氢气储存
打赌理论
傅里叶变换红外光谱
吸附
化学
化学工程
金属有机骨架
水溶液
纳米孔
比表面积
无机化学
催化作用
材料科学
核化学
氢
物理化学
有机化学
工程类
作者
Saisai Chen,Jin Liu,Yongfei Xu,Zhen Li,Wang Tai,Jiong Xu,Zhuo Wang
标识
DOI:10.1016/j.ijhydene.2018.06.106
摘要
Metal organic frameworks (MOF) are a type of nanoporous materials with large specific surface area, which are especially suitable for gas separation and storage. In this work, we report a new approach of crosslinking UiO-66-(OH)2 to enhance its hydrogen storage capacity. UiO-66-(OH)2 was synthesized using hafnium tetrachloride (HfCl4) and 2, 5-dihydroxyterephthalic acid (DTPA) through a canonical modulated hydrothermal method (MHT), followed by a post-synthesis modification, which is to form a crosslinking structure inside the porous structure of UiO-66-(OH)2. During the modification process, the phenolic hydroxyl groups on the UiO-66-(OH)2 reacted with methanal, and HCl aqueous solution and triethylamine served as catalyst (the products denoted as UiO-66-H and UiO-66-T, respectively). Powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), 13C nuclear magnetic resonance spectroscopy (13C NMR) proved that the crosslinking was formed. The BET specific surface area and the average adsorption pore size of UiO-66-H and UiO-66-T significantly increased after modification. The hydrogen storage capacity of UiO-66-H reached a maximum of 3.37 wt% (16.87 mmol/g) at 77 K, 2 MPa. Hydrogen adsorption enthalpy of UiO-66-T was 0.986 kJ/mol, which was higher than that of UiO-66-(OH)2 (0.695 kJ/mol). This work shows that UiO-66-(OH)2 is a promising candidate for potential application in high-performance hydrogen storage.
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