CN1763504A - Transmissive multi-beam confocal interference microscope with tens nanometer transverse resolution - Google Patents

Transmissive multi-beam confocal interference microscope with tens nanometer transverse resolution Download PDF

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Publication number
CN1763504A
CN1763504A CN 200510123582 CN200510123582A CN1763504A CN 1763504 A CN1763504 A CN 1763504A CN 200510123582 CN200510123582 CN 200510123582 CN 200510123582 A CN200510123582 A CN 200510123582A CN 1763504 A CN1763504 A CN 1763504A
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interference microscope
light source
confocal
confocal interference
microscope
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CN 200510123582
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赵维谦
冯政德
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Harbin Institute of Technology
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Harbin Institute of Technology
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Abstract

The invention discloses a transmission multiple-beam confocal interference microscope of tens of nanometer transverse resolution power in the microscope image-forming and microcosmic precise measuring technique domain, which comprises the following parts: light source (1), aligning beam expander (2) and polarizing beam splitter (10) on the emission end of light source sequently, one fourth wave plate (11) and microobjective lens (4) on the reflecting optical path of polarizing beam splitter (10), collecting lens (6) on the transmission optical path of polarizing beam splitter (10), pinhole (7) at the focal point position of collecting lens (6), photodetector (8) next to the back of pinhole and multiple-beam generator (12) between polarizing beam splitter (10) and collecting lens (6). The invention can be used in domain of microelectronic material, industry precision detection, biomedical and so on to finish high resolution power microscopic image-forming detection.

