Mo2C@C nanofibers film as durable self-supported electrode for efficient electrocatalytic hydrogen evolution

Self-supported electrocatalytic thin films consist 3D conducting network and well-embedded electrocatalysts, which endows the advantage in mass flow kinetics and durability for large-scale water splitting. Synthesis of such self-supported electrode still remains a big challenge due to the difficulty in the control over the 3D conducting network and the simultaneous growth of catalyst with well attachment on the conducting fibers. Herein, a self-supported Mo2C@carbon nanofibers (Mo2C@C NF) film has been successfully fabricated with outstanding electrocatalytic performance under optimized pyrolysis temperature and precursors mass ratio conditions. During the carbonation process, the Mo2C nanoparticles (~16 nm) are simultaneously grown and well dispersed on the inter-connected carbon nanofibers, which form 3D conducting network. The as-formed 3D carbon network is strong enough to support direct electrocatalytic application without additional ink or supporting substrates. This particular electrode structure facilitates easy access to the active catalytic sites, electron transfer, and hydrogen diffusion, resulting in the high hydrogen evolution reaction (HER) activity. A low overpotential of 86 mV is needed to achieve 10 mA cm-2 current density with outstanding kinetics metric (Tafel 43 mV dec-1) in 1M KOH. Additionally, the self-supported Mo2C@C NF film, a binder-free electrode, exhibits extraordinary stability of more than 340 h.

Biomarkers geochemistry of the Alpagut oil shale sequence: an evaluation of dispositional environments and source rock potential from Dodurga-Çorum basin (N-Turkey)

The Cenozoic Çankırı-Çorum basin, with sedimentary facies of varying thickness and distribution, contains raw matters such as coal deposits, oil shales and evaporate. Source rock and sedimentary environment characteristics of the oil shale sequence have been evaluated. The studied oil shales have high organic matter content (from 2.97 to 15.14%) and show excellent source rock characteristics. Oil shales are represented by very high hydrogen index (532–892 mg HC/g TOC) and low oxygen index (8–44 mgCO2/g TOC) values. Pyrolysis data indicate that oil shales contain predominantly Type I and little Type II kerogen. The biomarker data reveal the presence of algal, bacterial organic matter and terrestrial organic matter with high lipid content. These findings show that organic matters in the oil shales can generate hydrocarbon, especially oil. High C26/C25, C24/C23 and low C22/C21 tricyclic terpane, C31R/C30 hopane and DBT/P ratios indicate that the studied oil shales were deposited in a lacustrine environment, and very low Pr/Ph ratio is indicative of anoxic character for the depositional environment. Tmax values from the pyrolysis analysis are in the range of 418–443 °C, and production index ranges from 0.01 to 0.08. On the gas chromatography, high Pr/nC17 and Ph/nC18 ratios and CPI values significantly exceeding 1 were determined. Very low 22S/(22S + 22R) homohopane, 20S/(20S + 20R) sterane, diasterane/sterane and Ts/(Ts + Tm) ratios were calculated from the biomarker data. Results of all these analyses indicate that Alpagut oil shales have not yet matured and have not entered the oil generation window.

NIRS and Aquaphotomics Trace Robusta-to-Arabica Ratio in Liquid Coffee Blends

Coffee is both a vastly consumed beverage and a chemically complex matrix. For a long time, an arduous chemical analysis was necessary to resolve coffee authentication issues. Despite their demonstrated efficacy, such techniques tend to rely on reference methods or resort to elaborate extraction steps. Near infrared spectroscopy (NIRS) and the aquaphotomics approach, on the other hand, reportedly offer a rapid, reliable, and holistic compositional overview of varying analytes but with little focus on low concentration mixtures of Robusta-to-Arabica coffee. Our study aimed for a comparative assessment of ground coffee adulteration using NIRS and liquid coffee adulteration using the aquaphotomics approach. The aim was to demonstrate the potential of monitoring ground and liquid coffee quality as they are commercially the most available coffee forms. Chemometrics spectra analysis proved capable of distinguishing between the studied samples and efficiently estimating the added Robusta concentrations. An accuracy of 100% was obtained for the varietal discrimination of pure Arabica and Robusta, both in ground and liquid form. Robusta-to-Arabica ratio was predicted with R2CV values of 0.99 and 0.9 in ground and liquid form respectively. Aquagrams results accentuated the peculiarities of the two coffee varieties and their respective blends by designating different water conformations depending on the coffee variety and assigning a particular water absorption spectral pattern (WASP) depending on the blending ratio. Marked spectral features attributed to high hydrogen bonded water characterized Arabica-rich coffee, while those with the higher Robusta content showed an abundance of free water structures. Collectively, the obtained results ascertain the adequacy of NIRS and aquaphotomics as promising alternative tools for the authentication of liquid coffee that can correlate the water-related fingerprint to the Robusta-to-Arabica ratio.

