(446b) Transition Metal Nitrides Catalyzed Electrochemical Nitrogen Reduction Reaction | AIChE

(446b) Transition Metal Nitrides Catalyzed Electrochemical Nitrogen Reduction Reaction

Authors 

Xu, B. - Presenter, University of Delaware
Yang, X., University of Delaware
Nash, J., University of Delaware
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 × 10−10 mol s−1 cm−2 and 6.0% at −0.1 V within 1 h,
respectively. ENRR with 15N2 as the feed produces both 14NH3 and 15NH3, which indicates that the reaction follows a Mars−van 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 × 10−10 mol s−1 cm−2 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.