Effects of Sulfation Level on the Desulfation Behavior of Presulfated Pt-BaO/Al2O3 Lean NOx Trap Catalysts: A Combined H2 Temperature-Programmed Reaction, in Situ Sulfur K-Edge X-ray Absorption Near-Edge Spectroscopy, X-ray Photoelectron Spectroscopy, and Time-Resolved X-ray Diffraction Study

2009 ◽  
Vol 113 (17) ◽  
pp. 7336-7341 ◽  
Author(s):  
Do Heui Kim ◽  
Janos Szanyi ◽  
Ja Hun Kwak ◽  
Xianqin Wang ◽  
Jonathan C. Hanson ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Lean Nox Trap ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Lean Nox ◽  
Temperature Programmed ◽  
Temperature Programmed Reaction ◽  
X Ray Absorption

A dispenser–reactor apparatus applied forin situXAS monitoring of Pt nanoparticle formation

2015 ◽  
Vol 22 (3) ◽  
pp. 736-744 ◽  
Author(s):  
Jocenir Boita ◽  
Marcus Vinicius Castegnaro ◽  
Maria do Carmo Martins Alves ◽  
Jonder Morais
Keyword(s):  
Photoelectron Spectroscopy ◽  
Metallic Nanoparticles ◽  
Pt Nanoparticles ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Two Stages ◽  
X Ray Absorption

In situtime-resolved X-ray absorption spectroscopy (XAS) measurements collected at the PtL3-edge during the synthesis of Pt nanoparticles (NPs) in aqueous solution are reported. A specially designed dispenser–reactor apparatus allowed for monitoring changes in the XAS spectra from the earliest moments of Pt ions in solution until the formation of metallic nanoparticles with a mean diameter of 4.9 ± 1.1 nm. By monitoring the changes in the local chemical environment of the Pt atoms in real time, it was possible to observe that the NPs formation kinetics involved two stages: a reduction-nucleation burst followed by a slow growth and stabilization of NPs. Subsequently, the synthesized Pt NPs were supported on activated carbon and characterized by synchrotron-radiation-excited X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS). The supported Pt NPs remained in the metallic chemical state and with a reduced size, presenting slight lattice parameter contraction in comparison with the bulk Pt values.

A reaction cell for time-resolvedin situXAS studies during wet chemical synthesis: the Cu2(OH)3Cl case

2013 ◽  
Vol 21 (1) ◽  
pp. 254-258 ◽  
Author(s):  
Jocenir Boita ◽  
Maria do Carmo Martins Alves ◽  
Jonder Morais
Keyword(s):  
Chemical Synthesis ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Reaction Cell ◽  
Time Resolved ◽  
X Ray ◽  
Wet Chemical Synthesis ◽  
X Ray Absorption ◽  
Electronic And Structural Properties

The use ofin situtime-resolved dispersive X-ray absorption spectroscopy (DXAS) to monitor the formation of Cu2(OH)3Cl particles in an aqueous solution is reported. The measurements were performed using a dedicated reaction cell, which enabled the evolution of the CuK-edge X-ray absorption near-edge spectroscopy to be followed during mild chemical synthesis. The formed Cu2(OH)3Cl particles were also characterized by synchrotron-radiation-excited X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. The influence of polyvinylpyrrolidone (PVP) on the electronic and structural properties of the formed particles was investigated. The results indicate clearly the formation of Cu2(OH)3Cl, with or without the use of PVP, which presents very similar crystalline structures in the long-range order. However, depending on the reaction, dramatic differences were observed byin situDXAS in the vicinities of the Cu atoms.

scholarly journals “PdO vs. PtO”—The Influence of PGM Oxide Promotion of Co3O4 Spinel on Direct NO Decomposition Activity

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 62 ◽  
Author(s):  
Gunugunuri K. Reddy ◽  
Torin C. Peck ◽  
Charles A. Roberts
Keyword(s):  
Photoelectron Spectroscopy ◽  
No Decomposition ◽  
Single Element ◽  
X Ray Diffraction ◽  
X Ray ◽  
Promotional Effect ◽  
Ft Ir ◽  
Temperature Programmed ◽  
Thermal Stability Of

Direct decomposition of NO into N2 and O2 (2NO→N2 + O2) is recognized as the “ideal” reaction for NOx removal because it needs no reductant. It was reported that the spinel Co3O4 is one of the most active single-element oxide catalysts for NO decomposition at higher reaction temperatures, however, activity remains low below 650 °C. The present study aims to investigate new promoters for Co3O4, specifically PdO vs. PtO. Interestingly, the PdO promoter effect on Co3O4 was much greater than the PtO effect, yielding a 4 times higher activity for direct NO decomposition at 650 °C. Also, Co3O4 catalysts with the PdO promoter exhibit higher selectivity to N2 compared to PtO/Co3O4 catalysts. Several characterization measurements, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), H2-temperature programmed reduction (H2-TPR), and in situ FT-IR, were performed to understand the effect of PdO vs. PtO on the properties of Co3O4. Structural and surface analysis measurements show that impregnation of PdO on Co3O4 leads to a greater ease of reduction of the catalysts and an increased thermal stability of surface adsorbed NOx species, which contribute to promotion of direct NO decomposition activity. In contrast, rather than remaining solely as a surface species, PtO enters the Co3O4 structure, and it promotes neither redox properties nor NO adsorption properties of Co3O4, resulting in a diminished promotional effect compared to PdO.

