ZIF-8@Zn-MOF-74 core–shell metal–organic framework (MOF) with open metal sites: Synthesis, characterization, and gas adsorption performance

金属有机骨架 高分辨率透射电子显微镜 吸附 打赌理论 多孔性 介孔材料 金属 傅里叶变换红外光谱 分子 化学工程 比表面积 选择性 化学 材料科学 无机化学 催化作用 纳米技术 有机化学 透射电子显微镜 工程类
作者
Somayeh Norouzbahari,Zohreh Mehri Lighvan,Ali Ghadimi,Behrouz Sadatnia
出处
期刊:Fuel [Elsevier BV]
卷期号:339: 127463-127463 被引量:52
标识
DOI:10.1016/j.fuel.2023.127463
摘要

In this paper, an efficient hierarchical metal–organic framework (MOF), namely ZIF-8@Zn-MOF-74 with core–shell structure and coordinately open/unsaturated metal sites (OMS) was successfully synthesized. For this purpose, the facile post-synthetic ligand exchange (PSE) method at ambient temperature was applied. In the fabricated core–shell porous structure, the SOD-type ZIF-8 acts as the core, providing molecular sieving features, resulting in greater adsorption selectivity values. On the other hand, Zn-MOF-74 as the shell part, owing to the larger pore size, makes entrance and diffusion of the guest gas molecules more convenient. In addition, due to the presence of OMS in the Zn-MOF-74 structure, a greater adsorption capacity would be achieved. The prepared MOFs were characterized by FESEM, EDS, HRTEM, FTIR, XRD, BET, and TGA analyses, and formation of the core–shell structure was confirmed. The FESEM and HRTEM images demonstrated rather smooth coverage of the core (ZIF-8) with a layer of the shell (Zn-MOF-74). The rather high BET surface area (633.2 m2/g) and total pore volume (0.671 cm3 g−1) of the core–shell structure, make it promising for gas adsorption applications. The gas adsorption measurements were conducted for CO2, N2, H2, O2, CH4, C2H6, C3H8, C2H4, and C3H6 pure gases at 308 K and equilibrium pressures up to 4 bar. It was found that the CO2 adsorption capacity of ZIF-8@Zn-MOF-74 nanoparticles (3.27 mmol g−1) has enhanced ∼63.5 % compared to the pristine ZIF-8 (∼2 mmol/g). The CO2/N2 and CO2/CH4 selectivity values were also increased by 85.4 % and 74.4 %, respectively, that indicates overcoming the trade-off between adsorption capacity and selectivity.
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