Microscopes TRIZ Cases

A convex and concave mirror pair with a 2.5:1 radius ratio directs light normal to an image receptor.

A lens array demagnifies intermediate optical spots onto a photodetector, resolving alignment complexity while enhancing resolving power.

Pivotable and interleaved panels in a deployable shade assembly reduce vertical space consumption while protecting optical components from stray light.

Automated rangefinder measurements replace manual focus adjustments on transparent carriers, resolving slow operational efficiency.

Movable liquid pouring means adjust positions automatically to prevent interference during objective lens exchange.

Separates wavelength bands for imaging and height sensing to eliminate signal confusion in high aspect ratio trenches.

A concentrator with fractional phase index of refraction increases the absorption cross-section of nanoresonators beyond conventional limits.

A multi-index optical element steers radiation through adjacent portions with graded refractive indices to guide light toward an image plane.

Separate focusing lenses in a stereoscopic microscope allow independent focal plane adaptation, preventing intermediate image drift during focusing.

Spatial light modulators replace mechanical lens groups to change magnification ratios, reducing adjustment time and device complexity.

Continuous sample movement at constant speed reduces recording time by eliminating step-by-step acceleration cycles that cause motion blur.

Oblique detection locates tissue samples before high-magnification scanning, reducing total image count and increasing throughput.

An immersion set merges a fluid tank, pump, and control electronics into a compact unit fastened directly to the objective.

Spatial light modulator compensates meniscus refraction to maintain image clarity during time-lapse culture vessel observation.

Independent installation units with shifted abutting reference surfaces allow optical device replacement without altering the microscope configuration.

A multi-well plate auto-focusing method computes an in-focus plane from a subset of wells to enable rapid scanning with lower magnification objectives.

Aperture structure adjusts diffraction order intensities to resolve blurred edges on periodic semiconductor substrates.

Resilient springs counterbalance the infinity lens weight while a fixed axial focusing aid device maintains consistent focus across non-planar sample surfaces.

A localization microscope captures image frames while continuously translating the sample to generate composite data covering larger spatial regions.

Merging the optical component with the scanner maintains beam profiles during lateral movement, covering larger sample areas without translation.

Three lens groups with cemented elements resolve the trade-off between high numerical aperture and working distance for deep tissue imaging.

A receiving apparatus transports active objectives along an orthogonal path to reduce mechanical loads.

Inclined cuvette walls align optical paths perpendicular to samples, reducing refraction errors and improving imaging throughput.

Asymmetrical numerical aperture design expands field of view and inspection speed while maintaining high optical resolution for semiconductor packages.

Aperture member positioning eliminates modulator dependency, resolving alignment complexity while enabling unrestricted shadow direction.

Adjustable sleeve mechanism compensates for tripod thread offset, aligning optical pupils to resolve cropped field of view issues.

A microlens array integrates light sources between lenses on a transparent base to emit parallel illumination.

Ring elementary illuminators direct light toward the objective lens, reducing energy loss and image background in reflective dark field microscopy.

Light deflection systems in afocal modules adjust beam path length to fix the exit pupil position, enabling stable SLM integration.

A laser autofocus device detects scattered light from nonfocal positions to determine source location and adjust the focusing lens.

An open-stage near-TIRF microscope positions optical components beneath the sample to enable physical access and environmental control.

An optical assembly uses adjustable deflectors to route light into selectable beam paths for structured illumination.

A medical stereomicroscope optical system uses imaging lens groups with single aspheric surfaces to correct spherical aberration and field curvature.

Sensor feedback adjusts front lens position to prevent corneal contact and ensure clear retinal visualization.

A light beam generator uses an optical phase modulation element to produce structured electromagnetic waves with specific spatial distributions.

A multi-focal light-sheet module uses a Wollaston prism to generate structured illumination patterns for simultaneous 3D imaging.

A surgical microscope tube uses a telesystem lens configuration to guide imaging beams through pivotable segments.

A compact focusing unit uses a rigid arm and lever mechanism to drive vertical movement of an objective lens.

A light input assembly directs intense beams into the optical path of a scanning confocal microscope.

A detachable reference surface unit with adjustable inclined angles integrates into an interference objective lens.

A scanning molecule counting method detects individual fluorescent particles using a rapidly moved photodetection region and triplet quenching agents.

A remote focusing microscope splits fluorescence into polarized beams for aberration-free volumetric imaging.

Segmented monochromatic sources provide oblique illumination to remove dichroic mirrors, reducing light energy loss and improving image accuracy.

A surgical microscopy system registers focal points and stores spatial coordinates for precise microscope repositioning.

An automatic image optimization system adjusts an additional lens position via a CCD camera and analyzing unit to reduce reflections in retinal imaging.

A microscopy system isolates fluorescent radiation from excitation light using specialized optical filters and variable angle illumination paths.

An infinity-corrected optical system with variable parfocal distance detects feeble light signals from biological specimens.

A multi-wavelength optical arrangement superimposes synchronized laser pulses to enable precise object examination.

A microscope slider integrates a polarizer, analyzer, and shearing elements into a single interchangeable stack.

A plasmonic sample holder with sub-micron structures produces wavelength-shifted resonance peaks, enabling high-contrast imaging of unstained specimens.