(446b) Transition Metal Nitrides Catalyzed Electrochemical Nitrogen Reduction Reaction
AIChE Annual Meeting
2019
2019 AIChE Annual Meeting
Catalysis and Reaction Engineering Division
Catalysis for Nitrogen Chemistry I: Electrocatalytic Nitrogen Reduction
Wednesday, November 13, 2019 - 8:18am to 8:36am
Renewable production of ammonia, a building block for most fertilizers, via the electrochemical nitrogen reduction reaction (ENRR) is desirable; however, selective electrocatalysts are lacking. Here we show that transition metal nitrides are a family of active, selective, and stable ENRR catalysts. In particular, vanadium nitride nanoparticles have an ENRR rate and a Faradaic efficiency of 3.3 Ã 10â10 mol sâ1 cmâ2 and 6.0% at â0.1 V within 1 h,
respectively. ENRR with 15N2 as the feed produces both 14NH3 and 15NH3, which indicates that the reaction follows a Marsâvan Krevelen mechanism. Ex situ X-ray photoelectron spectroscopy characterization of fresh and spent VN catalysts reveals that multiple vanadium oxide, oxynitride, and nitride species are present on the surface and identified vanadium oxynitride as the active phase in the ENRR, which is supported by operando X-ray absorption spectroscopic results. An ammonia production rate of 1.1 Ã 10â10 mol sâ1 cmâ2 can be maintained on VN for 116 h, with a steady-state turnover number of 431. The deactivation mechanisms of transition metal nitrides in ENRR will also be discussed.
respectively. ENRR with 15N2 as the feed produces both 14NH3 and 15NH3, which indicates that the reaction follows a Marsâvan Krevelen mechanism. Ex situ X-ray photoelectron spectroscopy characterization of fresh and spent VN catalysts reveals that multiple vanadium oxide, oxynitride, and nitride species are present on the surface and identified vanadium oxynitride as the active phase in the ENRR, which is supported by operando X-ray absorption spectroscopic results. An ammonia production rate of 1.1 Ã 10â10 mol sâ1 cmâ2 can be maintained on VN for 116 h, with a steady-state turnover number of 431. The deactivation mechanisms of transition metal nitrides in ENRR will also be discussed.