Mechanistic Insights into Electrochemical Nitrogen Reduction Reaction on Vanadium Nitride Nanoparticles

• Published in: Journal of the American Chemical Society Vol. 140; no. 41; pp. 13387 - 13391
• Main Authors: Yang, Xuan, Nash, Jared, Anibal, Jacob, Dunwell, Marco, Kattel, Shyam, Stavitski, Eli, Attenkofer, Klaus, Chen, Jingguang G, Yan, Yushan, Xu, Bingjun
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 17.10.2018; American Chemical Society (ACS)
• Subjects: ammonia; catalysts; durability; electrochemistry; fertilizers; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; nanoparticles; nitrides; nitrogen; stable isotopes; vanadium; X-ray absorption spectroscopy; X-ray photoelectron spectroscopy
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.8b08379

Renewable production of ammonia, a building block for most fertilizers, via the electrochemical nitrogen reduction reaction (ENRR) is desirable; however, a selective electrocatalyst is lacking. Here we show that vanadium nitride (VN) nanoparticles are active, selective, and stable ENRR catalysts with an ENRR rate and a Faradaic efficiency (FE) 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 catalysts reveals that multiple vanadium oxide, oxynitride, and nitride species are present on the surface and identified VN0.7O0.45 as the active phase in the ENRR. Operando X-ray absorption spectroscopy and catalyst durability test results corroborate this hypothesis and indicate that the conversion of VN0.7O0.45 to the VN phase leads to catalyst deactivation. We hypothesize that only the surface N sites adjacent to a surface O are active in the ENRR. An ammonia production rate of 1.1 × 10–10 mol s–1 cm–2 can be maintained for 116 h, with a steady-state turnover number of 431.