Low-temperature hydrogen release exceeding 7 wt% from LiBH4-mannitol composites

被引:2
作者
Yan, Chengguo [1 ]
Zheng, Jiaguang [1 ,2 ]
Xia, Ao [1 ]
Zhang, Qingbo [1 ]
Lv, Meiling [1 ]
Ma, Zhenxuan [1 ]
Su, Chao [1 ]
Yao, Zhendong [3 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Energy & Power, Zhenjiang 212003, Peoples R China
[2] Nankai Univ, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
[3] China Jiliang Univ, Coll Mat & Chem, Hangzhou 310018, Peoples R China
基金
中国国家自然科学基金;
关键词
STORAGE PROPERTIES; LIBH4; HYDROLYSIS; GENERATION; NANOCONFINEMENT; CAPACITY; MICRO; DESTABILIZATION; DEHYDROGENATION; DECOMPOSITION;
D O I
10.1016/j.ijhydene.2024.07.045
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
Among conventional hydrogen storage materials, LiBH 4 has been regarded as one of the best hydrogen transporters due to its relatively large hydrogen capacities. However, because of its extraordinarily high dehydrogenation temperatures, LiBH 4 was not suitable for hydrogen storage due to its stable thermodynamic features. Herein, we present a novel approach to LiBH 4 that uses solid-state multi-hydroxyl mannitol as a reactant, regulating hydrogen release below 69.9 degrees C. More than 7 wt % H 2 could be released with ultra-fast rates at 140 degrees C from the LiBH 4-mannitol composite. XRD, FTIR, and SEM tests revealed that the reaction between mannitol (H delta+ ) and LiBH 4 (H delta- ) to produce hydrogen was accompanied by the generation of large amounts of heat in situ, which further promoted the decomposition of LiBH 4 for hydrogen production, exceeding the theoretical dehydrogenation amount of H delta+- H delta- reaction. This work indicates possibilities for the development of fast and easy high-capacity hydrogen generation systems based on complex hydrides.
引用
收藏
页码:346 / 352
页数:7
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