Flue gas denitrification represents an environmentally friendly and economically viable strategy for alleviating energy crises and advancing carbon neutrality goals. Although traditional selective catalytic reduction (SCR) catalysts demonstrate excellent denitrification efficiency and catalytic stability, they still face significant challenges, including high cost and ammonia slip. In this study, the high-entropy oxide (HEO) NiCoZnVCrOx was synthesized via the sol–gel method and evaluated for the reduction of NO to N2. The effects of varying reaction conditions on the NO reduction performance of this material were systematically investigated alongside the underlying reaction mechanism. The results reveal that the reduced oxygen carrier (OC) achieves optimal performance at an oxidation temperature of 800 °C, oxidizing gas flow rate of 200 mL/min and reduction time of 60 min, yielding the highest NO conversion and N2 selectivity while simultaneously minimizing NO2 selectivity. The reaction mechanism was further elucidated through a series of characterization techniques, including DRIFTS. Overall, this HEO demonstrates significant potential as a candidate OC for flue gas denitrification.
Cai et al. (Wed,) studied this question.