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dc.contributor.author김종호-
dc.date.accessioned2019-01-07T05:17:59Z-
dc.date.available2019-01-07T05:17:59Z-
dc.date.issued2018-06-
dc.identifier.citationNATURE COMMUNICATIONS, v. 9, Article no. 2549en_US
dc.identifier.issn2041-1723-
dc.identifier.urihttps://www.nature.com/articles/s41467-018-04997-w-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/81098-
dc.description.abstractThe ability to control the dimensions and properties of nanomaterials is fundamental to the creation of new functions and improvement of their performances in the applications of interest. Herein, we report a strategy based on glucan multivalent interactions for the simultaneous exfoliation and functionalization of two-dimensional transition metal dichal-cogenides (TMDs) in an aqueous solution. The multivalent hydrogen bonding of dextran with bulk TMDs (WS2, WSe2, and MoSe2) in liquid exfoliation effectively produces TMD monolayers with binding multivalency for pathogenic bacteria. Density functional theory simulation reveals that the multivalent hydrogen bonding between dextran and TMD monolayers is very strong and thermodynamically favored (Delta E-b = -0.52 eV). The resulting dextran/TMD hybrids (dex-TMDs) exhibit a stronger affinity (K-d = 11 nM) to Escherichia coli O157:H7 (E. coli) than E. coli-specific antibodies and aptamers. The dex-TMDs can effectively detect a single copy of E. coli based on their Raman signal.en_US
dc.description.sponsorshipThis work was supported by the Samsung Research Funding Center of Samsung Electronics under project number SRFCTA1503-02.en_US
dc.language.isoen_USen_US
dc.publisherNATURE PUBLISHING GROUPen_US
dc.subjectINITIO MOLECULAR-DYNAMICSen_US
dc.subjectTOTAL-ENERGY CALCULATIONSen_US
dc.subjectAUGMENTED-WAVE METHODen_US
dc.subjectESCHERICHIA-COLIen_US
dc.subjectMONOLAYER MOS2en_US
dc.subjectBASIS-SETen_US
dc.subjectEXFOLIATIONen_US
dc.subjectNANOSHEETSen_US
dc.subjectWS2en_US
dc.subjectPHOTOLUMINESCENCEen_US
dc.title2D Transition Metal Dichalcogenides with Glucan Multivalency for Antibody-free Pathogen Recognitionen_US
dc.typeArticleen_US
dc.relation.no2549-
dc.relation.volume9-
dc.identifier.doi10.1038/s41467-018-04997-w-
dc.relation.page1-10-
dc.relation.journalNATURE COMMUNICATIONS-
dc.contributor.googleauthorKang, Tae Woog-
dc.contributor.googleauthorHan, Juhee-
dc.contributor.googleauthorLee, Sin-
dc.contributor.googleauthorHwang, In-Jun-
dc.contributor.googleauthorJeon, Su-Ji-
dc.contributor.googleauthorJu, Jong-Min-
dc.contributor.googleauthorKim, Man-Jin-
dc.contributor.googleauthorYang, Jin-Kyoung-
dc.contributor.googleauthorJun, Byoengsun-
dc.contributor.googleauthorKim, Jong-Ho-
dc.contributor.googleauthorLee, Chi Ho-
dc.contributor.googleauthorLee, Sang Uck-
dc.relation.code2018003595-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF ENGINEERING SCIENCES[E]-
dc.sector.departmentDEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING-
dc.identifier.pidkjh75-
Appears in Collections:
COLLEGE OF ENGINEERING SCIENCES[E](공학대학) > MATERIALS SCIENCE AND CHEMICAL ENGINEERING(재료화학공학과) > Articles
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