Phase Transition Analysis between LiFePO4and FePO4by In-Situ Time-Resolved X-ray Absorption and X-ray Diffraction

2013 ◽  
Vol 160 (5) ◽  
pp. A3061-A3065 ◽  
Author(s):  
Yuki Orikasa ◽  
Takehiro Maeda ◽  
Yukinori Koyama ◽  
Taketoshi Minato ◽  
Haruno Murayama ◽  
...  
Keyword(s):  
Phase Transition ◽  
X Ray Diffraction ◽  
Transition Analysis ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Absorption

scholarly journals Expanding the Mechanochemical Toolbox: Combining X-Ray Absorption Spectroscopy and Scattering for in Situ Time-Resolved Monitoring of Gold Nanoparticle Mechanosynthesis

2020 ◽  
Author(s):  
Paulo F M de Oliveira ◽  
Adam Michalchuk ◽  
Ana de Oliveira Guilherme Buzanich ◽  
Ralf Bienert ◽  
Roberto M. Torresi ◽  
...  
Keyword(s):  
Absorption Spectroscopy ◽  
Electronic Materials ◽  
Early Stage ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
Subsequent Formation ◽  
X Ray ◽  
Detection Capabilities ◽  
X Ray Absorption

<div>The development of time-resolved in situ approaches for monitoring mechanochemical</div><div>transformations has revolutionized the field of mechanochemistry. Currently, the established in</div><div>situ approaches greatly limit the scope of investigations that are possible. Here we develop a new</div><div>approach to simultaneously follow the evolution of bulk atomic and electronic structure during a</div><div>mechanochemical synthesis. This is achieved by coupling two complementary synchrotron-based</div><div>X-ray methods: X-ray absorption spectroscopy and X-ray diffraction. We apply this method to</div><div>investigate the bottom-up mechanosynthesis of technologically important Au nanoparticles in the</div><div>presence of three different reducing agents. Moreover, we demonstrate how X-ray absorption</div><div>spectroscopy offers unprecedented insight into the early stage generation of growth species (e.g.</div><div>monomers and clusters), which lead to the subsequent formation of nanoparticles. These</div><div>processes are beyond the detection capabilities of diffraction methods. The approach is general,</div><div>and not limited to monitoring NP mechanosynthesis. This combined X-ray approach paves the</div><div>way to new directions in mechanochemical research of advanced electronic materials.</div>

scholarly journals RISING beamline (BL28XU) for rechargeable battery analysis

2013 ◽  
Vol 21 (1) ◽  
pp. 268-272 ◽  
Author(s):  
H. Tanida ◽  
K. Fukuda ◽  
H. Murayama ◽  
Y. Orikasa ◽  
H. Arai ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Rechargeable Batteries ◽  
Time Range ◽  
Rechargeable Battery ◽  
X Ray Diffraction ◽  
Battery Charging ◽  
X Ray ◽  
And Performance ◽  
X Ray Absorption

The newly installed BL28XU beamline at SPring-8 is dedicated toin situstructural and electronic analysis of rechargeable batteries. It supports the time range (1 ms to 100 s) and spatial range (1 µm to 1 mm) needed for battery analysis. Electrochemical apparatus for battery charging and discharging are available in experimental hutches and in a preparation room. Battery analysis can be carried out efficiently and effectively using X-ray diffraction, X-ray absorption fine-structure analysis and hard X-ray photoelectron spectroscopy. Here, the design and performance of the beamline are described, and preliminary results are presented.

scholarly journals Expanding the Mechanochemical Toolbox: Combining X-Ray Absorption Spectroscopy and Scattering for in Situ Time-Resolved Monitoring of Gold Nanoparticle Mechanosynthesis

2020 ◽  
Author(s):  
Paulo F M de Oliveira ◽  
Adam Michalchuk ◽  
Ana de Oliveira Guilherme Buzanich ◽  
Ralf Bienert ◽  
Roberto M. Torresi ◽  
...  
Keyword(s):  
Absorption Spectroscopy ◽  
Electronic Materials ◽  
Early Stage ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
Subsequent Formation ◽  
X Ray ◽  
Detection Capabilities ◽  
X Ray Absorption

<div>The development of time-resolved in situ approaches for monitoring mechanochemical</div><div>transformations has revolutionized the field of mechanochemistry. Currently, the established in</div><div>situ approaches greatly limit the scope of investigations that are possible. Here we develop a new</div><div>approach to simultaneously follow the evolution of bulk atomic and electronic structure during a</div><div>mechanochemical synthesis. This is achieved by coupling two complementary synchrotron-based</div><div>X-ray methods: X-ray absorption spectroscopy and X-ray diffraction. We apply this method to</div><div>investigate the bottom-up mechanosynthesis of technologically important Au nanoparticles in the</div><div>presence of three different reducing agents. Moreover, we demonstrate how X-ray absorption</div><div>spectroscopy offers unprecedented insight into the early stage generation of growth species (e.g.</div><div>monomers and clusters), which lead to the subsequent formation of nanoparticles. These</div><div>processes are beyond the detection capabilities of diffraction methods. The approach is general,</div><div>and not limited to monitoring NP mechanosynthesis. This combined X-ray approach paves the</div><div>way to new directions in mechanochemical research of advanced electronic materials.</div>

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