Evaluation of tin nitride (Sn3N4) via atomic layer deposition using novel volatile Sn precursors

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dc.contributor.authorPark, Hyeonbinko
dc.contributor.authorChoi, Heenangko
dc.contributor.authorShin, Sunyoungko
dc.contributor.authorPark, Bo Keunko
dc.contributor.authorKang, Kibumko
dc.contributor.authorRyu, Ji Yeonko
dc.contributor.authorEom, Taeyongko
dc.contributor.authorChung, Taek-Moko
dc.date.accessioned2023-12-06T01:00:30Z-
dc.date.available2023-12-06T01:00:30Z-
dc.date.created2023-12-06-
dc.date.issued2023-10-
dc.identifier.citationDALTON TRANSACTIONS, v.52, no.41, pp.15033 - 15042-
dc.identifier.issn1477-9226-
dc.identifier.urihttp://hdl.handle.net/10203/315779-
dc.description.abstractNovel Sn precursors, Sn(tbip)(2), Sn(tbtp)(2), and Sn(tbta)(2), were synthesized and characterized using various analytical techniques and density functional theory calculations. These precursors contained cyclic amine ligands derived from iminopyrrolidine. X-ray crystallography revealed the formation of monomeric SnL2 with distorted seesaw geometry. Thermogravimetric analysis demonstrated the exceptional volatility of all complexes. Sn(tbtp)(2) showed the lowest residual weight of 2.7% at 265 degrees C. Sn3N4 thin films were successfully synthesized using Sn(tbtp)(2) as the Sn precursor and NH3 plasma. The precursor exhibited ideal characteristics for atomic layer deposition, with a saturated growth per cycle value of 1.9 & Aring; cy(-1) and no need for incubation when the film was deposited at 150-225 degrees C. The indirect optical bandgap of the Sn3N4 film was approximately 1-1.2 eV, as determined through ultraviolet-visible spectroscopy. Therefore, this study suggests that the Sn3N4 thin films prepared using the newly synthesized Sn precursor are suitable for application in thin-film photovoltaic devices.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleEvaluation of tin nitride (Sn3N4) via atomic layer deposition using novel volatile Sn precursors-
dc.typeArticle-
dc.identifier.wosid001081052000001-
dc.identifier.scopusid2-s2.0-85174550297-
dc.type.rimsART-
dc.citation.volume52-
dc.citation.issue41-
dc.citation.beginningpage15033-
dc.citation.endingpage15042-
dc.citation.publicationnameDALTON TRANSACTIONS-
dc.identifier.doi10.1039/d3dt02138f-
dc.contributor.localauthorKang, Kibum-
dc.contributor.nonIdAuthorPark, Hyeonbin-
dc.contributor.nonIdAuthorChoi, Heenang-
dc.contributor.nonIdAuthorShin, Sunyoung-
dc.contributor.nonIdAuthorPark, Bo Keun-
dc.contributor.nonIdAuthorRyu, Ji Yeon-
dc.contributor.nonIdAuthorEom, Taeyong-
dc.contributor.nonIdAuthorChung, Taek-Mo-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTHIN-FILMS-
dc.subject.keywordPlusNEGATIVE ELECTRODE-
dc.subject.keywordPlusVAPOR-DEPOSITION-
dc.subject.keywordPlusSN-119 NMR-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusCOPPER-
dc.subject.keywordPlusGERMANIUM-
dc.subject.keywordPlusNITROGEN-
dc.subject.keywordPlusALD-
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