Influence of meromixia on the distribution of zoobenthos and zooplankton in the salt soda lake Doroninskoe

Meromictic soda lakes are considered models of reservoirs of the Early Proterozoic. Lake Doroninskoe belongs to a rare type of moderately salty alkaline soda lake with a carbonate type of salinity and pronounced meromixia. Studies and publications on the zoobenthos of the lake are rare. In 2005–2007, studies of zoobenthos and zooplankton of the lake were carried out. Meromixia of the water column caused the stable presence of zooplankton only in a layer up to 4 m. The distribution of the taxonomic abundance, quantitative development and structure of zoobenthos in the lake corresponds to the stratification of the water column into mixolimnion, chemocline and monimolimnion. Bottom biotopes and water column layers deeper than 4 m were uninhabited, which is probably due to the lack of oxygen and high hydrogen sulphide content in the bottom water layers due to meromixia. A similar distribution of zooplankton in Lake Doroninskoe and its mesocosm model was revealed.

Progress in Mo/W-based electrocatalysts for nitrogen reduction to ammonia under ambient conditions

Ammonia (NH3), possessing high hydrogen content and energy density, has been widely employed as fertilizers and value-added chemicals in green energy carriers and fuels. However, the current NH3 synthesis largely...

The enhanced thermal stability and reduced hygroscopicity of aluminum hydride coated with Vinyltrimethoxysilane

Alpha-aluminum hydride (α-AlH3) is an excellent high-energy additive for solid propellants because of its high hydrogen content (10.8 wt%) and energy density, low decomposition temperature, and good combustion performance. However,...

Hydrogen Recovery by Mixed Matrix Membranes Made from 6FCl-APAF HPA with Different Contents of a Porous Polymer Network and Their Thermal Rearrangement

Mixed matrix membranes (MMMs) consisting of a blend of a hydroxypolyamide (HPA) matrix and variable loads of a porous polymer network (PPN) were thermally treated to induce the transformation of HPA to polybenzoxazole (β-TR-PBO). Here, the HPA matrix was a hydroxypolyamide having two hexafluoropropyilidene moieties, 6FCl-APAF, while the PPN was prepared by reacting triptycene (TRP) and trifluoroacetophenone (TFAP) in a superacid solution. The most probable size of the PPN particles was 75 nm with quite large distributions. The resulting membranes were analyzed by SEM and AFM. Up to 30% PPN loads, both SEM and AFM images confirmed quite planar surfaces, at low scale, with limited roughness. Membranes with high hydrogen permeability and good selectivity for the gas pairs H2/CH4 and H2/N2 were obtained. For H2/CO2, selectivity almost vanished after thermal rearrangement. In all cases, their hydrogen permeability increased with increasing loads of PPN until around 30% PPN with ulterior fairly abrupt decreasing of permeability for all gases studied. Thermal rearrangement of the MMMs resulted in higher permeabilities but lower selectivities. For all the membranes and gas pairs studied, the balance of permeability vs. selectivity surpassed the 1991 Robeson’s upper bound, and approached or even exceeded the 2008 line, for MMMs having 30% PPN loads. In all cases, the HPA-MMMs before thermal rearrangement provided good selectivity versus permeability compromise, similar to their thermally rearranged counterparts but in the zone of high selectivity. For H2/CH4, H2/N2, these nonthermally rearranged MMMs approach the 2008 Robeson’s upper bound while H2/CO2 gives selective transport favoring H2 on the 1991 Robeson’s bound. Thus, attending to the energy cost of thermal rearrangement, it could be avoided in some cases especially when high selectivity is the target rather than high permeability.