Abstract
The electrochemical conversion of nitrate to value-added ammonia is a green alternative to the energy-intensive Haber-Bosch process. However, due to inefficient catalysts, guiding the reaction route towards selective ammonia synthesis is still challenging. Here, we report a highly efficient Cu-infused V(2)C catalyst, synthesized via the molten salt synthesis method using selective CuCl(2) etching. The optimized catalyst exhibits a faradaic efficiency of ∼83% and an ammonia yield of 320 μg cm(-2) h(-1) at -0.7 V vs RHE. We performed (15)N isotopic labeling to ensure the purity and origin of ammonium ions. The synthesis approach was further applied to Ti(3)C(2) MXene, which, upon Cu infusion, achieved a faradaic efficiency of ∼70% and an improved ammonia yield of approximately 450 μg cm(-2) h(-1) at -0.6 V vs RHE. Our results demonstrate that Cu-infused MXene catalysts achieve high selectivity, faradaic efficiency, and ammonia yield, highlighting the broad applicability of this method across different MXenes derived from various transition metals. Moreover, the Cu infusion approach can be expanded to incorporate other metals, offering versatile potential for developing MXene-based catalysts for a range of applications, from ammonia synthesis to CO(2) reduction.