Constitution and mechanism of the selenium rectifier photocell

This paper describes experiments to elucidate the exact physical and chemical structure of the selenium rectifier photocell, especially that of the thin surface film. A technique is described for sputtering films of cadmium oxide which, though transparent in the thickness required for a cell, have an electrical conductivity exceeding that of graphite. The thickness of the films can be closely controlled. With such films, on pure crystalline selenium, cells were produced with white-light sensitivities of over 700 µA per lumen, open-circuit voltages up to 0.5 V under high illumination, and maximum quantum efficiencies up to 70 %. The optical properties of the films are described, and the way in which the technique may be used to produce other non-metallic films is indicated. The cadmium oxide is found to have a negative Hall coefficient, and is therefore an N type semi-conductor. Further experiments with single films of gold, and double films of zinc oxide and gold, illustrate the behaviour of these, in intimate contact with selenium. The metal-selenium contact yields a poor photocell, the metal-zinc oxide-selenium contact one whose properties are critically dependent on the thickness of the intermediate oxide layer, and the N type cadmium oxide-selenium contact one for which the efficiency is high, and the thickness of cadmium oxide not critical. It is suggested therefore that in the practical photocell, the essential mechanism is a contact between two suitable semi-conductors of dissimilar types, any extra metal film when present serving simply to raise the lateral conductivity of the intermediate semi-conducting film when this is not high enough to eliminate undesirable effects of a high internal resistance in the finished cell.

Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1463 ◽  
Author(s):  
Vishma Pratap Sur ◽  
Marketa Kominkova ◽  
Zaneta Buchtova ◽  
Kristyna Dolezelikova ◽  
Ondrej Zitka ◽  
...  

The physical and chemical synthesis methods of quantum dots (QDs) are generally unfavorable for biological applications. To overcome this limitation, the development of a novel “green” route to produce highly-fluorescent CdSe QDs constitutes a promising substitute approach. In the present work, CdSe QDs were biosynthesized in yeast Saccharomyces cerevisiae using a novel method, where we showed for the first time that the concentration of tryptone highly affects the synthesis process. The optimum concentration of tryptone was found to be 25 g/L for the highest yield. Different methods were used to optimize the QD extraction from yeast, and the best method was found to be by denaturation at 80 °C along with an ultrasound needle. Multiple physical characterizations including transmission electron microscopy (TEM), dynamic light scattering (DLS), energy-dispersive X-ray spectroscopy (EDX), and spectrophotometry confirmed the optical features size and shape distribution of the QDs. We showed that the novel conjugate of the CdSe QDs and a cell-penetrating peptide (hecate) can detect bacterial cells very efficiently under a fluorescent microscope. The conjugate also showed strong antibacterial activity against vancomycin-resistant Staphylococcus aureus (VRSA), methicillin-resistant Staphylococcus aureus (MRSA), and Escherichia coli, which may help us to cope with the problem of rising antibiotic resistance.


Author(s):  
Venkata Nagarjun PM ◽  
Hirshik Ram S ◽  
Pratik Uthan ◽  
Veeramani V ◽  
Senthilkumar Subramaniam

BIBECHANA ◽  
2015 ◽  
Vol 13 ◽  
pp. 23-28
Author(s):  
Leela Pradhan Joshi

Aluminium doped Zinc Oxide (AZO) seed layers were deposited on Fluorine doped Tin Oxide (FTO) substrates using a spin coating technique. These were then immersed in growth solutions of zinc nitrate, hexamethylenetetramine and distilled water to develop nanoplates of Zinc Oxide (ZnO). The nanostructures of ZnO grown on FTO were studied using x-ray diffraction techniques. Dye-sensitized solar cells (DSSC) were fabricated using two prepared electrodes, one of dye-loaded zinc oxide and another that was platinum coated. The electrolyte used was potassium iodide iodine solution. The performance of the assembled DSCCs was tested by drawing an IV curve. The results showed that the short circuit current and open circuit voltages were about 10 microamperes and 270 millivolts respectively.BIBECHANA 13 (2016) 23-28


2019 ◽  
Vol 10 (4) ◽  
pp. 69
Author(s):  
Ajeet Babu K. Parasumanna ◽  
Ujjwala S. Karle ◽  
Mangesh R. Saraf

Battery packaging in a vehicle depends on the cell chemistry being used and its behavior plays an important role in the safety of the entire battery pack. Chemical degradation of various parts of a cell such as the cathode or anode is a concern as it adversely affects performance and safety. A cell in its battery pack once assembled can have two different mechanical abuse condition. One is the vibration generated from the vehicle and the second is the intrusion of external elements in case of accident. In this paper, a commercially available 32,700 lithium ion cell with lithium iron phosphate (LFP) chemistry is studied for its response to both the abuse conditions at two different states of charge (SoC). The primary aim of this study is to understand their effect on the surface morphology of the cathode and the anode. The cells are also characterized to study impedance behavior before and after being abused mechanically. The cells tested for vibration were also analyzed for dynamic stiffness. A microscopy technique such as scanning electron microscopy (SEM) was used to study the surface morphology and electrochemical impedance spectroscopy (EIS) characterization was carried out to study the internal resistance of the cell. It was observed that there was a drop in internal resistance and increase in the stiffness after the cells subjected to mechanical abuse. The study also revealed different morphology at the center and at the corner of the cell subjected to nail penetration at 50% SoC.


