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dc.contributor.authorBabaryk, Artem A.es_ES
dc.contributor.authorAdawy, Alaaes_ES
dc.contributor.authorGarcía, Inéses_ES
dc.contributor.authorTrobajo, Caminoes_ES
dc.contributor.authorAmghouz, Zakariaees_ES
dc.contributor.authorColodrero, Rosario M. P.es_ES
dc.contributor.authorCabeza, Aurelioes_ES
dc.contributor.authorOlivera-Pastor, Pascuales_ES
dc.contributor.authorBazaga-García, Montsees_ES
dc.contributor.authorSantos-Gómez, Lucía doses_ES
dc.date.accessioned2022-01-31T10:39:53Z-
dc.date.available2022-01-31T10:39:53Z-
dc.date.issued2021-
dc.identifier.citationDalton Transactions 50(22): 7667-7677 (2021)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/259239-
dc.description.abstractAlthough the fibrous polymorphic modification of titanium phosphate, π-Ti2O(PO4)2·2H2O (π-TiP) has been known for decades, its crystal structure has remained unsolved. Herewith, we report the crystal structure of π-TiP at room temperature, as determined from synchrotron radiation powder X-ray diffraction, and corroborated by 31P solid state NMR and accurate density functional theory calculations. In contrast to the previously reported ρ-TiP polymorph, the as-synthesized hydrated phase crystallizes in the monoclinic system (P21/c, a = 5.1121(2) Å, b = 14.4921(9) Å, c = 12.0450(11), β = 115.31(1)°, Z = 4), and is composed of corner-sharing titanium octahedra and phosphate units arranged in a pattern that is unique to the ρ-TiP polymorph. The unit cell was confirmed by electron diffraction, while the formation of planar packing imperfections and stacking faults along the [101] plane was revealed by HRTEM analysis. An in situ dehydration study of π-TiP, monitored by high-temperature powder X-ray diffraction, led to a new anhydrous monoclinic (P21/c, a = 5.1187(13) Å, b = 11.0600(21) Å, c = 14.4556(26), β = 107.65(2)°, Z = 4) phase that crystallizes at 500 °C. The latter resembles the packing fashion of the parental π-TiP, albeit titanium atoms are present in both distorted tetrahedral and octahedral coordination environments. Anhydrous π-TiP was found to partially rehydrate at room temperature, reversibly adopting the structure of the initial phase. The studies carried out under different conditions of leaching and impregnation with H3PO4 showed that π-TiP exhibits an extrinsic proton conductivity (1.3 × 10−3 S cm−1 at 90 °C and 95% RH) due to the presence of the protonated phosphate species bound on the particles surface, as revealed by 31P MAS-NMR spectroscopy data. The composite membranes of Chitosan (CS) matrices filled with H3PO4-impregnated π-TiP solid show an increment of proton conductivity up to 4.5 × 10−3 S cm−1, at 80 °C and 95% RH, which is 1.8-fold higher than those of the bare CS membranes.es_ES
dc.description.sponsorshipThis work has been supported by Ministerio de Ciencia, Innovación y Universidades and Ministerio de Economía, Industria y Competitividad from Spain (MAT2016-78155-C2-1-R, MAT2016-77648-R and PID2019-110249RB-I00), Junta de Andalucía (FQM-113) research project and Principado de Asturias–FICYT-FEDER (IDI/2018/000170). Use of the Advanced Photon Source at Argonne National Laboratory was supported by the U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. Artem A. Babaryk would like to thank Prof. Santiago García-Granda (SYSTAM Group), the Department of Physical and Analytical Chemistry, University of Oviedo, for the SRPXRD data (APS 11 BM-B “Mail-In” program, under proposal no. GUP-65338). Prof. José Manuel Recio (MALTA-Consolider Team) is acknowledged for providing computational facilities at the University of Oviedo. The authors thank Prof. José R. García and S. Khainakov, Department of Organic and Inorganic Chemistry, University of Oviedo, for their generous scientific assistance. L. dos Santos-Gómez thanks the Ministerio de Ciencia, Innovación y Universidades for her Juan de la Cierva Formación grant (FJC2018-036746-I), M. Bazaga-García thanks Junta de Andalucía for her Postdoc PAIDI grant, and R. M. P. Colodrero thanks UMA Research Plan for her financial support.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO//MAT2016-78155-C2-1-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO//MAT2016-77648-Res_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-110249RB-I00/ES/DISEÑO Y DESARROLLO DE ELECTROCATALIZADORES Y MEMBRANAS POLIMERICAS DERIVADAS DE FOSFONATOS METALICOS Y OXIDOS CERAMICOS PARA PILAS DE COMBUSTIBLES Y ELECTROLIZADORES/es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO//FJC2018-036746-Ies_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccesses_ES
dc.titleStructural and proton conductivity studies of fibrous π-Ti2O(PO4)2·2H2O: application in chitosan-based composite membraneses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/D1DT00735A-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1039/D1DT00735Aes_ES
dc.identifier.e-issn1477-9234-
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)es_ES
dc.contributor.funderMinisterio de Economía, Industria y Competitividad (España)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderAgencia Estatal de Investigación (España)es_ES
dc.contributor.funderPrincipado de Asturiases_ES
dc.contributor.funderDepartment of Energy (US)es_ES
dc.contributor.funderJunta de Andalucíaes_ES
dc.relation.csices_ES
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dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011033es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100000015es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011011es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100010198es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100011941es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextopen-
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