Microscopes TRIZ Cases

Two cascaded phase-modulation spatial light modulators convert input light into arbitrary cross-sectional shapes without optical loss.

Objective lens unit with inclined lenses refracts measurement light to focus on the retina while dispersing reflection light away from the detector.

Dynamic touch panel layouts adapt to observation modes, resolving blind touch operability issues while maintaining precise stage positioning.

A pupil modulation element with varying transmittance regions refracts light to produce three-dimensional images of unstained cells.

A capillary channel objective cap manages immersion medium flow using hydraulic forces and suction.

Scanning illumination along a sample rough shape reduces image-taking time while maintaining high resolution for semiconductor wafers.

Smartphone microscope hardware captures magnified images of blood samples, enabling rapid diagnosis without specialized lab equipment.

Calculates parfocality offsets via z-stack contrast analysis, eliminating immersion liquid application and reducing calibration time.

Dual spatial light modulators shape the wavefront of an input light beam to control transverse distribution and axial position within a target volume.

A rotating sample container passes biological specimens through a defined observation volume to enable parallel detection and high-speed imaging.

Hall effect sensors detect manual microscope zoom positions to enable parameter storage without motorized drives.

Subpixel sensor-scanning synthetic aperture overcomes the inverse relationship between imaging resolution and field-of-view in conventional optical microscopy.

Galvanometric mirror switches light sheet direction under 10 ms to synchronize with detector integration time.

Conical diffraction combined with Bayesian reconstruction determines fluorophore spatial distribution, resolving precision versus operational complexity.

Digital signal processing merges multiple wavelengths into one component, reducing electronic complexity and energy consumption.

Connector maintains overpressure to prevent evaporation and encrustation during automated microscopy.

A phase contrast microscope system captures infrared images of hair samples to reveal internal structures without physical sectioning.

A line-scanning microscope rotates structured illumination to control phase position and scanning direction with minimal light loss.

A segmented diaphragm creates variable intensity distributions for mask inspection microscopes.

A multi-group immersion objective lens design achieves high numerical aperture through specific cemented lens configurations.

A dual optical medium component adjusts phase lag across multiple wavelengths to preserve specimen color information.

A microscope control unit automatically adjusts the iris diaphragm aperture based on zoom and lens parameters.

Lookup tables store pre-calculated correction values to resolve edge distortions and maintain precision across zoom levels.

Lateral detection captures high-contrast overview images while avoiding liquid meniscus aberrations that degrade image quality.

A fixed-focus lens uses a curved reflector to redirect light beams between spherical and aspheric lens groups.

A relay optical system with a rhomboid prism laterally shifts light beams from angled-polished fiber endfaces.

A confocal microscope switches light sources in a clocked sequence to read detection pixels in reverse order.

A portable dark tent restricts ambient light around microscope oculars to maintain image contrast.

Segmented conical recesses in a gel body maintain sample alignment during rotation, resolving trade-offs between image quality and throughput.

An adhesive bead centers optical fibers inside actuator tubes, eliminating surface tension pull that degrades scan pattern accuracy.

Segmented stage supports allow optical device attachment in inverted microscopes, preventing stage elevation that increases vibration susceptibility.

A microscope system adjusts electric zoom magnification to maintain constant total magnification during objective lens switching.

Integrated calibration device aligns test structure with focusing lens to compensate for thermal expansion and maintain stable microscope performance.

Three-subsystem immersion objective lens uses cemented elements and aperture stops to reduce veiling glare while maintaining 1.49 numerical aperture.

Segmenting the STED beam into hollow and filled cores isolates direct excitation noise, preserving high spatial frequency details.