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dc.contributor.authorShaw, Bikash Kumar
dc.contributor.authorCastillo-Blas, Celia
dc.contributor.authorThorne, Michael F
dc.contributor.authorRíos Gómez, María Laura
dc.contributor.authorForrest, Tom
dc.contributor.authorLopez, Maria Diaz
dc.contributor.authorChater, Philip A
dc.contributor.authorMcHugh, Lauren N
dc.contributor.authorKeen, David A
dc.contributor.authorBennett, Thomas D
dc.date.accessioned2022-04-21T01:03:36Z
dc.date.available2022-04-21T01:03:36Z
dc.date.issued2022-02-16
dc.identifier.issn2041-6520
dc.identifier.other35308849
dc.identifier.otherPMC8849004
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/336300
dc.descriptionFunder: European Social Fund
dc.descriptionFunder: University of Cambridge
dc.description.abstractFour novel dicyanamide-containing hybrid organic-inorganic ABX3 structures are reported, and the thermal behaviour of a series of nine perovskite and non-perovskite [AB(N(CN)2)3] (A = (C3H7)4N, (C4H9)4N, (C5H11)4N; B = Co, Fe, Mn) is analyzed. Structure-property relationships are investigated by varying both A-site organic and B-site transition metal cations. In particular, increasing the size of the A-site cation from (C3H7)4N → (C4H9)4N → (C5H11)4N was observed to result in a decrease in T m through an increase in ΔS f. Consistent trends in T m with metal replacement are observed with each A-site cation, with Co < Fe < Mn. The majority of the melts formed were found to recrystallise partially upon cooling, though glasses could be formed through a small degree of organic linker decomposition. Total scattering methods are used to provide a greater understanding of the melting mechanism.
dc.languageeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceessn: 2041-6539
dc.sourcenlmid: 101545951
dc.titlePrinciples of melting in hybrid organic-inorganic perovskite and polymorphic ABX3 structures.
dc.typeArticle
dc.date.updated2022-04-21T01:03:35Z
prism.endingPage2042
prism.issueIdentifier7
prism.publicationNameChem Sci
prism.startingPage2033
prism.volume13
dc.identifier.doi10.17863/CAM.83718
dcterms.dateAccepted2022-01-18
rioxxterms.versionofrecord10.1039/d1sc07080k
rioxxterms.versionVoR
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0/
dc.contributor.orcidShaw, Bikash Kumar [0000-0003-3249-2487]
dc.contributor.orcidThorne, Michael F [0000-0002-3188-2478]
dc.contributor.orcidChater, Philip A [0000-0002-5513-9400]
dc.contributor.orcidMcHugh, Lauren N [0000-0003-2032-0450]
dc.contributor.orcidKeen, David A [0000-0003-0376-2767]
dc.contributor.orcidBennett, Thomas D [0000-0003-3717-3119]
dc.identifier.eissn2041-6539
pubs.funder-project-idRoyal Society (RG94426, UF150021)
pubs.funder-project-idLeverhulme Trust (RPG-2020-005)
pubs.funder-project-idScience and Engineering Research Board (NIF/R1/180163)
cam.issuedOnline2022


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International