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Achieving high NO conversion and N2 selectivity in selective catalytic reduction of NO by CO (CO‐SCR) in a wide operating temperature window, particularly in the presence of high O2 concentration, remains a big challenge. Herein, guided by density functional theory (DFT) calculations, a catalyst is rationally developed with dual active centers consisting of both Co single‐atoms (SAs) and CoOx nanoclusters...
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