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An Eight-Atom Iridium-Aluminum Oxide Cluster IrAlO6+ Catalytically Oxidizes Six CO Molecules.
Li, Xiao-Na; Jiang, Li-Xue; Wang, Li Na; Ou, Shu-Hua; Zhang, Mei-Qi; Yang, Yuan; Ma, Tong-Mei; He, Sheng-Gui.
Afiliação
  • Li XN; State Key Laboratory for Structural Chemistry of Unstable and Stable Species , Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , China.
  • Jiang LX; Beijing National Laboratory for Molecular Sciences and CAS Research/Education Center of Excellence in Molecular Sciences , Beijing 100190 , China.
  • Wang LN; State Key Laboratory for Structural Chemistry of Unstable and Stable Species , Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , China.
  • Ou SH; University of Chinese Academy of Sciences , Beijing 100049 , China.
  • Zhang MQ; Beijing National Laboratory for Molecular Sciences and CAS Research/Education Center of Excellence in Molecular Sciences , Beijing 100190 , China.
  • Yang Y; State Key Laboratory for Structural Chemistry of Unstable and Stable Species , Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , China.
  • Ma TM; University of Chinese Academy of Sciences , Beijing 100049 , China.
  • He SG; Beijing National Laboratory for Molecular Sciences and CAS Research/Education Center of Excellence in Molecular Sciences , Beijing 100190 , China.
J Phys Chem Lett ; 10(24): 7850-7855, 2019 Dec 19.
Article em En | MEDLINE | ID: mdl-31790248
Fundamental understanding regarding oxygen storage capacity involving how and why an active site can buffer a large number of oxygen atoms in redox processes is vital to the design of advanced oxygen storage materials, while it is challenging because of the complexity of heterogeneous catalysis. Herein, we identified that an eight-atom iridium-aluminum oxide cluster IrAlO6+ can transfer all the oxygen atoms to catalytically oxidize six CO molecules. This finding represents a breakthrough in cluster catalysis where at most three oxygen atoms from a heteronuclear metal oxide cluster can be catalytically involved in CO oxidation. We found that oxygen prefers to be stored on aluminum to form an O3-• radical in the energetically unfavorable IrAlO6+ isomer and generate the low-coordinated iridium that is pivotal to capturing CO and triggering the catalysis. The powerful electron cycling capability of iridium and the cooperative iridium-aluminum interplay are emphasized to drive the oxygen atom-transfer behavior.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China
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