Synthesis of superficially modified Ce1−x(Zr + Y)xO2−δ solid solutions and thermogravimetric analysis of their performance in the catalytic soot combustion

In this work, solid solutions of general formula Ce _1−x (Zr + Y)xO _2− _δ were chemically synthesized through the so-called citrate-EDTA complexing method, wherein the doping cations Zr and Y were substituted in the ceria lattice with an equimolar amount of 0.05 ≤ x ≤ = 0.25. The ternary oxides were heat-treated, and those that showed the best textural properties were superficially impregnated with Fe _2 O _3 particles by the thermal decomposition method using a metalorganic precursor. The X-ray diffraction results suggest that co-doping with Zr ^4+ and Y ^3+ promotes a slight distortion of the CeO _2 cubic cell. Nevertheless, the fluorite cubic structure of the oxides remains stable after being exposed to heat treatments. Furthermore, using scanning electron microscopy and Raman techniques, the presence of deposited Fe _2 O _3 and the formation of extrinsic vacancies in the materials could be corroborated. Finally, the oxides’ catalytic evaluation in the soot oxidation reaction was carried out using the thermogravimetry technique. The ternary oxide with cerium molar content equal to 0.9 and impregnated with Fe _2 O _3 presented excellent catalytic behavior for soot oxidation. T _10 , T _50 , and T _90 temperatures were 310, 383, and 416 °C, respectively

Bimetallic PdCo and PdFe electrocatalysts for the electrochemical oxidation of formica acid

Pd, PdCo and PdFe catalysts were prepared by the impregnation method, using sodium borohydride (NaBH4) as the reducing agent and a commercial carbon material (Vulcan XC-72R) as support. The synthesized electrocatalysts were tested for the formic acid oxidation reaction (FAOR) in acid medium (H2SO4 0.5 M). The morphology, composition and particle size of the electrocatalysts were characterized by physicochemical techniques as X-ray diffraction (XRD), scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). The catalytic activity was evaluated by cyclic voltammetry (CV) and chronoamperometry techniques (CA)Catalizadores de Pd, PdFe y PdCo fueron preparados por el método de impregnación, usando borohidruro de sodio (NaBH4) como agente reductor y un material de carbono comercial, (Vulcan XC-72R) como soporte. Los electrocatalizadores sintetizados fueron probados para la reacción de oxidación de ácido fórmico (FAOR, por sus siglas en inglés) en medio ácido (H2SO4 0,5 M). La morfología, la composición y el tamaño de partícula de los electrocatalizadores se caracterizaron mediante técnicas físico-químicas como difracción de rayos X (XRD), microscopía electrónica de barrido con espectroscopia por energía dispersiva (SEM-EDS) y microscopia electrónica de transmisión (TEM). La actividad catalítica se evaluó mediante técnicas de voltamperometría cíclica (CV) y cronoamperometría (CA

Catalizadores bimetálicos de PdCo y PdFe para la oxidación electroquímica de ácido fórmico

4 Figuras, 1 Tabla.[EN] Pd, PdCo and PdFe catalysts were prepared by the impregnation method, using sodium borohydride (NaBH4) as the reducing agent and a commercial carbon material (Vulcan XC-72R) as support. The synthesized electrocatalysts were tested for the formic acid oxidation reaction (FAOR) in acid medium (H2SO4 0.5 M). The morphology, composition and particle size of the electrocatalysts were characterized by physicochemical techniques as X-ray diffraction (XRD), scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). The catalytic activity was evaluated by cyclic voltammetry (CV) and chronoamperometry techniques (CA).[ES] Catalizadores de Pd, PdFe y PdCo fueron preparados por el método de impregnación, usando borohidruro de sodio (NaBH4) como agente reductor y un material de carbono comercial, (Vulcan XC-72R) como soporte. Los electrocatalizadores sintetizados fueron probados para la reacción de oxidación de ácido fórmico (FAOR, por sus siglas en inglés) en medio ácido (H2SO4 0,5 M). La morfología, la composición y el tamaño de partícula de los electrocatalizadores se caracterizaron mediante técnicas físico-químicas como difracción de rayos X (XRD), microscopía electrónica de barrido con espectroscopia por energía dispersiva (SEM-EDS) y microscopia electrónica de transmisión (TEM). La actividad catalítica se evaluó mediante técnicas de voltamperometría cíclica (CV) y cronoamperometría (CA).LJM agradece a CONACyT por la beca otorgada para la realización de los estudios de Maestría, así como a UAM-A, ICB, IPN por el apoyo otorgado para la realización de este trabajo. MGMY, MRR, MEPP y AEM agradecen al SNI. MGMY agradece a L ́oreal-UNESCO-CONACyT-AMC por la beca en Mujeres en la Ciencia 2016. MJL and SPR agradecen al Gobierno de Aragón (DGA) y FEDER por la financiación a través del Grupo de Investigación Conversión de Combustibles (T06_17R)Peer reviewe

Electrocatalytic performance of palladium-based electrocatalysts supported on carbon nanotubes for formic acid oxidation

In the present work, Pd and PdFe nanoparticles supported on CNT with and without functionalization (CNT and CNTox) were used for Formic Acid Oxidation Reaction (FAOR) in acid media. Electrocatalysts were synthesized by the borohydride reduction method with 20 wt.% metal loading. The CNTs were synthesized by the methane catalytic decomposition, and subjected to an oxidation treatment with nitric acid, named as CNTox. Themorphology, composition and structural properties were studied by Transmission Electron Microscopy (TEM), Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX) and X-Ray Diffraction (XRD). The FAOR was evaluated in acid media in a conventional three-electrode cell by means of cyclic voltammetry and chronoamperometry. From the steady state current density, it was found that Pd and PdFe supported at CNTox allowed improving the catalytic activity in comparison with the nonoxidized support.Peer reviewe

Carbon supported PdM (M = Fe, Co) electrocatalysts for formic acid oxidation. Influence of the Fe and Co precursors

8 Figuras.- 4 TablasPd and PdM (M = Fe or Co) nanostructured electrocatalysts were synthesized by the impregnation method and supported on carbon black Vulcan XC-72R for the formic acid oxidation reaction, FAOR, in acid medium. Nitrates or chlorides were used as Fe and Co precursors to study the counter ion role on the physicochemical features and electrochemical performance of the electrocatalysts. TEM analysis showed that PdM was deposited on the carbon material with a particle size around 2–3 nm. From XRD, peaks associated with the fcc palladium planes were observed along with evidence of PdM alloy formation, particularly when the nitrate salts were used as metal precursors. Furthermore, XPS analyses indicated that nitrates promote the metal oxide formation to a greater extent than chlorides, mainly for Pd. PdCo electrocatalyst obtained from nitrates exhibited the highest performance for FAOR with a steady state current density of 451 and 313 μA cm−2 at 200 and 400 mV respectively, which is in both cases, 3 times larger than that developed for a commercial Pd/C catalyst.LJM is grateful to CONACYT for the grant awarded for this research, as well as to the UAM-A and the ICB for the support provided. MGMY, MRR, MPP and AEM thank the SNI for the distinction of their membership and the stipend provided. MGMY is indebted to L'oreál-UNESCO-CONACyT-AMC for the grant Women in Science 2016. MJL and SPR gratefully acknowledge financial support given by Spanish MINECO (ENE2014-52158-C2-1-R).Peer reviewe