Carbon-doped boron nitride nanosheets as an efficient metal-free catalyst for the selective oxidation of H2S.

We report the first use of carbon-doped boron nitride (BCN) for H2S-selective catalytic oxidation. The obtained carbon-doped BN with an ultrathin layer structure exhibits outstanding H2S elimination and high S yield. In particular, BN doped carbon nanosheets display better catalytic performance than traditional catalysts, such as iron- and carbon-based catalysts. The findings of the present work shed a new light on metal-free catalysts for efficient catalytic removal of toxic H2S.

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

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.

Highly Active and Sulfur-Resistant Fe-N4 Sites in Porous Carbon Nitride for the Oxidation of H2 S into Elemental Sulfur.

Iron-based catalysts have been widely studied for the oxidation of H2 S into elemental S. However, the prevention of iron sites from deactivation remains a big challenge. Herein, a facile copolymerization strategy is proposed for the construction of isolated Fe sites confined in polymeric carbon nitride (CN) (Fe-CNNχ). The as-prepared Fe-CNNχ catalysts possess unique 2D structure as well as electronic property, resulting in enlarged exposure of active sites and enhancement of redox performance. Combining systematic characterizations with density functional theory calculation, it is disclosed that the isolated Fe atoms prefer to occupy four-coordinate doping configurations (Fe-N4 ). Such Fe-N4 centers favor the adsorption and activation of O2 and H2 S. As a consequence, Fe-CNNχ exhibit excellent catalytic activity for the catalytic oxidation of H2 S to S. More importantly, the Fe-CNNχ catalysts are resistant to water and sulfur poisoning, exhibiting outstanding catalytic stability (over 270 h of continuous operation), better than most of the reported catalysts.

Polymeric carbon nitride nanomesh as an efficient and durable metal-free catalyst for oxidative desulfurization.

We report the first use of polymeric carbon nitride (CN) for the catalytic selective oxidation of H2S. The as-prepared CN with unique ultrathin "nanomeshes" structure exhibits excellent H2S conversion and high S selectivity. In particular, the CN nanomesh also displays better durability in the desulfurization reaction than traditional catalysts, such as carbon- and iron-based materials.