Metallic Co Nanoarray Catalyzes Selective NH3 Production from Electrochemical Nitrate Reduction at Current Densities Exceeding 2 A cm(-2)

Electrochemical nitrate reduction (NITRR) offers a promising alternative toward nitrogen recycling and ammonia production under ambient conditions, for which highly active and selective electrocatalyst is desired. In this study, metallic cobalt nanoarrays as facilely prepared from the electrochemical reduction of Co(OH)(2) nanoarrays (NAs) are demonstrated to exhibit unprecedented NH3 producing capability from catalyzing NITRR. Benefitting from the high intrinsic activity of Co-0, intimate contact between active species and conductive substrate and the nanostructure which exposes large number of active sites, the Co-NAs electrode exhibits current density of -2.2 A cm(-2) and NH3 production rate of 10.4 mmol h(-1) cm(-2) at -0.24 V versus RHE under alkaline condition and significantly surpasses reported counterparts. Moreover, the close-to-unity (>= 96%) Faradaic efficiency (FE) toward NH3 is achieved over wide application range (potential, NO3- concentration and pH). Density function theory calculation reveals the optimized adsorption energy of NITRR intermediates on Co surface over Co(OH)(2). Furthermore, it is proposed that despite the sluggish kinetics of Volmer step (H2O -> *H + *OH) which provides protons in conventional hydrogenation mechanism, the proton-supplying water dissociation process on Co surface is drastically facilitated following a concerted water dissociation-hydrogenation pathway.

Automated summary

The study demonstrates the high NH3 producing capability and close-to-unity Faradaic efficiency of metallic cobalt nanoarrays in electrochemical nitrate reduction. Density function theory calculation reveals the optimized adsorption energy of NITRR intermediates on Co surface. Additionally, the study proposes a water dissociation-hydrogenation pathway that facilitates proton-supplying in the process.