Water-based synthesis and enhanced CO2 capture performance of perfluorinated cerium-based metal–organic frameworks with UiO-66 and MIL-140 topology

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dc.contributor.author Donnadio, Anna
dc.contributor.author Carta, Mariolino
dc.contributor.author D'Amato, Roberto
dc.contributor.author Sangregorio, Claudio
dc.contributor.author Tiana, Davide
dc.contributor.author Vivani, Riccardo
dc.contributor.author Taddei, Marco
dc.contributor.author Costantino, Ferdinando
dc.date.accessioned 2019-01-18T14:31:13Z
dc.date.available 2019-01-18T14:31:13Z
dc.date.issued 2019-11-23
dc.identifier.citation D’Amato, R., Donnadio, A., Carta, M., Sangregorio, C., Tiana, D., Vivani, R., Taddei, M. and Costantino, F. (2019) 'Water-Based Synthesis and Enhanced CO2 Capture Performance of Perfluorinated Cerium-Based Metal–Organic Frameworks with UiO-66 and MIL-140 Topology', ACS Sustainable Chemistry & Engineering, 7(1), pp. 394-402. doi: 10.1021/acssuschemeng.8b03765 en
dc.identifier.volume 7 en
dc.identifier.issued 1 en
dc.identifier.startpage 394 en
dc.identifier.endpage 402 en
dc.identifier.issn 2168-0485
dc.identifier.uri http://hdl.handle.net/10468/7320
dc.identifier.doi 10.1021/acssuschemeng.8b03765
dc.description.abstract Reaction of cerium ammonium nitrate and tetrafluoroterephthalic acid in water afforded two new metal–organic frameworks with UiO-66 [F4_UiO-66(Ce)] and MIL-140 [F4_MIL-140A(Ce)] topologies. The two compounds can be obtained in the same experimental conditions, just by varying the amount of acetic acid used as crystallization modulator in the synthesis. Both F4_UiO-66(Ce) and F4_MIL-140A(Ce) feature pores with size <8 Å, which classifies them as ultramicroporous. Combination of X-ray photoelectron spectroscopy and magnetic susceptibility measurements revealed that both compounds contain a small amount of Ce(III), which is preferentially accumulated near the surface of the crystallites. The CO2 sorption properties of F4_UiO-66(Ce) and F4_MIL-140A(Ce) were investigated, finding that they perform better than their Zr-based analogues. F4_MIL-140A(Ce) displays an unusual S-shaped isotherm with steep uptake increase at pressure <0.2 bar at 298 K. This makes F4_MIL-140A(Ce) exceptionally selective for CO2 over N2: the calculated selectivity, according to the ideal adsorbed solution theory for a 0.15:0.85 mixture at 1 bar and 293 K, is higher than 1900, among the highest ever reported for metal–organic frameworks. The calculated isosteric heat of CO2 adsorption is in the range of 38–40 kJ mol–1, indicating a strong physisorptive character. en
dc.description.sponsorship Fondo Ricerca di Base FRB-2017 project en
dc.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher American Chemical Society, ACS en
dc.relation.uri https://pubs.acs.org/doi/10.1021/acssuschemeng.8b03765
dc.rights © 2018 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Sustainable Chemistry & Engineering, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acssuschemeng.8b03765 en
dc.subject Carbon dioxide capture en
dc.subject Gas separations en
dc.subject Green synthesis en
dc.subject Porous materials en
dc.subject Metal-organic frameworks en
dc.title Water-based synthesis and enhanced CO2 capture performance of perfluorinated cerium-based metal–organic frameworks with UiO-66 and MIL-140 topology en
dc.type Article (peer-reviewed) en
dc.internal.authorcontactother Davide Tiana, Chemistry, University College Cork, Cork, Ireland. +353-21-490-3000 Email: davide.tiana@ucc.ie en
dc.internal.availability Full text available en
dc.check.info Access to this article is restricted until 12 months after publication at the request of the publisher en
dc.check.date 2019-11-23
dc.date.updated 2019-01-18T12:53:17Z
dc.description.version Accepted Version en
dc.internal.rssid 469989561
dc.contributor.funder Horizon 2020 en
dc.contributor.funder H2020 Marie Skłodowska-Curie Actions en
dc.contributor.funder Università degli Studi di Perugia en
dc.description.status Peer reviewed en
dc.identifier.journaltitle Acs Sustainable Chemistry & Engineering en
dc.internal.copyrightchecked No !!CORA!! en
dc.internal.licenseacceptance Yes en
dc.internal.IRISemailaddress davide.tiana@ucc.ie en
dc.relation.project info:eu-repo/grantAgreement/EC/H2020::MSCA-COFUND-FP/663830/EU/Strengthening International Research Capacity in Wales/SIRCIW en


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