scholarly journals Effect of Chemisorbed Oxygen on Photovoltaic and Photoconductive Processes in Rutile

1964 ◽  
Vol 35 (6) ◽  
pp. 1866-1867 ◽  
Author(s):  
R. Keezer
Keyword(s):  
Chemisorbed Oxygen

Decomposition of hydrogen peroxide on a two-component NiO-CdO catalyst and the effect of ionizing radiation on its catalytic properties

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Nickel Oxide ◽  
Catalytic Properties ◽  
Cadmium Oxide ◽  
Chemisorb Oxygen ◽  
Composition Region ◽  
Chemisorbed Oxygen ◽  
Two Component

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.

scholarly journals Nanosheet-Like Ho2O3 and Sr-Ho2O3 Catalysts for Oxidative Coupling of Methane

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 388
Author(s):  
Yuqiao Fan ◽  
Changxi Miao ◽  
Yinghong Yue ◽  
Weiming Hua ◽  
Zi Gao
Keyword(s):  
Oxidative Coupling ◽  
Temperature Programmed Desorption ◽  
Oxidative Coupling Of Methane ◽  
Molar Ratio ◽  
Impregnation Method ◽  
Oxygen Species ◽  
N2 Adsorption ◽  
Basic Sites ◽  
Chemisorbed Oxygen ◽  
Temperature Programmed

In this work, Ho2O3 nanosheets were synthesized by a hydrothermal method. A series of Sr-modified Ho2O3 nanosheets (Sr-Ho2O3-NS) with a Sr/Ho molar ratio between 0.02 and 0.06 were prepared via an impregnation method. These catalysts were characterized by several techniques such as XRD, N2 adsorption, SEM, TEM, XPS, O2-TPD (temperature-programmed desorption), and CO2-TPD, and they were studied with respect to their performances in the oxidative coupling of methane (OCM). In contrast to Ho2O3 nanoparticles, Ho2O3 nanosheets display greater CH4 conversion and C2-C3 selectivity, which could be related to the preferentially exposed (222) facet on the surface of the latter catalyst. The incorporation of small amounts of Sr into Ho2O3 nanosheets leads to a higher ratio of (O− + O2−)/O2− as well as an enhanced amount of chemisorbed oxygen species and moderate basic sites, which in turn improves the OCM performance. The optimal catalytic behavior is achievable on the 0.04Sr-Ho2O3-NS catalyst with a Sr/Ho molar ratio of 0.04, which gives a 24.0% conversion of CH4 with 56.7% selectivity to C2-C3 at 650 °C. The C2-C3 yield is well correlated with the amount of moderate basic sites present on the catalysts.

scholarly journals Role of CO2 During Oxidative Dehydrogenation of Propane Over Bulk and Activated-Carbon Supported Cerium and Vanadium Based Catalysts

2021 ◽  
Author(s):  
Petar Djinović ◽  
Janez Zavašnik ◽  
Janvit Teržan ◽  
Ivan Jerman
Keyword(s):  
Catalytic Activity ◽  
Activated Carbon ◽  
Oxidative Dehydrogenation ◽  
Active Phase ◽  
Lattice Oxygen ◽  
Chemisorbed Oxygen ◽  
Catalytically Active ◽  
Temperature Programmed ◽  
Propane Cracking

AbstractCeO2, V2O5 and CeVO4 were synthesised as bulk oxides, or deposited over activated carbon, characterized by XRD, HRTEM, CO2-TPO, C3H8-TPR, DRIFTS and Raman techniques and tested in propane oxidative dehydrogenation using CO2. Complete oxidation of propane to CO and CO2 is favoured by lattice oxygen of CeO2. The temperature programmed experiments show the ~ 4 nm AC supported CeO2 crystallites become more susceptible to reduction by propane, but less prone to re-oxidation with CO2 compared to bulk CeO2. Catalytic activity of CeVO4/AC catalysts requires a 1–2 nm amorphous CeVO4 layer. During reaction, the amorphous CeVO4 layer crystallises and several atomic layers of carbon cover the CeVO4 surface, resulting in deactivation. During reaction, V2O5 is irreversibly reduced to V2O3. The lattice oxygen in bulk V2O5 favours catalytic activity and propene selectivity. Bulk V2O3 promotes only propane cracking with no propene selectivity. In VOx/AC materials, vanadium carbide is the catalytically active phase. Propane dehydrogenation over VC proceeds via chemisorbed oxygen species originating from the dissociated CO2. Graphic Abstract

