https://web.uvic.ca/~agbrolo/ACA_GFS_MF_2011.pdf

A review on the fabrication of substrates for surface enhanced Raman spectroscopy and their applications in analytical chemistry.

Highly active and low-cost catalysts for electrochemical reactions such as the hydrogen evolution reaction (HER) are crucial for the development of efficient energy conversion and storage technologies. Theoretical simulations have been instrumental in revealing the correlations between the electronic structure of materials and their catalytic activity, and guide the prediction and development of improved catalysts. However, difficulties in accurately engineering the desired atomic sites lead to challenges in making direct comparisons between experimental and theoretical results. In MoS2, the Mo-edge has been demonstrated to be active for HER whereas the S-edge is inert. Using a computational descriptor-based approach, we predict that by incorporating transition metal atoms (Fe, Co, Ni, or Cu) the S-edge site should also become HER active. Vertically standing, edge-terminated MoS2 nanofilms provide a well-defined model system for verifying these predictions. The transition metal doped MoS2 nanofilms show an increase in exchange current densities by at least two-fold, in agreement with the theoretical calculations. This work opens up further opportunities for improving electrochemical catalysts by incorporating promoters into particular atomic sites, and for using well-defined systems in order to understand the origin of the promotion effects.

/pdf/transition-metal-doped-edge-sites-in-vertically-aligned-mos2-47o8fdy795.pdf

Transition-metal Doped Edge Sites in Vertically Aligned MoS2 Catalysts for Enhanced Hydrogen Evolution

Biomass gasification is an interesting technology in the future development of a worldwide sustainable energy system, which can help to decrease our current dependence on fossil fuels. Biomass gasification is a thermal process where solid fuel is converted into a useful gas using several gasifying agents such as air, and steam. The producer gas has a great number of applications. The most important is being combustion for power and heat generation as well as raw gas for production of fuels or chemicals. This review mainly presents the recent progresses on tar elimination during the biomass gasification. Then, novel non-catalytic absorption and adsorption methods of tar removal under ambient temperature conducted by our laboratory members were also explained. In our opinion, the tar removal can be conducted by combination of catalytic reforming in the gasifier and oil materials adsorption in the scrubber. Furthermore, the tar catalytic reforming is a most significant step during biomass gasification or pyrolysis. Thus, the development of reasonable catalysts for tar elimination has been faced with a significant challenge in current society.

Recent progresses in catalytic tar elimination during biomass gasification or pyrolysis—A review

A series of manganese oxides (MnO, MnO2, Mn2O3 and Mn3O4) were synthesized and tested in heterogeneous activation of peroxymonosulfate (PMS) for phenol degradation in aqueous solutions. Their properties were characterized by several techniques such as X-ray diffraction (XRD), thermogravimetric-differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), and N2 adsorption/desorption isotherms. Catalytic activities of Mn oxides were found to be closely related to the chemical states of Mn. Mn2O3 is highly effective in heterogeneous activation of PMS to produce sulfate radicals for phenol degradation compared with other catalysts (MnO, MnO2, and Mn3O4). The activity shows an order of Mn2O3 > MnO > Mn3O4 > MnO2. Mn2O3 could completely remove phenol in 60 min at the conditions of 25 mg/L phenol, 0.4 g/L catalyst, 2 g/L PMS, and 25 °C. After heat regeneration, the activity could be fully recovered. A pseudo first order model would fit to phenol degradation kinetics and activation energy was obtained as 11.4 kJ/mol.

/pdf/manganese-oxides-at-different-oxidation-states-for-2bitr7kyli.pdf

Manganese oxides at different oxidation states for heterogeneous activation of peroxymonosulfate for phenol degradation in aqueous solutions

A facile, one-pot solvothermal method is developed to synthesize MoS2 nanoflowers (MoS2NFs) coated on reduced graphene oxide (rGO) paper. The resulting MoS2NF/rGO paper serves as a freestanding, flexible and durable working electrode for hydrogen evolution reaction (HER), exhibiting an overpotential lowered to −0.19 V with a Tafel slope of ∼95 mV per decade.

MoS2 nanoflower-decorated reduced graphene oxide paper for high-performance hydrogen evolution reaction

Three alkyltrimethylammonium thiomolybdates, [R–N(CH3)3]2MoS4 (where R = lauryl, myristyl or cetyl) were synthesized in aqueous solution, and characterized by 1H-NMR spectroscopy. These alkyltrimethylammonium thiomolybdates were used (the lauryl and myristyl thiomolybdates for the first time) as precursors for in situ prepared MoS2 catalysts, activated during the hydrodesulfurization of dibenzothiophene. The catalysts were analyzed by EDX, showing large voids and a S/Mo ratio around 2. High surface areas up to 443 m2/g and type IV adsorption–desorption nitrogen isotherms were obtained. X-ray diffraction showed that the catalysts are poorly crystalline, with a very weak (002) peak intensity for all samples except the MoS2 catalyst prepared from pure ammonium tetrathiomolybdate precursor. A high dibenzothiophene conversion (74%) was observed with the catalyst obtained from the lauryltrimethylammonium thiomolybdate precursor, attributed mainly to its high specific surface area. Selectivity results showed that all the prepared catalysts strongly favored the hydrogenation pathway.

G. Alonso

Papers

HDS of DBT with Molybdenum Disulfide Catalysts Prepared by In Situ Decomposition of Alkyltrimethylammonium Thiomolybdates