Electrochemical conversion of industrial nitrate wastewater to valuable ammonia (NH 3 ) is an attractive method for nitrate removal and NH 3 production. However, the energy efficiency is limited by the high reaction overpotential and poor selectivity. Herein, we demonstrate a tandem electrode composed of hierarchical Cu nanowires shelled with NiCo-layered double hydroxide (NiCo LDH/Cu NW) that exhibits an industrial-relevant NH 3 partial current density of 570 mA cm −2 while maintaining a Faradaic efficiency of 94.25% through the nitrate reduction reaction (NO 3 RR). The practical application of the NO 3 RR route in simulated wastewater with different NO 3 − concentrations and in membrane electrode assembly is developed, which demonstrates great potential for industrial application. Furthermore, online differential electrochemical mass spectrometry, in situ Fourier transform infrared spectroscopy, and density functional theory calculations confirm the tandem catalysis mechanism of NiCo LDH/Cu NW, suggesting that the activity of catalysts for NO 3 RR could be attributed to the synergy effects, in which Cu nanowires would preferentially catalyze the reduction of NO 3 − to NO 2 − and then NiCo LDH catalyzes the reduction of NO 2 − to NH 3 .