1996
DOI: 10.1007/s003400050119
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Single fluorescence centers on the tips of crystal needles: First observation and prospects for application in scanning one-atom fluorescence microscopy

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Cited by 31 publications
(15 citation statements)
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“…Such orientation dependence can potentially enable the study of protein folding and the environment effect on protein interactions. 266 Scanning FRET microscopy was developed with a SNOM fiber probe 271 and with an apertureless AFM tip. 272 In the fiber probe approach, a small crystal containing the donor or the acceptor was placed at the apex of the fiber probe.…”
Section: B Förster Resonance Energy Transfermentioning
confidence: 99%
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“…Such orientation dependence can potentially enable the study of protein folding and the environment effect on protein interactions. 266 Scanning FRET microscopy was developed with a SNOM fiber probe 271 and with an apertureless AFM tip. 272 In the fiber probe approach, a small crystal containing the donor or the acceptor was placed at the apex of the fiber probe.…”
Section: B Förster Resonance Energy Transfermentioning
confidence: 99%
“…272 In the fiber probe approach, a small crystal containing the donor or the acceptor was placed at the apex of the fiber probe. 271 In the apertureless approach, the AFM tip was coated with donor or acceptor molecules. 272 When the FRET-activated fiber probe or AFM tip scanned the sample, the complementary donor/acceptor deposited on the sample generated a FRET signal if it was within the Förster radius.…”
Section: B Förster Resonance Energy Transfermentioning
confidence: 99%
“…After the exposure to X‐rays, the LiF plate storing sample image is illuminated with blue light and the fluorescent CCs spatial distribution, which reproduces the absorption contrast image of the sample, is observed by an optical microscope in fluorescence mode. While using luminescent LiF as soft X‐ray imaging detector, the spatial resolution is limited by the image reading optical process; as a matter of fact, the intrinsic spatial resolution of LiF detectors is, in principle, limited only from the dimension of the produced CCs (a few nanometres; Sekatski & Letokhov, ). Anyway, by using as reading process of LiF luminescent detectors advanced optical microscopes, like confocal laser scanning microscope and scanning near‐field optical microscope, optical fluorescence images with micro‐ and nanometric spatial resolutions can be respectively obtained (Almaviva et al ., 2006; Ustione et al ., ).…”
Section: Methodsmentioning
confidence: 99%
“…Nowadays, a variety of different implementations of SNOM exists. Starting from the visionary work of Synge in 1929 [25] in which the basic idea of apertured SNOM was presented, the concept of a microscopy technique based on the local interaction of light mediated by a nanoprobe has been extended including, but not limited at, Scattering-type SNOM (s-SNOM) [26], collection mode SNOM [27], illumination-mode SNOM [28], PSTM (Photon Scanning Tunnelling Microscopy) [29], coupled to several detection methods ranging from interferometric homodyne [30], heterodyne [31,32], to spectrometric (fluorescence [33,34] and Raman [35]). A comprehensive description of SNOM-related techniques is outside the scope of this work.…”
Section: Techniques For the Characterization Of Surfaces At The Nanosmentioning
confidence: 99%