双金属片
路易斯酸
材料科学
X射线光电子能谱
金属有机骨架
催化作用
解吸
金属
化学工程
吸附
选择性
无机化学
化学
有机化学
冶金
工程类
作者
Ziyu Gao,Lin Liang,Xiao Zhang,Ping Xu,Jianmin Sun
标识
DOI:10.1021/acsami.1c20878
摘要
Bimetallic metal-organic frameworks (MOFs) containing two different inorganic metal nodes exhibited enhanced properties in CO2 adsorption and catalytic conversion compared with the corresponding monometallic MOFs. In this work, the novel bimetallic Zn/Mg-MOF-74 with different ratios of Zn/Mg was synthesized successfully by a facile one-pot method. Powder X-ray diffraction, Fourier transform infrared, X-ray photoelectron spectroscopy, scanning electron microscopy/transmission electron microscopy, N2/CO2 adsorption/desorption, and CO2/NH3-temperature-programmed desorption techniques thoroughly characterized the structure, morphology, and physicochemical properties of Zn/Mg-MOF-74. Besides the excellent CO2 adsorption capacity (128.3 cm3/g at 273 K and 1 bar), Zn0.75Mg0.25-MOF-74 also showed efficient catalytic activity for the cycloaddition reaction of CO2 and epoxides to cyclic carbonates with outstanding yield and selectivity all over 99% under solvent-free and mild conditions (60 °C, 0.8 MPa), outperforming the mechanical combination of Zn-MOF-74 and Mg-MOF-74 with the same metal contents, indicating the synergistic effect of two adjacent metals in bimetallic MOF-74. In addition, the Zn0.75Mg0.25-MOF-74 catalyst could be recycled for at least five runs and possess good versatility to various substrates. Finally, a feasible mechanism of the catalytic reaction was proposed. Thanks to the high surface area, affinity toward CO2, and accessibility of multiple active sites of the unsaturated metal centers as active Lewis acid sites and O atoms from Zn-O and Mg-O as Lewis basic sites, efficient chemical fixation of CO2 to cyclic carbonates was obtained over the Zn0.75Mg0.25-MOF-74 catalyst. The present facile synthesis and application of a robust bimetallic MOF catalyst offered a competitive avenue for the integration of CO2 adsorption and CO2 catalytic conversion.
科研通智能强力驱动
Strongly Powered by AbleSci AI