Full metadata record

DC Field Value Language
dc.contributor.authorCho, Jung Min-
dc.contributor.authorKo, Young Jin-
dc.contributor.authorLee, Hak Joo-
dc.contributor.authorChoi, Heon-­Jin-
dc.contributor.authorBaik, Young Joon-
dc.contributor.authorPARK, JONG KEUK-
dc.contributor.authorKwak, Joon Young-
dc.contributor.authorKim, Jae wook-
dc.contributor.authorPark, Jong kil-
dc.contributor.authorJeong, Yeon Joo-
dc.contributor.authorKim, In ho-
dc.contributor.authorLEE, KYEONG SEOK-
dc.contributor.authorLee, Wook­Seong-
dc.date.accessioned2024-01-12T03:32:37Z-
dc.date.available2024-01-12T03:32:37Z-
dc.date.created2022-03-07-
dc.date.issued2022-02-
dc.identifier.issn1613-6810-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/76800-
dc.description.abstractThe diamond-graphite hybrid thin film with low-dimensional nanostructure (e.g., nitrogen-included ultrananocrystalline diamond (N-UNCD) or the alike), has been employed in many impactful breakthrough applications. However, the detailed picture behind the bottom-up evolution of such intriguing carbon nanostructure is far from clarified yet. Here, the authors clarify it, through the concerted efforts of microscopic, physical, and electrochemical analyses for a series of samples synthesized by hot-filament chemical vapor deposition using methane-hydrogen precursor gas, based on the hydrogen-dependent surface reconstruction of nanodiamond and on the substrate-temperature-dependent variation of the growth species (atomic hydrogen and methyl radical) concentration near substrate. The clarified picture provides insights for a drastic enhancement in the electrochemical activities of the hybrid thin film, concerning the detection of important biomolecule, that is, ascorbic acid, uric acid, and dopamine: their limits of detections are 490, 35, and 25 nm, respectively, which are among the best of the all-carbon thin film electrodes in the literature. This work also enables a simple and effective way of strongly enhancing AA detection.-
dc.languageEnglish-
dc.publisherWiley - V C H Verlag GmbbH & Co.-
dc.titleBottom-Up Evolution of Diamond-Graphite Hybrid Two-Dimensional Nanostructure: Underlying Picture and Electrochemical Activity-
dc.typeArticle-
dc.identifier.doi10.1002/smll.202105087-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSmall, v.18, no.8-
dc.citation.titleSmall-
dc.citation.volume18-
dc.citation.number8-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000729090800001-
dc.identifier.scopusid2-s2.0-85120890718-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusASCORBIC-ACID-
dc.subject.keywordPlusSELECTIVE DETECTION-
dc.subject.keywordPlusHIGH-PERFORMANCE-
dc.subject.keywordPlusURIC-ACID-
dc.subject.keywordPlusC-H-
dc.subject.keywordPlusDOPAMINE-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusFILM-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordAuthorall-carbon electrochemical electrodes-
dc.subject.keywordAuthordehydrogenation-induced surface reconstruction-
dc.subject.keywordAuthordiamond?graphite hybrid thin films, nanodiamonds-
dc.subject.keywordAuthorsimultaneous electrochemical detection-
dc.subject.keywordAuthortwo-dimensional carbon nanostructure evolution mechanism-
Appears in Collections:
KIST Article > 2022
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE