Quantum Nondemolition Measurements of a Particle in an Inhomogeneous Gravitational Field

In this work we obtain a family of quantum nondemolition variables for the case of a particle moving in an inhomogeneous gravitational field. Afterwards, we calculate the corresponding propagator, and deduce the probabilities associated with the possible measurement outputs. The comparison, with the case in which the position is being monitored, will allow us to find the differences with respect to the case of a quantum demolition measuring process.     

Spectroscopy study of air plasma induced by IR CO2 laser pulses

A spectroscopic study of ambient air plasma, initially at room temperature and pressures ranging from 32 to 101 kPa, produced by high-power transverse excitation atmospheric (TEA) CO₂ laser (λ=9.621 and 10.591 μm; τ _FWHM≈64 ns; power densities ranging from 0.29 to 6.31 GW cm⁻²) has been carried out in an attempt to clarify the processes involved in laser-induced breakdown (LIB) air plasma. The strong emission observed in the plasma region is mainly due to electronic relaxation of excited N, O and ionic fragments N⁺. The medium-weak emission is due to excited species O⁺, N²⁺, O²⁺, C, C⁺, C²⁺, H, Ar and molecular band systems of N ₂⁺(_{2}^{+}( B ²\varSigma _u⁺^{2}\varSigma _{\mathrm{u}}^{+} –X ²\varSigma _g⁺)^{2}\varSigma _{\mathrm{g}}^{+}) , N₂(C³ Π _u–B³ Π _g), N ₂⁺(_{2}^{+}( D² Π _g–A² Π _u) and OH(A² Σ ⁺–X² Π). Excitation temperatures of 23400±700 K and 26600±1400 K were estimated by means of N⁺ and O⁺ ionic lines, respectively. Electron number densities of the order of (0.5–2.4)×10¹⁷ cm⁻³ and (0.6–7.5)×10¹⁷ cm⁻³ were deduced from the Stark broadening of several ionic N⁺ and O⁺ lines, respectively. Estimates of vibrational and rotational temperatures of N ₂⁺_{2}^{+} electronically excited species are reported. The characteristics of the spectral emission intensities from different species have been investigated as functions of the air pressure and laser irradiance. Optical breakdown threshold intensities in air at 10.591 μm have been measured.     

Laser induced breakdown spectroscopy of germane plasma induced by IR CO2 pulsed laser

Laser-induced breakdown spectroscopy (LIBS) in germane (GeH₄), initially at room temperature and pressures ranging from 2 to 10 kPa, was studied using a high-power transverse excitation atmospheric (TEA) CO₂ laser (λ=10.653 μm, τ _FWHM=64 ns and power densities ranging from 0.28 to 5.52 GW cm⁻²). The strong emission spectrum of the generated plasma is mainly due to electronic relaxation of excited Ge, H and ionic fragments Ge⁺, Ge²⁺ and Ge³⁺. The weak emission is due to molecular bands of H₂. Excitation temperatures of 8100±300 K and 23,500±2500 K were estimated by Ge atomic and Ge⁺ singly ionized lines, respectively. Electron number densities of the order of (0.7–6.2)×10¹⁷ cm⁻³ were deduced from the Stark broadening of several atomic Ge lines. The characteristics of the spectral emission intensities from different species have been investigated as functions of the germane pressure and laser irradiance. Optical breakdown threshold intensities in germane at 10.653 μm have been determined. The mechanism of initiation of the laser-induced plasma in germane has been analyzed.     

Thermal decomposition of the [Pt(NH3)4]2+ complex in nax zeolite: effect of calcination procedure

The effect of the calcination procedure on the decomposition of the [Pt(NH₃)₄]²⁺ complex in a NaX zeolite was studied by mass spectrometry (MS-TPDE) and diffuse reflectance spectroscopy (DRS). The decomposition of the complex took place in two steps. In the first step, under oxygen, the [Pt(NH₃)₄]²⁺ complex was first converted to [Pt(NH₃)₂]²⁺ complex, accompanied by nitrogen release. In the second step, corresponding to the decomposition of the remaining two amine ligands, NO formation was also observed. Under He, the decomposition also occurred in two steps with H₂ liberation. A reaction scheme was proposed for these results.     

Anodic electrodeposition of NiTSPP from aqueous basic media

The oxidative electrodeposition of NiTSPP (tetrakis(4-sulfonatophenyl) Ni porphyrin) on ITO electrode from 0.1 M NaOH aqueous solution has been studied, and UV-visible and reflection FTIR spectroscopies have been used to analyze the composition of such film. By use of UV-vis spectroscopy, small absorbance of the film and an almost nulling effect on the Soret band of the porphyrin along the Ni(III)/Ni(II) redox process were observed. The reflection FTIR spectroscopy detected the presence of Ni-OH groups in the reduced film and as well the state of the porphyrin molecules as radical cation. Moreover, the porphyrin has been quantified by means of the area of the vibration bands assigned to the sulfonate groups by using as reference a Langmuir-Blodgett film containing a known surface concentration of NiTSPP. These results lead us propose the formation of a conductor salt by electrocrystallization, with stoichiometries TSPP/Ni(II)(OH)2 and TSPP/Ni(III)OOH, for its reduced and oxidized forms, respectively. In these two forms, the porphyrin rings will be present as radical cation, which may be stabilized through its dimerization or polymerization.