scholarly journals Chemisorbed Oxygen or Surface Oxides Steer the Selectivity in Pd Electrocatalytic Propene Oxidation Observed by Operando Pd Ledge X‐ray Absorption Spectroscopy

2021 ◽  
Author(s):  
Sergey Koroidov ◽  
Anna Winiwarter ◽  
Oscar Alfonso Diaz-Morales ◽  
Mikaela Gorlin ◽  
Joakim Halldin Stenlid ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Absorption Spectroscopy ◽  
Propene Oxidation ◽  
X Ray ◽  
Chemisorbed Oxygen ◽  
Oxidation Of Hydrocarbons ◽  
Surface Oxides ◽  
X Ray Absorption

Controlled electrochemical oxidation of hydrocarbons to desired products is an attractive approach in catalysis. Here we study the electrochemical propene oxidation under operando conditions using Pd L‐edge X‐ray absorption spectroscopy...

Atom resolved evidence for a defective chemisorbed oxygen state at a Mg(0001) surface

2002 ◽  
pp. 2020-2021 ◽  
Author(s):  
Albert F. Carley ◽  
Philip R. Davies ◽  
Rhys V. Jones ◽  
K. R. Harikumar ◽  
M. Wyn Roberts
Keyword(s):  
Oxygen State ◽  
Chemisorbed Oxygen

Oxygen-plasma-assisted formaldehyde adsorption mechanism of SnO2 electrospun fibers

2021 ◽  
Author(s):  
Haiying Du ◽  
Yuxia Wu ◽  
Zhaorui Zhang ◽  
Wanmin He ◽  
Yanhui Sun ◽  
...  
Keyword(s):  
Oxygen Plasma ◽  
Adsorption Mechanism ◽  
Gas Sensing ◽  
High Energy ◽  
Plasma Modification ◽  
Electrospun Fibers ◽  
Chemisorbed Oxygen ◽  
Formaldehyde Sensing ◽  
Formaldehyde Adsorption ◽  
Sensing Performance

Abstract Abstract: Chemisorbed oxygen acts a crucial role in the redox reaction of semiconductor gas sensors, and which is of great significance for improving gas sensing performance. In this study, an oxygen-plasma-assisted technology is presented to enhance the chemisorbed oxygen for improving the formaldehyde sensing performance of SnO2 electropun fiber. An inductively coupled plasma device was used for oxygen plasma treatment of SnO2 electrospun fibers. The surface of SnO2 electrospun fibers was bombarded with high-energy oxygen plasma for facilitating the chemisorption of electronegative oxygen molecules on the SnO2 (110) surface to obtain an oxygen-rich structure. Oxygen-plasma-assisted SnO2 electrospun fibers exhibited excellent formaldehyde sensing performance. The formaldehyde adsorption mechanism of oxygen-rich SnO2 was investigated using density functional theory. After oxygen plasma modification, the adsorption energy and the charge transfer number of formaldehyde to SnO2 were increased significantly. And an unoccupied electronic state appeared in the SnO2 band structure, which could enhance the formaldehyde adsorption ability of SnO2. The gas sensing test revealed that plasma-treated SnO2 electrospun fibers exhibited excellent gas sensing properties to formaldehyde, low operating temperature, high response sensitivity, and considerable cross-selectivity. Thus, plasma modification is a simple and effective method to improve the gas sensing performance of sensors.

Photoconversions of chemisorbed oxygen on reduced anatase

1979 ◽  
Vol 12 (1) ◽  
pp. 1-4 ◽  
Author(s):  
A. M. Volodin ◽  
A. E. Cherkashin ◽  
V. S. Zakharenko
Keyword(s):  
Chemisorbed Oxygen
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