Understanding complete oxidation of methane on spinel oxides at a molecular level

  • Franklin Feng Tao
  • , Jun Jun Shan
  • , Luan Nguyen
  • , Ziyun Wang
  • , Shiran Zhang
  • , Li Zhang
  • , Zili Wu
  • , Weixin Huang
  • , Shibi Zeng
  • , P. Hu

Research output: Contribution to journalArticlepeer-review

296 Scopus citations

Abstract

It is crucial to develop a catalyst made of earth-abundant elements highly active for a complete oxidation of methane at a relatively low temperature. NiCo2O4 consisting of earth-abundant elements which can completely oxidize methane in the temperature range of 350-550 °C. Being a cost-effective catalyst, NiCo2O4 exhibits activity higher than precious-metal-based catalysts. Here we report that the higher catalytic activity at the relatively low temperature results from the integration of nickel cations, cobalt cations and surface lattice oxygen atoms/oxygen vacancies at the atomic scale. In situ studies of complete oxidation of methane on NiCo2O4 and theoretical simulations show that methane dissociates to methyl on nickel cations and then couple with surface lattice oxygen atoms to form -CH3O with a following dehydrogenation to -CH2O; a following oxidative dehydrogenation forms CHO; CHO is transformed to product molecules through two different sub-pathways including dehydrogenation of OCHO and CO oxidation.

Original languageEnglish
Article number7798
JournalNature Communications
Volume6
DOIs
StatePublished - Aug 4 2015

Funding

F.T. acknowledges the funding support from the Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy under Grant No. DE-FG02-12ER16353.

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