Percolative metal-organic framework/carbon composites for hydrogen storage

被引:12
|
作者
Xie, Shuqian [1 ]
Hwang, Jiann-Yang [2 ]
Sun, Xiang [2 ]
Shi, Shangzhao [2 ]
Zhang, Zheng [2 ]
Peng, Zhiwei [2 ]
Zhai, Yuchun [1 ]
机构
[1] Northeastern Univ, Sch Met & Mat, Shenyang 110819, Liaoning, Peoples R China
[2] Michigan Technol Univ, Dept Mat Sci & Engn, Houghton, MI 49931 USA
关键词
Hydrogen adsorption; Electric field; MOF; Polarization; CARBON NANOTUBES; ADSORPTION; CAPACITY; PHYSISORPTION;
D O I
10.1016/j.jpowsour.2013.12.072
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
Percolative Metal-organic framework/Carbon (MOFAC) composites are synthesized by IRMOF8 (isoreticular metal-organic frameworks) directly depositing on activated carbon via heterogeneous nucleation. Carbon content is calculated by TGA (Thermogravimetric analysis) tests. XRD (X-ray diffraction) and FESEM (Field emission-scanning electron microscope) are carried out to characterize the structures of the samples. BET surface areas and the pore size distribution are measured. The dielectric constant is measured with impedance analyzer and a specially designed sample holder. The dielectric constants of the MOFAC composites rise with increasing the carbon content, and the composites possess the insulator conductor transition as the carbon content increases from 17.77 wt% to 22.2 wt%. The composites are further tested for hydrogen storage capability under assist of the PMN-PT (single crystal lead magnesium niobate lead titanate) generated electric field. With help from the PMN-PT, the hydrogen uptake capability is increased about 31.5% over the MOFAC3 (MOF-Carbon composite with 22.2 wt% of carbon) without PMN-PT which is elucidated by the charge distribution mechanisms. The improved storage is due to a stronger electrostatic interaction between IRMOF8 and hydrogen molecule caused by field polarization. Meanwhile, rapid adsorption/desorption kinetics and total reversibility on the samples are observed in the present or absence of external electric field. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 137
页数:6
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