The effect of light scattering layers (400 nm, TiO_2 particle) of 4 mum thickness on the dye-sensitized solar cell has been investigated with a 12 mum thickness of photo-anode (20 nm, TiO_2 particle). Two different structures of scattering layers (separated and back) were applied to investigate the light transmitting behaviors and solar cell properties. The light transmittance and cell efficiency significantly improved with inserting scattering layers. The back scattering layer structure had more effective transmitting behavior, but separated scattering layer (center: 2 mum, back: 2 mum) structure (9.83% of efficiency) showing higher efficiency (0.6%), short circuit current density (0.26 mA/cm2) and fill factor (0.02). The inserting separating two scattering layers improved the light harvesting, and relatively thin back scattering layer (2 mum of thickness) minimized interruption of ion diffusion in liquid electrolyte.
Ultra-fine TiC/Co composite powder was synthesized by the carbothermal reduction process without wet chemical processing. The starting powder was prepared by milling of titanium dioxide and cobalt oxalate powders followed by subsequent calcination to have a target composition of TiC-15 wt.%Co. The prepared oxide powder was mixed again with carbon black, and this mixture was then heat-treated under flowing argon atmosphere. The changes in the phase, mass and particle size of the mixture during heat treatment were investigated using XRD, TG-DTA and SEM. The synthesized oxide powder after heat treatment at 700°C has a mixed phase of TiO_2 and CoTiO_3 phases. This composite oxide powder was carbothermally reduced to TiC/Co composite powder by the solid carbon. The synthesized TiC/Co composite powder at 1300°C for 9 hours has particle size of under about 0.4 mum.
Fe based (Fe_68.2C_5.9Si_3.5B_6.7P_9.6Cr_2.1Mo_2.0Al_2.0) amorphous powder, which is a composition of iron blast cast slag, were produced by a gas atomization process, and sequently mixed with ductile Cu powder by a mechanical ball milling process. The experiment results show that the as-prepared Fe amorphous powders less than 90 mum in size has a fully amorphous phase and its weight fraction was about 73.7%. The as-atomized amorphous Fe powders had a complete spherical shape with very clean surface. Differential scanning calorimetric results of the as-atomized Fe powders less than 90 mum showed that the glass transition, T_g, onset crystallization, T_x, and super-cooled liquid range DeltaT=T_x-T_g were 512, 548 and 36°C, respectively. Fe amorphous powders were mixed and deformed well with 10 wt.% Cu by using AGO-2 high energy ball mill under 500 rpm.
Fe based (Fe_68.2C_5.9Si_3.5B_6.7P_9.6Cr_2.1Mo_2.0Al_2.0) amorphous powder, which is a composition of iron blast cast slag, were produced by a gas atomization process, and sequently mixed with ductile Cu powder by a mechanical ball milling process. The Fe-based amorphous powders and the Fe-Cu composite powders were compacted by a spark plasma sintering (SPS) process. Densification of the Fe amorphous-Cu composited powders by spark plasma sintering of was occurred through a plastic deformation of the each amorphous powder and Cu phase. The SPS samples milled by AGO-2 under 500 rpm had the best homogeneity of Cu phase and showed the smallest Cu pool size. Micro-Vickers hardness of the as-SPSed specimens was changed with the milling processes.
To produce alloy powders with only Sm_2Fe_17 single phase by reduction-diffusion (R-D) method, the effect of excess samarium oxide on the preparation of Sm-Fe alloy powder during R-D heat treatment was studied. The quantity of samarium oxide was varied from 5% to 50% whereas iron and calcium were taken 0% and 200% in excess of chemical equivalent, respectively. The pellet type mixture of samarium, iron powders and calcium granulars was subjected to heat treatment at 1100°C for 5 hours. The R-D treated pellet was moved into deionized water and agitated to separate Sm-Fe alloy powders. After washing them in deionized water several times, the powders were washed with acetic acid to remove the undesired reaction products such as CaO. By these washing and acid cleaning treatment, only 0.03 wt% calcium remained in Sm-Fe alloy powders. It was also confirmed that the content of unreacted alpha-Fe in Sm_2Fe_17 matrix gradually decreased as the percentage of samarium oxide is increased. However, there was no significant change above 40% excess samarium oxide.
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Ti_50Cu_20Ni_20Al_10 quaternary amorphous alloy was prepared by high-energy ball milling process. A complete amorphization was confirmed for the composition of Ti_50Cu_20Ni_20Al_10 after milling for 30hrs. Differential scanning calorimetry showed a large super-cooled liquid region (DeltaT_x = T_x T_g, T_g and T_x: glass transition and crystallization onset temperatures, respectively) of 80 K. Prepared amorphous powders of Ti_50Cu_20Ni_20Al_10 were consolidated by spark-plasma sintering. Densification behavior and microstructure changes were investigated. Samples sintered at higher temperature of 713 K had a nearly full density. With increasing the sintering temperature, the compressive strength increased to fracture strength of 756 MPa in the case of sintering at 733 K, which showed a 'transparticle' fracture. The samples sintered at above 693 K showed the elongation maximum above 2%.
The amorphization process and the thermal properties of amorphous Ti_40Cu_40Ni_10Al_10 powder during milling by mechanical alloying were examined by X-ray diffractometry (XRD), differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). The chemical composition of the samples was examined by an energy dispersive X-ray spectrometry (EDX) facility attached to the scanning electron microscope (SEM). The as-milled powders showed a broad peak (2theta = 42.4°) with crystalline size of about 5.0 nm in the XRD patterns. The entire milling process could be divided into three different stages: agglomeration (0 < t_m ≤ 3 h), disintegration (3 h < t_m ≤ 20 h), and homogenization (20 h < t_m ≤ 40 h) (t_m: milling time). In the DSC experiment, the peak temperature T_p and crystallization temperature T_x were 466.9°C and 444.3°C, respectively, and the values of T_p, and T_x increased with a heating rate (HR). The activation energies of crystallization for the as-milled powder was 291.5 kJ/mol for T_p.