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Despite the revolutionary significance, the conventional far-field light microscopy is restricted by the diffraction limit based on the scale diffraction theory; that is, objects within a diffraction-limited spot, ∼250 nm, cannot be resolved.
Molecular imaging has been hampered by the diffraction limit, an intrinsic blurring of light that prevents two sources from being resolved when they are close together.
While 32 nm lithography technology is on the horizon for integrated circuit (IC) fabrication, matching the pace for miniaturization with optics has been hampered by the diffraction limit.
Although PL measurement on individual submicron structures is possible, the accuracy of the technique is limited by the diffraction limit and poor signal-to-noise ratio [6].
Typically, light microscopic methodologies using conventional optics are limited by the diffraction limit yielding resolutions that cannot be reached lower than approximately 200 nm.
To date, photolithography has been able to meet the demand for ever smaller devices despite the constraints imposed by the diffraction limit and the expense of deep and extreme UV light sources.
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Therefore, SPPs offer fascinating prospects for the photoelectronics, for example, by evading the diffraction limit and, thus, enabling the efficient integration with electronics, so far prevented by the size mismatch of the ever diminishing electrical but diffraction limited optical components.
In particular, the processes of antigen-induced receptor clustering and lipid-mediated transmembrane signaling are of fundamental immunological importance, but are dominated by interactions below the diffraction limit of light (∼200 nm).
We found that for initial aberrations with a root-mean-square wave front error of only one third of the wavelength the threshold energy can still be reduced by a factor of three if the aberrations are corrected to the diffraction limit by adaptive optics.
Such techniques have found remarkable success in surpassing the diffraction limit to achieve sub-diffraction limited resolution; however, they are predominantly limited to fluorescent samples.
This is because such a lens need not be limited by an imperfection known as the diffraction limit, which has set a ceiling on the accuracy of optical systems ever since lenses were first polished.That is an altogether more subtle claim.
More suggestions(15)
by the way limit
by the diffraction condition
by the diffraction peak
by the service limit
by the debt limit
by the diffraction diffraction
by the credit limit
by the convergence limit
by the exchange limit
by the commission limit
by the temperature limit
by the detection limit
by the diffraction analysis
by the diffraction barrier
by the diffraction profile
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