Graphitic Patterns on CVD Diamond Plate as Microheating/Thermometer Devices.

A simple compact temperature sensor and microheater in a wide temperature range has been developed, realizing a laser-patterned resistive structure on the surface of a synthetic polycrystalline diamond plate. Imaging and spectroscopy techniques used to investigate morphology, structure, and composition of the pattern showed that it incorporates different nondiamond carbon phases. Transport experiments revealed the semiconducting behavior of this microresistor. Thermal power measurements versus temperature are presented. A possible application of this device that may easily match compact experimental layouts avoiding both thermal anchoring offset and mechanical stress between sample and sensor is discussed. The patterned structure undergoes testing as a microthermometer, providing fast response and excellent stability versus time. It exhibits a good sensitivity that coupled to an easy calibration procedure minimizes errors and guarantees high accuracy. Plot of temperature versus input power of the resistive patterned line used as microheater shows a linear behavior in an extended temperature range.

Interaction of a long alkyl chain protic ionic liquid and water.

A combined experimental/theoretical approach has been used to investigate the role of water in modifying the microscopic interactions characterizing the optical response of 1-butyl-ammonium nitrate (BAN) water solutions. Raman spectra, dominated by the signal from the protic ionic liquid, were collected as a function of the water content, and the corresponding spatial organization of the ionic couples, as well as their local arrangement with water molecules, was studied exploiting classical molecular dynamics calculations. High quality spectroscopic data, combined with a careful analysis, revealed that water affects the vibrational spectrum BAN in solution: as the water concentration is increased, peaks assigned to stretching modes show a frequency hardening together with a shape narrowing, whereas the opposite behavior is observed for peaks assigned to bending modes. Calculation results clearly show a nanometric spatial organization of the ionic couples that is not destroyed on increasing the water content at least within an intermediate range. Our combined results show indeed that small water concentrations even increase the local order. Water molecules are located among ionic couples and are closer to the anion than the cation, as confirmed by the computation of the number of H-bonds which is greater for water-anion than for water-cation. The whole results set thus clarifies the microscopic scenario of the BAN-water interaction and underlines the main role of the extended hydrogen bond network among water molecules and nitrate anions.

E(1)(A) electronic band gap in wurtzite InAs nanowires studied by resonant Raman scattering.

We report on resonant Raman experiments carried out on wurtzite InAs nanowires. Resonant conditions have been obtained by tuning either the excitation energy or the band gap through external high pressure at fixed excitation energy. A complete azimuthal study of the Raman spectra with two laser excitation lines (2.41 and 1.92 eV) has also been performed on a single wire. The measured E2(H) mode resonance indicates that the E1(A) gap is about 2.4 eV, which is considerably reduced with respect to the zinc-blende InAs E1 gap. These findings confirm recent theoretical calculations of crystal phase induced bandstructure modifications.

Pathological biominerals: Raman and infrared studies of bioapatite deposits in human heart valves.

We studied pathological bioapatite from patients undergoing valvular replacement due to severe aortic and mitral stenosis. Three different types of mineralized human cardiac valves were analyzed. We used infrared and Raman spectroscopy to infer the presence of the carbonate group and evaluate the carbonate substitution in bioapatite structure. The Raman spectra showed that the pathological bioapatite is a B-type "carbonate-apatite" (CO(3)(2-) for PO(4)(3-)) similar to the major mineralized products derived from normal biomineralization processes occurring in the human body. Fourier transform infrared spectra (FT-IR) confirmed the B-type carbonate substitution (CO(3)(2-) for PO(4)(3-)) and showed evidence for the partial replacement of [OH] by [CO(3)] (A-type substitution). The carbonate content of the samples inferred by the spectroscopic measurements is in good agreement with the range of values estimated for biological apatite. On the contrary, the crystal size of the pathological apatite estimated using the percentage area of the component at 1059 cm(-1) of the infrared spectrum is in the nanometer range and it is significantly smaller than the crystal size of normal mineralized tissues.