Stability of sub‐micron‐thick CdTe solar cells

Sputtered CdS/CdTe cells with only 0.75 µm of CdTe have reached AM1.5 efficiencies over 12.5%. But the use of very thin absorber layers of CdTe raises questions about the possible impact on long‐term stability when the back contact is very close to the main junction. In this study, we have performed accelerated life testing (ALT) on unencapsulated CdTe dot cells with absorber thickness ranging from 0.7 to 2.1 µm. After 900 h of ALT at 85°C under continuous one‐sun illumination, with open circuit biasing and no encapsulation, we find that any decrease in stability as CdTe thickness decreases is within the ~10% statistical uncertainty shown by the sample sets of more than 20 cells each. Cells of all thicknesses exhibited some decrease in performance under these stress conditions, and open‐circuit voltage appears to be the key factor in decreased efficiency. These changes in performance under ALT at 85°C are found to be consistent with a projected field lifetime of about 40 years in typical conditions. Secondary ion mass spectroscopy depth profiles of several elements including Cu showed no evidence of ALT‐driven diffusion in these sputtered CdTe cells. Copyright © 2013 John Wiley & Sons, Ltd.     

Transmission line maintenance robots capable of crossing obstacles: State‐of‐the‐art review and challenges ahead

Power line inspection and maintenance already benefit from developments in mobile robotics. This paper presents a comprehensive review of the state of the art. It focuses on mobile robots designed to cross obstacles found on a typical transmission line while using the conductor as support for traveling. Promising areas of research and development as well as challenges that remain to be solved are discussed with a view to developing fully autonomous technologies. Maintenance tasks, including inspection and repairs, are identified as high‐value applications in transmission live‐line work. Conclusions are drawn from experience, and the future of mobile robotics applied to transmission line maintenance is discussed. © 2009 Wiley Periodicals, Inc.     

Assessing the Performance of Evapotranspiration Covers for Municipal Solid Waste Landfills in Northwestern Ohio

Evapotranspiration (ET) covers have gained considerable interest as an alternative to conventional covers for the final closure of municipal solid waste (MSW) landfills, but often produce higher rates of percolation in regions that receive more than 32??cm?year-1 of precipitation. The goal of this project is to design ET covers for MSW landfills in northwestern Ohio (long-term annual rate of precipitation of 83??cm?year-1) that produce rates of percolation <32??cm?year-1, the rate considered acceptable by the Ohio Environmental Protection Agency (OEPA), and promote habitat restoration. To attain this goal, an adequate soil water-storage capacity was provided using dredged sediment amended with organic material. Two plant mixtures were tested to evaluate the performance of ET covers immediately following construction (immature plants seeded onto the soil) and in the future (mature plants transplanted from a restored tall-grass prairie that is more than 10?years old). ET covers were constructed in drainage lysimeters (1.52-m diameter, 1.52-m depth) and watered at a rate of 91.12 to 95.72??cm?year-1, which included simulated 100-year rain events (11.7?cm over 24?h) in July and October. During the 1-year monitoring period, the ET covers using the mature plant mixture produced considerably less percolation (0.12 to 11.44??cm?year-1) than the covers with the immature plant mixture (6.71 to 24.16??cm?year-1). Thus far, all ET covers have produced rates of percolation less than the maximum standard by the OEPA, and they will continue to be monitored.     

Effect size measures for mediation models: Quantitative strategies for communicating indirect effects.

The statistical analysis of mediation effects has become an indispensable tool for helping scientists investigate processes thought to be causal. Yet, in spite of many recent advances in the estimation and testing of mediation effects, little attention has been given to methods for communicating effect size and the practical importance of those effect sizes. Our goals in this article are to (a) outline some general desiderata for effect size measures, (b) describe current methods of expressing effect size and practical importance for mediation, (c) use the desiderata to evaluate these methods, and (d) develop new methods to communicate effect size in the context of mediation analysis. The first new effect size index we describe is a residual-based index that quantifies the amount of variance explained in both the mediator and the outcome. The second new effect size index quantifies the indirect effect as the proportion of the maximum possible indirect effect that could have been obtained, given the scales of the variables involved. We supplement our discussion by offering easy-to-use R tools for the numerical and visual communication of effect size for mediation effects. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

A Joint Experimental and Computational Search for Authentic Nano‐electrocatalytic Effects: Electrooxidation of Nitrite and L‐Ascorbate on Gold Nanoparticle‐Modified Glassy Carbon Electrodes

The investigation of electrocatalytic nanoeffects is tackled via joint electrochemical measurements and computational simulations. The cyclic voltammetry of electrodes modified with metal nanoparticles is modeled considering the kinetics of the electrochemical process on the bulk materials of the different regions of the electrode, that is, the substrate (glassy carbon) and the nanoparticles (gold). Comparison of experimental and theoretical results enables the detection of changes in the electrode kinetics at the nanoscale due to structural and/or electronic effects. This approach is applied to the experimental assessment of electrocatalytic effects by gold nanoparticles (Au NPs) in the electrooxidation of nitrite and L‐ascorbate. Glassy carbon electrode is modified with Au NPs via seed‐mediated growth method. Divergence between the kinetics of these processes on gold macroelectrodes and gold nanoparticles is examined. Whereas claimed catalytic effects are not observed in the electrooxidation of nitrite, electrocatalytic nanoeffects are verified in the case of L‐ascorbate. This is probably due to that the electron transfer process follows an adsorptive mechanism. The combination of simulation with experiments is commended as a general strategy of authentification, or not, of nanoelectrocatalytic effects.     

