Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107923
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dc.contributorDepartment of Biomedical Engineering-
dc.contributorPhotonics Research Institute-
dc.creatorLiu, Yen_US
dc.creatorYu, Pen_US
dc.creatorWu, Yen_US
dc.creatorZhuang, Jen_US
dc.creatorWang, Zen_US
dc.creatorLi, Yen_US
dc.creatorLai, Pen_US
dc.creatorLiang, Jen_US
dc.creatorGong, Len_US
dc.date.accessioned2024-07-18T03:17:12Z-
dc.date.available2024-07-18T03:17:12Z-
dc.identifier.issn0027-8424en_US
dc.identifier.urihttp://hdl.handle.net/10397/107923-
dc.language.isoenen_US
dc.publisherNational Academy of Sciencesen_US
dc.rightsCopyright © 2023 the Author(s). Published by PNAS. This article is distributed under Creative Commons Attribution-NonCommercial- NoDerivatives License 4.0 (CC BY-NC- ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Liu, Y., Yu, P., Wu, Y., Zhuang, J., Wang, Z., Li, Y., Lai, P., Liang, J., & Gong, L. (2023). Optical single-pixel volumetric imaging by three-dimensional light-field illumination. Proceedings of the National Academy of Sciences, 120(31), e2304755120 is available at https://doi.org/10.1073/pnas.2304755120.en_US
dc.subject3D light-field illuminationen_US
dc.subjectSingle-pixel imagingen_US
dc.subjectVolumetric imagingen_US
dc.titleOptical single-pixel volumetric imaging by three-dimensional light-field illuminationen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume120en_US
dc.identifier.issue31en_US
dc.identifier.doi10.1073/pnas.2304755120en_US
dcterms.abstractThree-dimensional single-pixel imaging (3D SPI) has become an attractive imaging modality for both biomedical research and optical sensing. 3D-SPI techniques generally depend on time-of-flight or stereovision principle to extract depth information from backscattered light. However, existing implementations for these two optical schemes are limited to surface mapping of 3D objects at depth resolutions, at best, at the millimeter level. Here, we report 3D light-field illumination single-pixel microscopy (3D-LFI-SPM) that enables volumetric imaging of microscopic objects with a near-diffraction-limit 3D optical resolution. Aimed at 3D space reconstruction, 3D-LFI-SPM optically samples the 3D Fourier spectrum by combining 3D structured light-field illumination with single-element intensity detection. We build a 3D-LFI-SPM prototype that provides an imaging volume of ∼390 × 390 × 3,800 μm3 and achieves 2.7-μm lateral resolution and better than 37-μm axial resolution. Its capability of 3D visualization of label-free optical absorption contrast is demonstrated by imaging single algal cells in vivo. Our approach opens broad perspectives for 3D SPI with potential applications in various fields, such as biomedical functional imaging.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationProceedings of the National Academy of Sciences of the United States of America, 1 Aug. 2023, v. 120, no. 31, e2304755120en_US
dcterms.isPartOfProceedings of the National Academy of Sciences of the United States of Americaen_US
dcterms.issued2023-08-01-
dc.identifier.scopus2-s2.0-85165697888-
dc.relation.ispartofbookProceedings of the National Academy of Sciences of the United States of Americaen_US
dc.identifier.eissn1091-6490en_US
dc.identifier.artne2304755120en_US
dc.description.validate202407 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3059a-
dc.identifier.SubFormID49308-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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