Stimulated emission depletion microscopy with diamond silicon-vacancy centers
The spatial resolution and fluorescence signal amplitude in stimulated emission depletion (STED) microscopy is limited by the photostability of available fluorophores. Here, we show that negatively-charged silicon vacancy (SiV) centers in diamond are promising fluorophores for STED microscopy, owing...
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Abstract | The spatial resolution and fluorescence signal amplitude in stimulated emission depletion (STED) microscopy is limited by the photostability of available fluorophores. Here, we show that negatively-charged silicon vacancy (SiV) centers in diamond are promising fluorophores for STED microscopy, owing to their photostable, near-infrared emission and favorable photophysical properties. A home-built pulsed STED microscope was used to image shallow implanted SiV centers in bulk diamond at room temperature. The SiV stimulated emission cross section for 765-800 nm light is found to be (4.0 +/- 0.3) x 10^(-17) cm^2, which is approximately 2-4 times larger than that of the negatively-charged diamond nitrogen vacancy center and approaches that of commonly-used organic dye molecules. We performed STED microscopy on isolated SiV centers and observed a lateral full-width-at-half-maximum spot size of 89 +/- 2 nm, limited by the low available STED laser pulse energy (0.4 nJ). For a pulse energy of 5 nJ, the resolution is expected to be ~20 nm. We show that the present microscope can resolve SiV centers separated by <150 nm that cannot be resolved by confocal microscopy. |
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AbstractList | ACS Photonics, 6 2577 (2019) The spatial resolution and fluorescence signal amplitude in stimulated
emission depletion (STED) microscopy is limited by the photostability of
available fluorophores. Here, we show that negatively-charged silicon vacancy
(SiV) centers in diamond are promising fluorophores for STED microscopy, owing
to their photostable, near-infrared emission and favorable photophysical
properties. A home-built pulsed STED microscope was used to image shallow
implanted SiV centers in bulk diamond at room temperature. The SiV stimulated
emission cross section for 765-800 nm light is found to be (4.0 +/- 0.3) x
10^(-17) cm^2, which is approximately 2-4 times larger than that of the
negatively-charged diamond nitrogen vacancy center and approaches that of
commonly-used organic dye molecules. We performed STED microscopy on isolated
SiV centers and observed a lateral full-width-at-half-maximum spot size of 89
+/- 2 nm, limited by the low available STED laser pulse energy (0.4 nJ). For a
pulse energy of 5 nJ, the resolution is expected to be ~20 nm. We show that the
present microscope can resolve SiV centers separated by <150 nm that cannot be
resolved by confocal microscopy. The spatial resolution and fluorescence signal amplitude in stimulated emission depletion (STED) microscopy is limited by the photostability of available fluorophores. Here, we show that negatively-charged silicon vacancy (SiV) centers in diamond are promising fluorophores for STED microscopy, owing to their photostable, near-infrared emission and favorable photophysical properties. A home-built pulsed STED microscope was used to image shallow implanted SiV centers in bulk diamond at room temperature. The SiV stimulated emission cross section for 765-800 nm light is found to be (4.0 +/- 0.3) x 10^(-17) cm^2, which is approximately 2-4 times larger than that of the negatively-charged diamond nitrogen vacancy center and approaches that of commonly-used organic dye molecules. We performed STED microscopy on isolated SiV centers and observed a lateral full-width-at-half-maximum spot size of 89 +/- 2 nm, limited by the low available STED laser pulse energy (0.4 nJ). For a pulse energy of 5 nJ, the resolution is expected to be ~20 nm. We show that the present microscope can resolve SiV centers separated by <150 nm that cannot be resolved by confocal microscopy. |
Author | Acosta, Victor M Silani, Yaser rest, Hubert |
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BackLink | https://doi.org/10.1021/acsphotonics.9b01135$$DView published paper (Access to full text may be restricted) https://doi.org/10.48550/arXiv.1907.08604$$DView paper in arXiv |
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Snippet | The spatial resolution and fluorescence signal amplitude in stimulated emission depletion (STED) microscopy is limited by the photostability of available... ACS Photonics, 6 2577 (2019) The spatial resolution and fluorescence signal amplitude in stimulated emission depletion (STED) microscopy is limited by the... |
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SubjectTerms | Chemical compounds Depletion Diamonds Emission Fluorescence Microscopy Near infrared radiation Physics - Biological Physics Physics - Mesoscale and Nanoscale Physics Physics - Optics Physics - Quantum Physics Silicon Spatial resolution Stimulated emission Vacancies |
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