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Electrical Stimulation of Catalytic Activity of Platinum Nanocoatings in CO oxidation
— An increase in the rate of catalytic CO oxidation for platinum nanocoatings was measured when the electrical stress of various polarity and value was applied to a coating from an external source. Under conditions of the experiment at 250°C, atmospheric pressure and the starting composition mixture...
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Published in: | Russian journal of physical chemistry. B 2020-05, Vol.14 (3), p.547-551 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | —
An increase in the rate of catalytic CO oxidation for platinum nanocoatings was measured when the electrical stress of various polarity and value was applied to a coating from an external source. Under conditions of the experiment at 250°C, atmospheric pressure and the starting composition mixture of 4.8% CO + 10.2% O
2
+ Ar, applying the positive stress of +10 or +30 V on a coating leads to increase in the rate of CO oxidation by 18 or 54%, respectively. Applying the negative stress of –10 or –30 V leads to small acceleration in oxidation by 4 or 8%. It is shown that the effect of applied stress does not depend on particle size in a coating and grows linearly with stress. Quantum-chemical calculations of heats of association of CO and O
2
with electrically neutral or electrically charged platinum cluster were performed. It was found that the creation of the positive charge on Pt
2
leads to decrease in the heat of CO association by 6.4 kcal/mol and increase in the heat of O
2
association by 4.7 kcal/mol, while the creation of the negative charge on Pt
2
leads to a small effect of decrease in the heat of CO association by 3.0 kcal/mol and increase in the heat of O
2
association by 4.2 kcal/mol. From the results, it is proposed to explain increase in the rate of catalytic CO oxidation on platinum electrically charged with the help of the external stress source. |
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ISSN: | 1990-7931 1990-7923 |
DOI: | 10.1134/S1990793120030033 |