期刊
ACS CATALYSIS
卷 13, 期 11, 页码 7243-7255出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.3c00810
关键词
propylene hydroformylation; Rh; single-atomcatalysis; ceria; oxygen vacancies
This study tunes the local coordination environment of Rh single atoms on CeO2 through calcination, creating a highly active hydroformylation catalyst. Rh single atoms on CeO2 calcined at a high temperature exhibit more oxygen vacancies, leading to the formation of a large amount of low-coordination Rh active species that are more active for hydroformylation. The best Rh/CeO2 catalyst achieved a TOF of approximately 5000 h(-1) and 100% aldehyde selectivity in propylene hydroformylation.
Controlling the interactions between atomically dispersedmetalatoms and the support plays significant roles in determining the activityand selectivity of single-atom catalysts. In this report, we tunedthe local coordination environment of Rh single atoms on CeO2 via calcination to construct a highly active hydroformylation catalyst.Single-atom Rh/CeO2 calcined at a high temperature exhibitsmore oxygen vacancies, which lead to the formation of a large amountof low-coordination Rh active species that are more active for hydroformylation.Under the optimum conditions, the best Rh/CeO2 catalystachieved a TOF at approximately 5000 h(-1) with 100%aldehyde selectivity in propylene hydroformylation to butanal. Insitu FTIR spectroscopy and in situ XPS characterizations provide strongevidence that Rh on 800 degrees C-calcined CeO2 is easilyactivated to form surface HRh-(CO)(2) active species, favoringpropylene adsorption and CO insertion. This work highlights the significanceof engineering metal-support interactions in tuning the hydroformylationperformance of single-atom catalysts and contributes to mechanisticinsights into single-atom Rh-catalyzed hydroformylation reactions.
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