Characterization of the catalytic properties of ceria-zirconia mixed oxides by temperature-programmed techniques

2005 ◽  
Vol 80 (1) ◽  
pp. 225-228 ◽  
Author(s):  
J. I. Gutiérrez-Ortiz ◽  
B. de Rivas ◽  
R. López-Fonseca ◽  
J. R. González-Velasco
1986 ◽  
Vol 83 ◽  
Author(s):  
E. I. Altman ◽  
R. J. Gorte

ABSTRACTIndustrial metal catalysts are usually in the form of small metal particles supported on a porous oxide. The typical size of these metal particles ranges between 1.0 and 10.0 nm and it is well known that the particle size and the oxide substrate can affect the catalytic properties of the metal for some important reactions[1]. Previous work with adsorption on small particles has indicated that desorption temperatures[2–4] and the ability to dissociate CO[5,6] can also be affected by the particle size. To further investigate these size and substrate effects, we have examined the adsorption properties of several simple gases on small Pt particles supported on alumina using temperature programmed desorption (TPD). We will show that the desorption curves for CO, H2, and NO on these particles are very similar to curves measured on single crystals.


Langmuir ◽  
1994 ◽  
Vol 10 (1) ◽  
pp. 159-165 ◽  
Author(s):  
Christopher T. Fishel ◽  
Robert J. Davis

2021 ◽  
Author(s):  
Luciano Honorato Chagas ◽  
Sandra Shirley Ximeno Chiaro ◽  
Alexandre Amaral Leitão ◽  
Renata Diniz

This chapter covers a brief review of the definition, structural characteristics and main applications of hydrotalcite, an interesting multifunctional material which finds applicability in different areas. Particularly, some catalytic reactions using hydrotalcite or mixed oxides derived from these materials are addressed (Ethanol Steam Reforming, Photochemical conversions, Hydrodesulfurization). The use of Raman Spectroscopy associated with other techniques, such as powder X-ray diffraction (XRD), Extended X-ray Absorption Fine-Structure (EXAFS), Temperature Programmed Reduction of hydrogen (H2-TPR), Fourier-Transform Infrared (FTIR) and Density Functional Theory (DFT) simulations, to characterize this type of material is addressed through examples described in the current literature. In this sense, multidisciplinary efforts must be made in order to increase the understanding of the properties of these materials and the catalytic behavior in the most varied reactions.


Author(s):  
L.D. Schmidt ◽  
K. R. Krause ◽  
J. M. Schwartz ◽  
X. Chu

The evolution of microstructures of 10- to 100-Å diameter particles of Rh and Pt on SiO2 and Al2O3 following treatment in reducing, oxidizing, and reacting conditions have been characterized by TEM. We are able to transfer particles repeatedly between microscope and a reactor furnace so that the structural evolution of single particles can be examined following treatments in gases at atmospheric pressure. We are especially interested in the role of Ce additives on noble metals such as Pt and Rh. These systems are crucial in the automotive catalytic converter, and rare earths can significantly modify catalytic properties in many reactions. In particular, we are concerned with the oxidation state of Ce and its role in formation of mixed oxides with metals or with the support. For this we employ EELS in TEM, a technique uniquely suited to detect chemical shifts with ∼30Å resolution.


2020 ◽  
Author(s):  
Travis Marshall-Roth ◽  
Nicole J. Libretto ◽  
Alexandra T. Wrobel ◽  
Kevin Anderton ◽  
Nathan D. Ricke ◽  
...  

Iron- and nitrogen-doped carbon (Fe-N-C) materials are leading candidates to replace platinum in fuel cells, but their active site structures are poorly understood. A leading postulate is that iron active sites in this class of materials exist in an Fe-N<sub>4</sub> pyridinic ligation environment. Yet, molecular Fe-based catalysts for the oxygen reduction reaction (ORR) generally feature pyrrolic coordination and pyridinic Fe-N<sub>4</sub> catalysts are, to the best of our knowledge, non-existent. We report the synthesis and characterization of a molecular pyridinic hexaazacyclophane macrocycle, (phen<sub>2</sub>N<sub>2</sub>)Fe, and compare its spectroscopic, electrochemical, and catalytic properties for oxygen reduction to a prototypical Fe-N-C material, as well as iron phthalocyanine, (Pc)Fe, and iron octaethylporphyrin, (OEP)Fe, prototypical pyrrolic iron macrocycles. N 1s XPS signatures for coordinated N atoms in (phen<sub>2</sub>N<sub>2</sub>)Fe are positively shifted relative to (Pc)Fe and (OEP)Fe, and overlay with those of Fe-N-C. Likewise, spectroscopic XAS signatures of (phen<sub>2</sub>N<sub>2</sub>)Fe are distinct from those of both (Pc)Fe and (OEP)Fe, and are remarkably similar to those of Fe-N-C with compressed Fe–N bond lengths of 1.97 Å in (phen<sub>2</sub>N<sub>2</sub>)Fe that are close to the average 1.94 Å length in Fe-N-C. Electrochemical studies establish that both (Pc)Fe and (phen<sub>2</sub>N<sub>2</sub>)Fe have relatively high Fe(III/II) potentials at ~0.6 V, ~300 mV positive of (OEP)Fe. The ORR onset potential is found to directly correlate with the Fe(III/II) potential leading to a ~300 mV positive shift in the onset of ORR for (Pc)Fe and (phen<sub>2</sub>N<sub>2</sub>)Fe relative to (OEP)Fe. Consequently, the ORR onset for (phen<sub>2</sub>N<sub>2</sub>)Fe and (Pc)Fe is within 150 mV of Fe-N-C. Unlike (OEP)Fe and (Pc)Fe, (phen<sub>2</sub>N<sub>2</sub>)Fe displays excellent selectivity for 4-electron ORR with <4% maximum H<sub>2</sub>O<sub>2</sub> production, comparable to Fe-N-C materials. The aggregate spectroscopic and electrochemical data establish (phen<sub>2</sub>N<sub>2</sub>)Fe as a pyridinic iron macrocycle that effectively models Fe-N-C active sites, thereby providing a rich molecular platform for understanding this important class of catalytic materials.<p><b></b></p>


2020 ◽  
Author(s):  
Leelavathi Annamalai ◽  
Sopuruchukwu Ezenwa ◽  
Yanliu Dang ◽  
Haiyan Tan ◽  
Steven L. Suib ◽  
...  

MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.


Sign in / Sign up

Export Citation Format

Share Document