151 results about "Laser Microscopy" patented technology

A laser scanning microscope produces molecular excitation in a target material by simultaneous absorption of three or more photons to thereby provide intrinsic three-dimensional resolution. Fluorophores having single photon absorption in the short (ultraviolet or visible) wavelength range are excited by a beam of strongly focused subpicosecond pulses of laser light of relatively long (red or infrared) wavelength range. The fluorophores absorb at about one third, one fourth or even smaller fraction of the laser wavelength to produce fluorescent images of living cells and other microscopic objects. The fluorescent emission from the fluorophores increases cubicly, quarticly or even higher power law with the excitation intensity so that by focusing the laser light, fluorescence as well as photobleaching are confined to the vicinity of the focal plane. This feature provides depth of field resolution comparable to that produced by confocal laser scanning microscopes, and in addition reduces photobleaching and phototoxicity. Scanning of the laser beam by a laser scanning microscope, allows construction of images by collecting multi-photon excited fluorescence from each point in the scanned object while still satisfying the requirement for very high excitation intensity obtained by focusing the laser beam and by pulse time compressing the beam. The focused pulses also provide three-dimensional spatially resolved photochemistry which is particularly useful in photolytic release of caged effector molecules, marking a recording medium or in laser ablation or microsurgery. This invention refers explicitly to extensions of two-photon excitation where more than two photons are absorbed per excitation in this nonlinear microscopy.

An Agile-Beam Laser Array Transmitter (ABLAT) uses an array of emitters and an array of lenses to project electromagnetic beams over a wide angular coverage area in the far field. Differences in the separation pitches of the two arrays allows the ABLAT to project beams to contiguous and/or overlapping positions, depending on the ratio of the separation pitches and the lens focal length. Compared to other beam steering technology, the ABLAT is a smaller, lighter, and more efficient means of projecting beams over wider angular coverage areas. Various embodiments can be used in any beam steering application, including, but not limited to: free-space optical communications; light detection and ranging (lidar); optical scanning (e.g., retinal or bar-code scanning); display projection; image capture; optical character recognition; scanning laser microscopy; non-destructive testing; printing; facsimiles; map making; web inspection; color print processing; phototypesetting and platemaking; laser marking; material processing; DNA analysis; and drug discovery.

An enhanced resolution scanned image of an object is produced by a scanning laser microscope which includes an illumination arm for scanning an object with a focused probe beam and a detection arm for receiving light from the object. The detection arm includes a detector which collects and detects light from the object to produce pixel data for a plurality of pixels. In addition, the detection arm includes a wavefront sensor for sensing phase variations of the light from the object to produce wavefront data for scanned pixel locations. From the wavefront shape of the collected light at each pixel location, a high frequency spectrum is determined which corresponds to uncollected scattered light from small scale features of that pixel location. An enhanced resolution image of a region of interest is produced based on the high frequency spectra of the scanned pixel locations.

A laser microscope according to the present invention comprises a laser light source which generates a laser beam, an optical path split portion which has a plurality of optical path split elements with different characteristics for separating the laser beam irradiated to a sample from the laser light source and light returned from the sample and includes a selection mechanism to switch these optical path split elements on an optical path, an imaging lens to converge light which is returned from the sample and is separated in the optical path split portion, a spectrophotometric detection unit which obtains spectral data of light from the sample, an optical fiber which guides light from the sample imaged by the imaging lens to the spectrophotometric detection unit, wherein an incident end face of the fiber is arranged to a position substantially conjugate to the sample, and a transfer mechanism which moves an incident end face of the optical fiber in a plane orthogonal to an optical axis of light incident on the optical fiber.

A laser microscope comprises a laser light source emitting illumination light; an objective applying the illumination light on a sample; a light path compounding unit compounding a first illumination light path and a second illumination path between the laser light source and the objective; a phase-modulation type spatial light modulator placed on a position on the first illumination path, the position also being optically conjugate with a pupil position of the objective, modulating a phase of the illumination light; and a two-dimensional scanning unit placed on the second illumination light path, scanning the sample in a plane orthogonal to an optical axis of the objective.

