Wubritt7144

Nonfullerene acceptors (NFAs) have attracted great attention in high-efficiency organic solar cells (OSCs). While the effect of molecular properties including structures and energetics on charge transfer has been extensively investigated, the effect of macroscopic-phase properties is yet to be revealed. Here we have performed a correlation study of the nanoscale-phase morphology on the photoexcited hole transfer (HT) process and photovoltaic performance by combining ultrafast spectroscopy with high temporal resolution and photo-induced force microscopy (PiFM) with high spatial and chemical resolution. In PM6/IT-4F, we observe biphasic HT behavior with a minor ultrafast ( less then 100 fs) interfacial process and a major diffusion-mediated HT process until ∼100 ps, which depends strongly on phase segregation. Because of the interplay between charge transfer and transport, a compromised domain size of 20-30 nm for NFAs shows the best performance. This study highlights the critical role of phase morphology in high-efficiency OSCs.In the context of electron dynamics simulations, when the charge density of a molecule is subject to a perturbation in the form of a short electric field pulse, density fluctuations develop in time. In the absence of dissipation, these oscillations continue indefinitely, reflecting the resonances of the electronic system; as a matter of fact, from the Fourier transform of the time dependent dipole arising from them, the absorption spectrum of the molecule can be calculated. Since these oscillations are the result of the electrons moving through the molecular structrure, it seems plausible that they carry information on the transport properties of the system. This is the idea explored in the present article for the case of conjugated polymers. Specifically, we depart from a nonequilibrium state with the charge concentrated on the ends of the molecule, and estimate the currents flowing back and forth during the evolution of electron dynamics simulations. These show that the charge oscillates between the sides oic structure techniques.Scientific understanding of microbial biogeography and assembly is lacking for activated sludge microbial communities, even though the diversity of microbial communities in wastewater treatment plants (WWTPs) is thought to have a direct influence on system performance. Here, utilizing large-scale 16S rRNA gene data generated from 211 activated sludge samples collected from 15 cities across China, we show activated sludge microbes, whose growth and metabolism can be regulated followed with the metabolic theory of ecology with an apparent Ea value (apparent activation energy) of 0.08 eV. WWTPs at a lower latitude tend to harbor a more diverse array of microorganisms. In agreement with the general understanding, the activated sludge microbial assembly was mainly driven by deterministic processes and the mean annual temperature was identified as the most important factor affecting the microbial community structure. The treatment process types with similar microbial growth types and functions had a distinct impact on the activated sludge microbial community structure only when WWTPs were located near each other and received similar influent. Overall, these findings provide us with a deeper understanding of activated sludge microbial communities from an ecological perspective. Moreover, these findings suggest that, for a given set of performance characteristics (e.g., combined nitrification, denitrification, and phosphorus removal), it may be difficult to employ common engineering levers to control additional aspects of community structure due to the influence of natural environmental factors.Herbicides are a key element in agriculture but they do cause environmental problems and natural alternatives are being sought. In this context, invasive plants could provide an as yet unexplored source for the development of future herbicides. Urochloa humidicola has great invasive potential in Brazilian environments as it hampers the establishment of other plants. The phytotoxicity of U. humidicola root extracts has been evaluated, and the major components have been identified. MDV3100 The phytotoxicity of the extract was assessed in the wheat coleoptile assay on seeds of troublesome weeds and on Anadenanthera colubrina, a tree species used in ecological restoration programs. The ethyl acetate extract showed the highest activity, and the most affected weeds were E. crus-galli, M. maximus, and A. viridis with the latter weed more affected by the extract than by the herbicide Logran. Microscopic ultrastructural analysis of A. colubrina roots indicated possible signals of cell death. Seven compounds were identified in the ethyl acetate extract of which one diterpene and four saponins are new. Six of these compounds were tested in the wheat coleoptile bioassay. The most active were diterpene 1 and saponins 2, 3, and 6. The phytotoxic activity of U. humidicola explains the issues observed in ecological restoration with A. colubrina in the presence of Urochloa species, and its effect on weeds reinforces its potential use in agriculture.For food emulsions containing enzymatically modified egg yolk, the conventional Folch extraction does not fully recover the polar lysophospholipids. This can be overcome by repeated methanol extractions. After solvent evaporation, the extracted (lyso)phospholipids are solubilized into mixed micelles with cholate as a detergent. link2 The solubilized (lyso)phospholipids can be accurately quantified by 31P NMR with recoveries ranging between 96% and 108%. Detection at a high (16.4 T) relative to a mainstream (9.4 T) magnetic field strength did not offer a significant advantage since the slow molecular tumbling of the mixed micelles