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Article: A Two-Dimensional Polyimide-Graphene Heterostructure with Ultra-fast Interlayer Charge Transfer

TitleA Two-Dimensional Polyimide-Graphene Heterostructure with Ultra-fast Interlayer Charge Transfer
Authors
Keywords2D polymers
graphene
interfacial synthesis
transient absorption spectroscopy
van der Waals heterostructure
Issue Date2021
Citation
Angewandte Chemie - International Edition, 2021, v. 60, n. 25, p. 13859-13864 How to Cite?
AbstractTwo-dimensional polymers (2DPs) are a class of atomically/molecularly thin crystalline organic 2D materials. They are intriguing candidates for the development of unprecedented organic–inorganic 2D van der Waals heterostructures (vdWHs) with exotic physicochemical properties. In this work, we demonstrate the on-water surface synthesis of large-area (cm2), monolayer 2D polyimide (2DPI) with 3.1-nm lattice. Such 2DPI comprises metal-free porphyrin and perylene units linked by imide bonds. We further achieve a scalable synthesis of 2DPI-graphene (2DPI-G) vdWHs via a face-to-face co-assembly of graphene and 2DPI on the water surface. Remarkably, femtosecond transient absorption spectroscopy reveals an ultra-fast interlayer charge transfer (ca. 60 fs) in the resultant 2DPI-G vdWH upon protonation by acid, which is equivalent to that of the fastest reports among inorganic 2D vdWHs. Such large interlayer electronic coupling is ascribed to the interlayer cation–π interaction between 2DP and graphene.
Persistent Identifierhttp://hdl.handle.net/10722/349558
ISSN
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300

 

DC FieldValueLanguage
dc.contributor.authorLiu, Kejun-
dc.contributor.authorLi, Jiang-
dc.contributor.authorQi, Haoyuan-
dc.contributor.authorHambsch, Mike-
dc.contributor.authorRawle, Jonathan-
dc.contributor.authorVázquez, Adrián Romaní-
dc.contributor.authorNia, Ali Shaygan-
dc.contributor.authorPashkin, Alexej-
dc.contributor.authorSchneider, Harald-
dc.contributor.authorPolozij, Mirosllav-
dc.contributor.authorHeine, Thomas-
dc.contributor.authorHelm, Manfred-
dc.contributor.authorMannsfeld, Stefan C.B.-
dc.contributor.authorKaiser, Ute-
dc.contributor.authorDong, Renhao-
dc.contributor.authorFeng, Xinliang-
dc.date.accessioned2024-10-17T06:59:20Z-
dc.date.available2024-10-17T06:59:20Z-
dc.date.issued2021-
dc.identifier.citationAngewandte Chemie - International Edition, 2021, v. 60, n. 25, p. 13859-13864-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10722/349558-
dc.description.abstractTwo-dimensional polymers (2DPs) are a class of atomically/molecularly thin crystalline organic 2D materials. They are intriguing candidates for the development of unprecedented organic–inorganic 2D van der Waals heterostructures (vdWHs) with exotic physicochemical properties. In this work, we demonstrate the on-water surface synthesis of large-area (cm2), monolayer 2D polyimide (2DPI) with 3.1-nm lattice. Such 2DPI comprises metal-free porphyrin and perylene units linked by imide bonds. We further achieve a scalable synthesis of 2DPI-graphene (2DPI-G) vdWHs via a face-to-face co-assembly of graphene and 2DPI on the water surface. Remarkably, femtosecond transient absorption spectroscopy reveals an ultra-fast interlayer charge transfer (ca. 60 fs) in the resultant 2DPI-G vdWH upon protonation by acid, which is equivalent to that of the fastest reports among inorganic 2D vdWHs. Such large interlayer electronic coupling is ascribed to the interlayer cation–π interaction between 2DP and graphene.-
dc.languageeng-
dc.relation.ispartofAngewandte Chemie - International Edition-
dc.subject2D polymers-
dc.subjectgraphene-
dc.subjectinterfacial synthesis-
dc.subjecttransient absorption spectroscopy-
dc.subjectvan der Waals heterostructure-
dc.titleA Two-Dimensional Polyimide-Graphene Heterostructure with Ultra-fast Interlayer Charge Transfer-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.202102984-
dc.identifier.pmid33835643-
dc.identifier.scopuseid_2-s2.0-85105458606-
dc.identifier.volume60-
dc.identifier.issue25-
dc.identifier.spage13859-
dc.identifier.epage13864-
dc.identifier.eissn1521-3773-

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