Campanile probe

SEM image of a campanile probe.[1]
SEM image of a campanile probe.[1]
Comparison of photoluminescence maps recorded from a molybdenum disulfide flake using a campanile probe (top) and conventional confocal microscopy (bottom). Scale bars: 1 μm.[1]

In near-field scanning optical microscopy the campanile probe is a tapered optical probe with a shape of a campanile (a square pyramid). It is made of an optically transparent dielectric, typically silica, and its two facets are coated with a metal, typically gold. At the probe tip, the metal-coated facets are separated by a gap of a few tens of nanometers, which determines the spatial resolution of the probe. Such a probe design allows collecting optical signals, usually photoluminescence (PL) or Raman scattering, with a subwavelength resolution, breaking the diffraction limit.[1][2]

The campanile probe is attached to an optical fiber, which both provides a laser excitation of the studied sample and collects the measured signal. The probe is rastered over the sample with a standard scanning probe microscopy scanner, keeping the distance to the sample surface at a few nanometers.[1] Contrary to the traditional (circular) near-field probes, the campanile probe has no cut-off frequency and is insensitive to the spatial mode of the optical near field. Hence its application is not limited to thin-film samples.[2] Another advantage of the campanile probe is a high signal collection efficiency, which exceeds 90%.[3]

Campanile probes are typically fabricated as follows: a standard cylindrical single-mode optical fiber is etched with hydrofluoric acid to create a conical tip with a radius of ca. 100 nm. Then a square pyramid is carved on the tip using focused ion beam (FIB) milling, and its two facets are coated with a metal by shadow evaporation. A nanometer gap is the opened on the tip by FIB.[2]

References

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  1. 1 2 3 4 5 Bao, Wei; Borys, Nicholas J.; Ko, Changhyun; Suh, Joonki; Fan, Wen; Thron, Andrew; Zhang, Yingjie; Buyanin, Alexander; Zhang, Jie; Cabrini, Stefano; Ashby, Paul D.; Weber-Bargioni, Alexander; Tongay, Sefaattin; Aloni, Shaul; Ogletree, D. Frank; Wu, Junqiao; Salmeron, Miquel B.; Schuck, P. James (2015). "Visualizing nanoscale excitonic relaxation properties of disordered edges and grain boundaries in monolayer molybdenum disulfide". Nature Communications. 6: 7993. Bibcode:2015NatCo...6E7993B. doi:10.1038/ncomms8993. PMC 4557266Freely accessible. PMID 26269394.
  2. 1 2 3 Bao, W.; Melli, M.; Caselli, N.; Riboli, F.; Wiersma, D. S.; Staffaroni, M.; Choo, H.; Ogletree, D. F.; Aloni, S.; Bokor, J.; Cabrini, S.; Intonti, F.; Salmeron, M. B.; Yablonovitch, E.; Schuck, P. J.; Weber-Bargioni, A. (2012). "Mapping Local Charge Recombination Heterogeneity by Multidimensional Nanospectroscopic Imaging". Science. 338 (6112): 1317. Bibcode:2012Sci...338.1317B. doi:10.1126/science.1227977. PMID 23224550.
  3. ↑ Chapelle, Marc Lamy de la; Gucciardi, Pietro Giuseppe; Lidgi-Guigui, Nathalie (28 October 2015). Handbook of Enhanced Spectroscopy. Pan Stanford Publishing. pp. 366–. ISBN 978-981-4613-33-0.
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