Scanning microscope in which a sample is simultaneously and optically excited at various points

• US 6,262,423 B1
• Filed: 08/18/1998
• Issued: 07/17/2001
• Est. Priority Date: 12/22/1996
• Status: Expired due to Fees

• Current Assignee: Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften e.V. (Max-Planck-Gesellschaft zur Frderung der Wissenschaften e)
• Original Assignee: Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften e.V. (Max-Planck-Gesellschaft zur Frderung der Wissenschaften e)
• Inventors: Hell, Stefan, Bewersdorf, Jörg, Pick, Rainer
• Primary Examiner(s): Sugarman, Scott J.
• Assistant Examiner(s): HANIG, RICHARD E
• Application Number:
  US09/125,484
• Time in Patent Office: 1,064 Days
• Field of Search: 250/458.1, 250/459.1, 250/461.1, 250/461.2, 356/124, 356/239.2
• US Class Current: 250/458.1
• CPC Class Codes: G02B 21/002 Scanning microscopes scanning near field optical microscopes G01Q60/18

Abstract

An optical apparatus, especially a scanning microscope (1), wherein an expanded laser beam (2) is divided into several partial beams (4) by micro lenses (5) arranged next to one another. Each partial beam (4) is focused onto a focal point (11) by a common objective lens (7) to optically excite a sample (8). Fluorescent light emanating from the individual focal points (11) of the sample (8) is registered by a photo sensor (13) arranged behind the objective lens (7) as seen from the sample (8). Each photon of the fluorescent light coming from the sample (8) and being registered by the photo sensor (13) is excited by at least two photons of the laser beam (2).

Claims

1. An optical apparatus, wherein an expanded laser beam is divided into several partial beams by micro lenses arranged next to one another, wherein each partial beam is focused onto a focal point by a common objective lens to optically excite a sample, wherein fluorescent light emanating from the individual focal points of the sample is registered by a photo sensor arranged behind the objective lens as seen from the sample, and wherein each photon of the fluorescent light coming from the sample and being registered by the photo sensor is excited by at least two photons of the laser beam.

2. The apparatus of claim 1, wherein the wavelength of the laser beam is approximately twice as long as the wavelength of the fluorescent light coming from the sample and being registered by the photo sensor.

3. The apparatus of claim 1, wherein the micro lenses have a common focal length and are arranged in a plane oriented perpendicularly to the laser beam.

4. The apparatus of claim 1, wherein the micro lenses have different focal lengths and are arranged in parallel planes oriented perpendicularly to the laser beam.

5. The apparatus of claim 1, wherein the micro lenses are arranged side by side in one direction.

6. The apparatus of claim 1, wherein the micro lenses are arranged side by side in two directions.

7. The apparatus of claim 6, wherein the micro lenses are arranged to form a micro lens wheel, wherein the expanded laser beam is divided into the partial beams by some of the micro lenses, and wherein the sample is scanned in two dimensions by rotating the micro lens wheel about its axis extending in parallel to the laser beam.

8. The apparatus of claim 1, wherein the photo sensor is a CCD-array.

9. The apparatus of claim 1, wherein the laser beam divided into partial beams by the micro lenses is divided by a beam dividing device, and wherein the two divided partial beams coming from opposite directions are brought to interference in the region of the sample.

10. The apparatus of claim 6, wherein the micro lenses are arranged to form a micro lens wheel, wherein the expanded laser beam is divided into the partial beams by some of the micro lenses, and wherein the sample is scanned in three dimensions by rotating the micro lens wheel about its axis extending in parallel to the laser beam.

11. The apparatus of claim 1, wherein said common objective lens is a lens, a defect of which is to be determined, and wherein the sample comprises a fluorescent material having a defined, homogenous concentration.