A laser microscope according to an embodiment of the invention includes: a laser beam source; a phase plate providing a phase difference for laser beam from the laser beam source in accordance with an incident position; an objective lens focusing light transmitted through the phase plate onto a sample; a first separating unit separating second harmonic light emitted from the sample in a direction opposite to a traveling direction of the laser beams from a fundamental light reflected by the sample; and a photodetector detecting the second harmonic light separated from the fundamental light by the first separating unit.

A copper heat dissipation material having a satisfactory heat dissipation performance is provided. The copper heat dissipation material has an alloy layer containing at least one metal selected from Cu, Co, Ni, W, P, Zn, Cr, Fe, Sn and Mo on one or both surfaces, in which surface roughness Sz of the one or both surfaces, measured by a laser microscope using laser light of 405 nm in wavelength, is 5 μm or more.

Provided herein is a carrier-attached copper foil having desirable fine circuit formability. The carrier-attached copper foil includes a carrier, an interlayer, and an ultrathin copper layer in this order. The maximum ridge height Sp as measured with a laser microscope according to ISO 25178 on the surface of the carrier-attached copper foil on the side of the ultrathin copper layer is 0.193 to 3.082 [mu]m.

Observation is performed using bright, clear multiphoton fluorescence images produced by efficiently generating a multiphoton excitation effect, without the need for a complex interference film structure. The invention employs a laser microscope apparatus including a first dichroic mirror that reflects visible laser light guided via a first light path and that transmits IR pulsed laser light guided via a second light path to combine the first light path and the second light path; an XY galvanometer mirror that scans the laser light from the first dichroic mirror on a specimen; an objective lens that irradiates the specimen with the scanned laser light and that collects fluorescence produced in the specimen; a second dichroic mirror that reflects the visible laser light and transmits the fluorescence from the specimen; and a detection unit that detects the fluorescence transmitted through the second dichroic mirror.

The invention relates to a method for quantitatively analyzing inclusions in steel under laser microscope, comprising the following steps: 1) sampling; 2) polishing; 3) observing and imaging under a microscope; 4) analyzing data, wherein the data of inclusions in each digitalized photo is directly obtained after analysis, and the inclusion A method grading of single sample is obtained; and 5) splicing and analyzing the photo, wherein the inclusion B method grading of single sample is calculated through measurement. Through the application of the laser microscope and accessories, the surface of the whole metallic phase sample can be quickly scanned, the light microscope photos with different areas on a detection surface are obtained respectively by scanning one or more photos continuously, micro deviation of light on the surface of the sample is eliminated through software shadow rectification processing, the inclusions on the surface of the steel sample are sieved by utilizing the gray difference in the photo, the information of different types of inclusions in the whole surface to be detected such as size, length-diameter ratio, shape and the like are automatically calculated and counted through software after laser imaging, and the inclusions are graded with reference to national standard.

A scanning laser microscope of the present invention comprises at least one laser light source, a plurality of modulating sections for adjusting each laser light emitted from each laser light source, storage section for storing delay time information on an input/output of each modulating section, and signal production section for producing a driving signal to drive the modulating section selected from the plurality of modulating section based on the delay time information of the selected modulating section.

A solution for optical detection of the eye. Molecular markers are used for high-contrast diagnosis of eye diseases, other diseases, and other vital parameters which can be diagnosed in the eye. For optical detection of the eye, a molecular marker with spectral characteristics of absorption and/or scattering in the visual and infrared spectral region is introduced into the eye and bound to a specific target. The interaction of the molecular marker with the target is detected by means of optical imaging methods, such as fundus photography, confocal laser microscopy, polarisation-optical imaging methods, holographic methods or especially OCT methods. The use of optical methods is strongly preferred for the diagnosis of the eye as a result of the high transparency of the optical system of the eye compared to other body parts.

