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Selective catalytic oxidation of ammonia (NH3-SCO) to nitrogen (N2) represents a pivotal technology for abating ammonia-containing emissions from industrial and energy utilization sectors. While manganese oxides are environmentally benign catalysts with notable activity, they typically afford low N2 selectivity due to over-oxidation of NH3 to noxious nitrogen oxides. Herein, an efficient strategy integrating microwave-assisted hydrothermal synthesis with boric acid-etching was developed to construct high-performance MnO2-based catalysts. Boron species existed as MnBO3 on the surface of α-MnO2 or occupy the interstitial sites in the α-MnO2 lattice, with their distribution determined by the boric acid solution concentration. The optimal catalyst exhibited moderate crystallite sizes for boron-doped α-MnO2 and MnBO3, high Mn3+ and oxygen vacancy content, and enhanced moderate acid sites, collectively promoting NH3 adsorption/dissociation, providing key intermediate- NH2 for the proceeding of i-SCR pathway while inhibiting the formation of N2O. Remarkably, it achieved 100 % NH3 conversion at 165 °C with 95 % N2 selectivity, and demonstrating excellent stability and water resistance. This work offers a cost-effective approach to design transition metal oxide catalysts for practical applications. © 2025 Elsevier B.V.
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Chemical Engineering Journal
ISSN: 1385-8947
Year: 2025
Volume: 524
1 3 . 4 0 0
JCR@2023
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ESI Highly Cited Papers on the List: 0 Unfold All
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