Experimental investigation of the temperature coefficients of Vmpp and Impp in a silicon solar cell

Master's thesis Renewable Energy ENE500 - University of Agder 2019This thesis is meant to provide an experimental investigation of the temperature coefficient(b)of Vmpp compared to Voc in amulticrystallinesilicon solar cell.With the main question being: to what degree is the temperature coefficient equal for Voc and Vmpp and how does series losses(Rs)affect the two? Also investigating the same question for Isc and Impp. Three types of multicrystalline cells have been measured using a NeonSee AAA sun simulator, for a total of 18 tested cells all produced by Elkem SolarSilicon. I-V data wascollected using temperature scan, Suns-Voc and Isc-Voc measurements, with temperatures reflecting normal operation range for solar cells, from 25 to 65°C. The different cells tested have been Al-BSF, PERC 0.5 and PERC 1.3 cells. Theresultingdata hasbeen calculated using Excel providingbresults for Voc, Vmpp, Isc and Impp. For all bresults, standard deviation of slope was also calculated to say something about the accuracy of the measurements.Results from theanalysed data show a trend where bVoc is statistically significant different from bVmpp. This is concluded based on the results where the majority cells tested show bVoc having a larger value than bVmpp, without any overlapping instandard deviation. The degree of differencevaries with the different cells and the different measuring techniques. As for the effect of Rs, the difference in results between the Tscan measuring technique and the Suns-Voc and Isc-Voc techniques have been analysed. A trend of lower values for bVmppfrom Tscan measurements indicates that Rs has a negative effect on the bVmpp. Generally, the results show that bfor current is more varyingthan for voltage data. Results compared between the different measuring techniques are showing less visible trends for bIsc and bImpp than for bVocand bVmpp. There are less systematic differences between Tscan data and the two other methods. This is probably because Rs should have little or no effect on the current.For most of the cells calculated, standard deviation is very low for both current and voltage calculations, which is a sign that the measurements are accurate, however more testing is requiredto statemore conclusive evidence

X-ray Diffraction and Molecular Dynamics Study of Medium-range Order in Ambient and Hot Water

We have developed x-ray diffraction measurements with high energy-resolution and accuracy to study water structure at three different temperatures (7, 25 and 66 C) under normal pressure. Using a spherically curved Ge crystal an energy resolution better than 15 eV has been achieved which eliminates influence from Compton scattering. The high quality of the data allows a precise oxygen-oxygen pair correlation function (PCF) to be directly derived from the Fourier transform of the experimental data resolving shell structure out to ~12 {\AA}, i.e. 5 hydration shells. Large-scale molecular dynamics (MD) simulations using the TIP4P/2005 force-field reproduce excellently the experimental shell-structure in the range 4-12 {\AA} although less agreement is seen for the first peak in the PCF. The Local Structure Index [J. Chem. Phys. 104, 7671 (1996)] identifies a tetrahedral minority giving the intermediate-range oscillations in the PCF and a disordered majority providing a more featureless background in this range. The current study supports the proposal that the structure of liquid water, even at high temperatures, can be described in terms of a two-state fluctuation model involving local structures related to the high-density and low-density forms of liquid water postulated in the liquid-liquid phase transition hypothesis.Comment: Submitted to Phys. Chem. Chem. Phy

Measurement of positron lifetime to probe the mixed molecular states of liquid water

Positron lifetime spectra were measured in liquid water at temperatures between 0c and 50c. The long lifetime of ortho-positronium atoms (o-Ps) determined by electron pick-off in molecular substances decreases smoothly by 10% as the temperature is raised. This lifetime temperature dependence can be explained by combining the Ps-bubble model and the mixture state model of liquid water.Comment: 11 pages, 6 page

Entropy/IP: Uncovering Structure in IPv6 Addresses

In this paper, we introduce Entropy/IP: a system that discovers Internet address structure based on analyses of a subset of IPv6 addresses known to be active, i.e., training data, gleaned by readily available passive and active means. The system is completely automated and employs a combination of information-theoretic and machine learning techniques to probabilistically model IPv6 addresses. We present results showing that our system is effective in exposing structural characteristics of portions of the IPv6 Internet address space populated by active client, service, and router addresses. In addition to visualizing the address structure for exploration, the system uses its models to generate candidate target addresses for scanning. For each of 15 evaluated datasets, we train on 1K addresses and generate 1M candidates for scanning. We achieve some success in 14 datasets, finding up to 40% of the generated addresses to be active. In 11 of these datasets, we find active network identifiers (e.g., /64 prefixes or `subnets') not seen in training. Thus, we provide the first evidence that it is practical to discover subnets and hosts by scanning probabilistically selected areas of the IPv6 address space not known to contain active hosts a priori.Comment: Paper presented at the ACM IMC 2016 in Santa Monica, USA (https://dl.acm.org/citation.cfm?id=2987445). Live Demo site available at http://www.entropy-ip.com

Surface Induced Order in Liquid Metals and Binary Alloys

Measurements of the surface x-ray scattering from several pure liquid metals (Hg, Ga, and In) and from three alloys (Ga-Bi, Bi-In, and K-Na) with different heteroatomic chemical interactions in the bulk phase are reviewed. Surface-induced layering is found for each elemental liquid metal. The surface structure of the K-Na alloy resembles that of an elemental liquid metal. Bi-In displays pair formation at the surface. Surface segregation and a wetting film are found for Ga-Bi.Comment: 10 pages, 3 fig, published in Journal of Physics: Condensed Matte

Model of a fluid at small and large length scales and the hydrophobic effect

We present a statistical field theory to describe large length scale effects induced by solutes in a cold and otherwise placid liquid. The theory divides space into a cubic grid of cells. The side length of each cell is of the order of the bulk correlation length of the bulk liquid. Large length scale states of the cells are specified with an Ising variable. Finer length scale effects are described with a Gaussian field, with mean and variance affected by both the large length scale field and by the constraints imposed by solutes. In the absence of solutes and corresponding constraints, integration over the Gaussian field yields an effective lattice gas Hamiltonian for the large length scale field. In the presence of solutes, the integration adds additional terms to this Hamiltonian. We identify these terms analytically. They can provoke large length scale effects, such as the formation of interfaces and depletion layers. We apply our theory to compute the reversible work to form a bubble in liquid water, as a function of the bubble radius. Comparison with molecular simulation results for the same function indicates that the theory is reasonably accurate. Importantly, simulating the large length scale field involves binary arithmetic only. It thus provides a computationally convenient scheme to incorporate explicit solvent dynamics and structure in simulation studies of large molecular assemblies

Optimized random phase approximations for arbitrary reference systems: extremum conditions and thermodynamic consistence

The optimized random phase approximation (ORPA) for classical liquids is re-examined in the framework of the generating functional approach to the integral equations. We show that the two main variants of the approximation correspond to the addition of the same correction to two different first order approximations of the homogeneous liquid free energy. Furthermore, we show that it is possible to consistently use the ORPA with arbitrary reference systems described by continuous potentials and that the same approximation is equivalent to a particular extremum condition for the corresponding generating functional. Finally, it is possible to enforce the thermodynamic consistence between the thermal and the virial route to the equation of state by requiring the global extremum condition on the generating functional.Comment: 8 pages, RevTe