Proposals for a practical calibration method for mechanical torque measurement on the wind turbine drive train under test on a test bench

The mechanical torque input into the wind turbine drive train is a very useful measurement for tests performed on a test bench. To ensure the accuracy and the reliability, an accurate calibration of the torque measurement must be carried out and repeated within a certain period of time. However, owing to the high torque level and large structure size, such a calibration is both expensive and time consuming. To overcome this challenge, a new calibration method is proposed here. The method is based on the electrical power measurement, where a high level of accuracy is much easier to achieve. With the help of a special test process, a relationship between the torque-measuring signal and the electrical power can be established. The process comprises two tests with the drive train running in different operating modes. The calibration is possible by carrying out the same test process on several different torque levels. Detailed uncertainty analysis of the method is presented, whereby the uncertainty can be calculated by means of matrix operation and also numerically. As a demonstration, the implementation of the method on a test bench drive train that contains two 5-MW motors in tandem with the motors operating in a back-to-back configuration is also presented. Finally, some variations on the method and possible ways of achieving better accuracy are discussed. © 2020 The Authors. Wind Energy published by John Wiley & Sons Lt

The Impact of Stoichiometry on the Photophysical Properties of Ruddlesden-Popper Perovskites

2D Ruddlesden-Popper perovskites are interesting for a variety of applications owing to their tunable optical properties and their excellent ambient stability. As these materials are processable from solution, they hold the promise of procuring flexible and cost-effective films through large-scale fabrication techniques. However, such solution-based deposition techniques often induce large degrees of heterogeneity due to poorly controlled crystallization. The microscopic properties of films of (PEA)(2)PbI4 cast from precursor solutions of different stoichiometry are therefore investigated. The stoichiometry of the precursor solution is found to have a large impact on the crystallinity, morphology, and optical properties of the resulting thin films. Even for films cast from stoichiometric precursors, differences in photoluminescence intensities occur on a subgranular level. The heterogeneity in these films is found to be thermally activated with an activation energy of 0.4 eV for the emergence of local variations in nonradiative recombination rates. The spatial variation in the distribution of trap states is attributed to local fluctuations in the stoichiometry. In line with this, the surface can successfully be passivated by providing an excess of phenylethylammonium iodide (PEAI) to an as-cast film, enhancing the photoluminescence by as much as 85% without significantly altering the film's morphology.</p

Nuclear magnetic resonance as a quantitative tool to study interactions in biomacromolecules

High-resolution nuclear magnetic resonance (NMR) has emerged as one of the most versatile tools for the quantitative study of structure, kinetics, and thermodynamics of biomolecules and their interactions at atomic resolution. Traditionally, nuclear Overhauser enhancements (NOEs) and chemical shift perturbation methods are used to determine molecular geometries and to identify contact surfaces, but more recently, weak anisotropic orientation, anisotropic diffusion, and scalar couplings across hydrogen bonds provide additional information. Examples of such technologies are shown as applied to the quantitative characterization of function and thermodynamics of several biomacromolecules. In particular, (1) the structural and dynamical changes of the TipA multidrug resistance protein are followed upon antibiotic binding, (2) the trimer-monomer equilibrium and thermal unfolding of foldon, a small and very efficient trimerization domain of the T4 phagehead, is described in atomic detail, and (3) the changes of individual protein hydrogen bonds during thermal unfolding are quantitatively followed by scalar couplings across hydrogen bond

Influence of the stoichiometry of tin-based 2D/3D perovskite active layers on solar cell performance

2D/3D mixed tin perovskites have the advantages of high crystallinity and preferential orientation compared to pure 3D tin perovskite. However, solar cells based on 2D/3D mixed tin perovskites are still limited by low power conversion efficiency (PCE) when compared to their lead-based counterparts. It is essential to gain deeper insight into the factors that limit the performance of these solar cells in order to further improve them. In this work, we demonstrate that the starting stoichiometry of 2D/3D (PEA(0.08)FA(x)SnI(3)) tin perovskite films influences their crystallization and photophysical properties as well as the solar cell performance. The reference 2D/3D film (x = 0.92, where x refers to the stoichiometry of the precursors) is highly crystalline with the 3D phase preferentially oriented and a small amount of 2D phase located at the bottom of the film. The reference solar cell delivers a PCE of about 8.0%. 2D/3D films with even higher FA concentration (x > 1.0) mainly consist of poorly crystalline and randomly oriented 3D phases, with much higher trap density compared to the reference film. The corresponding solar cells therefore suffer from severe trap-assisted charge recombination, and deliver a poor PCE o

An experimental study to discriminate between the validity of diffraction theories for off-Bragg replay

We show that experiments clearly verify the assumptions made by the first-order two-wave coupling theory for one dimensional lossless unslanted planar volume holographic gratings using the beta-value method rather than Kogelnik's K-vector closure method. Apart from the fact that the diffraction process is elastic, a much more striking difference between the theories becomes apparent particularly in the direction of the diffracted beam in off-Bragg replay. We therefore monitored the direction of the diffracted beam as a function of the off-Bragg replay angle in two distinct cases: [a] the diffracted beam lies in the plane of incidence and [b] the sample surface normal, the grating vector and the incoming beam do not form a plane which calls for the vectorial theory and results in conical scattering.Comment: Corrected Eqs. (3) & (6); 14 pages, 8 figure

