Abbe Diffraction Limit Formula:
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Microscope resolution refers to the smallest distance between two points that can still be distinguished as separate entities. The Abbe diffraction limit describes the fundamental resolution limit of optical microscopes due to the wave nature of light.
The calculator uses the Abbe diffraction limit formula:
Where:
Explanation: This formula calculates the theoretical maximum resolution achievable by an optical microscope, determined by the wavelength of light used and the numerical aperture of the objective lens.
Details: Understanding microscope resolution is crucial for selecting appropriate microscopy techniques, interpreting imaging results, and determining the limitations of optical systems in biological and materials research.
Tips: Enter wavelength in nanometers (nm) and numerical aperture as a unitless value. Typical wavelengths: 400-700 nm (visible light), 550 nm (green light commonly used). Numerical aperture ranges from 0.1 to 1.4 for most objectives.
Q1: What Is The Rayleigh Criterion?
A: The Rayleigh criterion states that two point sources are resolvable when the principal diffraction maximum of one image coincides with the first minimum of the other.
Q2: How Can I Improve Microscope Resolution?
A: Use shorter wavelength light, higher numerical aperture objectives, immersion oil, or super-resolution techniques that overcome the diffraction limit.
Q3: What Is Typical Resolution For Light Microscopes?
A: For visible light (λ=550 nm) with NA=1.4 objective, resolution is approximately 0.24 μm (240 nm).
Q4: Does Magnification Affect Resolution?
A: No, magnification alone doesn't improve resolution. Empty magnification beyond the resolution limit doesn't reveal additional detail.
Q5: What Are Super-Resolution Techniques?
A: Techniques like STED, PALM/STORM, and SIM that bypass the diffraction limit to achieve resolution below 200 nm.