High-capacity hydrogen storage through molecularly restructured and confined hydrogen hydrates

被引:3
|
作者
Firuznia, Rojan [1 ]
Abutalib, Amir [2 ,3 ]
Hakimian, Alireza [1 ]
Nazifi, Sina [1 ]
Huang, Zixu [1 ]
Lee, T. Randall [3 ,4 ]
Rimer, Jeffrey D. [2 ,3 ]
Ghasemi, Hadi [1 ,2 ,5 ,6 ]
机构
[1] Univ Houston, Dept Mech Engn, 4226 Martin Luther King Blvd, Houston, TX 77204 USA
[2] Univ Houston, Dept Chem & Biomol Engn, 4226 Martin Luther King Blvd, Houston, TX 77204 USA
[3] Univ Houston, Dept Chem, 3585 Cullen Blvd,Room 112, Houston, TX 77204 USA
[4] Univ Houston, Texas Ctr Superconduct, 3369 Cullen Blvd,Suite 202, Houston, TX 77204 USA
[5] Univ Houston, Dept Mech Engn, Houston, TX 77204 USA
[6] Univ Houston, Dept Chem & Biomol Engn, Houston, TX 77204 USA
关键词
Hydrogen; Storage; Nanoconfinements; Mesoporous zeolite; Hydrates; WATER; DYNAMICS;
D O I
10.1016/j.mtphys.2023.101248
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In the future landscape of sustainable energies and in combating global climate challenges, hydrogen plays a crucial role in both stationary and portable energy systems that currently supply 18 % of the total energy de-mand. High-capacity, safe, and cost-effective hydrogen storage is critical for advancing the hydrogen economy but remains a dauting challenge. A range of advanced material systems including metal hydrides, metal-organic frameworks, and 2D materials have been explored in efforts to achieve high storage capacity, but high operating pressures, low charging/discharging rates, and energy intensive discharging processes have hindered their development and deployment. Here, we report a green material paradigm for high storage capacity with fast charging/discharging and ambient temperature discharging. The material platform is a modified zeolite with rationally tuned pores and modified surface chemistry that exhibits long-term stability and stores hydrogen gas in the form of hydrogen hydrates. The selected pore dimensions enhance the hydrogen solubility through restructuring of water molecules, and the surface chemistry of the material leads to enhanced double donor -acceptor bonds with water molecules for enhanced hydrogen storage capacity. The material enables hydrogen storage in hydrogen hydrate form at 8-10 bar dropping the required storage pressure by two orders of magnitude lower compared to state-of-the-art materials and addresses long-standing hurdles of high operating pressure and slow formation kinetics of hydrogen hydrates providing a promising platform for hydrogen storage.
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页数:8
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