Near Room-Temperature Liquid-Phase Deposition of Barium-Doped TiO2 on n-GaN and its Application to AlGaN/GaN MOSHEMTs

2019 ◽  
Vol 41 (3) ◽  
pp. 439-444 ◽  
Author(s):  
Chih C. Hu ◽  
Mon-Sen Lin ◽  
Tsu-Yi Wu ◽  
Feri Adriyanto ◽  
Po-Wen Sze ◽  
...  
Keyword(s):  
Liquid Phase ◽  
Room Temperature ◽  
Liquid Phase Deposition ◽  
Doped Tio2 ◽  
Temperature Liquid

Liquid phase deposition of iron and cobalt doped TiO2 epitaxial thin films

2008 ◽  
Vol 205 (10) ◽  
pp. 2405-2408 ◽  
Author(s):  
K. Y. S. Chan ◽  
G. K. L. Goh ◽  
M. Y. Han
Keyword(s):  
Thin Films ◽  
Liquid Phase ◽  
Epitaxial Thin Films ◽  
Liquid Phase Deposition ◽  
Doped Tio2

scholarly journals γ-Radiolysis of cyclohexane with electron scavengers. VII. Perfluorocyclohexane and perfluorobenzene as electron scavengers

1969 ◽  
Vol 47 (14) ◽  
pp. 2655-2660 ◽  
Author(s):  
N. H. Sagert ◽  
J. A. Reid ◽  
R. W. Robinson
Keyword(s):  
Liquid Phase ◽  
Electron Capture ◽  
Room Temperature ◽  
Large Change ◽  
Electron Scavenger ◽  
Free Ion ◽  
Neutralization Process ◽  
Temperature Liquid

The room temperature, liquid phase radiolysis of cyclohexane has been investigated using perfluorocyclohexane (C6F12) and perfluorobenzene (C6F6) as electron scavengers. Yields of the respective monohydrofluorocarbons were investigated over several orders of magnitude scavenger concentration. The C6F11H yield from the C6F12–cyclohexane system has previously been shown to result from electron capture by C6F12. The data over the extended concentration range were used to calculate a total ion yield of 4.3 ± 0.2 G units and a free ion yield of 0.14 ± 0.02 G units. With C6F6 as an electron scavenger, hydrogen, cyclohexene, and dicyclohexyl yields were all reduced. However, C6F5H yields were much lower than the C6F11H yields from C6F12. On changing the neutralization step by adding the proton scavenger ethanol, C6F5H yields were obtained equal to the C6F11H yields from C6F12. Thus C6F6 is as efficient an electron scavenger as C6F12. Since a change in the neutralization process produces a large change in yield, it is likely that C6F5H (or C6F5) is produced in the neutralization process.

γ-Radiolysis of cyclohexane with electron scavengers. IV. CO2 as an electron scavenger

1968 ◽  
Vol 46 (2) ◽  
pp. 336-338 ◽  
Author(s):  
N. H. Sagert
Keyword(s):  
Liquid Phase ◽  
Room Temperature ◽  
Electron Scavenger ◽  
Rate Of Reaction ◽  
Temperature Liquid

The room temperature liquid phase radiolysis of cyclohexane has been examined in the presence of CO2 and of CO2 with N2O. CO2 decreases the yields of all major products by scavenging electrons. It is concluded that the CO2 anion does not dissociate and that no precursors of cyclohexyl radicals are formed when it is finally neutralized by a hydrocarbon cation. No evidence that CO2 acts as an efficient O− scavenger in liquid phase cyclohexane was found. Its rate of reaction with O− appears comparable to its rate of reaction with electrons.

Room-temperature Synthesis of Monodispersed SnO2Nanoparticles by Liquid Phase Deposition

2009 ◽  
Vol 38 (10) ◽  
pp. 974-975 ◽  
Author(s):  
Minoru Mizuhata ◽  
Yuki Umekage ◽  
Akiyoshi Nakata ◽  
Ramanujam Kumaresan ◽  
Shigehito Deki
Keyword(s):  
Liquid Phase ◽  
Room Temperature ◽  
Liquid Phase Deposition ◽  
Temperature Synthesis ◽  
Room Temperature Synthesis

γ-Radiolysis of cyclohexane with electron scavengers. III. Perfluorocarbons as electron scavengers

1968 ◽  
Vol 46 (2) ◽  
pp. 95-99 ◽  
Author(s):  
N. H. Sagert
Keyword(s):  
Liquid Phase ◽  
Electron Capture ◽  
Solid Solutions ◽  
Room Temperature ◽  
Dissociative Electron Capture ◽  
Bond Breaking ◽  
Hydrogen Yield ◽  
Fluorocarbon Compounds ◽  
Temperature Liquid

The room temperature, liquid phase radiolysis of cyclohexane in the presence of three solutes, per fluorocyclohexane (PCH), perfluoromethylcyclohexane (PMCH), and perfluorocyclobutane (PCB) has been examined. All decrease the hydrogen yield from 5.6 to 2.6 G units by capturing electrons. However, with PMCH and PCB the yields of cyclohexene and bicyclohexyl are not decreased as much as the hydrogen yield and with PCH, dimer and olefin yields are increased. Furthermore, large yields of monohydrofluorocarbon (e.g. undecafluorocyclohexane) are produced, indicating that a carbon–fluorine bond has been broken. It is concluded that electron capture by these fluorocarbon compounds causes dissociation; possible mechanisms are discussed, but it was not possible to reach a clear conclusion on the basis of our results.The radiolysis of homogeneous solid solutions of these solutes at 77 °K has also been studied, but only PMCH was studied in detail. Under these conditions there is no evidence for dissociative electron capture and apparently the combination of solute anion and hydrocarbon cation on warming does not lead to bond breaking.

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