Practical H<sub>2</sub> supply from ammonia borane enabled by amorphous iron domain.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39438482.
- Also identified by DOI 10.1038/s41467-024-53574-x and PMC identifier 11496879.
- Licence recorded as CC BY-NC-ND.
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Abstract
Efficient catalysis of ammonia borane (AB) holds potential for realizing controlled energy release from hydrogen fuel and addressing cost challenges faced by hydrogen storage. Here, we report that amorphous domains on metallic Fe crystal structures (R-Fe<sub>2</sub>O<sub>3</sub> Foam) can achieve AB catalytic performances and stability (turnover frequency (TOF) of 113.6 min<sup>-1</sup>, about 771 L H<sub>2</sub> in 900 h, and 43.27 mL/(min·cm<sup>2</sup>) for 10×10 cm<sup>2</sup> of Foam) that outperform reported benchmarks (most <14 L H<sub>2</sub> in 45 h) by at least 20 times. These notable increases are enabled by the stable Fe crystal structure, while defects and unsaturated atoms in the amorphous domains form Fe-B intermediates that significantly lower the dissociation barriers of H<sub>2</sub>O and AB. Given that the catalyst lifetime is a key determinant for the practical use in fuel cells, our R-Fe<sub>2</sub>O<sub>3</sub> Foam also provides decent H<sub>2</sub> supply (180 mL H<sub>2</sub>/min, AB water solution of 7.5 wt% H<sub>2</sub>) in a driven commercial car fuel cell at stable power outputs (7.8 V and 1.6 A for at least 5 h). When considered with its facile synthesis method, these materials are potentially very promising for realizing durable high-performance AB catalysts and viable chemical storage in hydrogen powered vehicles.