4.7 Article

Boosting nitrous oxide direct decomposition performance based on samarium doping effects

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 414, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128643

Keywords

N2O decomposition; Sm-doping; In situ NAP-XPS; Redox cycle

Funding

  1. National Natural Science Foundation of China [21936005, 21876093]
  2. National Key Research and Development Program [2018YFC0213401, 2017YFC0212804]

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A series of Sm-doped Co3O4 catalysts were synthesized by the sol-gel method, with Sm significantly enhancing the N2O decomposition activity. The incorporation of Sm distorted the Co3O4 lattice and promoted oxygen vacancy generation, leading to a redox cycle between Co and Sm species. In situ Raman and in situ NAP-XPS results indicated that this redox cycle is the main reason for the accelerated N2O decomposition efficiency with Sm doping.
A series of Sm-doped Co3O4 catalysts for the N2O direct catalytic decomposition were synthesized by the sol?gel method using citric acid as a chelating agent and urea as a combustion agent. The doping of Sm significantly altered the activity of N2O decomposition on the Co3O4 catalyst. Sm was incorporated into the Co3O4 matrix, leading to the distortion of Co3O4 lattice with the spinel configuration maintained. Sm-doping can effectively promote the oxygen vacancy generation, and the electron interaction between Co and Sm species occurred as the Co3+ + Sm2+ ? Co2+ + Sm3+ redox cycle. Combined with in situ Raman and in situ NAP-XPS results proposed that this redox cycle is the main reason that the Sm-doping accelerates the high-efficiency N2O decomposition.

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