
Open access
Date
2023-12-15Type
- Journal Article
Abstract
The development of selective catalysts for direct conversion of ammonia into nitrous oxide, N₂O, will circumvent the conventional five-step manufacturing process and enable its wider utilization in oxidation catalysis. Deviating from commonly accepted catalyst design principles for this reaction, reliant on manganese oxide, we herein report an efficient system comprised of isolated chromium atoms (1 wt %) stabilized in the ceria lattice by coprecipitation. The latter, in contrast to a simple impregnation approach, ensures firm metal anchoring and results in stable and selective N₂O production over 100 h on stream up to 79% N₂O selectivity at full NH3 conversion. Raman, electron paramagnetic resonance, and in situ UV–vis spectroscopies reveal that chromium incorporation enhances the density of oxygen vacancies and the rate of their generation and healing. Accordingly, temporal analysis of products, kinetic studies, and atomistic simulations show lattice oxygen of ceria to directly participate in the reaction, establishing the cocatalytic role of the carrier. Coupled with the dynamic restructuring of chromium sites to stabilize intermediates of N₂O formation, these factors enable catalytic performance on par with or exceeding benchmark systems. These findings demonstrate how nanoscale engineering can elevate a previously overlooked metal into a highly competitive catalyst for selective ammonia oxidation to N2O, paving the way toward industrial implementation. Show more
Permanent link
https://doi.org/10.3929/ethz-b-000646442Publication status
publishedExternal links
Journal / series
ACS CatalysisVolume
Pages / Article No.
Publisher
American Chemical SocietySubject
single-atom catalysis; ammonia oxidation; nitrous oxide; chromium; ceriaOrganisational unit
03871 - Pérez-Ramírez, Javier / Pérez-Ramírez, Javier
03810 - Jeschke, Gunnar / Jeschke, Gunnar
Funding
180544 - NCCR Catalysis SNF Management KTT (SNF)
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