The solvation of carbon dioxide in sea water plays an important role in the carbon circle and the world climate. The salting-out/salting-in mechanism of CO2 in electrolyte solutions still remains elusive at molecule level. The ability of ion salting-out/salting-in CO2 in electrolyte solution follows Hofmeister Series and the change of water mobility induced by salts can be predicted by the viscosity B-coefficients. In this work, the chemical potential of carbon dioxide and the dynamic properties of water in aqueous NaCl, KF and NaClO4 solutions are calculated and analyzed. According to the viscosity B-coefficients, NaClO4 (0.012) should salt out the carbon dioxide relative to in pure water, but the opposite effect is observed for it. Our simulation results suggest that the salting-in effect of NaClO4 is due to the strongly direct anion-CO2 interaction. The inconsistency between Hofmeister Series and the viscosity B-coefficient suggests that it is not always right to indicate whether a salt belongs to salting-in or salting-out just from these properties of the salt solution in the absence of solute. 相似文献
The title complex [(C12H8N2)2Bi(O2NO)3] was synthesized by reaction of 1,10-phenanthroline (phen) and Bi(NO3)3·5H2O. The structure of the complex was characterized by single-crystal X-ray diffraction, IR spectroscopy, and elemental analysis. An advanced solution-reaction isoperibol microcalorimeter was applied to determine the standard molar enthalpies of formation at 298.15 K of the complex and Bi(NO3)3·5H2O, giving –(798.92 ± 5.99) and –(1986.87 ± 0.20) kJ mol−1, respectively. The biological effect of the complex was evaluated by microcalorimetry on the growth of Schizosaccharomyces pombe (S. pombe). According to thermogenic curves, the corresponding thermokinetics and thermodynamic parameters were derived. The complex had good bioactivity on the growth metabolism of S. pombe, with the value of IC50 being 2.8 × 10−5 mol L−1.
Nitrogen-doped porous carbons were prepared using a facile method, with low-biotechnology fulvic acid potassium salts as a precursor. The prepared carbons had a high surface area (1623 m2 g?1) and good electrochemical properties, making them suitable electrode materials for supercapacitors. Nitrogen-doped porous carbons were tested as an electrode in both 6 M KOH aqueous solution and different concentrations KNO3 aqueous solution. The nitrogen-doped porous carbons with unique microstructure and nitrogen functionalities exhibited a capacitance of 235 F g?1 in a 6 M KOH aqueous solution. Electrochemical investigation showed that the nitrogen-doped porous carbons exhibited a broad potential operational window in a 2.5 M KNO3 aqueous solution. Furthermore, a high capacitance retention of 88.1 % was achieved even after 5000 cycles at 1.7 V. Potassium nitrate solutions in a wide range of concentrations were also proven to be promising electrolytes for electrochemical capacitors because they are cheap, noncorrosive, electrochemically stable, and compatible to diverse current collectors. 相似文献
Hexagram-like CoS-MoS2 composites were prepared on indium tin oxide (ITO) conductive glasses via cyclic voltammetry electrodeposition using Co(NO3)2 and (NH4)2MoS2 as precursors and tested for application in hydrogen evolution reaction (HER). The structure of CoS-MoS2 composites was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and X-ray photoelectron spectrum (XPS). Electrochemical characterizations indicate that CoS-MoS2 composites exhibit more excellent catalytic activity and stability than MoS2. Compared with pure MoS2, the hexagram-like CoS-MoS2 composites with increased specific surface area improved the density of exposed active sites, and the Co binding S edges in CoS-MoS2 composites promote the number of highly catalytic edge sites and decreased the binding energy △GH. Moreover, the effects of different substrates on the CoS-MoS2 composites were also investigated. Our further understanding of this highly active hydrogen evolution catalyst can facilitate the development of economical electrochemical hydrogen production systems. 相似文献
Journal of Solid State Electrochemistry - Binder-free, high-performance electrode materials play a critical role for supercapacitors. In this paper, through the electrochemical anodization process,... 相似文献
The metallic 1T-MoS2 has attracted considerable attention as an effective catalyst for hydrogen evolution reactions (HERs). However, the fundamental mechanism about the catalytic activity of 1T-MoS2 and the associated phase evolution remain elusive and controversial. Herein, we prepared the most stable 1T-MoS2 by hydrothermal exfoliation of MoS2 nanosheets vertically rooted into rigid one-dimensional TiO2 nanofibers. The 1T-MoS2 can keep highly stable over one year, presenting an ideal model system for investigating the HER catalytic activities as a function of the phase evolution. Both experimental studies and theoretical calculations suggest that 1T phase can be irreversibly transformed into a more active 1T′ phase as true active sites in photocatalytic HERs, resulting in a “catalytic site self-optimization”. Hydrogen atom adsorption is the major driving force for this phase transition. 相似文献
In this paper, we study the inverse anisotropic curvature flow from strictly convex hypersurfaces. We show the long-time existence and the convergence to the Wulff shape after rescaling, under certain conditions on the general speed functions. 相似文献
The aim of this paper is to introduce and study Hom-Gel'fand–Dorfman super-bialgebras and Hom-Lie conformal superalgebras. In this paper, we provide different ways for constructing HomGel'fand–Dorfman super-bialgebras. Also, we obtain some infinite-dimensional Hom-Lie superalgebras from affinization of Hom-Gel'fand–Dorfman super-bialgebras. Finally, we give a general construction of Hom-Lie conformal superalgebras from Hom-Lie superalgebras and establish the equivalence between quadratic Hom-Lie conformal superalgebras and Hom-Gel'fand–Dorfman super-bialgebras. 相似文献