脱氢
氢气储存
材料科学
重量分析
氢
合金
催化作用
化学工程
解吸
物理化学
冶金
化学
有机化学
生物化学
工程类
吸附
作者
Nuo Xu,Kaiwen Wang,Yunfeng Zhu,Yao Zhang
标识
DOI:10.1002/adma.202303173
摘要
Abstract Hydrogen storage has long been a priority on the renewable energy research agenda. Due to its high volumetric and gravimetric hydrogen density, MgH 2 is a desirable candidate for solid‐state hydrogen storage. However, its practical use is constrained by high thermal stability and sluggish kinetics. Here, PdNi bilayer metallenes are reported as catalysts for hydrogen storage of bulk‐MgH 2 near ambient temperature. Unprecedented 422 K beginning dehydrogenation temperature and up to 6.36 wt.% reliable hydrogen storage capacity are achieved. Fast hydrogen desorption is also provided by the system (5.49 wt.% in 1 h, 523 K). The in situ generated PdNi alloy clusters with suitable d ‐band centers are identified as the main active sites during the de/re‐hydrogenation process by aberration‐corrected transmission electron microscopy and theoretical simulations, while other active species including Pd/Ni pure phase clusters and Pd/Ni single atoms obtained via metallene ball milling, also enhance the reaction. These findings present fundamental insights into active species identification and rational design of highly efficient hydrogen storage materials.
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