increased line widths. This was due to field-strength-dependent chemical shift anisotropy relaxation. Method precision is similar at 9.4 and 16.4 T, with within-laboratory reproducibilities of 7-22% and 12-25%, respectively. The method can be implemented as a routine analytical procedure at 9.4 T (400 MHz NMR spectrometer), and the limits of detection and quantification are adequate for the verification of the standard of identity of a mayonnaise prepared with enzymatically modified egg yolk.Imine and enamine bonds decorate the skeleton of numerous reagents, catalysts, and organic materials. However, it is difficult to isolate at will a single tautomer, as dynamic equilibria occur easily, even in the solid state, and are sensitive to electronic and steric effect, including π-conjugation and H-bonding. link3 Here, using as model Schiff bases generated from salicylaldehydes and TRIS in a set of linear free energy relationships (LFER), we disclose how the formation of either imines or enamines can be controlled and provide a comprehensive framework that captures the structural underpinning of this prediction. This work highlights the potentiality of tailor-made designs en route to compounds with desirable functionality.Optical voltage sensors with the ability to monitor neuronal activities are invaluable tools for studying information processing of the brain. However, the current genetically encoded voltage indicators usually require high-power visible light for excitation and are limited to genetically addressable model animals. Here, we report a near-infrared (NIR)-excited nongenetic voltage nanosensor that achieves stable recording of neuronal membrane potential in intact animals. The nanosensor is composed of a Förster resonance energy transfer (FRET) pair, the outer membrane-anchored upconversion nanoparticle (UCNP), and the membrane-embedded dipicrylamine (DPA). The negative charge of DPA allows membrane potential fluctuation to affect the distance between the DPA and UCNP, therefore changing the FRET efficiency. Consequently, the emission intensity of the nanosensor can report the membrane potential. Using the nanosensor, we monitor not only electrically evoked changes in the membrane potential of cultured cells but also sensory responses of neurons in intact zebrafish and brain state-modulated subthreshold activities of cortical neurons in intact mice.Polymeric metal-organic nanocapsule networks (polyMONCs), where metal-organic nanocapsules (MONCs) are connected by functional polymers, could possess the properties of traditional polymers and also retain the structures of MONCs. In this work, we constructed novel polyMONCs based on Mg-seamed pyrogallol[4]arene-containing MONCs through supramolecular coordination-driven self-assembly. The MONCs can be successfully polymerized using poly(ethylene glycol) as the linker, and the prepared polyMONCs can be further made into gels with self-healing properties and stimuli responsiveness. Advantageously, single crystals of MONCs cross-linked by ethylene glycol/diethylene glycol were obtained, giving us direct perspectives to mimic and investigate the self-assembly process of polyMONCs.With increasing utilization of silver nanomaterials, growing concerns are raised on their deleterious effects to the environment. Once discharged in an aquatic environment, the interactions between silver nanowires (AgNWs) and proteins may significantly affect the environmental behaviors, fate, and toxicities of AgNWs. In the present study, three representative model proteins, including ovalbumin (OVA), bovine serum albumin (BSA), and lysozyme (LYZ), were applied to investigate the impacts of the interactions between proteins and AgNWs on the transformations (oxidative dissolution and sulfidation) of AgNWs in an aquatic environment. Fluorescence spectroscopy and isothermal titration calorimetry analyses indicated that there was very weak interaction between OVA or BSA and AgNWs, but there was a strong interaction between the positively charged LYZ and the negatively charged AgNWs. The presence of LYZ not only reversed the surface charge of AgNWs but also resulted in the breakup of the nanowire structure and increased the reactive surface area. The positively charged surface of AgNWs in the presence of LYZ favored the access of sulfide ions. As a consequence, the kinetics of oxidative dissolution and sulfidation of AgNWs were not affected by OVA and BSA but were significantly facilitated by LYZ. The results shed light on the important roles of electrostatic interactions between AgNWs and proteins, which may have important implications for evaluating the fate and effects of silver nanomaterials in complicated environments.Naphthalene (NAP), as a surrogate of intermediate-volatility organic compounds (IVOCs), has been proposed to be an important precursor of secondary organic aerosol (SOA). However, the relative contribution of its emission sources is still not explicit. This study firstly conducted the source apportionment of atmospheric NAP using a triple-isotope (δ13C, δ2H, and Δ14C) technique combined with a Bayesian model in the Beijing-Tianjin-Hebei (BTH) region of China. At the urban sites, stable carbon (-27.7 ± 0.7‰, δ13C) and radiocarbon (-944.0 ± 20.4‰, Δ14C) isotope compositions of NAP did not exhibit significant seasonal variation, but the deuterium system showed a relatively more 2H depleted signature in winter (-86.7 ± 8.9‰, δ2H) in comparison to that in summer (-56.4 ± 3.9‰, δ2H). Radiocarbon signatures indicated that 95.1 ± 1.8% of NAP was emitted from fossil sources in these cities. The Bayesian model results indicated that the emission source compositions in the BTH urban sites had a similar pattern. The contribution of liquid fossil combustion was highest (46.