2011 ◽  
Vol 64 (6) ◽  
pp. 820 ◽  
Author(s):  
Fuzhi Huang ◽  
Yi-Bing Cheng ◽  
Rachel A. Caruso

Porous aluminium doped TiO2 was prepared through a sol–gel process in the presence of a template. The doping enlarges the band-gap of the anatase TiO2, which modifies the TiO2 electrical properties. The porous Al/TiO2 films were assembled into dye-sensitized solar cells. A 45 mV enhancement of open-circuit photovoltage and 11% increase of fill factor at 2 wt-% doping concentration, and 8.6% improvement of the overall efficiency at 0.5 wt-% doping concentration were achieved relative to that of a cell containing non-doped TiO2 under the same conditions. This advance is attributed to the increase in conductivity with the Al-doping of the TiO2 electrode.


2003 ◽  
Vol 762 ◽  
Author(s):  
Jessica M. Owens ◽  
Daxing Han ◽  
Baojie Yan ◽  
Jeffrey Yang ◽  
Kenneth Lord ◽  
...  

AbstractThe open-circuit voltage (Voc) of mixed-phase hydrogenated silicon solar cells has been found to increase after light soaking. In this study, we use micro-Raman to investigate the heterogeneous structure of solar cells in the amorphous-to-nanocrystalline transition region. For a cell with Voc = 0.981 V, Raman spectra show a typical broad Gaussian lineshape around 480 cm-1, a signature of typical amorphous material. A cell with Voc = 0.674 V displays a sharp Lorentzian peak around 516 cm-1, indicative of nanocrystallinity. A cell with Voc = 0.767 V was systematically scanned for 20 different positions in 500 μm increments. Most spectra show a typical Gaussian lineshape around 480 cm-1, several spectra reveal a hint of a nanocrystalline shoulder around 512 cm-1, and one spectrum exhibits a distinct nanocrystalline peak. We conclude that the nanocrystallite distribution in the mixed-phase material is very non-uniform even within a mm dot. This result provides direct evidence supporting a recently proposed two-diode equivalent-circuit model to explain the light-induced effect.


2016 ◽  
Vol 190 ◽  
pp. 269-289 ◽  
Author(s):  
Xiangling Yue ◽  
Ana Arenillas ◽  
John T. S. Irvine

Hybrid direct carbon/coal fuel cells (HDCFCs) utilise an anode based upon a molten carbonate salt with an oxide conducting solid electrolyte for direct carbon/coal conversion. They can be fuelled by a wide range of carbon sources, and offer higher potential chemical to electrical energy conversion efficiency and have the potential to decrease CO2 emissions compared to coal-fired power plants. In this study, the application of (La, Sr)(Cr, Mn)O3 (LSCM) and (Gd, Ce)O2 (GDC) oxide anodes was explored in a HDCFC system running with two different carbon fuels, an organic xerogel and a raw bituminous coal. The electrochemical performance of the HDCFC based on a 1–2 mm thick 8 mol% yttria stabilised zirconia (YSZ) electrolyte and the GDC–LSCM anode fabricated by wet impregnation procedures was characterized and discussed. The infiltrated oxide anode showed a significantly higher performance than the conventional Ni–YSZ anode, without suffering from impurity formation under HDCFC operation conditions. Total polarisation resistance (Rp) reached 0.8–0.9 Ω cm2 from DCFC with an oxide anode on xerogel and bituminous coal at 750 °C, with open circuit voltage (OCV) values in the range 1.1–1.2 V on both carbon forms. These indicated the potential application of LSCM–GDC oxide anode in HDCFCs. The chemical compatibility of LSCM/GDC with carbon/carbonate investigation revealed the emergence of an A2BO4 type oxide in place of an ABO3 perovskite structure in the LSCM in a reducing environment, due to Li attack as a result of intimate contact between the LSCM and Li2CO3, with GDC being stable under identical conditions. Such reaction between LSCM and Li2CO3 was not observed on a LSCM–YSZ pellet treated with Li–K carbonate in 5% H2/Ar at 700 °C, nor on a GDC–LSCM anode after HDCFC operation. The HDCFC durability tests of GDC–LSCM oxide on a xerogel and on raw bituminous coal were performed under potentiostatic operation at 0.7 V at 750 °C. The degradation mechanisms were addressed, especially on raw coal.


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