Light-induced changes in the solar cell parameters and temperature coefficient of n-C/p-Si heterojunction solar cell

Amorphous carbon (a-C) is a potential material for the development of low-cost and high-efficiency solar cell. We report the study of the influence of light soaking up to 100 h on n-C/p-Si heterojunction solar cell. It is observed that the deterioration in the fill factor and the efficiency are significantly smaller as compared to that observed in a-Si:H solar cell. Variations in the temperature coefficients of the I–V characteristics subjected to light degradation and recovery has also been investigated. A good correlation between change in the temperature coefficient and the degradation/recovery state of cell's conversion efficiency has been observed.     

Synthesis of nitrogen incorporated diamond-like carbon thin films using microwave surface-wave plasma CVD

Nitrogenated diamond-like (DLC:N) carbon thin films have been deposited by microwave surface wave plasma chemical vapor deposition on silicon and quartz substrates, using argon gas, camphor dissolved in ethyl alcohol composition and nitrogen as plasma source. The deposited DLC:N films were characterized for their chemical, optical, structural and electrical properties through X-ray photoelectron spectroscopy, UV/VIS/NIR spectroscopy, Raman spectroscopy, atomic force microscope and current–voltage characteristics. Optical band gap decreased (2.7 to 2.4 eV) with increasing Ar gas flow rate. The photovoltaic measurements of DLC:N / p-Si structure show that the open-circuit voltage (V_oc) of 168.8 mV and a short-circuit current density (J_sc) of 8.4 μA/cm² under light illumination (AM 1.5 100 mW/cm²). The energy conversion efficiency and fill factor were found to be 3.4 × 10^{− 4}% and 0.238 respectively.     

First-principles calculation of phase equilibria and phase separation of the Fe-Ni alloy system

Theoretical investigation of the phase equilibria of the Fe-Ni alloy has been performed by combining the FLAPW total energy calculations and the Cluster Variation Method through the Cluster Expansion Method. The calculations have proved the stabilization of the LIE phase at 1：3 stoichiometry, which is in agreement with the experimental result, and predicted the existence of L1 0 as a stable phase below 550 K; this L1 0 phase has been missing in the conventional phase diagram. The calculations are extended to the Fe-rich region that is characterized by a wide range phase separation and has drawn considerable attention because of the intriguing Invar property associated with a Fe concentration of 65%. To reveal the origin of the phase separation, a P-V curve in an entire concentration range is derived by the second derivative of free energy functional of the disordered phase with respect to the volume. The calculation confirmed that the phase separation is caused by the breakdown of the mechanical-stability criterion. The newly calculated phase separation line combined with the L1 0 and L12Eorder-disordered phase boundaries provides phase equilibria in the wider concentration range of the system. Furthermore, a coefficient of thermal expansion （CTE） is attempted by incorporating the thermal vibration effect through harmonic approximation of the Debye-Gruneisen model. The Invar behavior has been reproduced, and the origin of this anomalous volume change has been discussed.     

Study of the combined use of ground probing radar and electric profiling in soil exploration

Bulletin of Engineering Geology and the Environment - To explore the shallow structure of the ground, the combined use of ground probing radar and electric profiling was tested. As a result, it is...     

Thermal conductivity and phonon scattering mechanisms in La#x2212;x#x2212;x#x2212;xMxCuO4

The thermal conductivity of high density La_2–xM_xCuO₄ (M=Ba, Sr) sintered materials was measured between 15K and 150K for the various concentrations of Ba and the phonon thermal conductivity was analyzed comparing with that of Nd_2–xCe_xCuO₄. The pretty large value for pure La₂CuO₄ was drastically diminished by substituting La by a small amount of Ba atoms especially at low temperatures. It was found that a new type of the phonon scattering center such as a two-level tunneling must be taken account of in order to explain the observed reduction.     

