Subnanometric alkaline-earth oxide clusters for sustainable nitrate to ammonia photosynthesis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35232982.
- Also identified by DOI 10.1038/s41467-022-28740-8 and PMC identifier 8888631.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The limitation of inert N<sub>2</sub> molecules with their high dissociation energy has ignited research interests in probing other nitrogen-containing species for ammonia synthesis. Nitrate ions, as an alternative feedstock with high solubility and proton affinity, can be facilely dissociated for sustainable ammonia production. Here we report a nitrate to ammonia photosynthesis route (NO<sub>3</sub><sup>-</sup>RR) catalyzed by subnanometric alkaline-earth oxide clusters. The catalyst exhibits a high ammonia photosynthesis rate of 11.97 mol g<sub>metal</sub><sup>-1</sup> h<sup>-1</sup> (89.79 mmol g<sub>cat</sub><sup>-1</sup> h<sup>-1</sup>) with nearly 100% selectivity. A total ammonia yield of 0.78 mmol within 72 h is achieved, which exhibits a significant advantage in the area of photocatalytic NO<sub>3</sub><sup>-</sup>RR. The investigation of the molecular-level reaction mechanism reveals that the unique active interface between the subnanometric clusters and TiO<sub>2</sub> substrate is beneficial for the nitrate activation and dissociation, contributing to efficient and selective nitrate reduction for ammonia production with low energy input. The practical application of NO<sub>3</sub><sup>-</sup>RR route in simulated wastewater is developed, which demonstrates great potential for its industrial application. These findings are of general knowledge for the functional development of clusters-based catalysts and could open up a path in the exploitation of advanced ammonia synthesis routes with low energy consumption and carbon emission.
Medical subject headings
- Ammonia
- Nitrates