Back Surface Field (BSF) has been used as one of means to enhance solar cell performance by reducing surface recombination velocity (SRV). One of methods to produce BSF is by introducing highly doped layer on rear surface of the wafer. Depending on the type of the dopant in wafer, the BSF layer could be either p+ or n+. This research aims to compare the performance of BSF layer both in p-type and n-type wafer in order to understand the effect of BSF on both wafer types. Monociystalline silicon wafer with thickness of 300 μm. area of 1 cm2, bulk doping level NB = 1.5×1016/cm3 both for p-type wafer and n-type wafer are used. Both wafer then converted into solar cell by adding emitter layer with concentration NE =7.5×1018/cm3 both for p-type wafer and n-type wafer. Doping profile that is used for emitter layer is following complementary error function (erfc) distribution profile. BSF concentration is varied from 1×1017/cm3 to 1×1020/cm3 for each of the cell. Solar cell performance is tested under standard condition, with AM1.5G spectrum at 1000 W/m2. Its output is measured based on its open circuit voltage (Voc). short circuit current density (JSC), efficiency (η). and fill factor (FF). The result shows that the value of VOC is relatively constant along the range of BSF concentration, which is 0.694 V – 0.702 V. The same pattern is also observed in FF value which is between 0.828 – 0.831. On the other hand, value of JSC and efficiency will drop against the increase of BSF concentration. Highest JSC which is 0.033 A/cm2 and highest efficiency which is 18.6% is achieved when BSF concentration is slightly higher than bulk doping level. The best efficiency can be produced when BSF concentration is around 1×1017cm-3.. This result confirms that surface recombination velocity has been reduced due to the increase in cell’s short circuit current density and its efficiency. In general both p-type and n-type wafer will produce higher efficiency when BSF is applied. However, the increase is larger in p-type wafer than in n-type wafer. Better performance for solar cell is achieved when BSF concentration is slightly higher that bulk doping level because at very high BSF concentration the cell’s efficiency will be decreased.
One of the procedures to handle liquid radioactive waste is by filtration process. To do this process, suitable filter should be used because of radioactive nature of the waste. Ceramic filter is one of the suitable filters that could be used for this purpose. This paper will discuss about producing ceramic filter from local clay and test its performance. Performance of the filter is given by its flux, compressive strength, Decontamination Factor (DF) and adsorption efficiency. The results show that there are almost no effects of casting pressure on both flux and compressive strength of ceramic filter, but zeolite addition produces different effect. The higher concentration of zeolite will decrease the filter flux and increase filter compressive strength. The optimal composition from this research is 70% w/o clay-25% w/o zeolite-5% w/o charcoal. It has adsorption efficiency (60.36) and Decontamination Factor (2.52). Besides, Sr concentration after filtration is still higher than environmental standard for Sr-90 and more studies are still needed.
Ba0.5Sr0.5TiO3 (BST) film doped with variations in RuO2 concentration (0%, 2%, 4%, and 6%) has been successfully grown on a type-p silicon substrate (100) using the chemical solution deposition (CSD) method and spin-coating at a speed of 3000 rpm for 30 s. The film on the substrate was then heated at 850 °C for 15 h. The sensitivity of BST film + RuO2 variations as a gas sensor were characterized. The sensitivity characterization was assisted by various electronic circuitry with the purpose of producing a sensor that is very sensitive to gas. The responses from the BST film + RuO2 variation were varied, depending on the concentration of the RuO2 dope. BST film doped with 6% RuO2 had a very good response to halitosis gases; therefore, this film was applied as the Arduino-Nano-based bad-breath detecting sensor. Before it was integrated with the microcontroller, the voltage output of the BST film was amplified using an op-amp circuit to make the voltage output from the BST film readable to the microcontroller. The changes in the voltage response were then shown on the prototype display. If the voltage output was ≤12.9 mV, the display would read “bad breath”. If the voltage output >42.1 mV, the display would read “fragrant”. If 12.9 mV < voltage output ≤ 42.1 mV, the display would read “normal”.
Barium Strontium Titanate (BST) film has been successfully produced as a light sensor. The BST film was made by CSD method by reacting barium acetate, strontium acetate and titanium isopropoxide with mole fractions of 0.5; 0.5 and 1, respectively.The BST absorbance test showed that BST film is sensitive to visible light ranging from 475 to 750 nm. The film test showed maximum absorbance at three peak wavelengths, 475 nm, 593 nm, and 702 nm. The energy gap of the BST film was 1.9 eV which showed that the film produced was a semiconductor. The IV test showed that BST film is a photodiode. This was indicated by the shift of the curve when tested in light and dark conditions. The sensitivity test showed BST film is most sensitive to blue light, signified by the most significant change in resistance. The decrease in resistance of blue LED was 0.401KX/lux, while the resistance decrease of green light was 0.051KX/lux and red was 0.288KX/lux. By using optical and electrical properties, BST thin film could be used as light sensors to detect LED lights.
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