Resonance Effect on the Tunneling Reaction: H+H2→H2+H in Solid Hydrogen

The tunneling abstraction reaction: H+H₂H₂+H in -irradiated solid hydrogen has been studied using electron spin resonance (ESR) and electron-nuclear double resonance (ENDOR) spectroscopy and gas-chromatography. The rate constant for the tunneling reaction in solid hydrogen was found to decrease with the increase in the concentration of ortho-H₂ molecules in solid hydrogen. We concluded that the decrease in the rate constant is due to the energy level mismatching between reactant species of H+H₂ trapped and product species of H₂+H trapped in the reverse induced by inhomogeneous intermolecular interactions between ortho-H² molecules in solid hydrogen. This result indicates that resonance effects play an important role in tunneling reactions in solids.     

Investigation of the voltage life of mica-alumina composite insulation at high temperatures

Experiments and investigations were carried out on the voltage life of a bar-coil model with a nickel-plated copper conductor covered with mica-alumina composite insulation at a temperature range of 550–850 °C. Diffusion of copper into the insulation layer was observed on the specimens aged for a long period. Insulation with mica paper gave faster diffusion speed and shorter voltage life than insulation with mica flake. The diffusion speed became higher with an increase in temperature. The ac current gradually increased with aging time and increased rapidly just before breakdown. There was the relationship I = aEⁿ (a, n: constants) between ac current I and applied stress E, and n was approximately equal to 1 in the region where thermal unbalance did not occur. Arrhenius's law held in the relationship between ac current and aging time. Therefore, the breakdown mechanism might be that the effective insulation thickness decreased due to copper diffusion into the insulation layer and the ac current increased gradually until thermal breakdown in the last stage. If copper diffuses into the insulation layer, even with no voltage application, the aging time required to decrease the breakdown voltage to a certain level (the voltage life) obeys Arrhenius's law. If the voltage life is dominated by diffusion into the insulation layer, the activation energy for voltage life in the aging test becomes twice that for diffusion, both with and without voltage application. © 1999 Scripta Technica, Electr Eng Jpn, 129(4): 24–31, 1999     

Influence of tungsten–carbon mixed layer and irradiation defects on deuterium retention behavior in tungsten

The D₂⁺ fluence dependence on deuterium (D) retention was studied to clarify the D retention mechanism in tungsten. The additional D desorption stage was observed around 660 K in the TDS spectrum for a sample implanted with D₂⁺ up to the fluence of 10²³ D⁺ m^?2, which desorption stage was not observed the D₂⁺ implanted sample with the fluence less than 10²² D⁺ m^?2. The TEM observation showed that the highly dense voids were formed in tungsten by D₂⁺ implantation with the fluence of 10²³ D⁺ m^?2, considering that the D would be trapped by voids. To understand the D trapping by voids in C⁺ implanted tungsten, C⁺–D₂⁺ sequential implantation experiments at various C⁺ implantation temperatures were performed. It was found that the amount of D desorbed around 560 K was increased by increasing the C⁺ implantation temperature. The formation of the voids was observed with increasing the C⁺ implantation temperature by TEM, indicating that the increase of D desorption around 560 K was caused by the formation of voids. However, the desorption temperature of D trapped by voids in C⁺ implanted sample was lower than that in D₂⁺ implanted one. TEM observation and XPS measurement indicated that this difference was caused by the increase of void size and/or the presence of implanted carbon.     

Synthesis of iron nanoparticle: Challenge to determine the limit of hydrogen reduction in supercritical water

Supercritical hydrothermal syntheses of metal nanoparticles were investigated. Organic metal salt and hydrogen gas produced by water catalyzed decomposition of formic acid was employed as metal sources and reduction agent, respectively. The formation of iron was verified by measuring the magnetic property of the products by superconducting quantum interference device (SQUID) magnetometer as well as crystallographic analysis by X-ray diffraction (XRD). As predicted by the free energy calculation of reduction of metal oxides by hydrogen molecule, silver, palladium, copper, nickel and cobalt nanoparticles were synthesized without using surface modifier, whereas, iron could be synthesized at small yield. The main product was iron oxides (mainly magnetite). In order to increase the yield of iron, hexanoic acid was employed as an in situ surface modifier of the synthesis. The surface modification lessened the size of the synthesized nanoparticles and increased the yield of iron. The optimum condition for iron synthesis was also investigated, as a result, 7.6% yield of iron was achieved.