) bicrystal grain boundary junctions (GBJs), shunted with 60 nm (20 nm) thick Au, were fabricated by focused ion beam milling with widths 80 nm w 7.8 μm. At 4.2 K we find critical current densities j c in the 10 5 A cm −2 range (without a clear dependence on w) and an increase in resistance times junction area ρ n with an approximate scaling ρ n ∝ w 1/2. For the narrowest GBJs j c ρ n = I c R n ≈ 100 μV (with critical current I c and junction resistance R n), which is promising for the realization of sensitive nanoSQUIDs for the detection of small spin systems. We demonstrate that our fabrication process allows the realization of sensitive nanoscale dc SQUIDs; for a SQUID with w ≈ 100 nm wide GBJs we find an rms magnetic flux noise spectral density of S 1/2 ≈ 4 μ 0 Hz −1/2 in the white noise limit. We also derive an expression for the spin sensitivity S 1/2 μ , which depends on S 1/2 , on the location and orientation of the magnetic moment of a magnetic particle to be detected by the SQUID, and on the SQUID geometry. For the unoptimized SQUIDs presented here, we estimate S 1/2 μ = 390 μ B Hz −1/2 , which could be further improved by at least an order of magnitude.
Surface acoustic wave (SAW)-based fluid atomizers are ideally suited to generate micrometer-sized droplets without any moving parts or nozzles. Versatile application fields can be found for instance in biomedical, aerosol or thin film technology, including medical inhalators or particle deposition for advanced surface treatment. Such atomizers also show great potential for on-chip integration and can lead to economic production of hand-held and even disposable devices, with either a single functionality or integrated in more complex superior systems. However, this potential was limited in the past by fluid supply mechanisms inadequate for mass production, accuracy and reliability. In this work, we briefly discuss existing fluid supply methods and demonstrate a straightforward new approach suited for reliable and cost-effective mass-scale manufacturing of SAW atomizer chips. Our approach is based on a fluid supply at the boundary of the acoustic beam via SU-8 microchannels produced by a novel one-layer/double-exposure photolithography method. Using this technique, we demonstrate precise and stable fluid atomization with almost ideal aerosol plume geometry from a dynamically stabilized thin fluid film. Additionally, we demonstrate the possibility of in situ altering the droplet size distribution by controlling the amount of fluid available in the active region of the chip.
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