A laser microscope (10) having a laser light source (22) which generates laser light pulses (23) for the purpose of examining a sample (16). An optical element (25) is arranged in the beam path of the laser light pulses (23). The optical element (25) disperses the wavelength spectrum of the laser light pulses (23). Fractions (46, 48,60, 62) of the broad-band laser light pulses (32) having different wavelengths travel different path lengths upon passing through a compensation device (30), such that the different fractions (46, 48, 60, 62) arrive at the sample (16) at the same time.

A laser microscope includes: a light source that emits deep ultraviolet laser light to be irradiated on a sample; a limiting device that sets a limit to an intensity of the deep ultraviolet laser light irradiated on the sample; a detection device that detects the deep ultraviolet laser light having been reflected from the sample; a storage device that stores first information related to damage to the sample corresponding to the intensity of the deep ultraviolet laser light; and a control device that controls the limiting device based upon the first information when a sample damage limit is input from outside.

It is possible to achieve a required field number and numerical aperture for microscope observation at a scanning speed equal to video-rate or higher and also to change the scanning speed with a simple configuration. The invention provides a laser microscope including a laser light source; a scanning unit configured to scan a specimen with laser light emitted from the laser light source; and an objective lens configured to focus the laser light scanned by the scanning unit on the specimen. The scanning unit is provided with an electro-optical deflecting element including an electro-optical crystal in which a refractive index gradient is induced by injecting electric current.

To enable both observations of coherent anti-Stokes Raman scattering light and multiphoton fluorescence in a same apparatus so as to observe a specimen by various observation methods. There is provided a laser microscope apparatus comprising: two optical paths for guiding pulsed laser beams having two different frequencies whose frequency difference is approximately equal to a specific molecular vibration frequency in a specimen; a multiplexer for combining the pulsed laser beams guided through these two optical paths; and a frequency dispersion adjuster which is provided on at least one of these two optical paths, and is capable of adjustment to approximately equalize frequency dispersion quantities of the pulsed laser beams guided through the two optical paths.

A laser microscope includes a laser light emitting system which emits a pump beam and a Stokes beam having different frequencies, and a common optical fiber having one end and the other end. The pump beam and the Stokes beam emitted from the laser light emitting system are incident on the one end thereof and emitted from the other end thereof. A beam irradiating mechanism condenses and irradiates the pump beam and the Stokes beam emitted from the other end of the optical fiber, onto a sample via the objective lens, thereby making an anti-Stokes beam be emitted from the sample. A photo detector detects the anti-Stokes beam emitted from the sample. A beam selecting mechanism allows only the anti-Stokes beam of the pump beam, the Stokes beam and the anti-Stokes beam to be received on the photo detector.

It is possible to reduce a drop in output power in a positive-dispersion element used as a pulse compressor, thus improving multiphoton-excitation efficiency. Also, reducing the size of the positive-dispersion element makes it easier to attach it to a microscope main body and to accommodate it therein, thus improving maneuverability. The invention provides a laser microscope including a laser light source for emitting ultrashort-pulsed laser light; a pulse expander for expanding the ultrashort-pulsed laser light emitted from the laser light source; a large-diameter single-mode fiber for transmitting the ultrashort-pulsed laser light expanded by the pulse expander; a pulse compressor for compressing the ultrashort-pulsed laser light transmitted by the single-mode fiber; and a microscope main body for irradiating a specimen with the ultrashort-pulsed laser light compressed by the pulse compressor.

An aberration correction optical unit (3) disposed in an optical system includes: a first phase modulation element (3a) and a second phase modulation element (3c) each having a polarization characteristic; and a variable waveplate (3b) disposed between the first and second phase modulation elements so that an optical axis of the variable waveplate has a predetermined angle with respect to optical axes of the two phase modulation elements, in order to correct an aberration generated by the optical system.