Low‐Valent Manganese Atoms Stabilized on Ceria for Nitrous Oxide Synthesis

Author:

Surin Ivan1ORCID,Tang Zhenchen1ORCID,Geiger Julian2ORCID,Damir Suyash1ORCID,Eliasson Henrik3ORCID,Agrachev Mikhail4ORCID,Krumeich Frank5ORCID,Mitchell Sharon1ORCID,Kondratenko Vita A.6ORCID,Kondratenko Evgenii V.6ORCID,Jeschke Gunnar4ORCID,Erni Rolf3ORCID,López Núria2ORCID,Pérez‐Ramírez Javier1ORCID

Affiliation:

1. Institute for Chemical and Bioengineering Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich 8093 Switzerland

2. Institute of Chemical Research of Catalonia (ICIQ) The Barcelona Institute of Science and Technology Av. Països Catalans 16 Tarragona 43007 Spain

3. Electron Microscopy Center Empa – Swiss Federal Laboratories for Materials Science and Technology Überlandstrasse 129 Dübendorf 8600 Switzerland

4. Laboratory of Physical Chemistry Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich 8093 Switzerland

5. Laboratory of Inorganic Chemistry Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich 8093 Switzerland

6. Department of Catalyst Discovery and Reaction Engineering Leibniz‐Institut für Katalyse Albert‐Einstein‐Straße 29a 18059 Rostock Germany

Abstract

AbstractNitrous oxide, N2O, exhibits unique reactivity in oxidation catalysis, but the high manufacturing costs limit its prospective uses. Direct oxidation of ammonia, NH3, to N2O can ameliorate this issue but its implementation is thwarted by suboptimal catalyst selectivity and stability, and the lack of established structure–performance relationships. Systematic and controlled material nanostructuring offers an innovative approach for advancement in catalyst design. Herein low‐valent manganese atoms stabilized on ceria, CeO2, are discovered as the first stable catalyst for NH3 oxidation to N2O, exhibiting two‐fold higher productivity than the state‐of‐the‐art. Detailed mechanistic, computational and kinetic studies reveal CeO2 as the mediator of oxygen supply, while undercoordinated manganese species activate O2 and facilitate N2O evolution via NN bond formation between nitroxyl, HNO, intermediates. Synthesis via simple impregnation of a small metal quantity (1 wt%) predominantly generates isolated manganese sites, while full atomic dispersion is achieved upon redispersion of sporadic oxide nanoparticles during reaction, as confirmed by advanced microscopic analysis and electron paramagnetic resonance spectroscopy. Subsequently, manganese speciation is maintained, and no deactivation is observed over 70 h on stream. CeO2‐supported isolated transition metals emerge as a novel class of materials for N2O production, encouraging future studies to evaluate their potential in selective catalytic oxidations at large.

Funder

Generalitat de Catalunya

European Commission

Ministerio de Ciencia e Innovación

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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