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A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction

A series of Cu–Pd alloy nanoparticles supported on Al(2)O(3) were prepared and tested as catalysts for deNO(x) reactions. XRD, HAADF-STEM, XAFS, and FT-IR analyses revealed that a single-atom alloy structure was formed when the Cu/Pd ratio was 5, where Pd atoms were well isolated by Cu atoms. Compar...

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Detalles Bibliográficos
Autores principales: Xing, Feilong, Jeon, Jaewan, Toyao, Takashi, Shimizu, Ken-ichi, Furukawa, Shinya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006621/
https://www.ncbi.nlm.nih.gov/pubmed/32110288
http://dx.doi.org/10.1039/c9sc03172c
Descripción
Sumario:A series of Cu–Pd alloy nanoparticles supported on Al(2)O(3) were prepared and tested as catalysts for deNO(x) reactions. XRD, HAADF-STEM, XAFS, and FT-IR analyses revealed that a single-atom alloy structure was formed when the Cu/Pd ratio was 5, where Pd atoms were well isolated by Cu atoms. Compared with Pd/Al(2)O(3), Cu(5)Pd/Al(2)O(3) exhibited outstanding catalytic activity and N(2) selectivity in the reduction of NO by CO: for the first time, the complete conversion of NO to N(2) was achieved even at 175 °C, with long-term stability for at least 30 h. High catalytic performance was also obtained in the presence of O(2) and C(3)H(6) (model exhaust gas), where a 90% decrease in Pd use was achieved with minimum evolution of N(2)O. Kinetic and DFT studies demonstrated that N–O bond breaking of the (NO)(2) dimer was the rate-determining step and was kinetically promoted by the isolated Pd.