摘要
Magnesium-based hydrogen storage alloy serves as an ideal substance for hydrogen storage and transportation because of its high hydrogen storage capacity, low expense, and eco-friendly properties. However, the stable thermodynamic properties and poor kinetic properties during de/hydrogenation limit its application. In this work, a novel high-efficiency catalyst CeF3 was successfully synthesized and induced into Mg90Al10, which exhibited excellent performance during de/hydrogenation. In particular, the Mg90Al10 + 8 wt% CeF3 can absorb 4.0 wt% hydrogen within 600 s at 200 °C, and release 4.3 wt% hydrogen within 900 s at 275 °C, better than the Mg90Al10 that can only absorb 1.36 wt% and release 0.3 wt% hydrogen in similar conditions. Meanwhile, the introduction of CeF3 can also decrease the dehydrogenation apparent activation energy (Ea) of Mg90Al10 obviously from 155.95 kJ/mol to 79.31 kJ/mol. The Al4Ce and MgF2 formed in situ, combined with the high thermal conductivity of Al in charge of the good hydrogen storage behavior of Mg90Al10 + 8 wt% CeF3. The study results are of great importance for applying Mg-Al hydrides in solid-state hydrogen storage.
源语言 | 英语 |
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文章编号 | 133962 |
期刊 | Fuel |
卷 | 384 |
DOI | |
出版状态 | 已出版 - 15 3月 2025 |