Highly Poison-Resistant Single-Atom Co-N4 Active Sites with Superior Operational Stability over 460 h for H2 S Catalytic Oxidation

Small. 2021 Nov;17(46):e2104939. doi: 10.1002/smll.202104939. Epub 2021 Oct 19.

Abstract

Efficient catalytic elimination of hydrogen sulfide (H2 S) with high activity and durability in nature gas and blast-furnace gas is very critical for both fundamental catalytic research and applied environmental chemistry. Herein, atomically dispersed Co atom catalysts with Co-N4 sites that can transform H2 S into S with conversion rate of ≈100% are designed and prepared. The representative 4Co-N/NC achieves a sulfur yield of nearly 100% and TOF(Co) of 869 h-1 at 180 °C. Importantly, remarkable long-term durability is achieved as well, with no obvious loss of catalytic activity in the run of 460 h, outperforming most of the reported catalysts. The short bond length and strong cooperation of Co-N are beneficial to improve the structural stability of the Co-N4 centers, and significantly enhanced resistance of water and sulfation over single-atom Co-catalyst. The present mechanism involves the stepwise hydrogen transfer process via the adsorbed *HOO and *HS intermediates.

Keywords: Co-N 4 sites; elemental sulfur formation; oxidative desulfurization; porous nitrogen-doped carbon; single-atom Co catalysts.