氨硼烷
脱氢
化学
氢气储存
氢
沸石咪唑盐骨架
氨
聚合
化学工程
组合化学
有机化学
金属有机骨架
催化作用
吸附
聚合物
工程类
作者
Guanlin Li,Ankit Kumar Tripathi,Hao Chan,Sung-Tzu Chen,Jui-Ting Chang,Tessui Nakagawa,Chengyu Wang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2023-04-10
卷期号:11 (16): 6143-6152
被引量:2
标识
DOI:10.1021/acssuschemeng.2c06036
摘要
Ammonia borane (AB, NH3BH3) is considered a promising hydrogen storage material due to its high hydrogen capacity of 19.6 wt %. However, AB thermolysis for complete dehydrogenation requires high temperature. Moreover, AB regeneration is challenging because of the strong B–N bonding in the spent fuel, which causes low regeneration yield. It has been reported that combined effects of size control and basic functionality effectively facilitate AB dehydrogenation and regeneration. In this study, we focused on nanoconfined AB in porous zeolitic imidazolate frameworks (ZIF-8). The ligands of 2-methylimidazole (2-mlm) in ZIF-8 were partially replaced with 3-amino-1,2,4-triazole (ATZ) in order to introduce amino functionalities. The AB@ZIF composites successfully showed 50 and 20 °C lower onset and apex dehydrogenation temperatures, respectively, than the neat AB case. Since the AB dehydrogenation temperature can be controlled by nanoconfinement size, the interaction between primary amines on ATZ and AB may forcibly limit AB molecules from aggregating near the ZIF aperture, forming small particles. For AB regeneration, the spent AB confined in ZIFs can be regenerated by reacting with only liquid ammonia but not N2H4. It is expected that nanoconfined AB results in a low degree of polymerization in the spent fuel rich in B–H species.
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