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45 kJ mol-1 at maximum, which proves that the catalytic promotion effect of silicate was greater than the inhibition effect of carbonate. The pyrolysis products obtained by Flash pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS) under isothermal pyrolysis conditions were primarily composed of aliphatic hydrocarbon structures, which had different degrees of impact on the production of heteroatoms. This work provides a reliable theoretical basis for future studies on the influence of minerals on pyrolysis of organic matter in oil shale.Li-ion rechargeable batteries are promising systems for large-scale energy storage solutions. Understanding the electrochemical process in the cathodes of these batteries using suitable techniques is one of the crucial steps for developing them as next-generation energy storage devices. Due to the broad energy range, synchrotron X-ray techniques provide a better option for characterizing the cathodes compared to the conventional laboratory-scale characterization instruments. This work gives an overview of various synchrotron radiation techniques for analyzing cathodes of Li-rechargeable batteries by depicting instrumental details of X-ray diffraction, X-ray absorption spectroscopy, X-ray imaging, and X-ray near-edge fine structure-imaging. Analysis and simulation procedures to get appropriate information of structural order, local electronic/atomic structure, chemical phase mapping and pores in cathodes are discussed by taking examples of various cathode materials. Applications of these synchrotron techniques are also explored to investigate oxidation state, metal-oxygen hybridization, quantitative local atomic structure, Ni oxidation phase and pore distribution in Ni-rich layered oxide cathodes.From the perspective of crystallography, there exist crystals as well as boundary planes in NdFeB permanent magnets and accordingly, there should exist orientation textures of Nd2Fe14B crystals and orientation texture of boundary planes. This work therefore aims to study the misorientations across boundary planes in a sintered NdFeB permanent magnet. As an interdisciplinary study, serial stereological methods are developed to extract more structural information from the material and as the result, spreading wetting and penetration of Nd-Rich phases to the Nd2Fe14B phase are quantificationally characterized. The entire boundaries are sorted into Nd2Fe14B/Nd2Fe14B grain boundaries (N/N boundaries) and Nd2Fe14B/(thin-layer-like)Nd-Rich phase boundaries (N/R boundaries). 31°/[0 0 1] and 60°/[0 0 1] twist boundaries are preferred among N/N boundaries, while 31°/[0 0 1] and 72°/[0 0 1] misorientations are preferred among N/R boundaries. The structural features of these misorientations are elaborated via the Five Parameter Analysis (FPA) method. The potential correlations between the grain boundary plane distributions (GBPDs) and magnetic properties are then discussed regarding how the anisotropic features at boundary locations impact coercivity, domain and remanence.By combining the anionic salt meso-tetra(4-carboxyphenyl)porphyrin (TCPP4-) and the Keggin polyoxometalate cation cluster [Al13O4(OH)24(H2O)12]7+ via a simple ion-exchange method, a hybrid (C48H26N4O8)[Al13O4(OH)24(H2O)12]2(OH)10·18H2O (Al13-TCPP) was prepared and thoroughly characterized as a prototype of polyoxometalate-porphyrin hybrids for the photocatalytic degradation of the mustard gas simulant 2-chloroethyl ethyl sulfide (CEES). The experimental results showed that the catalytic degradation rate of CEES in the presence of Al13-TCPP reached 96.16 and 99.01% in 180 and 90 min in methanol and methanol-water solvent mixture (v/v = 1  1), respectively. The reaction followed first-order reaction kinetics, and the half-life and kinetic constant in methanol and solvent mixture were 39.8 min, -0.017 min-1 and 14.7 min, -0.047 min-1. Mechanism analysis indicated that under visible light irradiation in air, CEES was degraded through a combination of oxidation and alcoholysis/hydrolysis in methanol and the methanol-water solvent mixture. The superoxide radical (O2˙-) and singlet molecular oxygen (1O2) generated by Al13-TCPP selectively oxidized CEES into a non-toxic sulfoxide. The singlet oxygen capture experiments showed that Al13-TCPP (Φ = 0.236) had a higher quantum yield of singlet oxygen generation than H4TCPP (Φ = 0.135) under visible light irradiation in air. The material Al13-TCPP has good reusability, and the degradation rate of CEES can still reach 98.37% after being recycled five times.This study aimed to promote the separation of photogenerated carriers and improve the redox performance of graphite carbon nitride (g-C3N4) by synthesizing a double-heterojunction-structure photocatalyst, g-C3N4/(101)-(001)-TiO2, through the solvothermal method. The photocatalyst comprised a Z-system formed from g-C3N4 and the (101) plane of TiO2, as well as a surface heterojunction formed from the (101) and (001) planes of TiO2. The results showed that g-C3N4/(101)-(001)-TiO2 had strong photocatalytic activity and stable performance in the photodegradation of paracetamol. The active species ·O2 - and ·OH were found to play important roles in the photocatalytic degradation of paracetamol through a radical-quenching experiment. The charge-transfer mechanism was also described in detail. Overall, this work provided a new strategy for the Z-system heterojunction and opened up the application of this structure in the degradation of organic pollutants.Metal complexes have gradually been attracting interest from researchers worldwide as potential