Catalyst-free efficient stoichiometric synthesis of ammonia and oxygen from nitrogen and water driven by γ-rays

Sustainable energy-driven ammonia synthesis from N<sub>2</sub> and H<sub>2</sub>O at mild conditions is desirable but challenging. Herein, we report an efficient γ-ray-driven stoichiometric N<sub>2</sub> + H<sub>2</sub>O reaction to produce NH<sub>3</sub> and O<sub>2</sub> at room temperature with a high NH<sub>3</sub> formation rate of 70.3 µmol h<sup>-1</sup> without the use of catalysts. Tannic acid was added as the ˙OH scavenger to shift the water radiolysis reaction equilibrium to maximize the concentrations of e<sub>aq</sub><sup>-</sup>, H<sub>aq</sub><sup>+</sup> and ˙H species for N<sub>2</sub> reduction and meanwhile suppress the side ˙OH-mediated NH<sub>3</sub> oxidation reaction. Isotope labelling, radical capture and theoretical modelling demonstrates that NH<sub>3</sub> was formed <i>via</i> ˙N<sub>2</sub>H, NHNH, ˙NHNH<sub>2</sub>, NH<sub>2</sub>NH<sub>2</sub> and ˙NH<sub>2</sub> intermediates, while O<sub>2</sub> was formed <i>via</i> ˙OH, H<sub>2</sub>O<sub>2</sub> and ˙OOH intermediates. Our catalyst-free γ-ray-driven N<sub>2</sub> + H<sub>2</sub>O reaction provides an alternative convenient and efficient route to synthesize NH<sub>3</sub> and O<sub>2</sub> driven by sustainable nuclear energy.

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Publication Details

Journal
Physical Chemistry Chemical Physics
Published
2025-12-18
DOI
https://doi.org/10.1039/d5cp04807a
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
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article

Catalyst-free efficient stoichiometric synthesis of ammonia and oxygen from nitrogen and water driven by γ-rays

Physical Chemistry Chemical Physics
Ammonia Synthesis and Nitrogen Reduction
article

Catalyst-free efficient stoichiometric synthesis of ammonia and oxygen from nitrogen and water driven by γ-rays

article en

Abstract

Sustainable energy-driven ammonia synthesis from N<sub>2</sub> and H<sub>2</sub>O at mild conditions is desirable but challenging. Herein, we report an efficient γ-ray-driven stoichiometric N<sub>2</sub> + H<sub>2</sub>O reaction to produce NH<sub>3</sub> and O<sub>2</sub> at room temperature with a high NH<sub>3</sub> formation rate of 70.3 µmol h<sup>-1</sup> without the use of catalysts. Tannic acid was added as the ˙OH scavenger to shift the water radiolysis reaction equilibrium to maximize the concentrations of e<sub>aq</sub><sup>-</sup>, H<sub>aq</sub><sup>+</sup> and ˙H species for N<sub>2</sub> reduction and meanwhile suppress the side ˙OH-mediated NH<sub>3</sub> oxidation reaction. Isotope labelling, radical capture and theoretical modelling demonstrates that NH<sub>3</sub> was formed <i>via</i> ˙N<sub>2</sub>H, NHNH, ˙NHNH<sub>2</sub>, NH<sub>2</sub>NH<sub>2</sub> and ˙NH<sub>2</sub> intermediates, while O<sub>2</sub> was formed <i>via</i> ˙OH, H<sub>2</sub>O<sub>2</sub> and ˙OOH intermediates. Our catalyst-free γ-ray-driven N<sub>2</sub> + H<sub>2</sub>O reaction provides an alternative convenient and efficient route to synthesize NH<sub>3</sub> and O<sub>2</sub> driven by sustainable nuclear energy.

Physical Chemistry Chemical PhysicsVol. 28(2)
University of Science and Technology of China (CN), Tsinghua University (CN)
Clean water and sanitation
Openalex Percentile: Top 54%
Ammonia Synthesis and Nitrogen Reduction
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