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dc.contributor.authorLin, Huang-Shenen_US
dc.contributor.authorKao, Chih-Chiangen_US
dc.contributor.authorKuo, Hao-Chungen_US
dc.contributor.authorWang, Shing-Chungen_US
dc.contributor.authorLin, Gong-Ruen_US
dc.date.accessioned2019-04-03T06:47:23Z-
dc.date.available2019-04-03T06:47:23Z-
dc.date.issued2006-01-01en_US
dc.identifier.isbn0-8194-6251-9en_US
dc.identifier.issn0277-786Xen_US
dc.identifier.urihttp://dx.doi.org/10.1117/12.663339en_US
dc.identifier.urihttp://hdl.handle.net/11536/150824-
dc.description.abstractBy rapid thermal annealing the Ni film evaporated on thin SiO2 layer covered Si substrate, we have successfully demonstrated the self-aggregation of two-dimensional randomized Ni nano-dots on Si wafer. The thin oxide layer prevents the formation of NiSi2 compounds and facilitates the self-assembly of Ni nanodots from retaining the thermal power on SiO2 layer. This greatly shrinks the annealing time required for metallic nanodot formation from > 10 min to < 30 sec. With the advantage of the self-assemble Ni/SiO2 nano-dots based nano-mask, a large-area Si nano-pillar array with rod size of < 50 nm can be formatted on Si substrate through the induced coupled plasma reactive ion etching (ICPRIE) procedure. After removing Ni dots and the SiO2 film on the Si substrate, both the visible and near infrared photoluminescence from the Si nano-pillar sample were observed and analyzed.en_US
dc.language.isoen_USen_US
dc.subjectself-assembleen_US
dc.subjectNi nano-doten_US
dc.subjectSi nano-pillaren_US
dc.subjectreactive ion etchingen_US
dc.subjectmasken_US
dc.subjectSiO2en_US
dc.subjectSien_US
dc.titleSelf-assembled Ni nanodot on SiO2 film-a novel reactive ion etching mask for Si nanopillar formation on Si substrateen_US
dc.typeProceedings Paperen_US
dc.identifier.doi10.1117/12.663339en_US
dc.identifier.journalNANOPHOTONICS-USAen_US
dc.citation.volume6195en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000239287700058en_US
dc.citation.woscount0en_US
Appears in Collections:Conferences Paper


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