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dc.contributor.authorFa, Shixinen
dc.contributor.authorYamamoto, Masanorien
dc.contributor.authorNishihara, Hirotomoen
dc.contributor.authorSakamoto, Ryotaen
dc.contributor.authorKamiya, Kazuhideen
dc.contributor.authorNishina, Yutaen
dc.contributor.authorOgoshi, Tomokien
dc.contributor.alternative生越, 友樹ja
dc.date.accessioned2021-02-15T05:26:13Z-
dc.date.available2021-02-15T05:26:13Z-
dc.date.issued2020-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/2433/261686-
dc.description.abstractCarbon-rich materials, which contain over 90% carbon, have been mainly synthesized by the carbonization of organic compounds. However, in many cases, their original molecular and ordered structures are decomposed by the carbonization process, which results in a failure to retain their original three-dimensional (3D) ordering at the angstrom level. Recently, we successfully produced carbon-rich materials that are able to retain their 3D ordering at the angstrom level even after the calcination of organic porous pillar[6]arene supramolecular assemblies and cyclic porphyrin dimer assemblies. Other new pathways to prepare carbon-rich materials with 3D ordering at the angstrom level are the controlled polymerization of designed monomers and redox reaction of graph. Electrocatalytic application using these materials is described.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry (RSC)en
dc.rightsThis article is licensed under a Creative Commons Attribution 3.0 Unported Licence.en
dc.titleCarbon-rich materials with three-dimensional ordering at the angstrom levelen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA12555653-
dc.identifier.jtitleChemical Scienceen
dc.identifier.volume11-
dc.identifier.spage5866-
dc.identifier.epage5873-
dc.relation.doi10.1039/d0sc02422h-
dc.textversionpublisher-
dc.identifier.pmid32953007-
dcterms.accessRightsopen access-
dc.identifier.pissn2041-6520-
dc.identifier.eissn2041-6539-
出現コレクション:学術雑誌掲載論文等

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