The Atmospheric Thermal Oxidation of Nitric Oxide

1963 ◽  
Vol 85 (19) ◽  
pp. 2901-2904 ◽  
Author(s):  
William A. Glasson ◽  
Charles S. Tuesday
1970 ◽  
Vol 4 (9) ◽  
pp. 752-757 ◽  
Author(s):  
Paul M. Yavorsky ◽  
Nestor J. Mazzocco ◽  
Gerald D. Rutledge ◽  
Everett Gorin

2013 ◽  
Vol 740-742 ◽  
pp. 707-710 ◽  
Author(s):  
Sarah Kay Haney ◽  
Veena Misra ◽  
Daniel J. Lichtenwalner ◽  
Anant K. Agarwal

MOSFETs and capacitors have been fabricated to investigate the atomic layer depositon (ALD) of SiO2onto SiC compared to thermal oxidation of SiC. Devices were fabricated on 4H-SiC with the following oxidation treatments: thermal oxidation at 1175°C, thermal oxidation at 1175°C followed by a nitric oxide (NO) anneal at 1175°C, and ALD of SiC at 150°C followed by an NO post oxidation anneal (POA) at 1175°C. ALD of the SiO2was performed using 3-aminopropyltriethoxysiliane (3-APTES), ozone and water. Capacitors fabricated with NO annealed ALD oxide and thermal oxide with NO POA exhibited similar CV behavior and yielded similar Dit of 1e11 at 0.5 eV from the conduction band. MOSFETs fabricated with NO PDA ALD oxide exhibited peak field effect mobilities ranging from 32 – 40.5 cm2/Vs compared to 30 –34.5 cm2/Vs for the MOSFETs with NO annealed thermal oxide. The higher mobilities exhibited by the ALD gate oxides were linked through SIMS to higher nitrogen concentrations at the SiO2/SiC interface.


1995 ◽  
Vol 34 (5) ◽  
pp. 1882-1888 ◽  
Author(s):  
Klaus Hjuler ◽  
Peter Glarborg ◽  
Kim Dam-Johansen

1997 ◽  
Vol 70 (3) ◽  
pp. 384-386 ◽  
Author(s):  
Kiran Kumar ◽  
Anthony I. Chou ◽  
Chuan Lin ◽  
Prasenjit Choudhury ◽  
Jack C. Lee ◽  
...  

1982 ◽  
Vol 16 (8) ◽  
pp. 1957-1972 ◽  
Author(s):  
Oliver Lindqvist ◽  
Evert Ljungström ◽  
Roger Svensson

Author(s):  
Chi-Ming Wei ◽  
Margarita Bracamonte ◽  
Shi-Wen Jiang ◽  
Richard C. Daly ◽  
Christopher G.A. McGregor ◽  
...  

Nitric oxide (NO) is a potent endothelium-derived relaxing factor which also may modulate cardiomyocyte inotropism and growth via increasing cGMP. While endothelial nitric oxide synthase (eNOS) isoforms have been detected in non-human mammalian tissues, expression and localization of eNOS in the normal and failing human myocardium are poorly defined. Therefore, the present study was designed to investigate eNOS in human cardiac tissues in the presence and absence of congestive heart failure (CHF).Normal and failing atrial tissue were obtained from six cardiac donors and six end-stage heart failure patients undergoing primary cardiac transplantation. ENOS protein expression and localization was investigated utilizing Western blot analysis and immunohistochemical staining with the polyclonal rabbit antibody to eNOS (Transduction Laboratories, Lexington, Kentucky).


2001 ◽  
Vol 28 (5-6) ◽  
pp. 459-462
Author(s):  
Pini Orbach ◽  
Charles E Wood ◽  
Maureen Keller-Wood
Keyword(s):  

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