Alvarezlynch6785

The electrochemical behavior of platinum single crystal surfaces can be taken as a model response for the interpretation of the activity of heterogeneous electrodes. The cyclic voltammogram of a given platinum electrode can be considered a fingerprint characteristic of the distribution of sites on its surface. We start this review by providing some simple mathematical descriptions of the voltammetric response in the presence of adsorption processes. We then describe the voltammogram of platinum basal planes, followed by the response of stepped surfaces. The voltammogram of polycrystalline materials can be understood as a composition of the response of the different basal contributions. Further resolution in the discrimination of different surface sites can be achieved with the aid of surface modification using adatoms such as bismuth or germanium. The application of these ideas is exemplified with the consideration of real catalysts composed of platinum nanoparticles with preferential shapes. Expected final online publication date for the Annual Review of Analytical Chemistry, Volume 13 is June 12, 2020. Please see http//www.annualreviews.org/page/journal/pubdates for revised estimates.Accurate, rapid, and reliable quantification of saccharides is essential for understanding their behaviors and roles in environmental processes. However, the conventional colorimetric method for saccharide quantification fails to discriminate between fructose and glucose, resulting in the misestimation of total saccharides. To solve this problem, a fluorescence approach, that is, parallel factor framework-linear regression analysis, was developed in this work to quantify the specific fluorescence signatures of the fluorescent products generated from the reaction between saccharides and sulfuric acid. The fluorescent derivatives of saccharides were recognized and the simultaneous quantification of glucose and fructose was achieved with a detection limit of 2.9 μg/mL and 1.3 μg/mL, respectively. Furthermore, 200 μg/mL of the treated sorbitol and gluconic acid only, respectively, equaled to 6 μg/mL and 3 μg/mL of the treated glucose, indicating their negligible interference for the saccharide quantification using this method. In addition, the feasibility and robustness of this method in environmental applications were validated with the recovery tests using spiked real water samples. This fluorescence-based approach offers a new tool to monitor saccharides in complex environments.Cereal grains and their processed food products are frequently contaminated with mycotoxins produced by the Fusarium genus. Enniatins (ENNs), which belong to the so-called "emerging mycotoxins" family, are among the most frequently found in small grain cereals. Health hazards induced by a chronic exposure to ENNs or an association of ENNs with other major mycotoxins is a risk that cannot be excluded given the current toxicological data. Thus, efforts must be pursued to define efficient control strategies to mitigate their presence in cereal grains. A key condition for achieving this aim is to gain deep and comprehensive knowledge of the factors promoting the appearance of ENNs in crop harvests. selleck inhibitor After an update of ENN occurrence data, this review surveys the scientific literature on the Fusarium species responsible for ENN contamination and covers the recent advances concerning the abiotic determinants and the genetic regulation of ENN biosynthesis.The role of dipolar motion of organic cations in the A-sites of halide perovskites has been debated in an effort to understand why these materials possess such remarkable properties. Here, we show that the dipolar motion of cations such as methylammonium (MA) or formamidinium (FA) versus cesium (Cs) does not influence large polaron binding energies, delocalization lengths, formation times, or bimolecular recombination lifetimes in lead bromide perovskites containing only one type of A-site cation. We directly probe the transient absorption spectra of large polarons throughout the entire mid-infrared and resolve their dynamics on time scales from sub-100 fs to sub-μs using time-resolved mid-infrared spectroscopy. Our findings suggest that the improved optoelectronic properties reported of halide perovskites with mixed A-site cations may result from synergy among the cations and how their mixture modulates the structure and dynamics of the inorganic lattice rather than from the dipolar properties of the cations themselves.Coordination geometries of transition metals play vital roles in the self-assembly process of supramolecular coordination complexes. Herein, seven-coordinate 3d metal ions were applied as templates and catalytically active sites for subcomponent self-assembly that resulted in a new category of covalent metallacycles. Single-crystal structures showed that the sizes, configurations, and functionalization of covalent metallacycles could be tuned by the selection of rigid dihydrazide, transition metal ions, and prefunctionalized subcomponents, respectively. Moreover, metallacycles decorated with carboxylic groups could be employed as precursors to prepare aerogels through hierarchical self-assembly, which also exhibited high catalytic activity for cycloaddition of CO2 into cyclic carbonates.Recent studies have shown the potential of the photosensitizer chemistry of humic acid, as a proxy for humic-like substances in atmospheric aerosols, to contribute to secondary organic aerosol mass. The mechanism requires particle-phase humic acid to absorb solar radiation and become photoexcited, then directly or indirectly oxidize a volatile organic compound (VOC), resulting in a lower volatility product in the particle phase. We performed experiments in a photochemical chamber, with aerosol-phase humic acid as the photosensitizer and limonene as the VOC. In the presence of 26 ppb limonene and under atmospherically relevant UV-visible irradiation levels, there is no significant change in particle diameter. Calculations show that SOA production via this pathway is highly sensitive to VOC precursor concentrations. Under the assumption that HULIS is equally or less reactive than the humic acid used in these experiments, the results suggest that the photosensitizer chemistry of HULIS in ambient atmospheric aerosols is unlikely to be a significant source of secondary organic aerosol mass.