Tailoring CO2 adsorption and activation properties of ceria nanocubes by coating with nanometre-thick yttria layers

[EN] Ceria (CeO2) is a ubiquitous component in catalysts for environmental protection processes, especially those devoted to CO2 valorisation. Aimed at preparing ceria-based nanomaterials with enhanced CO2 adsorption and activation properties, both the surface acid-base and redox features of ceria nanocubes were modulated by a novel, simple, wet chemistry synthetic strategy consisting of their coating with yttria (Y2O3) layers of variable thickness in the nanometre scale. The as-synthesised samples were characterised with special attention to their surface basicity and reducibility. Characterisation results revealed that the surface doping with yttria not only improved both the reducibility at low temperature and CO2 adsorption capacity of ceria nanocubes, but also introduced a variety of basic sites with different strength. Finally, the careful control of the yttria layer thickness allowed to modulate these effects and thereby the ability of nanostructured ceria to adsorb and activate the CO2 molecule

Size-Controlled Water-Soluble Ag Nanoparticles

Ag nanoparticles of two different sizes (1 and 4 nm) were prepared within an apoferritin cavity by using an Ag+-loaded apoferritin as a nanoconfined environment for their construction. The initial amount of Ag' ions injected in the apoferritin cavity dictates the size of the final Ag particles. The protein shell prevents bulk aggregation of the metal particles, which renders them water soluble and extremely stable

Catalytic Performance of Ni/CeO2/X-ZrO2 (X = Ca, Y) Catalysts in the Aqueous-Phase Reforming of Methanol

In this study, we reported on the effect of promoting Ni/ZrO2 catalysts with Ce, Ca (two different loadings), and Y for the aqueous-phase reforming (APR) of methanol. We mainly focused on the effect of the redox properties of ceria and the basicity provided by calcium or yttrium on the activity and selectivity of Ni in this reaction. A systematic characterization of the catalysts was performed using complementary methods such as XRD, XPS, TPR, CO2-TPD, H-2 chemisorption, HAADF-STEM, and EDS-STEM. Our results reveal that the improvement in reducibility derived from the incorporation of Ce did not have a positive impact on catalytic behaviour thus contrasting with the results reported in the literature for other Ce-based catalytic compositions. On the contrary, the available Ni-metallic surface and the presence of weak basic sites derived from Ca incorporation seem to play a major role on the catalytic performance for APR of methanol. The best performance was found for a Ce-free catalyst with a molar Ca content of 4%

Using the ℓ1-norm for Image-based tomographic reconstruction

This paper introduces an ℓ1-norm model based on Total Variation Minimization for tomographic reconstruction. The reconstructions produced by the proposed model are more accurate than those obtained with classical reconstruction models based on the ℓ2-norm. This model can be linearized and solved by linear programming techniques. Furthermore, the complementary slackness conditions can be exploited to reduce the dimension of the resulting formulation by removing unnecessary variables and constraints. Since the efficacy of the reduced formulation strongly depends on the quality of the dual-multipliers used when applying the reduction method, Lagrangian relaxation is used to obtain near-optimal multipliers. This allows solving larger instances in an efficient way

Combining Deep Learning and Compressed SensingMethods for the 3D Characterization of Ultra-ThinEpitaxial Layers Grown on Controlled-Shape Nano-Oxides

Using a nanostructured platform (a controlled-shape nano-oxide) and conventional wet impregnation techniques, powder-type materials have been prepared in which atomically thin surface layers are deposited under very mild conditions. More importantly, an advanced methodology, combining energy dispersive X-ray spectroscopy-scanning transmission electron tomography (STEM-EDX ET) and deep learning denoising techniques, has been developed for the 3D compositional characterization of these unique nanosystems. The complex case of LaOx-coated CeO2 nanocubes is illustrated. For these, aberration corrected 2D STEM-EDX evidence that ceria nanocubes become covered with a 2–4 atom-thick layer of a La, Ce-mixed oxide with spatially varying composition. However, STEM-EDX ET reveals that this layer distributes unevenly, patching most of the available nanocube surface. The large flexibility and spread availability of the involved synthetic techniques enables, using the tools here developed, a wide exploration of the wealth of questions and applications of these intriguing, atomically thin, surface oxide phases10 página

Understanding the potential-induced activation of a cobalt MOF electrocatalyst for the oxygen evolution reaction

Metal–organic frameworks (MOFs) are attractive porous materials for electrocatalytic applications associated with carbon-free energy storage and conversion. This type of material usually requires a post-treatment to be used as electrocatalyst. The present work comprehensively investigates the electrochemical activation of a cobalt-MOF@Nafion composite that produces outstanding electrocatalytic performance for the water oxidation reaction at neutral pH. A detailed electrochemical characterization reveals that the electroactivation of the composite requires the participation of the oxygen evolution reaction (OER) and leads to a significant increase in the electroactive population of cobalt centers. It is shown that an increase of the applied activation potential in the OER region results in a faster electroactivation of the Co-MOF without affecting the intrinsic electrocatalytic properties of the active cobalt centers, as evidenced by the unique linear correlation between the electrocatalytic OER current and the population of electroactive cobalt. In addition, at structural level, it is shown that the electrochemical activation causes the partial disruption of the Nafion adlayer, as well as morphological changes of the Co–MOF particles from a compact, rounded morphology, before electrochemical activation, to a more open and expanded structure, after electroactivation; with the concomitant increase of the number of surface–exposed cobalt centers. Interestingly, these cobalt centers retain their coordinative chemistry and their laminar distribution in the nanosheets at the nanoscale, which is consistent with the preservation of their intrinsic electrocatalytic activity after potential–induced activation. In this scenario, these results suggest that only the electroactivated cobalt centers with good accessibility to the electrolyte are electrochemically active. This work provides a better understanding of the processes and structural changes underlying the electrochemical activation at neutral pH of a Co–MOF for boosting the electrocatalytic water oxidation reaction9 página

