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Journal Article

Solid immersion facilitates fluorescence microscopy with nanometer resolution and sub-Ångström emitter localization.

MPS-Authors
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Wildanger,  D.
Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society;

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Schill,  H.
Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society;

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Schönle,  A.
Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society;

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Hell,  S. W.
Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society;

External Resource

http://onlinelibrary.wiley.com/doi/10.1002/adma.201203033/pdf
(Publisher version)

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Supplementary Material (public)

1563822_sm_suppl.pdf
(Supplementary material), 350KB

Citation

Wildanger, D., Patton, B. R., Schill, H., Marseglia, L., Hadden, J. P., Knauer, S., et al. (2012). Solid immersion facilitates fluorescence microscopy with nanometer resolution and sub-Ångström emitter localization. Advanced Materials, 24(4), OP309-OP313. doi:10.1002/adma.201203033.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-1922-E
Abstract
Exploring the maximum spatial resolution achievable in far-field optical imaging, we show that applying solid immersion lenses (SIL) in stimulated emission depletion (STED) microscopy addresses single spins with a resolution down to 2.4 ± 0.3 nm and with a localization precision of 0.09 nm.