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Correlation between structure, surface defect chemistry and 18O/16O exchange for La2Mo2O9 and La2(MoO4)3
Natalia M Porotnikova1, Maxim I Vlasov, Yuri Zhukov
1Institute of High Temperature Electrochemistry, Ural Branch of Russian Academy of Sciences, 620990 Ekaterinburg, Russia. Porotnikova@ihte.uran.ru.
This study investigated lanthanum molybdate ceramics, revealing surface defect chemistry influences oxygen exchange rates. Understanding these kinetics is crucial for advanced material applications.
Area of Science:
- Materials Science
- Surface Chemistry
- Solid-State Chemistry
Background:
- Lanthanum molybdates (La2Mo2O9 and La2(MoO4)3) are synthesized via solid-state reactions.
- Dense ceramics are prepared from these powders for advanced applications.
Purpose of the Study:
- To analyze the chemical composition and elemental charge states in the subsurface of lanthanum molybdate ceramics.
- To investigate the kinetics of oxygen exchange on the surface of these materials.
Main Methods:
- Solid-state reaction method for powder synthesis.
- X-ray photoelectron spectroscopy (XPS) for surface analysis under varying vacuum and oxygen partial pressures.
- Kinetic analysis using a two-step model for oxygen adsorption and incorporation.
Main Results:
- High-resolution XPS spectra for La 3d, Mo 3d, and O 1s states were obtained and analyzed.
- Oxygen adsorption (ra) and incorporation (ri) rates were calculated.
- Correlations between oxide surface defect chemistry and oxygen exchange rates were established.
Conclusions:
- Surface defect chemistry significantly impacts the rates of oxygen adsorption and incorporation in lanthanum molybdates.
- The findings provide insights into the surface processes governing oxygen exchange in these ceramic materials.
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