cancer therapeutics. Driven by the many side effects of the popular platinum-based anticancer drug cisplatin, the tireless endeavours of researchers have afforded strategies for the design of appropriate metal complexes with minimal side effects compared to cisplatin and its congeners to limit the unrestricted propagation of cancer. In this regard, transition metal complexes, especially rhenium-based complexes are being identified and highlighted as promising cancer theranostics, which are endowed with the ability to detect and annihilate cancer cells in the body. This is attributed the amazing photophysical properties of rhenium complexes together with their ability to selectively attack different organelles in cancer cells. TPCA-1 mw Therefore, this review presents the properties of different rhenium-based complexes to highlight their recent advances as anticancer agents based on their cytotoxicity results.This investigation is concerned with designing efficient catalysts for direct formic acid fuel cells. A ternary catalyst containing iron (nano-FeOx) and nickel (nano-NiOx) nanowire oxides assembled sequentially onto a bare platinum (bare-Pt) substrate was recommended for the formic acid electro-oxidation reaction (FAOR). While nano-NiOx appeared as fibrillar nanowire bundles (ca. 82 nm and 4.2 μm average diameter and length, respectively), nano-FeOx was deposited as intersecting nanowires (ca. 74 nm and 400 nm average diameter and length, respectively). The electrocatalytic activity of the catalyst toward the FAOR depended on its composition and loading sequence. The FeOx/NiOx/Pt catalyst exhibited ca. 4.8 and 1.6 times increases in the catalytic activity and tolerance against CO poisoning, respectively, during the FAOR, relative to the bare-Pt catalyst. Interestingly, with a simple activation of the FeOx/NiOx/Pt catalyst at -0.5 V vs. Ag/AgCl/KCl (sat.) in 0.2 mol L-1 NaOH, a favorable Fe2+/Fe3+ transformation succeeded in mitigating the permanent CO poisoning of the Pt-based catalysts. Interestingly, this activated a-FeOx/NiOx/Pt catalyst had an activity 7 times higher than that of bare-Pt with an ca. -122 mV shift in the onset potential of the FAOR. The presence of nano-FeOx and nano-NiOx enriched the catalyst surface with extra oxygen moieties that counteracted the CO poisoning of the Pt substrate and electronically facilitated the kinetics of the FAOR, as revealed from CO stripping and impedance spectra.Nano-porous aerogels are an advantageous approach to produce low-density materials with high surface area, particularly when using biobased materials. Frequently, most biobased aerogels are synthesized through a bottom-up approach, which requires high energy inputs to break and rebuild the raw materials, and for elimination of water. To curb this, this work focused on generating aerogels by a top-down approach through the delignification of a wood substrate while eliminating water by solvent exchange. To diversify the surface chemistry for use in water treatment, the delignified wood-nanowood-was coated with a chitosan-cyclodextrin co-polymer and tested in the capture of microcystin-LR. The generated nanowood structure had 75% porosity after coating, with up to 339% water swelling and an adsorption capacity of 0.12 mg g-1 of the microcystin. This top-down technique enables the generation of low-cost aerogels by reducing steps, using a biobased self-assembled coating with hydrophobic active sites, and avoiding costly energetic input.Flexible molds with micro-nano hierarchical structures on the surface were fabricated by a two-step template process using anodic porous alumina as a starting material. The obtained flexible molds could be used to form micro-nano hierarchical pillar arrays on the surface of glass tubes and convex lenses by photo-nanoimprinting. The contact angle characteristics of the surfaces with hierarchical pillar arrays were measured, and it was confirmed that they exhibit superhydrophobic properties with a water-droplet contact angle exceeding 150°. The flexible molds obtained in this study can be used repeatedly and efficiently to form micro-nano hierarchical surfaces with superhydrophobic properties on the surfaces of substrates with various curvatures.The anticorrosion efficiency of two polymer compounds, namely polystyrene (PS), polybutylene terephthalate (PBT), against the corrosion of SABIC iron (S-Fe) in 1.0 M HCl solution was investigated. The anticorrosion efficiency was estimated by chemical and electrochemical measurements. The anticorrosion efficiency increased with the increase in the concentration of the polymer compounds and reduction in temperature. All the obtained corrosion data confirmed the anticorrosion strength in the presence of PS and PBT compounds, such as the decreasing values of the corrosion current density, capacity of the double layer, and weight reduction, while the values of the charge-transfer resistance increased. Also, the pitting potential values moved in the noble (+) direction. The anticorrosion efficiency of the PBT compound was higher than that of the PS compound, which was 95.98% at 500 ppm concentration for PBT while for PS it was 93.34% according to polarization measurements. The anticorrosion activity occurred by the adsorption of PS and PBT compounds on the surface of S-Fe according to the Langmuir isotherm. The polarization curves indicated that the PS and PBT compounds were mixed-type inhibitors. Density functional theory (DFT) and Monte Carlo simulation (MC) were performed for the two polymer compounds. The computational quantum functions were found to be in agreement with the experimental results.