Indirect photodegradation of dissolved free amino acids: the contribution of singlet oxygen and the differential reactivity of DOM from various sources

The role of photochemically generated singlet oxygen (1O2) in the DOM-sensitized degradation of eighteen dissolved free amino acids was investigated. The fraction of total sensitized degradation due to reaction with 1O2 was determined through a kinetic analysis based on a measured reaction rate constant for each amino acid coupled with measured 1O2 concentrations and was confirmed through quenching experiments. Only four of the eighteen free amino acid residues examined were found to be photolabile under environmentally relevant conditions: histidine, methionine, tyrosine, and tryptophan. The fraction of Suwannee River Humic Acid (SRHA)-sensitized degradation due to reaction with 1O2 ranged from an upper value of 110 +/- 10% for histidine to 8 +/- 1% for tryptophan, with 26 +/- 3% contribution for methionine and 33 +/- 4% for tyrosine. In addition to degradation through reaction with 1O2, other reactive intermediates involved in the SRHA-photosensitized degradation of these amino acids were identified. Methionine was thought to be additionally degraded through reaction with H2O2 and triplet excited-state DOM, and 67% of tyrosine's indirect photodegradation was assigned to an oxygen-dependent type I photooxidation reaction. The majority of tryptophan indirect degradation was due to reaction with 3DOM. Photodegradation experiments with various DOM sources including Pony Lake (Antarctica) fulvic acid and a synthetic estuarine sample, as well as Minnesota freshwater samples (lakes Itasca, Superior, Josephine, and the St Louis River), demonstrated distinct reactivity patterns, indicating that DOM's 1O2-generation efficiency is not strongly coupled to its ability to promote other photooxidation pathways. These four amino acids highlightthe differential photoreactivity of DOM from various sources.     

In situ mechanical property measurements of amorphous carbon-boron nitride nanotube nanostructures

To understand the mechanical properties of amorphous carbon (a-C)/boron nitride nanotube (BNNT) nanostructures, in?situ mechanical tests are conducted inside a transmission electron microscope equipped with an integrated atomic force microscope system. The nanotube structure is modified with amorphous carbon deposited by controlled electron beam irradiation. We demonstrate multiple in situ tensile, compressive, and lap shear tests with a-C/BNNT hybrid nanostructures. The tensile strength of the a-C/BNNT hybrid nanostructure is 5.29?GPa with about 90?vol% of a-C. The tensile strength and strain of the end-to-end joint structure with a-C welding is 0.8?GPa and 5.2% whereas the lap shear strength of the side-by-side joint structure with a-C is 0.25?GPa.     

Near IR scanning angle total internal reflection Raman spectroscopy at smooth gold films

Total internal reflection (TIR) Raman and reflectivity spectra were collected for nonresonant analytes as a function of incident angle at sapphire or sapphire/smooth 50 nm gold interfaces using 785 nm excitation. For both interfaces, the Raman signal as a function of incident angle is well-modeled by the calculated interfacial mean square electric field (MSEF) relative to the incident field times the thickness of the layer being probed in the Raman measurement (D(RS)). The Raman scatter was reproducibly enhanced at the interface containing a gold film relative to the sapphire interface by a factor of 4.3-4.6 for aqueous pyridine or 2.2-3.7 for neat nitrobenzene, depending on the analyzed vibrational mode. The mechanism for the increased Raman signal is the enhanced MSEF at incident angles where propagating surface plasmons are excited in the metal film. The background from the TIR prism was reduced by 89-95% with the addition of the gold film, and the percent relative uncertainty in peak area was reduced from 15 to 1.7% for the 1347 cm(-1) mode of nitrobenzene. Single monolayers of benzenethiol (S/N = 6.8) and 4-mercaptopyridine (S/N = 16.5) on gold films were measured by TIR Raman spectroscopy with 785 nm excitation (210 mW) without resonant enhancement in 1 min.     

Triplet-sensitized photodegradation of sulfa drugs containing six-membered heterocyclic groups: identification of an SO2 extrusion photoproduct

The aquatic photochemical behavior of a class of sulfa drugs containing six-membered heterocyclic substituents (sulfamethazine, sulfamerazine, sulfadiazine, sulfachloropyridazine, and sulfadimethoxine) was investigated. Photodegradation of the sulfa drugs in a natural water sample was significantly enhanced relative to the degradation in deionized water, with the exception of sulfadimethoxine. This indicated an indirect photochemical process that was identified through the use of quenchers to be attributable to interaction with triplet excited-state dissolved organic matter (3DOM). The direct photolysis rate constant and quantum yield for both the neutral and anionic species of each sulfa drug were calculated using matrix deconvolution methods. The quantum yield values range from 0.01 x 10(-3) for the neutral form of sulfadimethoxine to 5 x 10(-3) for the anionic form of sulfamethazine and are significantly lower than those observed in a previous study for sulfa drugs containing five-membered heterocyclic substituents, although the rate constants are of similar magnitude. The primary product formed in both direct and indirect photodegradation for all five compounds was identified as a sulfur dioxide extrusion product. The predicted environmental half-lives solely attributable to direct photolysis range from 8.6 h in midsummer at 30 degrees latitude in pH 7 surface water for sulfachloropyridazine to 420 h in midwinter at 45 degrees in pH 7 surface water for sulfadimethoxine. These half-lives, except for sulfadimethoxine, will be decreased by interaction with 3DOM.