| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
|---|---|---|---|---|---|---|
| 1 | Jack Zhong | -- | 231 | 2026-09-22 05:18:38 | | | |
| 2 | Catherine Yang | -10 word(s) | 221 | 2026-09-22 05:39:41 | | |
Nitrogen reduction reaction is the conversion of dinitrogen (N2) into ammonia or related nitrogen-containing products, most often studied as a six-proton, six-electron process driven electrochemically or photocatalytically at ambient temperature and pressure [1]. Because the N2 triple bond is among the strongest in small molecules, and because the adsorbed N2H, NH2 and NH3 intermediates bind either too weakly or too strongly on most metal surfaces, the attainable rate is constrained by the scaling relations that link their adsorption energies [2]. Rates and Faradaic efficiencies are therefore usually low, and in aqueous electrolytes most of the applied current is consumed by hydrogen evolution rather than by ammonia formation [1]. Reported ammonia yields for metal, carbon-based and single-atom catalysts span several orders of magnitude, and the electrolyte, cell geometry and applied potential shift the measured value substantially; alkali-metal and nitrate or nitrite impurities can also contribute to the detected ammonia, so quantitative control experiments are required [3]. Catalysts examined to date range from transition metals and their nitrides to metal-free carbon materials, and no single material has yet combined high selectivity, high current density and long-term stability [4]. Standardised procedures for ammonia quantification have accordingly become part of how the field reports performance, including isotope labelling with 15N2 and rigorous blank measurements [5].