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Sarfus is an optical quantitative imaging technique based on the association of: *an upright or inverted optical microscope in crossed polarization configuration and *specific supporting plates – called surfs – on which the sample to observe is deposited. Sarfus visualization is based on the perfect control of the reflection properties of polarized light on a surface, which leads to an increase in the axial sensitivity of optical microscope by a factor of around 100 without reducing its lateral resolution. Thus this new technique increases the sensitivity of standard optical microscope to a point that it becomes possible to directly visualize thin films (down to 0.3 micrometer) and isolated nano-objects in real-time, be it in air or in water.


Principles

A recent study on polarized light coherence leads to the development of new supports – the surfs – having contrast amplification properties for standard optical microscopy in cross polarizers mode. Made of optical layers on an opaque or transparent substrate, these supports do not modify the light polarization after reflection even if the numerical aperture of the incident source is important. This property is modified when a sample is present on a surf, a non-null light component is then detected after the analyzer rendering the sample visible. The performances of these supports are estimated from the measurement of the contrast (C) of the sample defines by: C = (I1-I0)/(I0+I1) where I0 and I1 represent the intensities reflected by the bare surf and by the analyzed sample on the surf, respectively. For a one nanometer-film thickness, the surfs display a contrast 200 times higher than on silicon wafer. This high contrast increase allows the visualization with standard optical microscope of films with thicknesses down to 0.3 nm, as well as nano-objects (down to 2 nm diameter) and this, without any kind of sample labelling (neither fluorescence, nor radioactive marker). An illustration of the contrast enhance is given hereafter with the observation in optical microscopy between cross polarizers of a Langmuir-Blodgett structure on a silicon wafer and on a surf. In addition to visualization, recent developments have allowed accessing to the thickness measurement of the analyzed sample. A colorimetric correspondence is carried out between a calibration standard made of nano-steps and the analyzed sample. Indeed, due to optical interference, a correlation exists between RGB (red, green, blue) parameters of the sample and its optical thickness. This leads to 3D-representation of the analyzed samples, the measurement of profile sections, roughness and other topological measurements.


Experimental setup

The experimental set-up is simple: the sample to be characterized is deposited by usual deposit techniques such as dip-coating, spin-coating, deposit pipette, evaporation... on a surf instead of the traditional microscope slide. The support is then placed on the microscope stage.


Synergy with existing equipment

The sarfus technique can be integrated in existing analysis equipment (
atomic force microscope Atomic force microscopy (AFM) or scanning force microscopy (SFM) is a very-high-resolution type of scanning probe microscopy (SPM), with demonstrated resolution on the order of fractions of a nanometer, more than 1000 times better than the diffr ...
(AFM),
Raman spectroscopy Raman spectroscopy () (named after Indian physicist C. V. Raman) is a spectroscopic technique typically used to determine vibrational modes of molecules, although rotational and other low-frequency modes of systems may also be observed. Raman sp ...
, etc.) to add new functionalities, such as optical image, thickness measurement, kinetic study, and also for sample pre-localization to save time and consumables (AFM tips, etc.).


Applications


Life sciences

*Biological films *
Biochip In molecular biology, biochips are engineered substrates ("miniaturized laboratories") that can host large numbers of simultaneous biochemical reactions. One of the goals of biochip technology is to efficiently screen large numbers of biological a ...
* Phospholipids *
Soft lithography In technology, soft lithography is a family of techniques for fabricating or replicating structures using "elastomeric stamps, molds, and conformable photomasks". It is called "soft" because it uses elastomeric materials, most notably PDMS. So ...
*
Cell adhesion Cell adhesion is the process by which cells interact and attach to neighbouring cells through specialised molecules of the cell surface. This process can occur either through direct contact between cell surfaces such as cell junctions or indir ...


Thin films and surface treatment

* Polymers films * Langmuir-Blodgett films * Liquid crystals *Plasma treatment * Self-assembled monolayers


Nanomaterials

* Carbon nanotubes *
Nanoparticles A nanoparticle or ultrafine particle is usually defined as a particle of matter that is between 1 and 100 nanometres (nm) in diameter. The term is sometimes used for larger particles, up to 500 nm, or fibers and tubes that are less than 1 ...
* Nanowires * Graphene * DNA molecules


Advantages

Optical microscopy has several advantages compared to the usual techniques of nanocharacterization. It is easy-to-use and directly visualizes the sample. The analysis in real-time allows kinetic studies (real-time crystallization, dewetting, etc.). The broad choice of magnification (2.5 to 100x) allows fields of view from several mm2 to a few tens µm2. Observations can be performed in controlled atmosphere and temperature.


References

{{Optical microscopy Nanotechnology Microscopy Laboratory techniques Scientific techniques Biological techniques and tools Laboratory equipment Optical microscopy