Methane Activation at the Metal-Support Interface of Ni 4 -CeO 2 (111) Catalyst: A Theoretical Study

Rajib Kumar Singha, Yuta Tsuji, Muhammad Haris Mahyuddin, Kazunari Yoshizawa

研究成果: Contribution to journalArticle査読

13 被引用数 (Scopus)


Methane activation is usually assumed to take place on top of metal surfaces or metal clusters. It can also occur at the metal-support interface in metal-supported catalysts with reducible oxides, such as CeO 2 . In the present work, we exploit density functional theory with an additional Hubbard-like parameter (DFT + U) to calculate the activation of methane at an O site interfacing a Ni 4 metal cluster on a support, CeO 2 (111) surface. Two reaction routes, namely, radical and nonradical routes, are taken into account. We show that the nonradical route is favored with an apparent activation energy of 18.1 kcal/mol, which is lower than that for the radical route by 15.0 kcal/mol. In the nonradical route, the formation of a four-centered transition-state structure is observed while a C-H bond of methane is being cleaved to form an OH moiety and a CH 3 fragment that is being bound to the interfacial Ni atom. It is also found that the interfacial O atoms are out of the CeO 2 surface plane with Ce-O bond distances being much longer than those in the crystalline bulk CeO 2 , which allows them to be easily reduced, and hence, the interfacial O atoms become more reactive toward methane, as compared to the surface O atoms. The interactions between Ni 4 cluster and the CeO 2 (111) surface result in the reduction of two Ce 4+ ions to Ce 3+ , improving the reducibility of the interfacial O atoms. This should be an important key to the facile methane activation.

ジャーナルJournal of Physical Chemistry C
出版ステータス出版済み - 4 18 2019

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Energy(all)
  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films

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