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곽상규

Kwak, Sang Kyu
Kyu’s MolSim Lab @ UNIST
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dc.citation.number 6 -
dc.citation.startPage 2001911 -
dc.citation.title ADVANCED OPTICAL MATERIALS -
dc.citation.volume 9 -
dc.contributor.author Shang, Xiaobo -
dc.contributor.author Song, Inho -
dc.contributor.author Han, Myeonggeun -
dc.contributor.author Lee, Jeong Hyeon -
dc.contributor.author Ohtsu, Hiroyoshi -
dc.contributor.author Choi, Wanuk -
dc.contributor.author Kim, Jin Chul -
dc.contributor.author Ahn, Jaeyong -
dc.contributor.author Kwak, Sang Kyu -
dc.contributor.author Oh, Joon Hak -
dc.date.accessioned 2023-12-21T16:11:35Z -
dc.date.available 2023-12-21T16:11:35Z -
dc.date.created 2021-01-26 -
dc.date.issued 2021-03 -
dc.description.abstract Supramolecular chirality has attracted a great deal of attention as a platform for both fundamental study and chirality amplification in various research fields. Compared with the "sergeants-and-soldiers" principle, the "majority-rules" principle, which affects chirality amplification in supramolecular systems, is rarely reported for nano/microstructures. Here, chiral tetrachloro-substituted perylene diimides are synthesized that self-assemble into chiral supramolecules with different degrees of enantiomeric excess (ee). Interestingly, it is found that quasi-2D crystals are gradually transferred to 1D nanowires (NWs) with ee from 100% to 0%. In the racemic system, chiral self-discrimination is observed due to the greater thermodynamic stability of heterochiral crystals than the homochiral counterparts, judging from the theoretical studies. Circular dichroism analysis indicates that the self-assembled system with different ee values shows different peaks due to their unique molecular ordering for supramolecular exciton coupling. On measurement in optoelectronic devices, racemic 1D NWs show better charge transport ability than enantiomeric quasi-2D crystals. These results provide guidelines for tuning the supramolecular chirality and optoelectronic performance of self-assembled systems via the "majority-rules" principle. -
dc.identifier.bibliographicCitation ADVANCED OPTICAL MATERIALS, v.9, no.6, pp.2001911 -
dc.identifier.doi 10.1002/adom.202001911 -
dc.identifier.issn 2195-1071 -
dc.identifier.scopusid 2-s2.0-85098155104 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/49947 -
dc.identifier.url https://onlinelibrary.wiley.com/doi/full/10.1002/adom.202001911 -
dc.identifier.wosid 000602648100001 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title "Majority-Rules" Effect on Supramolecular Chirality and Optoelectronic Properties of Chiral Tetrachloro-Perylene Diimides -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Materials Science, Multidisciplinary; Optics -
dc.relation.journalResearchArea Materials Science; Optics -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor majority -
dc.subject.keywordAuthor rules -
dc.subject.keywordAuthor principle -
dc.subject.keywordAuthor organic phototransistors -
dc.subject.keywordAuthor organic single crystals -
dc.subject.keywordAuthor self -
dc.subject.keywordAuthor assembly -
dc.subject.keywordAuthor supramolecular chirality -
dc.subject.keywordPlus PERFORMANCE -
dc.subject.keywordPlus NANOWIRES -

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