Salasmcdougall7152

(PsycInfo Database Record (c) 2022 APA, all rights reserved).With the development of electric vehicles and products, lithium metal batteries with solid-state electrolytes have shown a broad application prospect. However, the uneven deposition of lithium, low ion conductivity, narrow electrochemical window, and high interfacial impedance limit the safety and performance of the solid-state batteries. Herein, we develop a non-ceramic solid electrolyte based on the graphene oxide aerogel frame filling with polyethylene oxide (GSPE). The resulting uniform and resilient framework structure form a continuous Li-ion adsorption zone, which ensures uniform ion-current distribution at the interface while obtaining the relatively high ionic conductivity, effectively preventing the uneven deposition of lithium, and thus greatly improving the battery stability. Comprehensive electrochemical analysis showed that GSPE achieved an ionic conductivity of 4.12 × 10-4 S cm-1 at 50 °C. The assembled LiFePO4(LFP) |GSPE| Li full battery can stably cycle for more than 100 cycles at 0.1 C, and the lithium symmetrical battery can continuously be plating-peeling for more than 600 h at 0.1 mA cm-2. The method of using the carbon aerogel structure to achieve the uniform deposition of lithium ions has explored a new possible research direction for all-solid-state batteries.Alzheimer's disease is a chronic disease, and the long-term treatment of chronic diseases has always been a concern. Memantine (Mem) is approved by the US Food and Drug Administration for the treatment of moderate to severe Alzheimer's disease. In this study, reactions of memantine (Mem) with pamoic acid (Pam) were carried out to form insoluble salts (Mem-Pam). Four polymorphic forms (Forms I-IV) of Mem-Pam were successfully obtained through polymorphic screening, which were systematically characterized by X-ray powder diffraction (PXRD), thermal analysis (TGA and DSC), single-crystal X-ray diffraction (SXRD), and solid-state fluorescence. Compared with the hydrochloride form, the dissolution and release rates of these four forms are lower. The presence of pamoic acid reduces the release rate of memantine and makes it possible to achieve a sustained release of the drug. learn more Interestingly, because of the presence of memantine, each polymorphic solid crystal of Mem-Pam has unique fluorescence emission. Therefore, memantine and pamoic acid have a synergistic effect on the fluorescence performance and can be expected to be used for real-time monitoring in continuous and controlled release drug delivery systems. In addition, the polymorphic solid crystals also exhibit reversible mechanochromic luminescence under the fumigation of acetonitrile vapor, which has a guiding role in the fluorescence design and synthesis of Pam substances and is expected to be used for information security, visual inspection of organic substances, etc.Materials with crystalline structures of circular symmetry are rare in nature; however, they are highly desired in optical applications with structured lights, whose characteristics are of cylindrical symmetry. In this work, using a naturally existing circular anisotropy from a spherulite formed by molecular self-assembly, we obtain a cylindrical vector optical vortex beam generation transformed from the spin angular momentum in the wide visible range. The proposed strategy provides promising and broad opportunities for the applications of spherulites in the generation of structured lights and modulations of both the polarization and the angular momentum.The advent of data-driven science in the 21st century brought about the need for well-organized structured data and associated infrastructure able to facilitate the applications of artificial intelligence and machine learning. We present an effort aimed at organizing the diverse landscape of physics-based and data-driven computational models in order to facilitate the storage of associated information as structured data. We apply object-oriented design concepts and outline the foundations of an open-source collaborative framework that is (1) capable of uniquely describing the approaches in structured data, (2) flexible enough to cover the majority of widely used models, and (3) utilizes collective intelligence through community contributions. We present example database schemas and corresponding data structures and explain how these are deployed in software at the time of this writing.We report an experimental and computational study of the electron-induced chemistry of methanesulfonic acid (MSA, MeSO3H) in clusters. We combine the mass spectra after the 70 eV electron ionization with the negative ion spectra after electron attachment (EA) at low electron energies of 0-15 eV of the MSA molecule, small MSA clusters, and microhydrated MSA clusters to reveal the solvation effects. The MSA/He coexpansion only generates small MSA clusters with up to four molecules, but adding water substantially hydrates the MSA clusters, resulting in clusters composed of 1-2 MSA molecules accompanied by quite a few water molecules. The clustering strongly suppresses the fragmentation of the MSA molecules upon both the positive ionization and EA. The electron-energy-dependent ion yield for different negative ions is measured. For the MSA molecule and pure MSA clusters, EA leads to an H-abstraction yielding MeSO3-. It proceeds efficiently at low electron energies below 2 eV with a shoulder at 3-4 eV and a broad, almost 2 orders of magnitude weaker, peak around 8 eV. The hydrated (H2O)nMeSO3- ions with n ≤ 3 exhibit only a broad peak around 7 eV similar to EA of pure water clusters. Thus, for the small clusters, the electron attachment and hydrogen abstraction from water occur. On the other hand, the larger clusters with n > 4 display a peak below 2 eV, which quickly dominates the spectrum with increasing n. This peak is related to the formation of the H3O+·MeSO3- ion pair upon hydration and