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dc.contributor.authorLee, Jong-Young-
dc.contributor.authorKim, Jong Hun-
dc.contributor.authorJung, Yeonjoon-
dc.contributor.authorShin, June Chul-
dc.contributor.authorLee, Yangjin-
dc.contributor.authorKim, Kwanpyo-
dc.contributor.authorKim, Namwon-
dc.contributor.authorvan der Zande, Arend M.-
dc.contributor.authorSon, Jangyup-
dc.contributor.authorLee, Gwan-Hyoung-
dc.date.accessioned2024-01-19T14:30:51Z-
dc.date.available2024-01-19T14:30:51Z-
dc.date.created2021-10-21-
dc.date.issued2021-07-
dc.identifier.issn2662-4443-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/116817-
dc.description.abstractDesulfurization of MoS2 alters its chemical and physical properties by breaking structural symmetry. Here, the atomic-scale mechanistic pathway by which this occurs is investigated during plasma etching, and changes in chemical structure and physical properties are revealed. Structural symmetry-breaking is a key strategy to modify the physical and chemical properties of two-dimensional transition metal dichalcogenides. However, little is known about defect formation during this process. Here, with atomic-scale microscopy, we investigate the evolution of defect formation in monolayer MoS2 exposed indirectly to hydrogen plasma. At the beginning of the treatment only top-layer sulfur atoms are removed, while vacancies and the molybdenum atomic layer are maintained. As processing continues, hexagonal-shaped nanocracks are generated along the zigzag edge during relaxation of defect-induced strain. As defect density increases, both photoluminescence and conductivity of MoS2 gradually decreases. Furthermore, MoS2 showed increased friction by 50% due to defect-induced contact stiffness. Our study reveals the details of defect formation during the desulfurization of MoS2 and helps to design the symmetry-breaking transition metal dichalcogenides, which is of relevance for applications including photocatalyst for water splitting, and Janus heterostructures.-
dc.languageEnglish-
dc.publisherSPRINGERNATURE-
dc.titleEvolution of defect formation during atomically precise desulfurization of monolayer MoS2-
dc.typeArticle-
dc.identifier.doi10.1038/s43246-021-00185-4-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCommunications Materials, v.2, no.1-
dc.citation.titleCommunications Materials-
dc.citation.volume2-
dc.citation.number1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000681390800002-
dc.identifier.scopusid2-s2.0-85118880642-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusHYDROGEN EVOLUTION-
dc.subject.keywordPlusSULFUR VACANCIES-
dc.subject.keywordPlusTHERMOELECTRIC PROPERTIES-
dc.subject.keywordPlus2-DIMENSIONAL MATERIALS-
dc.subject.keywordPlusCATALYTIC-ACTIVITY-
dc.subject.keywordPlusPHOTOLUMINESCENCE-
dc.subject.keywordPlusFRICTION-
dc.subject.keywordAuthorMoS2-
dc.subject.keywordAuthorHydrogen plasma-
dc.subject.keywordAuthorDesulfurization-
dc.subject.keywordAuthorDefect-
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