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A mechanochemical synthesis method has been used to synthesize CoRu nanoparticles supported on CeO2 for methane dry reforming. In this work, we study the effect of Ru addition to Co/CeO2-based catalysts and of the synthesis method by screening their catalytic activity, using synchrotron X-ray diffraction (XRD), and operando near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS). Ruthenium addition directly impacts the reducibility of cobalt species and results in smaller particle sizes, as demonstrated by H2-temperature programmed reduction and XRD. NAP-XPS shows that Ru modifies the metal-support interaction, as evidenced by the higher Ce3+/Ce ratios for the bimetallic samples and tuning the oxidation state of Ru. The synthesis method also influences the dispersion of Co and Ru on the surface. Mechanochemically-prepared samples (mono- and bimetallic) outperformed the conventionally-synthesized counterparts by reaching higher CH4 and CO2 conversions, resulting in a stable CoRu/CeO2 catalyst for 24 h at 700 °C and yielding an H2/CO ratio close to 1., Peer Reviewed, Postprint (published version)

Ni-Fe nanocatalysts supported on CeO2 have been prepared for the catalysis of methane steam reforming (MSR) aiming for coke-resistant noble metal-free catalysts. The catalysts have been synthesized by traditional incipient wetness impregnation as well as dry ball milling, a green and more sustainable preparation method. The impact of the synthesis method on the catalytic performance and the catalysts’ nanostructure has been investigated. The influence of Fe addition has been addressed as well. The reducibility and the electronic and crystalline structure of Ni and Ni-Fe mono- and bimetallic catalysts have been characterized by temperature programmed reduction (H2-TPR), in situ synchrotron X-ray diffraction (SXRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Their catalytic activity was tested between 700 and 950 °C at 108 L gcat-1 h-1 and with the reactant flow varying between 54 and 415 L gcat-1 h-1 at 700 °C. Hydrogen production rates of 67 mol gmet-1 h-1 have been achieved. The performance of the ball-milled Fe0.1Ni0.9/CeO2 catalyst was similar to that of Ni/CeO2 at high temperatures, but Raman spectroscopy revealed a higher amount of highly defective carbon on the surface of Ni-Fe nanocatalysts. The reorganization of the surface under MSR of the ball-milled NiFe/CeO2 has been monitored by in situ near-ambient pressure XPS experiments, where a strong reorganization of the Ni-Fe nanoparticles with segregation of Fe toward the surface has been observed. Despite the catalytic activity being lower in the low-temperature regime, Fe addition for the milled nanocatalyst increased the coke resistance and could be an efficient alternative to industrial Ni/Al2O3 catalysts., Peer Reviewed, Postprint (published version)

The generation of methane fuel using surplus renewable energy with CO as the carbon source enables both the decarbonization and substitution of fossil fuel feedstocks. However, high temperatures are usually required for the efficient activation of CO. Here we present a solid catalyst synthesized using a mild, green hydrothermal synthesis that involves interstitial carbon doped into ruthenium oxide, which enables the stabilization of Ru cations in a low oxidation state and a ruthenium oxycarbonate phase to form. The catalyst shows an activity and selectivity for the conversion of CO into methane at lower temperatures than those of conventional catalysts, with an excellent long-term stability. Furthermore, this catalyst is able to operate under intermittent power supply conditions, which couples very well with electricity production systems based on renewable energies. The structure of the catalyst and the nature of the ruthenium species were acutely characterized by combining advanced imaging and spectroscopic tools at the macro and atomic scales, which highlighted the low-oxidation-state Ru sites (Ru, 0 < n < 4) as responsible for the high catalytic activity. This catalyst suggests alternative perspectives for materials design using interstitial dopants.

Curved crystals are a simple but powerful approach to bridge the gap between single crystal surfaces and nanoparticle catalysts, by allowing a rational assessment of the role of active step sites in gas-surface reactions. Using a curved Rh(111) crystal, here, we investigate the effect of A-type (square geometry) and B-type (triangular geometry) atomic packing of steps on the catalytic CO oxidation on Rh at millibar pressures. Imaging the crystal during reaction ignition with laser-induced CO2 fluorescence demonstrates a two-step process, where B-steps ignite at lower temperature than A-steps. Such fundamental dissimilarity is explained in ambient pressure X-ray photoemission (AP-XPS) experiments, which reveal partial CO desorption and oxygen buildup only at B-steps. AP-XPS also proves that A-B step asymmetries extend to the active stage: at A-steps, low-active O–Rh–O trilayers buildup immediately after ignition, while highly active chemisorbed O is the dominant species on B-type steps. We conclude that B-steps are more efficient than A-steps for the CO oxidation.

