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      Improving the mechanical stability of zirconium-based metal–organic frameworks by incorporation of acidic modulators

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          Abstract

          Acidic modulating ligands have been shown to stabilize UiO metal-organic frameworks against structural collapse under ball-milling.

          Abstract

          The ability to retain structural integrity under processing conditions which involve mechanical stress, is essential if metal–organic frameworks (MOFs) are to fulfil their potential as serious candidates for use in gas sorption, separation, catalysis and energy conversion applications. A series of zirconium dicarboxylates, predicted to be amongst the more mechanically robust MOFs, have been found to undergo rapid collapse upon ball-milling, resulting in catastrophic losses of porosity. An inverse relationship between collapse time and framework porosity has been found. Addition of acidic modulator ligands ( e.g. trifluoroacetic acid) to UiO-66 provided a striking increase in mechanical robustness, the degree of which is inversely related to modulator p K a. This effect, caused by an increased strength of the zirconium–carboxylate bond, provides an important concept to design microporous hybrid frameworks capable of retaining their structure under harsh processing conditions.

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          Disclosing the Complex Structure of UiO-66 Metal Organic Framework: A Synergic Combination of Experiment and Theory

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            Iron-based cathode catalyst with enhanced power density in polymer electrolyte membrane fuel cells.

            H(2)-air polymer-electrolyte-membrane fuel cells are electrochemical power generators with potential vehicle propulsion applications. To help reduce their cost and encourage widespread use, research has focused on replacing the expensive Pt-based electrocatalysts in polymer-electrolyte-membrane fuel cells with a lower-cost alternative. Fe-based cathode catalysts are promising contenders, but their power density has been low compared with Pt-based cathodes, largely due to poor mass-transport properties. Here we report an iron-acetate/phenanthroline/zeolitic-imidazolate-framework-derived electrocatalyst with increased volumetric activity and enhanced mass-transport properties. The zeolitic-imidazolate-framework serves as a microporous host for phenanthroline and ferrous acetate to form a catalyst precursor that is subsequently heat treated. A cathode made with the best electrocatalyst from this work, tested in H(2)-O(2,) has a power density of 0.75 W cm(-2) at 0.6 V, a meaningful voltage for polymer-electrolyte-membrane fuel cells operation, comparable with that of a commercial Pt-based cathode tested under identical conditions.
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              Unusual and highly tunable missing-linker defects in zirconium metal-organic framework UiO-66 and their important effects on gas adsorption.

              UiO-66 is a highly important prototypical zirconium metal-organic framework (MOF) compound because of its excellent stabilities not typically found in common porous MOFs. In its perfect crystal structure, each Zr metal center is fully coordinated by 12 organic linkers to form a highly connected framework. Using high-resolution neutron power diffraction technique, we found the first direct structural evidence showing that real UiO-66 material contains significant amount of missing-linker defects, an unusual phenomenon for MOFs. The concentration of the missing-linker defects is surprisingly high, ∼10% in our sample, effectively reducing the framework connection from 12 to ∼11. We show that by varying the concentration of the acetic acid modulator and the synthesis time, the linker vacancies can be tuned systematically, leading to dramatically enhanced porosity. We obtained samples with pore volumes ranging from 0.44 to 1.0 cm(3)/g and Brunauer-Emmett-Teller surface areas ranging from 1000 to 1600 m(2)/g, the largest values of which are ∼150% and ∼60% higher than the theoretical values of defect-free UiO-66 crystal, respectively. The linker vacancies also have profound effects on the gas adsorption behaviors of UiO-66, in particular CO2. Finally, comparing the gas adsorption of hydroxylated and dehydroxylated UiO-66, we found that the former performs systematically better than the latter (particularly for CO2) suggesting the beneficial effect of the -OH groups. This finding is of great importance because hydroxylated UiO-66 is the practically more relevant, non-air-sensitive form of this MOF. The preferred gas adsorption on the metal center was confirmed by neutron diffraction measurements, and the gas binding strength enhancement by the -OH group was further supported by our first-principles calculations.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2015
                2015
                : 3
                : 4
                : 1737-1742
                Article
                10.1039/C4TA06396A
                1dead164-f409-450d-a377-ba22baea0533
                © 2015
                History

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