Parallelising Electrocatalytic Nitrogen Fixation Beyond Heterointerfacial Boundary

TL;DR

This paper proposes a parallelized reaction approach using a V2O3/VN hybrid system to enhance nitrogen reduction to ammonia, overcoming energy barriers in traditional pathways and significantly improving yield and efficiency.

Contribution

It introduces a novel multi-phase V2O3/VN system that parallelizes NRR pathways, demonstrating improved ammonia production over single-phase catalysts.

Findings

Increased ammonia yield rate of 18.36 μmol h^-1 cm^-2

Faraday efficiency of 26.62% at -0.3 V vs RHE

FE is 16.95 and 6.22 times higher than single-phase V2O3 and VN

Abstract

The nitrogen (N2) reduction reaction (NRR) is an eco-friendly alternative to the Haber-Bosch process to produce ammonia (NH3) with high sustainability. However, the significant magnitude of uphill energies in the multi-step NRR pathways is a bottleneck of its serial reactions. Herein, the concept of a parallelized reaction is proposed to actively promote NH3 production via the NRR using a multi-phase vanadium oxide-nitride (V2O3/VN) hybrid system. Density functional theory calculations revealed that the V2O3/VN junction parallelizes NRR pathways by exchanging intermediate N2H4* and NH2* products to avoid massive uphill energies towards final NH3 generation. Such an exchange is driven by the difference in coverage of the two species. The impact of the reaction parallelization strategy for multi-step nitrogen reduction is demonstrated with the V2O3/VN junction by an increased ammonia yield rate of 18.36 micro mol h^-1 cm^-2 and a Faraday efficiency (FE) of 26.62% at -0.3 V versus a reversible hydrogen electrode in a 0.1 M aqueous KOH electrolyte, of which FE value exhibits 16.95 times and 6.22 times higher than that of single-phase V2O3 and VN, respectively. The introduction of multi-phase oxides/nitrides into a transition metal-based electrocatalyst can thus be a promising approach to realizing an alternative method for N2 fixation.