Quantitative Evaluation of Supported Catalysts Key Properties from Electron Tomography Studies: Assessing Accuracy Using Material-Realistic 3D-Models

Electron Tomography (ET) reconstructions can be analysed, via segmentation techniques, to obtain quantitative, 3D-information about individual nanoparticles in supported catalysts. This includes values of parameters out of reach for any other technique, like their volume and surface, which are required to determine the dispersion of the supported particle system or the specific surface area of the support; two figures that play a major role in the performance of this type of catalysts. However, both the experimental conditions during the acquisition of the tilt series and the limited fidelity of the reconstruction and segmentation algorithms, restrict the quality of the ET results and introduce an undefined amount of error both in the qualitative features of the reconstructions and in all the quantitative parameters measured from them. Here, a method based on the use of well-defined 3D geometrical models (phantoms), with morphological features closely resembling those observed in experimental images of an Au/CeO2 catalyst, has been devised to provide a precise estimation of the accuracy of the reconstructions. Using this approach, the influence of noise and the number of projections on the errors of reconstructions obtained using a Total Variation Minimization in 3D (TVM-3D) algorithm have been determined. Likewise, the benefits of using smart denoising techniques based on Undecimated Wavelet Transforms (UWT) have been also evaluated. The results clearly reveal a large impact of usual noise levels on both the quality of the reconstructions and nanometrological measurement errors. Quantitative clues about the key role of UWT to largely compensate them are also provided.This work has received support from Projects: PID2020-113006-RB-I00, PID2019-110018GA-I00, PID2020-114594GB-C22, funded by MCIN/AEI/https://doi.org/10.13039/501100011033.This work has also been co-financed by Project ref: MAT2017-87579-R and by the 2014 -2020 ERDF Operational Programme and by the Department of Economy, Knowledge, Business and University of the Regional Government of Andalusia, Project references: FEDER-UCA18-107139, FEDERUCA18-106895 and P18-FR-1422. STEM ET experiments were recorded at the DME-UCA Node of the Spanish Singular Infrastructure for Electron Microscopy of Materials (ICTS ELECMI)

In-Depth Structural and Optical Analysis of Ce-modified ZnO Nanopowders with Enhanced Photocatalytic Activity Prepared by Microwave-Assisted Hydrothermal Method

Pure and Ce-modified ZnO nanosheet-like polycrystalline samples were successfully synthesized by a simple and fast microwave-based process and tested as photocatalytic materials in environmental remediation processes. In an attempt to clarify the actual relationships between functionality and atomic scale structure, an in-depth characterization study of these materials using a battery of complementary techniques was performed. X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM), high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM), energy-dispersive X-Ray spectroscopy-scanning transmission electron microscopy (STEM-XEDS), photoluminescence spectroscopy (PL) and UV-Visible absorption spectroscopy were used to evaluate the effect of Ce ions on the structural, morphological, optical and photocatalytic properties of the prepared ZnO nanostructures. The XRD results showed that the obtained photocatalysts were composed of hexagonal, wurtzite type crystallites in the 34-44 nm size range. The SEM and TEM showed nanosheet-shaped crystallites, a significant fraction of them in contact with bundles of randomly oriented and much smaller nanoparticles of a mixed cerium-zinc phase with a composition close to Ce0.68Zn0.32Ox. Importantly, in clear contrast to the prevailing proposals regarding this type of materials, the STEM-XEDS characterization of the photocatalyst samples revealed that Ce did not incorporate into the ZnO crystal lattice as a dopant but that a heterojunction formed between the ZnO nanosheets and the Ce-Zn mixed oxide phase nanoparticles instead. These two relevant compositional features could in fact be established thanks to the particular morphology obtained by the use of the microwave-assisted hydrothermal synthesis. The optical study revealed that in the ZnO:Ce samples optical band gap was found to decrease to 3.17 eV in the samples with the highest Ce content. It was also found that the ZnO:Ce (2 at.%) sample exhibited the highest photocatalytic activity for the degradation of methylene blue (MB), when compared to both the pure ZnO and commercial TiO2-P25 under simulated sunlight irradiation. The kinetics of MB photodegradation in the presence of the different photocatalysts could be properly described using a Langmuir-Hinshelwood (LH) model, for which the ZnO:Ce (2 at.%) sample exhibited the highest value of effective kinetic constant

Ultrathin Washcoat and Very Low Loading Monolithic Catalyst with Outstanding Activity and Stability in Dry Reforming of Methane

A Ni/CeO2/ZrO2 catalyst with improved redox properties has been washcoated onto a honeycomb cordierite monolith in the form of a nonconventional alumina-catalyst layer, just a few nanometers thick. In spite of the very low active phase loading, the monolith depicts outstanding performance in dry reforming of methane, both in terms of activity, with values reaching the thermodynamic limit already at 750 degrees C, even under extreme Weight Hourly Space Velocities (WHSV 115-346 Lg(F -1)h(-1)), as well as in terms of stability during prolonged Time on Stream (TOS 24-48 h)