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New Forms of CdSe: Molecular Wires, Gels, and Ordered Mesoporous Assemblies

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dc.contributor.authorHudson, Margaret H.-
dc.contributor.authorDolzhnikov, Dmitriy S.-
dc.contributor.authorFilatov, Alexander S.-
dc.contributor.authorJanke, Eric M.-
dc.contributor.authorJang, Jaeyoung-
dc.contributor.authorLee, Byeongdu-
dc.contributor.authorSun, Chengjun-
dc.contributor.authorTalapin, Dmitri V.-
dc.date.accessioned2021-07-30T05:25:57Z-
dc.date.available2021-07-30T05:25:57Z-
dc.date.created2021-05-12-
dc.date.issued2017-03-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/4808-
dc.description.abstractThis work investigates the structure and properties of soluble chalcogenidocadmates, a molecular form of cadmium chalcogenides with unprecedented one-dimensional bonding motifs. The single crystal X-ray structure reveals that sodium selenocadmate consists of infinite one-dimensional wires of (Cd2Se3)(n)2(n-) charge balanced by Na+ and stabilized by coordinating solvent molecules. Exchanging the sodium cation with tetraethylammonium or didodecyldimethylammonium expands the versatility of selenocadmate by improving its solubility in a variety of polar and nonpolar solvents without changing the anion structure and properties. The introduction of a micelle-forming cationic surfactant allows for the templating of selenocadmate, or the analogous telluride species, to create ordered organic-inorganic hybrid CdSe or CdTe mesostructures. Finally, the interaction of selenocadmate "wires" with Cd2+ ions creates an unprecedented gel-like form of stoichiometric CdSe. We also demonstrate that these low-dimensional CdSe species show characteristic semiconductor behavior, and can be used in photodetectors and field-effect transistors.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleNew Forms of CdSe: Molecular Wires, Gels, and Ordered Mesoporous Assemblies-
dc.typeArticle-
dc.contributor.affiliatedAuthorJang, Jaeyoung-
dc.identifier.doi10.1021/jacs.6b10077-
dc.identifier.scopusid2-s2.0-85014716659-
dc.identifier.wosid000396185700016-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.139, no.9, pp.3368 - 3377-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume139-
dc.citation.number9-
dc.citation.startPage3368-
dc.citation.endPage3377-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusFIELD-EFFECT TRANSISTORS-
dc.subject.keywordPlusCOLLOIDAL NANOCRYSTALS-
dc.subject.keywordPlusQUANTUM DOTS-
dc.subject.keywordPlusSOLAR-CELLS-
dc.subject.keywordPlusMETAL CHALCOGENIDES-
dc.subject.keywordPlusPORE ORGANIZATION-
dc.subject.keywordPlusSCALE SYNTHESIS-
dc.subject.keywordPlusGAS SEPARATION-
dc.subject.keywordPlusSEEDED GROWTH-
dc.subject.keywordPlusCDE E-
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