Assembly of SnO2 Rod using Optical Tweezers and Laser Curing of Metal Nanoparticles

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dc.contributor.authorNam, Chanhyuk-
dc.contributor.authorHong, Daehie-
dc.contributor.authorChung, Jaeik-
dc.contributor.authorHwang, Insung-
dc.contributor.authorLee, Jongheun-
dc.contributor.authorKo, Seung Hwan-
dc.contributor.authorGrigoropoulos, Costas P.-
dc.contributor.authorChung, Jaewon-
dc.date.accessioned2010-06-20T19:45:07Z-
dc.date.available2010-06-20T19:45:07Z-
dc.date.issued2010-05-20-
dc.identifier.citationJapanese Journal of Applied Physics, Vol.49, pp.05EA12en
dc.identifier.issn1347-4065-
dc.identifier.urihttp://hdl.handle.net/10203/18929-
dc.description.abstractAcicular tin dioxide (SnO2) rods (1–2 µm in diameter, 5–20 µm long) were assembled and fused on the patterned gold electrode by an optical tweezer. In addition, the electrical contact between the assembled SnO2 rod and the gold electrode was improved by laser curing of gold nanoparticles and the subsequent sintering in the oven. Here, the nanoparticles covered the entire area of the assembled SnO2 rod by evaporating a droplet of nanoparticle solution dripped on the assembled SnO2 rod. Subsequently, nanoparticles near the contact area between the rod and electrode were locally cured by direct heating with a focused infrared laser beam, which induced desorption of the surface monolayer. Therefore, the cured gold nanoparticles could be sintered after the non-laser irradiated nanoparticles were cleaned by the initial solvent application. Without sintering of the nanoparticles, the resistance of the assembled SnO2 rod was measured over several MΩ. After the nanoparticle sintering it could be reduced to a few hundred kΩ, which was in agreement with the resistance of the assembled SnO2 rod.en
dc.language.isoen_USen
dc.publisherJapan Society of Applied Physicsen
dc.subjectoptical tweezeren
dc.subjectnanoparticleen
dc.subjectselective laser pricessingen
dc.subjectSnO2 roden
dc.subjectlaser curingen
dc.titleAssembly of SnO2 Rod using Optical Tweezers and Laser Curing of Metal Nanoparticlesen
dc.typeArticleen
dc.identifier.doi10.1143/JJAP.49.05EA12-
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