Investigation on achieving super-resolution by solid immersion lens based STED microscopy
DC Field | Value | Language |
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dc.contributor.author | Kim, Wan-Chin | - |
dc.contributor.author | Moon, Hyungbae | - |
dc.contributor.author | Lee, Won-Sup | - |
dc.contributor.author | Lim, Geon | - |
dc.contributor.author | Choi, Guk-Jong | - |
dc.contributor.author | Kang, Donyoung | - |
dc.contributor.author | Lee, Hyungsuk | - |
dc.contributor.author | Park, No-Cheol | - |
dc.date.accessioned | 2023-04-21T01:40:25Z | - |
dc.date.available | 2023-04-21T01:40:25Z | - |
dc.date.issued | 2017-07 | - |
dc.identifier.issn | 1094-4087 | - |
dc.identifier.uri | https://yscholarhub.yonsei.ac.kr/handle/2021.sw.yonsei/6645 | - |
dc.description.abstract | The feasibility of stimulated emission depletion( STED) microscopy using a solid immersion lens was investigated. First, the theoretical feasibility of the considered system is discussed based on a vectorial field algorithm that uses a stratified medium composed of a SIL air-gap and test sample. Using the simulation, we verified that evanescent waves with much higher spatial frequencies corresponding to the high numerical aperture in the air-gap can be utilized to achieve a higher resolution than a confocal fluorescent image without a depletion beam. The simulated expectation was supported by actual imaging on two types of samples: fluorescent beads with a 20 nm diameter and an actin sample with a filamentous structure. The lateral resolution of the system was determined to be 34 nm via the imaging results on the nano-beads. The system was quite promising for achieving nano-scale surface imaging of biological samples; an even higher resolution was achieved by adjusting the wavelength and the intensity of the depletion beam. (C) 2017 Optical Society of America | - |
dc.format.extent | 14 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | OPTICAL SOC AMER | - |
dc.title | Investigation on achieving super-resolution by solid immersion lens based STED microscopy | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1364/OE.25.016629 | - |
dc.identifier.scopusid | 2-s2.0-85022043137 | - |
dc.identifier.wosid | 000407815100090 | - |
dc.identifier.bibliographicCitation | OPTICS EXPRESS, v.25, no.14, pp 16629 - 16642 | - |
dc.citation.title | OPTICS EXPRESS | - |
dc.citation.volume | 25 | - |
dc.citation.number | 14 | - |
dc.citation.startPage | 16629 | - |
dc.citation.endPage | 16642 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Optics | - |
dc.relation.journalWebOfScienceCategory | Optics | - |
dc.subject.keywordPlus | NEAR-FIELD READOUT | - |
dc.subject.keywordPlus | FLUORESCENCE MICROSCOPY | - |
dc.subject.keywordPlus | STIMULATED-EMISSION | - |
dc.subject.keywordPlus | RESOLUTION | - |
dc.subject.keywordPlus | APERTURE | - |
dc.subject.keywordPlus | LIMIT | - |
dc.subject.keywordAuthor | STED | - |
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