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Corrosion is one of the main PV module failure mechanisms, as it can cause severe electrical performance degradation in PV modules exposed to hot and humid environments. Moisture penetrating a photovoltaic (PV) module may react with the metallic components causing corrosion. In addition, acetic acid which is produced by hydrolysis of ethylene vinyl acetate (EVA), the most common encapsulant, may further degrade metallic components. Corrosion is one of the main PV module failure mechanisms, as it can cause severe electrical performance degradation in PV modules exposed to hot and humid environments. The specific chemical reactions involved in the corrosion mechanisms for the different components are well understood. However, which of these causes the most serious degradation in the field, and therefore, most severe power loss is unknown. Moreover, the severity of corrosion in the absence of acetic acid is not yet well researched. This work distinguished between the front and rear side corrosion mechanisms and identified the different electrical signatures observed due to them. The experiment included damp-heat (DH) conditioning of single-cell mini-modules, containing passivated emitter and rear contact (PERC) solar cells, laminated with a polyethylene terephthalate (PET) based backsheet. Furthermore, half-encapsulated PERC PV cells were tested, with either the front or the rear side exposed. Electrical and material characterisation were conducted for the investigation of the sample degradation, and the performance decrease, related to the degradation of the rear surface passivation, was examined.

Objective: To observe the efficacy and safety of Lishi Oral Liquid (LOL), a Chinese herbs formula, combined with levocetirizine, an antihistamine drug, in patients with damp-heat atopic dermatitis (AD). Methods: A randomized double-blind placebo-controlled clinical trial was conducted. Ninety patients diagnosed with damp-heat atopic dermatitis were randomly assigned to Lishi Oral Liquid group and control group at the ratio of 1:1. Patients were given one Lishi Oral Liquid or placebo three times per day. Both groups were treated with allantoin and vitamin E cream by topical use and levocetirizine by oral administration. Patients were followed up at the second and fourth week. The primary outcome was the scoring of atopic dermatitis (SCORAD). The secondary outcomes were visual analogue scale (VAS) and dermatology life quality index (DLQI). Results: After two weeks of treatment, there were statistical differences in SCORAD between these two groups ([Formula: see text]), whereas VAS and DLQI showed no statistical differences. There were significant differences in SCORAD and VAS between two groups at the end of four weeks of treatment ([Formula: see text]). However, no significant differences were observed in DLQI after four weeks of treatment. No serious adverse event was found during this clinical trial. Conclusion: LOL combined with levocetirizine is effective and safe for damp-heat AD treatment.

Long-term photovoltaic (PV) module reliability is highly determined by the durability of the polymeric components (backsheet and encapsulation materials). This paper presents the result of experiments on encapsulant degradation influenced by the backsheet permeation properties. Towards this goal, one type of ethylene/vinyl acetate copolymer (EVA) was aged in glass/EVA/backsheet laminates in accelerated aging tests (up to 4000 h for Damp-Heat (DH) and up to 480 kWh/m2 for UV and UV-DH combined). The samples contained three backsheets with different permeation properties to examine their impact on EVA degradation. Thermal and chemical characterization shows that the EVA degradation is stronger with the glass&ndash, EVA&ndash, polyamide (PA)-based backsheet than with the polyethylene terephthalate (PET)-based backsheets. The higher oxygen transmission rate (OTR) of the PA-based backsheet may increase photo-oxidation and aggravating the degradation of EVA in the laminates. Furthermore, FTIR results were used to demonstrate the effect of damp heat exposure on the EVA interfaces, showing an accelerated degradation at the glass&ndash, EVA interface. The comparison of accelerated aging stress factors reveals that EVA suffers the strongest chemical and optical degradation when high UV, high temperature and high relative humidity are combined simultaneously.

The electrical ageing of photovoltaic modules during extended damp-heat tests at different stress levels is investigated for three types of crystalline silicon photovoltaic modules with different backsheets, encapsulants and cell types. Deploying different stress levels allows determination of an equivalent stress dose function, which is a first step towards a lifetime prediction of devices. The derived humidity dose is used to characterise the degradation of power as well as that of the solar cell's equivalent circuit parameters calculated from measured current–voltage characteristics. An application of this to the samples demonstrates different modes in the degradation and thus enables better understanding of the module's underlying ageing mechanisms. The analysis of changes in the solar cell equivalent circuit parameters identified the primary contributors to the power degradation and distinguished the potential ageing mechanism for each types of module investigated in this paper. © 2016 The Authors. Progress in Photovoltaics: Research and Applications published by John Wiley & Sons Ltd. © 2016 The Authors. Progress in Photovoltaics: Research and Applications published by John Wiley & Sons Ltd. This work was supported in part by the European Commission under FP7 grant N° 262533 SOPHIA (INFRA-2010- 1.1.22_CP-CSA-Infra) and by the Research Councils UK (RCUK) under project ‘Stability and Performance of Photovoltaics (STAPP)’ (contract no: EP/H040331/1).

