scholarly journals Rotationally resolved photoelectron spectroscopy of the2Σ−Rydberg states of OH: The role of Cooper minima

1991 ◽  
Vol 95 (1) ◽  
pp. 714-716 ◽  
Author(s):  
E. de Beer ◽  
C. A. de Lange ◽  
J. A. Stephens ◽  
Kwanghsi Wang ◽  
V. McKoy
2020 ◽  
Vol 6 (1) ◽  
pp. 34-49
Author(s):  
Abul Arafat ◽  
Sabrin A. Samad ◽  
Jeremy J. Titman ◽  
Andrew L. Lewis ◽  
Emma R. Barney ◽  
...  

AbstractThis study investigates the role of yttrium in phosphate-based glasses in the system 45(P2O5)–25(CaO)– (30-x)(Na2O)–x(Y2O3) (0≤x≤5) prepared via melt quenching and focuses on their structural characterisation and degradation properties. The structural analyses were performed using a combination of solid-state nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). 31P NMR analysis showed that depolymerisation of the phosphate network occurred which increased with Y2O3 content as metaphosphate units (Q2) decreased with subsequent increase in pyrophosphate species (Q1). The NMR results correlated well with structural changes observed via FTIR and XPS analyses. XRD analysis of crystallised glass samples revealed the presence of calcium pyrophosphate (Ca2P2O7) and sodium metaphosphate (NaPO3) phases for all the glass formulations explored. Yttrium-containing phases were found for the formulations containing 3 and 5 mol% Y2O3. Degradation analyses performed in Phosphate buffer saline (PBS) and Milli-Q water revealed significantly reduced rates with addition of Y2O3 content. This decrease was attributed to the formation of Y-O-P bonds where the octahedral structure of yttrium (YO6) cross-linked phosphate chains, subsequently leading to an increase in chemical durability of the glasses. The ion release studies also showed good correlation with the degradation profiles.


1999 ◽  
Vol 8 (3) ◽  
pp. 384-391 ◽  
Author(s):  
W X Ding ◽  
L A Pinnaduwage ◽  
C Tav ◽  
D L McCorkle
Keyword(s):  

1999 ◽  
Vol 567 ◽  
Author(s):  
Masayuki Suzuki ◽  
Yoji Saito

ABSTRACTWe tried direct oxynitridation of silicon surfaces by remote-plasma-exited nitrogen and oxygen gaseous mixtures at 700°C in a high vacuum. The oxynitrided surfaces were investigated with in-situ X-ray photoelectron spectroscopy. With increase of the oxynitridation time, the surface density of nitrogen gradually increases, but that of oxygen shows nearly saturation behavior after the rapid increase in the initial stage. We also annealed the grown oxynitride and oxide films to investigate the role of the contained nitrogen. The desorption rate of oxygen from the oxynitride films is much less than that from oxide films. We confirmed that nitrogen stabilizes the thermal stability of these oxynitride films.


2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Richard P. Oleksak ◽  
Rafik Addou ◽  
Bharat Gwalani ◽  
John P. Baltrus ◽  
Tao Liu ◽  
...  

AbstractCurrent and future power systems require chromia-forming alloys compatible with high-temperature CO2. Important questions concerning the mechanisms of oxidation and carburization remain unanswered. Herein we shed light onto these processes by studying the very initial stages of oxidation of Fe22Cr and Fe22Ni22Cr model alloys. Ambient-pressure X-ray photoelectron spectroscopy enabled in situ analysis of the oxidizing surface under 1 mbar of flowing CO2 at temperatures up to 530 °C, while postexposure analyses revealed the structure and composition of the oxidized surface at the near-atomic scale. We found that gas purity played a critical role in the kinetics of the reaction, where high purity CO2 promoted the deposition of carbon and the selective oxidation of Cr. In contrast, no carbon deposition occurred in low purity CO2 and Fe oxidation ensued, thus highlighting the critical role of impurities in defining the early oxidation pathway of the alloy. The Cr-rich oxide formed on Fe22Cr in high purity CO2 was both thicker and more permeable to carbon compared to that formed on Fe22Ni22Cr, where carbon transport appeared to occur by atomic diffusion through the oxide. Alternatively, the Fe-rich oxide formed in low purity CO2 suggested carbon transport by molecular CO2.


2012 ◽  
Vol 116 (11) ◽  
pp. 2808-2818 ◽  
Author(s):  
Toshifumi Mori ◽  
William J. Glover ◽  
Michael S. Schuurman ◽  
Todd J. Martinez
Keyword(s):  

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