subsequent dipole-supported electron attachment followed by the hydronium neutralization and H3O• radical dissociation. The size-resolved experimental data indicate that the ionic dissociation of MSA starts to occur in the neutral MeSO3H(H2O)N clusters with about four water molecules.The generation of reactive oxygen species (ROS) in photodynamic therapy (PDT) involves excited-state intermediates with both singlet and triplet spin configurations, which provides possibilities to modulate the ROS production in PDT under an external magnetic field. Here, we present that magnetically modulated ROS production can promote PDT efficacy and develop a magnetic-field-assisted PDT (magneto-PDT) method for effectively and selectively killing cancer cells. The photosensitization reaction between excited-state riboflavin and oxygen molecules is influenced by the applied field, and the overall magnetic field effect (MFE) shows a moderate increase at a low field (1000 G). It is found that the spin precession occurring in radical ion pairs (electron transfer from riboflavin to oxygen) facilitates the O2•- generation at the low field. In comparison, the spin splitting in an encounter complex (energy transfer from riboflavin to oxygen) benefits the production of 1O2 species at the high field. The field modulation on the two types of ROS in PDT, i.e., O2•- and 1O2, is also demonstrated in living cells. The magneto-PDT strategy shows the capability to inhibit the proliferation of cancer cells (e.g., HeLa, RBL-2H3, and MCF-7) effectively and selectively, which reveals the potential of using the MFE on chemical reactions in biological applications.Merging existing catalysts together as a cascade catalyst may achieve "one-pot" synthesis of complex but functional molecules by simplifying multistep reactions, which is the blueprint of sustainable chemistry with low pollutant emission and consumption of energy and materials only when the smooth mass exchange between different catalysts is ensured. Effective strategies to facilitate the mass exchange between different active centers, which may dominate the final activity of various cascade catalysts, have not been reached until now, even though charged interfaces due to work function driven electron exchange have been widely observed. Here, we successfully constructed mass (reactants and intermediates) exchange paths between Pd/N-doped carbon and MoC/N-doped carbon induced by interfacial electron exchange to trigger the mild and cascade methylation of amines using CO2 and H2. Theoretical and experimental results have demonstrated that the mass exchange between electron-rich MoC and electron-deficient Pd could prominently improve the production of N,N-dimethyl tertiary amine, which results in a remarkably high turnover frequency value under mild conditions, outperforming the state-of-the-art catalysts in the literature by a factor of 5.9.Asymmetric catalytic azidation has increased in importance to access enantioenriched nitrogen containing molecules, but methods that employ inexpensive sodium azide remain scarce. This encouraged us to undertake a detailed study on the application of hydrogen bonding phase-transfer catalysis (HB-PTC) to enantioselective azidation with sodium azide. So far, this phase-transfer manifold has been applied exclusively to insoluble metal alkali fluorides for carbon-fluorine bond formation. Herein, we disclose the asymmetric ring opening of meso aziridinium electrophiles derived from β-chloroamines with sodium azide in the presence of a chiral bisurea catalyst. The structure of novel hydrogen bonded azide complexes was analyzed computationally, in the solid state by X-ray diffraction, and in solution phase by 1H and 14N/15N NMR spectroscopy. With N-isopropylated BINAM-derived bisurea, end-on binding of azide in a tripodal fashion to all three NH bonds is energetically favorable, an arrangement reminiscent of the corresponding dynamically more rigid trifurcated hydrogen-bonded fluoride complex. Computational analysis informs that the most stable transition state leading to the major enantiomer displays attack from the hydrogen-bonded end of the azide anion. All three H-bonds are retained in the transition state; however, as seen in asymmetric HB-PTC fluorination, the H-bond between the nucleophile and the monodentate urea lengthens most noticeably along the reaction coordinate. Kinetic studies corroborate with the turnover rate limiting event resulting in a chiral ion pair containing an aziridinium cation and a catalyst-bound azide anion, along with catalyst inhibition incurred by accumulation of NaCl. This study demonstrates that HB-PTC can serve as an activation mode for inorganic salts other than metal alkali fluorides for applications in asymmetric synthesis.Vast attention from researchers is being given to the development of suitable oxygen evolution reaction (OER) electrocatalysts via water electrolysis. Being highly abundant, the use of transition-metal-based OER catalysts has been attractive more recently. Among the various transition-metal-based electrocatalysts, the use of layered double hydroxides (LDHs) has gained special attention from researchers owing to their high stability under OER conditions. In this work, we have reported the synthesis of trimetallic NiCoV-LDH via a simple wet-chemical method. The synthesized NiCoV-LDH possesses aggregated sheet-like structures and is screened for OER studies in alkaline medium. In the study of OER activity, the as-prepared catalyst demanded 280 mV overpotential and this was 42 mV less than the overpotential essential for pristine NiCo-LDH. Moreover, doping of a third metal into the NiCo-LDH system might lead to an increase in TOF values by almost three times. Apart from this, the electronic structural evaluation confirms that the doping of V3+ into NiCo-LDH could synergistically favor the electron transfer among the metal ions, which in turn increases the activity of the prepared catalyst toward the OER.