Microscopes TRIZ Cases

A four-polarization detection scheme retrieves 3D dipole orientation parameters without deforming the point spread function.

Multi-depth Z-plane scanning creates 3D virtual slides that resolve focus control latency and time lag during remote specimen examination.

A microscope objective integrates a phase plate into an air space between the first two lenses to shift the real pupil and reduce scattered light.

A microscope hinged door unfolds into a horizontal work surface for direct sample manipulation.

An acousto-optical beam combiner diffracts light bundles onto a common optical axis using a single mechanical wave.

A light modulation element generates patterned and uniform measurement light, eliminating separate projecting sections to reduce device weight.

A microscope objective lens uses cemented low and high dispersion materials to achieve wide field of view.

Segmented lens groups balance chromatic and spherical aberrations, enabling wide field of view resolution.

A wedge-shaped component generates spatially offset scanning beams through multiple reflections at a partially reflecting surface.

Standardized mounting devices equalize focal positions across interchangeable objective lenses, preventing focus drift during exchange.

A dry microscope objective uses a three-group lens configuration to enhance resolution and brightness.

A microscopy system uses beam splitters to separate emission and reflection wavelengths for simultaneous fluorescence and white-light detection.

A dry microscope objective uses cemented doublets to correct axial chromatic aberrations across wide wavelength ranges.

Segmented lens slots on a sliding base enable independent plate orientation, resolving mechanical complexity limits while maintaining precise alignment.

A Fourier ptychography method corrects image quality by accounting for beam shape properties during evaluation.

Microlens array doubles numerical aperture to halve point spread function width, eliminating spurious resolution artifacts from image processing.

An identification filter blocks specific fluorescence spectra to enable simultaneous biomarker detection using a single light source and camera.

A microscope controller manages objective lens movement across distinct imaging modes to ensure safe operation.

A relay optical system corrects aberrations generated by scanning devices moving focusing positions in microscope illumination.

A specimen observation apparatus aligns the imaging field of view with the specimen container using pre-focus luminance detection.

A microscope controller manages bright-field and fluorescence illumination systems using a shutter mechanism to switch optical paths.

A transmitted light illumination apparatus uses a movable diaphragm element to cover a planar light source, directing reflected light via a concave mirror surface.

Segmented microlens arrays and dry air gap apertures eliminate dead time and striping artifacts while maintaining constant image intensity.

Preliminary scanning identifies fluorescence markers, allowing targeted inhibition light application that reduces phototoxicity and bleaching in living samples.

A fiducial-based surface fitting algorithm determines optimal z positions for probe array imaging.

Sequential wavelength measurement segments spatial and spectral resolution, reducing device complexity without losing multi-spectral data.

A fly-eye integrator distributes light from small-area sources across the optical path.

Segmented protrusion design reduces contact area in solid immersion lens holders.

A microscope system adjusts camera focus by capturing images at multiple depths to calculate defocusing amounts.

Structured illumination generates sub-diffraction-limited images while minimizing photodamage and out-of-focus background noise in biological samples.

Segmented design with vibration isolating mounts and optical fiber illumination resolves weight stability trade-offs.

A biological specimen observation apparatus adjusts magnification rates dynamically to track changing regions accurately.

A fluorescence endoscopy optical scanner uses a partially coated objective lens to direct excitation and emission light paths.

A gel member fills the space between an objective lens and a sample to maintain high refractive index.

A supercontinuum source generates broadband light via a nonlinear waveguide to enable multiphoton excitation.

Segmented apertures block paraxial rays to prevent thermal heating and back-reflections, maintaining imaging contrast in super-resolution microscopy.

A beam array generator produces an M×N light beam array that illuminates a sample and maps to a corresponding sensor array for whole microscopy image capture.

Dark field illumination generates high-contrast macro images to set accurate image pickup conditions for microscopes.

A concave-convex lens with optimized curvature changes focus rapidly without transmitting vibrations to the sample or degrading image quality.

Interference light beams with distinct beat frequencies expand detection bandwidth in laser microscopy systems.

A calibration slide featuring quadrant-divided aperture arrays standardizes focus alignment across automated microscope systems.

Adjustable illuminating arrangement directs light through the microscope main objective to optimize incidence angles.

A scanner arrangement rotates the scanning field via a mechanical pivot device to maintain beam centering.

Reflective axicon systems transform solid light beams into hollow profiles using conical mirrors and total internal reflection.

An electrowetting lens element replaces mechanical actuators to achieve high-speed axial focusing within a compact optical imaging device.

Matching the beam diameter to the pixelated photon detector effective area reduces photon count loss and widens the detectable light-intensity range.

Pre-calculated holograms applied by spatial light modulators suppress condensing intensity loss and shape spreading inside non-flat biological samples.

Segmenting piezo actuators for coarse and fine movements accelerates focusing speed while maintaining positioning precision.