Efficiently treating methane emissions in transportation remains a challenge. Here, we investigate palladium and platinum mono- and bimetallic ceria-supported catalysts synthesized by mechanical milling and by traditional impregnation for methane total oxidation under dry and wet conditions, reproducing those present in the exhaust of natural gas vehicles. By applying a toolkit of in situ synchrotron techniques (X-ray diffraction, X-ray absorption and ambient pressure photoelectron spectroscopies), together with transmission electron microscopy, we show that the synthesis method greatly influences the interaction and structure at the nanoscale. Our results reveal that the components of milled catalysts have a higher ability to transform metallic Pd into Pd oxide species strongly interacting with the support, and achieve a modulated PdO/Pd ratio than traditionally-synthesized catalysts. We demonstrate that the unique structures attained by milling are key for the catalytic activity and correlate with higher methane conversion and longer stability in the wet feed., Peer Reviewed, Postprint (published version)

Curved crystals are a simple but powerful approach to bridge the gap between single crystal surfaces and nanoparticle catalysts, by allowing a rational assessment of the role of active step sites in gas-surface reactions. Using a curved Rh(111) crystal, here, we investigate the effect of A-type (square geometry) and B-type (triangular geometry) atomic packing of steps on the catalytic CO oxidation on Rh at millibar pressures. Imaging the crystal during reaction ignition with laser-induced CO2 fluorescence demonstrates a two-step process, where B-steps ignite at lower temperature than A-steps. Such fundamental dissimilarity is explained in ambient pressure X-ray photoemission (AP-XPS) experiments, which reveal partial CO desorption and oxygen buildup only at B-steps. AP-XPS also proves that A-B step asymmetries extend to the active stage: at A-steps, low-active O-Rh-O trilayers buildup immediately after ignition, while highly active chemisorbed O is the dominant species on B-type steps. We conclude that B-steps are more efficient than A-steps for the CO oxidation.

In this work, the preparation of regular nanosized columnar structures of titanium dioxide by means of glancing angle deposition with magnetron sputtering (MS-GLAD) followed by thermal annealing is reported. MS-GLAD gives rise to metallic titanium columnar structures with regular width and length that after thermal treatment are fully oxidized to form TiO2 nanocolumns that maintain the morphological features of the original metallic ones. Further functionalization with gold by means of multiple ion cluster source results in well-dispersed Au nanoparticles across the nanocolumns’ surface with a narrow size distribution centered at ca. 8.5 nm. The obtained nanostructures show photocatalytic self-cleaning activity as shown by the elimination of an organic layer deposited on their surface and the detection of hydroxyl radicals. Photoelectrochemical measurements show a better charge separation at the Au/TiO2 interface. In addition, wettability studies show that the degree of hydrophobicity of the surface is increased by the presence of nanocolumns, both in the dark and under UV illumination. This behavior is not modified by the presence of Au nanoparticles on the surface. The obtained results open up interesting implications in the tunability of the properties of nanostructured thin films for this kind of photo-activated application.

In this study, epoxy fatty acid esters of cassava starch were synthesized by reacting cassava starch with vernonia oil methyl ester (epoxy ester) using 1‐butyl‐3‐methylimidazolium hexafluorophosphate, [C4C1Im][PF6] ionic liquid (IL) as a reaction medium and DMSO as co‐solvent. Lipase Candida antarctica fraction B (Novozyme 435) was used as a catalyst for the esterification reaction. In the optimized reaction conditions, a degree of substitution (DS) of 0.95 was achieved, at a reaction temperature of 40°C within 72 h of reaction time. The new cassava starch esters were characterized by infrared (FTIR), solid state NMR (CP/MAS 13C NMR), SEM, XRD, thermogravimetric analysis (TGA), and DSC. FTIR and NMR spectroscopy analyses confirmed the successful esterification of starch and the DS was calculated to be 0.95 by titration methods. SEM and XRD studies showed that the morphology and crystallinity of native cassava starch were significantly changed upon esterification producing a continuous and amorphous material. Finally, the thermal behavior of the native and the starch vernolate was investigated using TGA and DSC techniques. The results revealed a change in the characteristic melting point and decomposition pattern of the new polymer. The onset decomposition temperature of the new starch vernolate is similar to the native form.