Critical to the feasibility of electrochemical reduction of waste NO x (NO xRR), as a sustainable pathway and to close the NO x cycle for the emerging NH 3 economy, is the requirement of inexpensive, scalable and selective catalysts that can generate NH 4 + with high yield, as indicated by our economic modelling.
Critical to the feasibility of electrochemical reduction of waste NO x (NO xRR), as a sustainable pathway and to close the NO x cycle for the emerging NH 3 economy, is the requirement of inexpensive, scalable and selective catalysts that can generate NH 4 + with high yield, as indicated by our economic modelling. To this end, we carry out density functional theory (DFT) calculations to investigate the possible contribution of oxygen vacancy (OV) defects in NO xRR catalysis, discovering that an increase in defect density within CuO is leading to a decrease in adsorption energy for NO 3 − reactants. Using these findings as design guidelines, we develop defective CuO nanomaterials using flame spray pyrolysis (FSP) and mild plasma treatment, that can attain a NH 4 + yield of 520 μmol cm −2 h −1 at a cell voltage of 2.2 V within a flow electrolyser with good stability over 10 h of operation. Through our mechanistic investigation, we establish the beneficial role of oxygen vacancy defects (with one free electron) in CuO for NO xRR and we reveal a direct correlation of oxygen vacancy density with the NH 4 + yield, arising from improved NO 3 − adsorption, as evidenced from our theoretical calculations. Our findings on defect engineering to improve NH 4 + yield and its economic feasibility display the potential of NO xRR as an alternative pathway to generate green NH 3, which can also serve as an energy vector for the emerging hydrogen economy and close the NO x cycle.