Vacancy engineering of WO3−x nanosheets for electrocatalytic NRR process – a first-principles study

Abstract

It has been proved experimentally that tungsten oxide (WO₃) in a defective state has a positive effect on nitrogen reduction reactions (NRRs) owing to the surface modification by adding oxygen vacancies and doping. However, the role of different oxygen vacancies in the electrocatalytic NRR is still behind the scenes. In this study, we have carried out first-principles calculations to grapple with its causes and consequences, focusing on the two-dimensional WO_3−x surface on an atomic scale. Our study shows that WO₃ does not promote nitrogen reduction simply by a dimension reduction without oxygen vacancy. Two NRR processes, which are found to follow the associative mechanism in various pathways, are initiated at relatively lower potentials at two possible vacancies. It is the polarized electrons after being adsorbed over the dangling oxygen vacancy, which weaken the NN bond and enables N₂ reduction with a rate-limiting potential as large as −1.89 V. In contrast, the desorption of NH₃ from the planar vacancy is kinetically challenging at a cost of 1.47 eV, in which case the d orbitals of under-coordinated W match the p orbitals of N and form both bonding state and anti-bonding state. It demonstrates that P–V_O–WO₃ and N₂ can bond firmly but NH₃ desorption ought to pay a price. Two alternative schemes are accordingly proposed to balance good nitrogen adsorption and desorption. This noble metal-free system, by regulating vacancy sites, demonstrates its potential as an eco-friendly and fine-grained artificial material for electrochemical nitrogen reduction.