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Selective Formation of Cu Active Sites with Different Coordination States on Pseudospinel CuAl2O4 and Their NO Reduction Catalysis.


ABSTRACT: In the spinel framework, copper (Cu) in two distinct coordination states exhibits catalytic activity for NO reduction through different mechanisms. However, detailed exploration of their respective catalytic properties, such as the redox behavior of Cu and substrate molecule adsorption, has been challenging due to difficulties in their separate formation. In this study, we present the controlled formation of pseudospinel CuAl2O4, containing exclusively tetrahedrally or octahedrally coordinated Cu, achieved by manipulating aging temperature and O2 concentration. Through these materials, we observed that in the CO-NO reaction, the step primarily determining the rate differs: NO reduction dominates with octahedrally coordinated Cu, whereas carbon monoxide (CO) oxidation is prominent with tetrahedrally coordinated Cu. The lower coordination number of Cu significantly benefits NO reduction but negatively impacts the CO-NO reaction, albeit positively influencing NO reduction in three-way catalytic reactions.

SUBMITTER: Okuda A 

PROVIDER: S-EPMC10938440 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Selective Formation of Cu Active Sites with Different Coordination States on Pseudospinel CuAl<sub>2</sub>O<sub>4</sub> and Their NO Reduction Catalysis.

Okuda Aoi A   Furuyama Taniyuki T   Sakai Toshiaki T   Machida Masato M   Yoshida Hiroshi H  

ACS omega 20240304 10


In the spinel framework, copper (Cu) in two distinct coordination states exhibits catalytic activity for NO reduction through different mechanisms. However, detailed exploration of their respective catalytic properties, such as the redox behavior of Cu and substrate molecule adsorption, has been challenging due to difficulties in their separate formation. In this study, we present the controlled formation of pseudospinel CuAl<sub>2</sub>O<sub>4</sub>, containing exclusively tetrahedrally or octa  ...[more]

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