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Improved N Selectivity of MnO Catalysts for NO Reduction by Engineering Bridged Mn Sites. | LitMetric

Improved N Selectivity of MnO Catalysts for NO Reduction by Engineering Bridged Mn Sites.

Langmuir

International Joint Laboratory of Catalytic Chemistry, State Key Laboratory of Advanced Special Steel, Department of Chemistry, College of Sciences, Shanghai University, Shanghai 200444, China.

Published: May 2023

AI Article Synopsis

  • Mn-based catalysts are effective for reducing NO with NH at low temperatures, but they struggle with N selectivity due to excessive oxidizability.
  • A new catalyst, Mn/ZrTi-A, uses amorphous ZrTiO as a support, enhancing both low-temperature NO conversion and N selectivity.
  • The unique structure of ZrTiO improves the interaction with MnO, preventing the formation of harmful ammonium nitrate and promoting better overall performance in NO reduction.

Article Abstract

Mn-based catalysts are promising for selective catalytic reduction (SCR) of NO with NH at low temperatures due to their excellent redox capacity. However, the N selectivity of Mn-based catalysts is an urgent problem for practical application owing to excessive oxidizability. To solve this issue, we report a Mn-based catalyst using amorphous ZrTiO as the support (Mn/ZrTi-A) with both excellent low-temperature NO conversion and N selectivity. It is found that the amorphous structure of ZrTiO modulates the metal-support interaction for anchoring the highly dispersed active MnO species and constructs a uniquely bridged Mn bonded with the support through oxygen linked to Ti and Zr, respectively, which regulates the optimal oxidizability of the MnO species. As a result, Mn/ZrTi-A is not conducive to the formation of ammonium nitrate that readily decomposes to NO, thus further increasing N selectivity. This work investigates the role of an amorphous support in promoting the N selectivity of a manganese-based catalyst and sheds light on the design of efficient low-temperature deNO catalysts.

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Source
http://dx.doi.org/10.1021/acs.langmuir.3c00663DOI Listing

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