Atomic reconstruction for realizing stable solar-driven reversible hydrogen storage of magnesium hydride
Reversible solid-state hydrogen storage of magnesium hydride, traditionally driven by external heating, is constrained by massive energy input and low systematic energy density. Herein, a single phase of Mg 2 Ni(Cu) alloy is designed via atomic reconstruction to achieve the ideal integration of phot...
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Veröffentlicht in: | Nature communications 2024-04, Vol.15 (1), p.2815-2815, Article 2815 |
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Sprache: | eng |
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Zusammenfassung: | Reversible solid-state hydrogen storage of magnesium hydride, traditionally driven by external heating, is constrained by massive energy input and low systematic energy density. Herein, a single phase of Mg
2
Ni(Cu) alloy is designed via atomic reconstruction to achieve the ideal integration of photothermal and catalytic effects for stable solar-driven hydrogen storage of MgH
2
. With the intra/inter-band transitions of Mg
2
Ni(Cu) and its hydrogenated state, over 85% absorption in the entire spectrum is achieved, resulting in the temperature up to 261.8 °C under 2.6 W cm
−2
. Moreover, the hydrogen storage reaction of Mg
2
Ni(Cu) is thermodynamically and kinetically favored, and the imbalanced distribution of the light-induced hot electrons within CuNi and Mg
2
Ni(Cu) facilitates the weakening of Mg-H bonds of MgH
2
, enhancing the “hydrogen pump” effect of Mg
2
Ni(Cu)/Mg
2
Ni(Cu)H
4
. The reversible generation of Mg
2
Ni(Cu) upon repeated dehydrogenation process enables the continuous integration of photothermal and catalytic roles stably, ensuring the direct action of localized heat on the catalytic sites without any heat loss, thereby achieving a 6.1 wt.% H
2
reversible capacity with 95% retention under 3.5 W cm
−2
.
Researchers demonstrate a single phase Mg
2
Ni(Cu) alloy via atomic reconstruction to achieve the ideal integration of photothermal and catalytic effects, leading to a 6.1 wt. % H
2
reversible capacity with 95 % retention under 3.5 W cm
−2
. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-024-47077-y |