In this study, the influence of the PV laminate design on the silicon cell degradation was investigated. Laminates consisting of two different kinds of encapsulation (EVA and PVB) and three different back-sheet materials (TAPT, PA and a TPT foils) were manufactured. Standard cells with a two and three bus bar design were used as well as MWT cells. The laminates were subjected to a UV, heat and damp-heat aging tests. The degradation of the cell metallization was investigated by means of electroluminescence imaging, the degree of polymeric aging was determined by Raman spectroscopy. Special attention was paid to the spatial distribution of corrosion effects on the cell. A severe influence of the solar cell type, i.e. the metallization paste, could be shown. Furthermore, a strong dependence of the degree of metallization degradation on the type of back-sheet material was found. An extensive UV aging for up to 180 kWh appeared to have no influence on the metallization corrosion.

This thesis investigates the link between the plasma deposition conditions and microcrystalline silicon (μc-Si:H) material quality for thin-film silicon photovoltaic applications. The role of interfaces and the μc-Si:H material quality on the device performance are analyzed in detail. The low absorption of μc-Si:H at long wavelengths requires the deposition of absorber layers with thicknesses of typically a few micrometers for use in multi-junction TF Si solar cells. The growth typically takes place on highly textured surfaces, which provide increased light absorption—often called light trapping—but which potentially induce structural defects in the film during its growth. Therefore, to further improve the TF Si technology, one of the main challenges is the identification of the determinant plasma deposition parameters that result in the growth of very high-quality μc-Si:H at an increased deposition rate on textured substrates that guarantee efficient light trapping. As a first approach to better understand the plasma conditions necessary for the growth of high-quality μc-Si:H, the roles of both the silane depletion fraction and the deposition pressure are studied in an industrial-type large-area KAI reactor. With increasing pressure and silane depletion, the μc-Si:H defect density is significantly lowered leading to improved solar cell performance. An estimation of the average energy with which ions impinge on the substrate supports the hypothesis that ion bombardment is mainly responsible for the observed differences. Then, a fundamental aspect of μc-Si:H deposition on highly textured substrates is highlighted: two different phases of μc-Si:H material contribute to the overall solar cell efficiency, both of which can drive cell performance. The first phase relates to the bulk material and dominates the performance of cells on flat substrates. However, on rough morphologies, substrate-induced defective localized nanoporous regions—the second phase—develop and are found to be significantly more sensitive to the plasma process conditions and substrate morphology than the bulk phase. The relative importance of this secondary defective phase is shown through the use of new damp-heat experiments. Silicon oxide doped layers are demonstrated to mitigate the influence of these nanoporous regions on the solar cell performance. Next, a comparative study of the plasma excitation frequencies of 13.56 MHz (RF) and 40.68 MHz (VHF) shows that, while both allow for the growth of very good-quality bulk material, the efficiency of VHF-prepared cells is always poorer compared to that of RF-prepared cells within the range of our study for growth rates below 5 Å s−1. This decrease in solar cell performance is related to a higher density of nanoporous regions in the VHF-prepared cells as evidenced by damp-heat experiments, leading to strong open-circuit voltage instabilities. Still, the use of VHF is shown to be beneficial at increased deposition rates, thanks to reduced ion bombardment and improved bulk material quality. The crucial interplay between μc-Si:H growth rate and substrate morphology with regard to the formation of nanoporous regions is further discussed for regimes with high deposition rates of around 10 Ås−1. It is shown that high-silane-depletion regimes with significantly reduced H2 flow rate or increased pressure lead to a denser μc-Si:H material but are associated with increased secondary gas-phase reactions and powder formation. The use of a reduced interelectrode distance is demonstrated to allow for the growth of μc-Si:H with significantly improved bulk material quality at higher growth rates. Plasma simulations performed in collaboration with the University of Patras are presented and suggest that improvements observed in the μc-Si:H material quality are related mainly to an increased contribution of less reactive silane monoradicals, such as SiH3 and Si2H5, to the growing film, as compared to highly reactive ones such as SiH2 and SiH. Then, in an effort to better understand the formation of these two distinct μc-Si:H phases, the intrinsic stress within μc-Si:H i-layers is studied and correlated with the bulk defect density. Further improvements to both μc-Si:H and a-Si:H solar cells are obtained by introducing a novel intrinsic silicon oxide buffer layer at the p -i interface. For μc -Si:H solar cells, all electrical parameters are improved unless the i -layer is significantly more amorphous-rich and high quality, in which case an improvement only in carrier collection in the blue region is observed. In a-Si:H solar cells the silicon oxide buffer is shown to lower light-induced degradation, which is one of the weak points of TF Si technology. Furthermore, for both a-Si:H and μc-Si:H solar cells, the buffer can also act as an efficient barrier to boron cross-contamination, eliminating the need for additional time-consuming processing steps such as a water flush for single-chamber processes. Overall, this work contributes to a better understanding of the μc-Si:H material requirements for PV applications and how they relate to the plasma deposition conditions. Based on all the aforementioned developments, significant progress has been made in the understanding and the fabrication of thin-film silicon solar cells based on μc-Si:H. An outstanding single-junction μc-Si:H solar cell of 10.9% was attained; to our knowledge this is the highest reported in the literature. This work also contributed to the development of very high-efficiency tandem and triple-junction thin-film silicon solar cells at PV-Lab.