Theoretical insights into the electroreduction mechanism of N(2) to NH(3) from an improved Au(111)/H(2)O interface model

An improved H coverage-dependent Au(111)/H(2)O electrochemical interface model is proposed in this paper, which is firstly used to study electroreduction mechanisms of N(2) into NH(3) at the thermodynamical equilibrium potential in cooperation with electronic structure analysis. The results show that the associative mechanism is more favorable on Au(111) and therein alternating and distal pathways may be able to parallelly occur in gas phase and the present simulated electrochemical interface. The initial N(2) reduction into the N(2)H intermediate is the rate determining step, which may be able to be regarded as the origin of the observed experimentally high overpotential during N(2) electroreduction. The presence of an electrochemical environment can significantly change the N(2) reduction pathway and decrease the barrier of the rate determining step, which can be ascribed to the significant electron accumulation and interaction between N(2) molecules and H(2)O clusters. The theoretical results display excellent consistency with the available experimental data, confirming the rationality of the present proposed electrochemical model. The comparison of the barrier between the hydrogen evolution reaction and rate determining step well explains why the activity of Au electrodes is usually unsatisfactory. Accordingly, a single descriptor can be proposed, in which an ideal electrocatalyst should be able to reduce the barrier for initial N(2) electroreduction into N(2)H. In this way, N(2) electroreduction pathways can be facilitated and the yield of NH(3) can be enhanced. We believe that the present study can represent progress to study N(2) electroreduction mechanisms from an improved electrochemical model.