Tuning clathrate hydrates for hydrogen storage

被引:740
作者
Lee, H [1 ]
Lee, JW
Kim, DY
Park, J
Seo, YT
Zeng, H
Moudrakovski, IL
Ratcliffe, CI
Ripmeester, JA
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
[2] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
基金
美国国家航空航天局;
关键词
D O I
10.1038/nature03457
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
The storage of large quantities of hydrogen at safe pressures(1) is a key factor in establishing a hydrogen-based economy. Previous strategies-where hydrogen has been bound chemically(2), adsorbed in materials with permanent void space(3) or stored in hybrid materials that combine these elements(3)-have problems arising from either technical considerations or materials cost(2-5). A recently reported(6-8) clathrate hydrate of hydrogen exhibiting two different-sized cages does seem to meet the necessary storage requirements; however, the extreme pressures (similar to 2 kbar) required to produce the material make it impractical. The synthesis pressure can be decreased by filling the larger cavity with tetrahydrofuran (THF) to stabilize the material(9), but the potential storage capacity of the material is compromised with this approach. Here we report that hydrogen storage capacities in THF-containing binary-clathrate hydrates can be increased to similar to 4wt% at modest pressures by tuning their composition to allow the hydrogen guests to enter both the larger and the smaller cages, while retaining low-pressure stability. The tuning mechanism is quite general and convenient, using water-soluble hydrate promoters and various small gaseous guests.
引用
收藏
页码:743 / 746
页数:4
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