Publications by authors named "Shubo Geng"

Article Synopsis
  • - A new metal-organic framework (MOF) has been developed to effectively purify methane (CH) from natural gas and coal mine methane, which is important for the chemical industry but traditionally difficult to achieve.
  • - The MOF can be produced easily at room temperature and demonstrates exceptional separation performance, achieving a purity level of 154.7 cm³/g for methane in a mix of methane, ethane, and propane, and a higher capacity for methane compared to nitrogen.
  • - Detailed analysis using single-crystal X-ray data and molecular simulations revealed that the MOF utilizes multiple hydrogen bonds and specific interactions between the gases and its structure, making it a promising material for high-capacity methane purification.
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Article Synopsis
  • * A new double-walled network, [NiL(μ-HO)], featuring a unique azo linker and 8-connected building blocks, enables reversible transformations, increasing pore volume by 33%.
  • * The material demonstrates impressive gas uptake capacities, achieving 200 cm/cm for methane at high pressure, ranking among the top FMOMs for methane storage performance.
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Removal of carbon dioxide (CO) from a CO/N mixture by utilizing CO-selective sorbents is important from the perspective of energy security and environmental sustainability. Herein, a microporous metal-organic framework (MOF) composed of manganese(II) and a bifunctional linker 5-(4-1,2,4-triazol-4-yl)benzene-1,3-dicarboxylic acid (HL), [Mn(HL)] () is designed and synthesized using a hydrothermal method. Characterized by single-crystal X-ray diffraction (SCXRD), a microporous channel was found in the structure of compound along the -axis.

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One-step adsorptive purification of ethylene (CH) from a ternary mixture of acetylene (CH), CH, and ethane (CH) by a single material is of great importance but challenging in the petrochemical industry. Herein, a chemically robust olefin-linked covalent organic framework (COF), NKCOF-62, is designed and synthesized by a melt polymerization method employing tetramethylpyrazine and terephthalaldehyde as cheap monomers. This method avoids most of the disadvantages of classical solvothermal methods, which enable the cost-effective kilogram fabrication of olefin-linked COFs in one pot.

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Adsorption-based removal of carbon dioxide (CO ) from gas mixtures has demonstrated great potential for solving energy security and environmental sustainability challenges. However, due to similar physicochemical properties between CO and other gases as well as the co-adsorption behavior, the selectivity of CO is severely limited in currently reported CO -selective sorbents. To address the challenge, we create a bioinspired design strategy and report a robust, microporous metal-organic framework (MOF) with unprecedented [Mn ] nanocages.

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Two C H -selective metal-organic framework (MOF) adsorbents with ultrahigh stability, high surface areas, and suitable pore size have been designed and synthesized for one-step separation of ethane/ethylene (C H /C H ) under humid conditions to produce polymer-grade pure C H . Experimental results reveal that these two MOFs not only adsorb a high amount of C H but also display good C H /C H selectivity verified by fixed bed column breakthrough experiments. Most importantly, the good water stability and hydrophobic pore environments make these two MOFs capable of efficiently separating C H /C H under humid conditions, exhibiting the benchmark performance among all reported adsorbents for separation of C H /C H under humid conditions.

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Efficient propyne/propylene separation to obtain polymer-grade propylene is a crucial and challenging process in industrial production, but it has not yet been realized in the covalent organic framework (COF) field. Addressing this challenge, we synthesize two three-dimensional COF adsorbents via a [8 + 4] construction approach based on an octatopic aldehyde monomer. Upon using the continuous rotation electron diffraction technique and structural simulation, both COFs are successfully determined as rare topology.

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Regarding the global energy crisis, it is of profound significance to develop spontaneous power generators that harvest natural energy. Fabricating humidity-responsive actuators that can conduct such energy transduction is of paramount importance. Herein, we incorporate covalent organic frameworks with flexible polyethylene glycol to fabricate rigid-flexible coupled membrane actuators.

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Developing cost-/energy-efficient separation techniques for purifying ethylene from an ethylene/ethane mixture is highly important but very challenging in the industrial process. Herein, using a bottom-up [8 + 2] construction approach, we rationally designed and synthesized three three-dimensional covalent organic frameworks (COFs) with 8-connected networks, which can selectively remove ethane from an ethylene/ethane mixture with high efficiency. These COF materials, which are fabricated by the condensation reaction of a customer-designed octatopic aldehyde monomer with linear diamino linkers, possess high crystallinity, good structural robustness, and high porosity.

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Self-assembly of N,N,N',N'-tetrakis(4-carboxyphenyl)-1,4-phenylenediamine with the help of different solvents provides isostructural hydrogen-bonded organic frameworks (HOF-30). Single-crystal X-ray diffraction (SCXRD) analysis reveals HOF-30 possesses 3D ten-fold interpenetrated dia nets connected by two kinds of hydrogen bonds, namely solvent-bridged carboxyl dimers and carboxyl⋅⋅⋅carboxyl dimers. Degassing treatment for HOF-30 yields HOF-30a with 3D ten-fold interpenetrated dia nets but linked with sole carboxyl⋅⋅⋅carboxyl dimers.

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The development of new techniques and materials that can separate ethylene from ethane is highly relevant in modern applications. Although adsorption-based separation techniques using metal-organic frameworks (MOFs) have gained increasing attention, the relatively low stability (especially water resistance) and unscalable synthesis of MOFs severely limit their application in real industrial scenarios. Addressing these challenges, we rationally designed and synthesized two new CH-selective MOF adsorbents ( and ) with ultrahigh chemical and thermal stability, including water resistance.

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Two-dimensional (2D) metal-organic frameworks (MOFs) belong to a subgroup of MOFs reminiscent of graphite and covalent organic frameworks (COFs). In the past decade, conductive 2D MOFs have received increasing attention due to their relatively high charge carrier mobility and low resistivity that originate from in-plane charge delocalization and extended π conjugation within the layers. This review comprises the current state-of-the-art of the representative progress in theoretical exploration and electronic applications of conductive 2D MOFs.

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We aimed to develop new effective catalysts for the synthesis of propylene carbonate from propylene oxide and carbon dioxide. A kind of MCl coordination complex was fabricated based on the chelating tridentate ligand 2,6-bis[1-(phenylimino)ethyl] pyridine (). The obtained products were characterized by elemental analysis, infrared spectroscopy, ultraviolet spectroscopy, thermogravimetric analysis, and single-crystal X-ray diffraction.

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