Влияние параллельного слоям магнитного поля на фототок в GaAs/AlAs p-i-n-структурах

The behavior of the photocurrent in GaAs / AlAs p-i-n heterostructures is studied in a magnetic field parallel to the heterolayers in the wavelength range from 395 to 650 nm. A strong dependence of the non-oscillating component of the photocurrent on the radiation wavelength associated with the suppression of the diffusion current by the magnetic field was found. It is shown that the behavior of the oscillating component of the photocurrent in a magnetic field does not depend on the wavelength of light and is determined by the transfer of electrons through the dimensional quantization level in a triangular near-barrier well. It is shown that the suppression of the oscillating component by the magnetic field is due to the smearing of the level in the triangular well due to the motion of electrons parallel to the walls of the well and perpendicular to the magnetic field.

The Thermodynamic and pH Metric Binding Studies of Cu+2 Ions with Egg Protein by Spectrometric and Diffusion Current Techniques

Transition metals have unique efficacy in catalyzing various industrial reactions and also in living system, the redox reaction and redox changes in the metal ions catalyzed valence changes in the substrate molecule. The survey of the existing literature revealed that the binding of Molybdenum, Vanadium, Zinc, Cadmium, Copper, Nickel and Cobalt with the protein is well known but no binding studies of copper metal with egg protein are reported. With a view to extend the existing knowledge of ecological nature of metal-protein system, it was thought of interest to investigate the properties of metal-protein mixture. Investigations on the aspects of these binding problems were planned and their bindings constants have been determined using suitable physico-chemical methods. The pH metric, diffusion current measurements, spectrophotometric methods have been used on the binding of copper ions with albumin. The effect of physico-chemical factors on interaction between divalent metal ion i.e. copper with albumin has been discussed. On the basis of observed results, it is found that the binding data were dependent on pH and temperature. From scatchard plots, the intrinsic association constants (k) and the number of binding sites (n) were calculated and found high at lower pH and temperatures. Therefore, a lower temperature and lower pH offered more sites in the protein molecule for interaction with copper (II) ions. The enthalpy (ΔH), entropy (ΔS) changes, free energy change (ΔG°) have been calculated.

Copper deposits obtained by pulsating overpotential regime with a long pause and pulse duration from sulfated solutions

The morphologies of the copper deposits obtained by pulsating overpotential regime with prolonged pulse and pause durations from the solution of 0.15 M CuSO4 in 0.50 M H2SO4 at overpotentials lower, higher and belonging to the plateau of limiting diffusion current density were compared with those obtained by the same electrodeposition regime from solutions of 0.075 and 0.30 M CuSO4 in 0.50 M H2SO4 and 0.15 M CuSO4 in 0.25 and 1.00 M H2SO4 at overpotentials outside the plateau of limiting diffusion current density. These samples were characterized by scanning electron microscopic (SEM) analysis and the cathodic polarization characteristics from solutions compared. Increasing the Cu(II) concentration led to an increase in the limiting diffusion current density. Decreasing the H2SO4 concentration shifts both beginning and the end of the plateau of the limiting diffusion current density towards higher electrodeposition overpotentials. Also, electrodeposition in solutions of 0.15 M CuSO4 in 0.25 and 1.00 M H2SO4 led to the formation of morphological forms of copper deposits characteristic for electrodeposition of copper from higher CuSO4 or lower H2SO4 in solution at some higher overpotentials.

Relationship between cathodic protection current and limit diffusion current as an additional criteria of cathodic protection

The influence of the temperature and oxygen concentration in NS4 solution on the electrochemical characteristics of X70 steel for pipelines and the relationship of cathodic protection current density to limiting diffusion current density, in the normalized DSTU 4219 range of protective polarization potentials from -0.75 V to -1.05 V (сh.s.е.) were investigated. It has been established that with increasing of the temperature from 20 to 80 °C, the corrosion activity of X70 steel increases, which is confirmed by more negative values of corrosion potential and an increasing of the corrosion rate, and indicates on the prevailing effect of temperature on the corrosion process compared to the effect of oxygen concentration. In the temperature range considered, the limiting diffusion current has a maximum value at 40 °C and decreases with increasing of temperature, correlating with a decreasing of the oxygen concentration. Under conditions of free oxygen access to the NS4 solution in the normalized DSTU 4219 range of protective polarization potentials, the ratio of cathodic protection to limiting diffusion current varies from 0.4 to 1.3 at temperatures (20-40) oС, at temperatures (60-80) oC the ratio is less than 1. Under conditions of limited oxygen access, the ratio increases from 1.1 to 4.7. Using calculated and experimental results, it was shown that, at various values of relationship , conditions for excessive hydrogen evolution can be created, which represents a threat to the safe operation of the pipeline over time. Data on the ratio values should be taken into account when analyzing the protection state of pipelines.