Metal Nitride as a Mediator for the Electrochemical Synthesis of NH3
Source abstract
Abstract
The Haber-Bosch process has a massive carbon footprint, and it is highly desired to decentralize NH 3 synthesis in a more sustainable manner. Li-mediated NH 3 electrosynthesis is a promising approach to making NH 3 under ambient conditions, but it suffers from poor energy efficiency owing to the highly reducing electroplating potential of Li. In this Letter, we report a combined theoretical and experimental investigation into other mediators beyond Li, such as Ca, Mg, Sr, Y, and V. The density functional theory results suggest that, besides Li, Ca and Mg can also activate N 2 at room temperature and have a stable surface nitride vacancy necessary for NH 3 synthesis. NH 3 faradaic efficiencies of 50% ± 0.2% and 27% ± 2% are obtained from Ca and Mg, respectively, at an applied current density of 15 mA/cm 2 . This Letter serves as a proof-of-concept for Li-free NH 3 synthesis and will motivate further research in metal-nitride-mediated processes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Hydrogen Storage and Materials · Muon and positron interactions and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, University of Illinois Chicago, Chicago, Illinois 60607, United States
Department of Chemical Engineering, Texas Tech University, Lubbock, Texas 79409, United States
Department of Chemistry, University of Illinois Chicago, Chicago, Illinois 60607, United States
Chemical Sciences and Engineering, Argonne National Laboratory, Lemont, Illinois 60439, United States
Dow Inc., Midland, Michigan 48686, United States
Funding
Division of Chemistry
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