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Improved dehydrogenation performance of LiAlH4 doped with BaMnO3
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作者:

Sazelee, N. A.
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Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia

Rather, Sami-ullah
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King Abdulaziz Univ, Dept Chem & Mat Engn, POB 80204, Jeddah 21589, Saudi Arabia Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia

Sinin, A. M.
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Univ Malaysia Terengganu, STEM Fdn Ctr, Kuala Nerus 21030, Terengganu, Malaysia Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia

Ismail, M.
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Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia
机构:
[1] Univ Malaysia Terengganu, Fac Ocean Engn Technol, Energy Storage Res Grp, Kuala Nerus 21030, Terengganu, Malaysia
[2] King Abdulaziz Univ, Dept Chem & Mat Engn, POB 80204, Jeddah 21589, Saudi Arabia
[3] Univ Malaysia Terengganu, STEM Fdn Ctr, Kuala Nerus 21030, Terengganu, Malaysia
来源:
关键词:
Solid-state hydrogen storage;
LiAlH4;
Metal oxide;
Desorption kinetics;
HYDROGEN STORAGE PROPERTIES;
COMPOSITE;
D O I:
10.1016/j.heliyon.2024.e31190
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Due to its high gravimetric capacity of hydrogen (10.5 wt%), LiAlH4 has been regarded as a promising material for solid-state hydrogen storage material for onboard usage. However, high decomposition temperature, poor kinetics and irreversibility retard its application. To counter this problem, various weight percentages of BaMnO3 are introduced into the LiAlH4 system as an additive in this work. As a result, the starting hydrogen release of LiAlH4 was reduced to 109-115 degrees C and the second desorption temperature occurred at around 134-158 degrees C, much lower than pure LiAlH4. The isothermal desorption kinetics also proved that faster desorption kinetics can be observed at 90 degrees C for 80 min. About 2.00-2.60 wt% of H-2 could be desorbed by the composite, whereas only <1.00 wt% of H-2 was desorbed by undoped LiAlH4. Additionally, adding BaMnO3 reduced the activation energies by 30 kJ/mol for the first stages and 34 kJ/mol for the second stages. Based on the X-ray diffraction result, the active species formed of MnO2 and Ba or Ba-containing materials are believed to be responsible for the noticeable enhancement in the desorption properties of LiAlH4.
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