Gram-Scale Synthesis of CoO/C as Base for PtCo/C High-Performance Catalysts for the Oxygen Reduction Reaction

The composition, structure, catalytic activity in the ORR and stability of PtCo/C materials, obtained in two stages and compared with commercial Pt/C analogs, were studied. At the first stage of the synthesis performed by electrodeposition of cobalt on a carbon support, a CoOx/C composite containing 8% and 25 wt% cobalt oxide was successfully obtained. In the second step, PtCoOx/C catalysts of Pt1.56Co and Pt1.12Co composition containing 14 and 30 wt% Pt, respectively, were synthesized based on the previously obtained composites. According to the results of the composition and structure analysis of the obtained PtCoOx/C catalysts by X-ray diffraction (XRD), X-ray fluorescence analysis (XRF), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) methods, the formation of small bimetallic nanoparticles on the carbon support surface has been proved. The resulting catalysts demonstrated up to two times higher specific catalytic activity in the ORR and high stability compared to commercial Pt/C analogs.

Hybrid Supercapacitor Electrode Materials via Molecular Imprinting of Nitrogenous Ligands and Iron Complexes into Carbon Support

Novel hybrid supercapacitor materials were made by the covalent immobilization of nitrogenous ligands onto the surface of commercial carbon support (Vulcan XC-72), then coordinated to iron. The covalent attachment of the nitrogenous ligands allows for the controlled deposition of nitrogen functionalities on the surface of the carbon. The supercapacitor tests in acidic media showed significant growth of the capacitance as a result of the nitrogenous ligands on the support. Notably, the increase of the capacitance values directly correlates with the molecular loading on the surface. Following coordination of the iron to the ligands on the surface further elevated the capacitance via Faradaic reactions of the metal center. Remarkably, the overall capacitance of materials significantly increased after the course of long-term cycling tests (ca. 110% or higher). At the beginning of durability studies, a small decline in capacitance was observed, due to some extent of molecular decomposition on the surface of the electrode. However, the intense cycling further propagates a steady growth of the overall capacitance. This could be attributed to the process of polymerization of physisorbed molecules/ radicals that result in the formation of a 3D network structure that eventually boosts the overall capacitance and charge storage of the electrode.

Carbon-Supported KCoMoS2 for Alcohol Synthesis from Synthesis Gas

KCoMoS2 was supported on various carbon support materials to study the support effect on synthesis gas conversion. Next to two activated carbons with high micropore volume, a traditional alumina (γ-Al2O3) support and its carbon coated form (CCA) were studied for comparison. Coating alumina with carbon increases the selectivity to alcohols, but the AC-supported catalysts show even higher alcohol selectivities and yields, especially at higher temperatures where the conversions over the AC-supported catalysts increase more than those over the γ-Al2O3-based catalysts. Increasing acidity leads to decreased CO conversion yield of alcohols. The two activated-carbon-supported catalysts give the highest yield of ethanol at the highest conversion studied, which seems to be due to increased KCoMoS2 stacking and possibly to the presence of micropores and low amount of mesopores.

H2 Production from Formic Acid Using Highly Stable Carbon-Supported Pd-Based Catalysts Derived from Soft-Biomass Residues: Effect of Heat Treatment and Functionalization of the Carbon Support

The production of hydrogen from liquid organic hydrogen carrier molecules stands up as a promising option over the conventional hydrogen storage methods. In this study, we explore the potential of formic acid as a convenient hydrogen carrier. For that, soft-biomass-derived carbon-supported Pd catalysts were synthesized by a H3PO4-assisted hydrothermal carbonization method. To assess the impact of the properties of the support in the catalytic performance towards the dehydrogenation of formic acid, three different strategies were employed: (i) incorporation of nitrogen functional groups; (ii) modification of the surface chemistry by performing a thermal treatment at high temperatures (i.e., 900 °C); and (iii) combination on both thermal treatment and nitrogen functionalization. It was observed that the modification of the carbon support with these strategies resulted in catalysts with enhanced performance and outstanding stability even after six consecutive reaction cycles, thus highlighting the important effect of tailoring the properties of the support.