Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2008 Jan 6;8(2):711-738.
doi: 10.3390/s8020711.

Evanescent field Sensors Based on Tantalum Pentoxide Waveguides - A Review

Affiliations
Review

Evanescent field Sensors Based on Tantalum Pentoxide Waveguides - A Review

Katrin Schmitt et al. Sensors (Basel). .

Abstract

Evanescent field sensors based on waveguide surfaces play an important rolewhere high sensitivity is required. Particularly tantalum pentoxide (Ta₂O₅) is a suitablematerial for thin-film waveguides due to its high refractive index and low attenuation.Many label-free biosensor systems such as grating couplers and interferometric sensors aswell as fluorescence-based systems benefit from this waveguide material leading toextremely high sensitivity. Some biosensor systems based on Ta₂O₅ waveguides alreadytook the step into commercialization. This report reviews the various detection systems interms of limit of detection, the applications, and the suitable surface chemistry.

Keywords: Ta2O5.; biosensors; evanescent field; label-free detection.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Refractive index n and extinction coefficient k of a thin Ta2O5 layer on glass (n = 1.52) versus wavelength (light source: Xe arc lamp with corresponding interference filters); measurements performed at an angle of incidence of 50° by means of spectroscopic ellipsometry (EP3, Nanofilm Technologie GmbH, Göttingen, Germany).
Figure 2.
Figure 2.
Three-layer planar waveguide system comprising substrate, waveguide and cover layer, with refractive indices ns, nw, and nc, respectively.
Figure 3.
Figure 3.
The principle of evanescent field sensing. A waveguide layer on a substrate is guiding a light mode with phase velocity v1. A change in the effective refractive index and thus a decrease in the phase velocity v2 < v1 is caused by either a change in the cover refractive index Δnc or a change in the adlayer thickness Δtad due to molecule adsorption, e.g. binding of an antigen to a capture antibody. From [21].
Figure 4.
Figure 4.
Theoretical sensitivities of a waveguide to a) cover refractive index changes and b) surface adlayer changes versus waveguide thickness. Parameters for calculation: ns = 1.52, nw = 2.1, nc = 1.333 and λ = 675 nm. From [21].
Figure 5.
Figure 5.
(a) Schematic of the input grating coupler instrument. In an angular scan, the TE0 and TM0 modes are successively excited by an s- and a p-polarized laser beam. L = lever arm; MS = micrometer screw; SM = stepping motor; Cu = cuvette; Laser = He-Ne laser (λ = 632.8 nm); FP = Foster prism; M1 and M2 = mirrors; P = incident power; P′ = power of incoupled guided mode; α = angle of incidence; D1 and D2 = silicon photodetectors. (b) Detailed view of the sensor: C = liquid cover; F = waveguiding film of thickness dF on glass substrate S. From [34], Copyright Elsevier (1990).
Figure 6.
Figure 6.
(a) Schematic of output grating coupler sensor; F = waveguide; S = substrate; C = sample; Lc = cylindrical lens of short focal length fc (e.g. fc = 5 mm); L = cylindrical lens of focal length f (e.g. f = 300 mm); α = outcoupling angle; Δα = change in outcoupling angle proportional to the effective index change Δn; PSD = position-sensitive-detector; Δu = displacement of centre of the light spot on the PSD. (b) Schematics of output grating coupler measuring the effective index changes Δn(TE0) and Δn(TM0) of the TE0 and TM0 modes; M, M′ = mirrors. From [39], Copyright Elsevier (1990).
Figure 7.
Figure 7.
Optical arrangement for reflected-mode operation of integrated optical grating coupler. From [41], Copyright Elsevier (1996).
Figure 8.
Figure 8.
Schematic of wavelength interrogated optical sensor WIOS. From [46], Copyright Elsevier (2003).
Figure 9.
Figure 9.
(a) Cut through dual period sensor chip. (b) Cut through thickness-modulated sensor chip. From [46], Copyright Elsevier (2003).
Figure 10.
Figure 10.
Young interferometer as described in [21]. Light from a light source is coupled into the waveguide sensor chip by a grating after being split in two beams by a double slit. The two beams are guided separately down the waveguide, forming sensing and reference path, and coupled out by a second grating. The interference pattern is recorded behind another double slit by a CCD line sensor.
Figure 11.
Figure 11.
left: Schematic optical set-up used for first model-assays for volume detection’, interference filters were used for selection of the excitation or emission light and photodiodes or photomultiplier for signal detection; right: comparison of set-ups for volume detection and detection of backcoupled and guided luminescence light, using a second outcoupling grating where different wavelength can be discriminated by the outcoupling angle. From [31], Copyright Elsevier (1997).
Figure 12.
Figure 12.
Detection principle of evanescent field fluorescence on planar waveguides (principle of ZeptoREADER): excitation light is coupled into a thin-film waveguide; surface confined fluorescence of bound labeled molecules is detected by a CCD camera. Adapted from [2, 19]
Figure 13.
Figure 13.
Schematic of the Waveguide Excitation Fluorescence Microscope (WExFM); photograph of the system on a standard inverted microscope. From [10], Copyright Elsevier (2005).
Figure 14.
Figure 14.
Bidentate und monodentate phosphate coordination to tantalum ions. Adapted from [61].

Similar articles

Cited by

References

    1. Ehrat M., Kresbach G.M. DNA and protein microarrays and their contributions to proteomics and genomics. Chimia. 2001;55:35–39.
    1. Pawlak M., Schick E., Bopp M.A., Schneider M.J., Oroszlan P., Ehrat M. Zeptosens' protein microarrays: A novel high performance microarray platform for low abundance protein analysis. Proteomics. 2002;2:383–393. - PubMed
    1. Miklos G.L., Maleszka R. Protein functions and biological contexts. Proteomics. 2001;1:169–178. - PubMed
    1. Weissenstein U., Schneider M.J., Pawlak M., Cicenas J., Eppenberger-Castori S., Oroszlan P., Ehret S., Geurts-Moespot A., Sweep F.C.G.J., Eppenberger U. Protein chip based miniaturized assay for simultaneous quantitative monitoring of cancer biomarkers in tissue extracts. Proteomics. 2006;6:1427–1436. - PubMed
    1. Templin M.F., Stoll D., Pawlak M., Joos T.O. Protein Microarrays: Neue Systeme für die Proteomforschung. GIT Labor-Fachzeitschrift. 2006;50:890–892.

LinkOut - more resources