Swinging objective retarding immersion lens electron optics...

Radiant energy – Inspection of solids or liquids by charged particles – Electron probe type

Reexamination Certificate

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C250S3960ML

Reexamination Certificate

active

06392231

ABSTRACT:

FIELD OF THE INVENTION
This invention relates generally to scanning electron microscopes, and in particular, to a swinging objective retarding immersion lens electron optics focusing and deflection system and method that can provides a high current low voltage primary electron beam, high resolution scanning, large scan field, and high signal capture efficiency.
BACKGROUND OF THE INVENTION
Scanning electron microscopes are used in many applications that require inspection of very small structures of an object in great detail. Some of these applications include defect review and inspection of specimens such as very large scale integrated (VLSI) circuits, or wafers, or other articles, critical dimensioning of features in these specimens and also design and process verification of the specimens. Scanning electron microscopes are considered superior to optical microscopes for viewing features in sub-micron dimensions, currently about 0.2 &mgr;m (1 &mgr;m=10
−6
meters) or less, due to the short wavelength that helps the scanning electron microscope to generate a small spot size. Scanning electrons microscopes typically employ an objective lens system for focusing the electron beam onto the specimen under examination.
A scanning electron microscope typically includes a primary electron beam source, an accelerating anode, an objective lens for focusing the beam onto the specimen, a plurality of deflection units that enable the positioning and scanning movement of the primary beam over the specimen, and a detection system for capturing secondary electrons (SE) or backscattered electrons (BSE) from the specimen to produce an image of the specimen. In some cases a condenser lens system is used to provide a focused beam for the objective lens system. As known to those skilled in the pertinent art, the electron beam source generates a supply of electrons for the primary beam. The condenser lens system, if used, forms an image of the primary electron beam source for the objective lens and the objective lens focuses the condenser lens image onto the specimen. The deflection system moves the focused beam over a portion of the specimen in a scanning motion and secondary and backscattered electrons are released from the specimen material. These electrons are detected, amplified and the resulting signal used to modulate the beam of an imaging system operating synchronously with the scanning electron beam. The result is an image of the scanned area based on the electrons emitted or scattered from the specimen.
Prior art scanning electron microscopes have several drawbacks. First, in order to obtain high resolution for the prior art objective lens, a relatively high beam energy, say 15KeV or more, primary electron beam source is required. However, applying such a higher energy electron beam directly to the specimen is undesirable because it can cause damage to the specimen, which consequently leads to a reliability problem in the engineering, manufacturing and production of integrated circuits. Using a low energy primary electron beam source avoids the reliability problem but limits the spatial resolution due to chromatic aberration of the objective lens and by electron-electron interaction within the beam. Chromatic aberration of the objective lens arises from electrons of different velocity experiencing different focal points for the same lens. This effect creates a disk of confusion at the image plane on the specimen and limits resolution of the system. Both electron-electron interaction (space-charge effect) and chromatic aberration are reduced by using a higher energy electron beam. Second, it is difficult to achieve high secondary and backscattered electron capture efficiency with a low energy primary electron beam source. If a multi-channel plate is used, there is a severe reliability problem due to contaminants collecting in the holes (channels) of the plate.
As stated above, spatial resolution of current low voltage scanning electron microscopes is essentially limited by the chromatic aberration of the objective lens and by the electron-electron interaction, or Boersch effect. One way to improve the spatial resolution is to reduce the electron-electron interaction by using a high-energy primary bean which is subjected to a retarding field. Another way to improve spatial resolution is to use a snorkel (center pole) magnetic lens to reduce the loss in resolution due to chromatic and spherical aberration.
Conventional retarding field scanning electron microscopes which are equipped with a snorkel magnetic lens, a retarding electrostatic plate and pre-lens double deflection units are currently used for critical dimension measurement, defect review and defect inspection system in VLSI (very large scale integrated) wafer manufacturing. These conventional units still have several drawbacks.
First, it is difficult to generate a large deflection field with these units, where the deflection field is the reachable area in the plane of the specimen over which the primary beam can be moved by the deflection system. As a consequence, only a relatively small portion of the specimen can be examined at a time without repositioning the specimen. Second, because of the inherently small deflection field, the time required for inspecting, reviewing and measuring a specimen is substantially long. This results in increased engineering, testing, troubleshooting, and production costs, as well as an increase in integrated circuit turnaround time.
Thus, there is a need for an objective lens for an electron scanning microscope and method therefore that provides high primary beam current, lower energy electron beam on the specimen, relatively high resolution, a relative large scanning field, and a high signal capture efficiency.
SUMMARY OF THE INVENTION
A scanning electron microscope having a swinging objective retarding immersion lens electron optics focusing, deflection and signal capture system is disclosed herein that overcomes the drawbacks discussed above with regard to prior art objective lens. Specifically, the objective lens system of the invention converts a high energy primary electron beam to a lower energy electron beam at the specimen to minimize damage to the specimen. It also has relatively high resolution for clear examination of submicron features. Moreover, a scanning electron microscope, in accordance with the present invention, provides a relatively large deflection field to reduce the time to fully examine the specimen and includes a detection unit to more efficiently capture secondary electrons (SE) and backscattered electrons from the specimen (BSE).
One aspect of the invention includes a Swinging Objective Retarding Immersion Lens (SORIL) system for examination of a specimen including a a magnetic lens for generating a magnetic field in the vicinity of the specimen to focus the particles of the particle beam on the specimen, the magnetic lens having a central bore through which the particle beam travels; an electrode for providing a retarding field to the particle beam near the specimen to reduce the energy of the particle beam when the beam collides with the specimen; and a deflection system including a plurality of deflection units situated along the beam axis for deflecting the particle beam to allow scanning of the specimen, at least one of the deflection units located in the retarding field of the beam, the remainder of the deflection units located within the central bore of the magnetic lens; and an annular detection unit with a small aperture to capture SE and BSE.
Another aspect of the invention includes a method for increasing a scan field of an objective lens system over a specimen having the steps of: generating a magnetic field in the vicinity of the specimen to focus the particles of the particle beam on the specimen; providing a retarding electric field to reduce the energy of the particle beam prior to the beam colliding with the specimen; positioning the focused particle beam over area to be scanned, the area being within the deflection field of the specimen, a

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