Photochromism in Ruddlesden-Popper copper-based perovskites:A light-induced change of coordination number at the surface

Ruddlesden-Popper organic-inorganic hybrid copper-based perovskites have been studied for decades owing to a variety of interesting properties, such as thermochromism and piezochromism, and the mechanisms behind these phenomena have been explained. Another possible property of these materials that has seldomly been investigated is photochromism. In this work, the photochromic properties of bis(phenethylammonium) tetrachlorocuprate (also known as phenethylammonium copper chloride) are reported for the first time. This material has attracted scientific interest owing to the fact that it shows both ferroelectric and ferromagnetic behavior. This work highlights the difference in stability between two Ruddlesden-Popper copper-based perovskites - with phenethylammonium (PEA) or methylammonium (MA) as the cations - during external stimuli. Various techniques, such as Raman and X-ray photoelectron spectroscopy, and grazing-incidence wide-angle X-ray scattering, combined with optical studies, were used to investigate the underlying photochemical processes at a molecular level. It is found that for the PEA compound, ultraviolet illumination causes a color change from yellow to brown. This is the result of two independent events, namely a Cu2+ reduction reaction and a transition from an octahedral copper-chloride structure to square-planar CuCl42-. After illumination, the material (brown color) is unstable in air, which is evident from a color change back to yellow. Interestingly, the similar compound bis(methylammonium) tetrachlorocuprate does not display photochromic behavior, which is attributed to the different nature of the two organic cations

Body Shape and Life Style of the Extinct Balearic Dormouse Hypnomys (Rodentia, Gliridae): New Evidence from the Study of Associated Skeletons

Hypnomys is a genus of Gliridae (Rodentia) that occurred in the Balearic Islands until Late Holocene. Recent finding of a complete skeleton of the chronospecies H. morpheus (Late Pleistocene-Early Holocene) and two articulated skeletons of H. cf. onicensis (Late Pliocene) allowed the inference of body size and the calculation of several postcranial indexes. We also performed a Factorial Discriminant Analysis (FDA) in order to evaluate locomotory behaviour and body shape of the taxa. Using allometric models based on skull and tooth measurements, we calculated a body weight between 173 and 284 g for H. morpheus, and direct measurements of articulated skeletons yielded a Head and Body Length (HBL) of 179 mm and a Total Body Length of 295 mm for this species. In addition to the generally higher robustness of postcranial bones already recorded by previous authors, H. morpheus, similar to Canariomys tamarani, another extinct island species, displayed elongated zygopodium bones of the limbs and a wider distal humerus and femur than in an extant related taxon, Eliomys quercinus. Indexes indicated that Hypnomys was more terrestrial and had greater fossorial abilities than E. quercinus. This was also corroborated by a Discriminant Analysis, although no clear additional inference of locomotory abilities could be calculated

Threats posed by the fungal kingdom to humans, wildlife, and agriculture

The fungal kingdom includes at least 6 million eukaryotic species and is remarkable with respect to its profound impact on global health, biodiversity, ecology, agriculture, manufacturing, and biomedical research. Approximately 625 fungal species have been reported to infect vertebrates, 200 of which can be human associated, either as commensals and members of our microbiome or as pathogens that cause infectious diseases. These organisms pose a growing threat to human health with the global increase in the incidence of invasive fungal infections, prevalence of fungal allergy, and the evolution of fungal pathogens resistant to some or all current classes of antifungals. More broadly, there has been an unprecedented and worldwide emergence of fungal pathogens affecting animal and plant biodiversity. Approximately 8,000 species of fungi and Oomycetes are associated with plant disease. Indeed, across agriculture, such fungal diseases of plants include new devastating epidemics of trees and jeopardize food security worldwide by causing epidemics in staple and commodity crops that feed billions. Further, ingestion of mycotoxins contributes to ill health and causes cancer. Coordinated international research efforts, enhanced technology translation, and greater policy outreach by scientists are needed to more fully understand the biology and drivers that underlie the emergence of fungal diseases and to mitigate against their impacts. Here, we focus on poignant examples of emerging fungal threats in each of three areas: human health, wildlife biodiversity, and food security

Photophysics of Two-Dimensional Perovskites—Learning from Metal Halide Substitution

Whereas their photophysics exhibits an intricate interplay of carriers with the lattice, most reports have so far relied on single compound studies. With the exception of variations of the organic spacer cations, the effect of constituent substitution on the photophysics and the nature of emitting species, in particular, has remained largely under-explored. Here PEA$_2$PbBr$_4$, PEA$_2$PbI$_4$, and PEA$_2$SnI$_4$ are studied through a variety of optical spectroscopy techniques to reveal a complex set of excitonic transitions at low temperature. We attribute the emergence of weak high energy features to a vibronic progression breaking Kasha's rule and highlight that the responsible phonons cannot be accessed through simple Raman spectroscopy. Bright peaks at lower energy are due to two distinct excitons, of which the upper is a convolution of a bright exciton and a localised state, whereas the lower is attributed to shallow defects. Our study offers deeper insights into the photophysics of two-dimensional perovskites through compositional substitution and highlights critical limits to the communities' current understanding of the photophysics of these compounds