An X-Ray Photoelectron Spectroscopic and Chemical Reactivity Study of Routes to Functionalization of Etched InP Surfaces

1996 ◽  
Vol 118 (12) ◽  
pp. 3045-3046 ◽  
Author(s):  
Marcel Sturzenegger ◽  
Nathan S. Lewis
Symmetry ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1315
Author(s):  
Takafumi Miyanaga

X-ray absorption fine structure (XAFS) is a powerful technique used to analyze a local electronic structure, local atomic structure, and structural dynamics. In this review, I present examples of XAFS that apply to the local structure and dynamics of functional materials: (1) structure phase transition in perovskite PbTiO3 and magnetic FeRhPd alloys; (2) nano-scaled fluctuations related to their magnetic properties in Ni–Mn alloys and Fe/Cr thin films; and (3) the Debye–Waller factors related to the chemical reactivity for catalysis in polyanions and ligand exchange reaction. This study shows that the local structure and dynamics are related to the characteristic function of the materials.


2017 ◽  
Vol 887 ◽  
pp. 24-31
Author(s):  
Omar Ben Mya ◽  
Mahmoud Omari ◽  
Lucia dos Santos-Gomez ◽  
David Marerro-Lopezd

Perovskite La1-xSrxFe0.7Ni0.3O3-δ with x = 0.0, 0.1 &0.2 denoted LSFNx has been investigated as potential symmetrical electrode in solid fuel cells (SOFCs). The crystal structure is in pure orthorhombic phase for x = 0.0, orthorhombic-cubic phase coexist for x = 0.1 and pure cubic phase for x = 0.2. Structural properties are studied by X-ray powder diffraction (XRPD), refined by Rietveld analysis. SEM images show the morphology of as prepared and calcined samples either the compatibility between those electrodes and LSGM electrolyte in presence of 50% wt of Ce0.8Gd0.2O2-δ, so that, lower chemical reactivity was found. Total conductivity, impedance in high, medium and low frequencies HF, MF and LF respectively, and resistance polarization (Rp) are determined in air. LaFe0.7Ni0.3O3-δ has a good response in all ranges of frequencies but La0.9Sr0.1Fe0.7Ni0.3O3-δ and La0.8Sr0.2Fe0.7Ni0.3O3-δ have response only in HF and MF and exhibit Rp values as low as LaFe0.7Ni0.3O3-δ .


Ceramics ◽  
2019 ◽  
Vol 2 (2) ◽  
pp. 246-259 ◽  
Author(s):  
Cyril Gaudillere ◽  
Julio Garcia-Fayos ◽  
Jorge Plaza ◽  
José M. Serra

An original asymmetric tubular membrane for oxygen production applications was manufactured in a two-step process. A 3 mol% Y2O3 stabilized ZrO2 (3YSZ) porous tubular support was manufactured by the freeze-casting technique, offering a hierarchical and radial-oriented porosity of about 15 µm in width, separated by fully densified walls of about 2 µm thick, suggesting low pressure drop and boosted gas transport. The external surface of the support was successively dip-coated to get a Ce0.8Gd0.2O2−δ – 5mol%Co (CGO-Co) interlayer of 80 µm in thickness and an outer dense layer of La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) with a thickness of 30 µm. The whole tubular membrane presents both uniform geometric characteristics and microstructure all along its length. Chemical reactivity between each layer was studied by coupling X-Ray Diffraction (XRD) analysis and Energy Dispersive X-Ray spectroscopy (EDX) mapping at each step of the manufacturing process. Cation interdiffusion between different phases was discarded, confirming the compatibility of this tri-layer asymmetric ceramic membrane for oxygen production purposes. For the first time, a freeze-cast tubular membrane has been evaluated for oxygen permeation, exhibiting a value of 0.31 ml·min−1·cm−2 at 1000ºC under air and argon as feed and sweep gases, respectively. Finally, under the same conditions and increasing the oxygen partial pressure to get pure oxygen as feed, the oxygen permeation reached 1.07 ml·min−1·cm−2.


2009 ◽  
Vol 2009 ◽  
pp. 1-6 ◽  
Author(s):  
A. R. Chourasia ◽  
J. L. Hickman ◽  
R. L. Miller ◽  
G. A. Nixon ◽  
M. A. Seabolt

About 20 Å of hafnium were deposited on silicon substrates using the electron beam evaporation technique. Two types of samples were investigated. In one type, the substrate was kept at the ambient temperature. After the deposition, the substrate temperature was increased to 100, 200, and 300∘C. In the other type, the substrate temperature was held fixed at some value during the deposition. For this type, the substrate temperatures used were 100, 200, 300, 400, 500, 550, and 600∘C. The samples were characterized in situ by the technique of X-ray photoelectron spectroscopy. No trace of elemental hafnium is observed in the deposited overlayer. Also, there is no evidence of any chemical reactivity between the overlayer and the silicon substrate over the temperature range used. The hafnium overlayer shows a mixture of the dioxide and the suboxide. The ratio of the suboxide to dioxide is observed to be more in the first type of samples. The spectral data indicate that hafnium has a strong affinity for oxygen. The overlayer gets completely oxidized to form HfO2 at substrate temperature around 300∘C for the first type of samples and at substrate temperature greater than 550∘C for the second type.


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