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Growth behavior during metalorganic chemical vapor deposition of MoS2 using di-tert-butyl sulfide as organic sulfur precursor

 
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cris.virtual.orcid0000-0003-1461-5703
cris.virtual.orcid0000-0002-5781-7594
cris.virtual.orcid0000-0001-9739-7419
cris.virtualsource.departmentab262bc7-16ae-4482-b008-e896f1bbfe6a
cris.virtualsource.department5a858383-b569-42cd-8788-c2e90735c7e5
cris.virtualsource.department36689418-e07f-4cc4-8c33-f09792001dfb
cris.virtualsource.orcidab262bc7-16ae-4482-b008-e896f1bbfe6a
cris.virtualsource.orcid5a858383-b569-42cd-8788-c2e90735c7e5
cris.virtualsource.orcid36689418-e07f-4cc4-8c33-f09792001dfb
dc.contributor.authorDeijkers, Sanne
dc.contributor.authorMedina Silva, Henry
dc.contributor.authorManasi, A
dc.contributor.authorPasko, S.
dc.contributor.authorKessels, W. M. M. (Erwin)
dc.contributor.authorMackus, A. J. M.
dc.contributor.authorGroven, Benjamin
dc.contributor.authorDelabie, Annelies
dc.date.accessioned2026-04-23T09:14:58Z
dc.date.available2026-04-23T09:14:58Z
dc.date.createdwos2026-01-21
dc.date.issued2026
dc.description.abstractMetalorganic chemical vapor deposition is a promising synthesis technique for two-dimensional materials such as MoS2. In this study, we controlled the growth mode of MoS2 on SiO2 using Mo(CO)6 and di-tert-butyl sulfide as precursors by adjusting the process conditions. The growth was directed from amorphous deposition at 400 ∘C and 500 ∘C, to crystalline MoS2 at 600 ∘C and higher. From 750 ∘C, not only MoS2 grains were deposited, but Mo metal nuclei were also formed during the process. An enhancement of the grain size was achieved by increasing the S/Mo precursor ratio. A more effective method to enlarge the grains and to lower the number density of crystals was to anneal the SiO2 substrate in Ar atmosphere prior to deposition. The reduced number density suggested that the pretreatment increased the diffusion length of Mo adatom species on the surface. Furthermore, addition of H2 to the N2 carrier gas had two effects on the growth mode, without altering the amount of deposited Mo. On one hand, due to a higher fraction of H2 in the carrier gas, the grain size slightly increased, and on the other hand, a change towards Mo metal deposition was observed. Control of the process conditions offers the opportunity to deposit large MoS2 grains without co-depositing Mo metal.
dc.description.wosFundingTextThe authors kindly acknowledge the vital support from the imec lab and fab teams, the supply chain team, and the facility, process, and hardware engineering teams, the imec pilot line and the materials and components analysis teams. This work was performed in the imec Industrial Affiliation Program (IIAP) core CMOS and received funding from the European Union's Graphene Flagship 2D-PL (Grant Agreement No. 101189797). We kindly acknowledge the measurements and analysis by RBS from Johan Meersschaut and Johan Desmet, by AFM from Stefanie Sergeant, Danielle Vanhaeren, and Inge Vaesen, XPS from Thierry Conard and by SEM from Ehsan Jazaeri, Hans Billington and Eva Grieten.
dc.identifier.doi10.1088/1361-6528/ae2e05
dc.identifier.issn0957-4484
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/59175
dc.language.isoeng
dc.provenance.editstepusergreet.vanhoof@imec.be
dc.publisherIOP Publishing Ltd
dc.source.beginpage035601
dc.source.issue3
dc.source.journalNANOTECHNOLOGY
dc.source.numberofpages11
dc.source.volume37
dc.subject.keywordsPYROLYSIS
dc.title

Growth behavior during metalorganic chemical vapor deposition of MoS2 using di-tert-butyl sulfide as organic sulfur precursor

dc.typeJournal article
dspace.entity.typePublication
imec.internal.crawledAt2026-04-07
imec.internal.sourcecrawler
imec.internal.wosCreatedAt2026-04-07
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