Improving the desorption properties of LiAlH4 by the addition of Ni0.6Zn0.4O

被引:4
|
作者
Sazelee, N. A. [1 ]
Ali, N. A. [1 ]
Liu, Haizhen [2 ,3 ]
Ismail, M. [1 ]
机构
[1] Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia
[2] Guangxi Univ, Guangxi Coll & Univ Key Lab Blue Energy & Syst Int, Guangxi Novel Battery Mat Res Ctr Engn Technol, Sch Phys Sci & Technol, Nanning 530004, Peoples R China
[3] State Key Lab Featured Met Mat & Life cycle Safety, Nanning 530004, Peoples R China
关键词
Lithium alanate; Metal oxide; Solid -state hydrogen storage; Additive; HYDROGEN STORAGE PROPERTIES; DEHYDROGENATION PROPERTIES; MWCNTS ADDITION; RECENT PROGRESS; BEHAVIOR; NI; PERFORMANCE; NICKEL; NANOCOMPOSITES; SUBSTITUTION;
D O I
10.1016/j.ijhydene.2023.12.181
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium alanate (LiAlH4) is one of the most preferred materials for solid-state hydrogen storage materials owing to its relatively high hydrogen capacity (10.5 wt%). However, its high decomposition temperature and sluggish desorption kinetic restrict its potential application as a hydrogen storage medium for on-board hydrogen-powered applications. To overcome these problems, the impacts of Ni0.6Zn0.4O synthesized via a solid-state method on the desorption properties of LiAlH4 have been examined in this study. It was found that after the introduction of 10 wt% of Ni0.6Zn0.4O to LiAlH4, hydrogen started to release at 124 degrees C and 170 degrees C for the first two stages, respectively. Isothermal desorption kinetics also revealed that faster desorption kinetics can be observed at 90 degrees C for 120 min LiAlH4+10 wt% of Ni0.6Zn0.4O can desorb 3.1 wt% of H2, whereas undoped LiAlH4 can release approximately less than 0.5 wt% of H2 in the same time frame. According to the Kissinger method, the apparent activation energies for the first two steps of the LiAlH4+10 wt% of Ni0.6Zn0.4O composites have been found to be 73 kJ/mol and 85 kJ/mol, respectively, 32 kJ/mol and 40 kJ/mol less than milled LiAlH4. The in-situ formation of NiO and Zn or Zn-containing compounds during the heating process might contribute to the kinetic improvement of LiAlH4.
引用
收藏
页码:543 / 551
页数:9
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