Description

Transmissive multi-beam confocal interference microscope with tens nanometer transverse resolution
Technical field
The invention belongs to micro-imaging and microcosmic Technology of Precision Measurement field, be a kind of method and apparatus of realizing that transverse super resolution imaging detects, it can be used for carrying out the high resolution micro-imaging in the fields such as microelectronics, material, the accurate detection of industry, biomedicine and detects.
Background technology
In recent years, along with rapid development of science and technology, semiconductor technology involves the quantum device development to VLSI (very large scale integrated circuit), millimeter, Micrometer-Nanometer Processing Technology has also entered deep-submicron, the three-dimensional processing technique field of nanometer, the development of biomedicine, materialogy and superelevation precise light memory technology has simultaneously all proposed more and more higher requirement to optical imaging system and resolving power thereof, therefore presses for imaging with hyperresolution and the detection technique that research adapts to its demand for development.
And confocal microscope is used widely at above-mentioned numerous areas with its distinctive three-dimensional chromatography imaging capability, but owing to limited by the principle of diffraction phenomena, has restricted the further raising of its imaging resolution characteristic.In order fundamentally to break through diffraction limit, improve the imaging resolution characteristic of confocal microscope, in recent years, domestic and international many scholars are devoted to the research of confocal microscope, and have proposed numerous unconventional confocal microscopic imaging principles and ultra-resolution method.
At present, several typical confocal microscopes have appearred, for example: confocal interference microscope, 4PI confocal microscope, θ confocal microscope, based on the two-photon of optical nonlinearity behavior and multi-photon confocal microscope etc.The thought that interference technique and confocal microscope technology are merged mutually is (see " the three-dimensional imaging principle of confocal microscopy " for details, M. turns round and look at work, and Wang Guiying etc. translate, New Age Press, in January, 2000 publication) that Min Gu proposes the earliest.Domesticly also obtaining some achievements in research aspect the confocal interference microscopy, for example: Chinese patent " confocal microscope " (application number: 01122439.8, publication number: CN 1395127A) propose interferometric method is introduced in traditional confocal micro imaging system, be used to improve the method for azimuthal resolution; Chinese patent: " double-frequency confocal step height microscope measuring device " (application number: 02120884.0, publication number: CN 1384334A) disclose a kind of double-frequency confocal step and interfered microscopic system; Chinese patent " confocal interference microscope " (application number: 200410096338.8) etc. with high-space resolution imaging ability.
Traditional confocal interference microscope principle as shown in Figure 1, the pointolite that light source 1 sends becomes parallel beam through collimator and extender device 2, this parallel beam is divided into measuring beam and reference beam by spectroscope 3, measuring beam is reflected to collector lens 6 after object lens 4 focus on measured object 9 surfaces, reference beam arrives collector lens 6 after reference mirror 5 reflections, collector lens 6 can produce interference by coalescence with measuring beam and reference beam, the focus that photodetector 8 is positioned at collector lens 6 is used to survey the confocal interference signal, and its big or small corresponding measured object is with respect to the relative displacement at object lens 4 focus places.This confocal interference microscope improves the azimuthal resolution of confocal microscope by interference technique under the prerequisite that keeps the intrinsic horizontal resolution characteristic of confocal microscope.This traditional confocal interference microscope exists many deficiencies, as: the reflection that reference beam that is concerned with in traditional confocal interference microscope and measuring beam come from level crossing 5 respectively and the reflection on measured object 9 surfaces, two-beam is focused at generation interference on the photodetector 8 along different optic path through collector lens 6.Because reference light is from fixing plane mirror, its intensity is more stable, and the measuring beam Strength Changes is bigger, and what therefore traditional confocal interference microscope reference light and measuring light formed is that variable strength is interfered, its interference fringe poor contrast is a little less than the simultaneity factor antijamming capability.The more important thing is that traditional confocal interference microscope has only improved the azimuthal resolution of system, its transverse resolution still is subjected to the restriction of diffraction limit, and its resolving power is than often low two orders of magnitude of azimuthal resolution, and this has limited its range of application greatly.
In order to improve the transverse resolution of confocal microscope, Chinese scholars has also been carried out many research, and has proposed a series of research method and technology.Mainly contain spatial frequency lambda limiting process, iris filter method and the confocal method of 4PI.Recently, the DongKyun of Korea S University of Science and Technology (KAIST) proposed again a kind of novel relevant certainly confocal microscopy CSIM system based on two polarized light interferences (OPT.LETT.2003,28:2470-2472).Show that by numerical simulation the transverse resolution of the conventional relatively confocal microscope of the transverse resolution of this system has strengthened 38%.Although these methods and technology have certain effect to the transverse resolution that improves confocal microscope, but its transverse resolution is still limited, and these imaging systems are more complicated often, involve great expense, sometimes make when improving transverse resolution that the secondary lobe height increases, thereby reduced image quality.
Summary of the invention:
The objective of the invention is for overcoming the deficiency of above-mentioned prior art, provide a kind of transmissive multi-beam confocal interference microscope, to realize to carrying out the detection of high resolution micro-imaging in the fields such as microelectronics, material, the accurate detection of industry, biomedicine, life science with tens nanometer transverse resolution.
The transmissive multi-beam confocal interference microscope that the present invention has tens nanometer transverse resolution comprises light source 1, be successively placed on collimator and extender device 2, the polarization spectroscope 10 of light emitted end, be placed on quarter wave plate 11, microcobjective 4 on polarization spectroscope 10 reflected light paths, and collector lens on polarization spectroscope 10 transmitted light paths 6 and the pin hole 7 that is positioned at collector lens 6 focal positions, press close to the photodetector 8 of pin hole back, also comprise the multiple beam generator 12 that is placed between polarization spectroscope 10 and the collector lens 6.
Also comprise the telescope group 16 that is placed on 12 in polarization spectroscope 10 and multiple beam generator, the incident angle that is used to amplify the relative multiple beam generator 12 of incident light.
Comprise also being placed on the x-y two-dimentional work bench 13 of measuring the microcobjective front that the x-y two dimension that is used for sample moves.
Multiple beam generator wherein can be the device of parallel flat, clapboard or other all generation multiple beams.
Light source wherein can be a LASER Light Source, also can be general ordinary light source.
The present invention has following remarkable advantage:
1. significantly improve the transverse resolution of confocal interference microscope;
2. be total to light path can significantly improve system from relevant light path arrangement stability and antijamming capability;
3. multiple beam makes relevant multiple beam all from measured object surface same point, and forms approximate equal strength interference from the employing of coherent approach, can significantly improve the contrast of interference fringe, is convenient to detected with high accuracy.
4. compare from relevant confocal microscopy CSIM system with existing, apparatus of the present invention multiple-beam interference belongs to nonpolarized light and interferes, and has avoided like this adding analyzer before photodetector, has reduced the light path adjustment of introducing therefrom and the loss of system capacity.
Describe the present invention in detail below in conjunction with embodiment and accompanying drawing.
Description of drawings
Fig. 1 is the synoptic diagram of existing confocal interference microscope.
Fig. 2 is the synoptic diagram of the embodiment of the invention one.
Fig. 3 is the synoptic diagram of the embodiment of the invention two.
Fig. 4 is the horizontal normalized intensity response curve shown in confocal microscope, relevant certainly confocal microscopy CSIM system and the embodiment of the invention two.
Fig. 5 is the point spread function synoptic diagram of confocal microscopy mirror system.
Fig. 6 is the point spread function synoptic diagram of transmissive multi-beam confocal interference microscope CMTIM of the present invention system.
Wherein, 1 light source, 2 collimator and extender devices, 3 spectroscopes, 4 microcobjectives, 5 reference mirrors, 6 collector lenses, 7 pin holes, 8 photodetectors, 9 measured objects, 10 polarization spectroscopes, 111/4 wave plate, 12 multiple beam generators, the 13x-y two-dimentional work bench, 14 photodetector detector signal processing and amplifying systems, 15 computer measurement control system, 16 telescope groups, the horizontal normalized intensity response curve of 17 common confocal microscopes, 18 horizontal normalized intensity response simulation curves, the horizontal normalized intensity response simulation curve of 19 embodiment of the invention two based on the relevant certainly confocal microscopy CSIM system of two-beam interference.
Embodiment:
Basic thought of the present invention is that the multiple-beam interference technology is introduced in the confocal microscopy receiving light path system, produce multiple beam by the multiple beam generating means, and the condenser of multiple beam by confocal microscope system converged on the pin hole of confocal microscope system, multiple beam is produced interferes, utilize that the multiple-beam fringe width is narrow, characteristics such as good contrast and strong interference immunity, reach sharpening confocal microscope system Airy disk main lobe width, reach the purpose of improving confocal microscope system transverse super-resolution power then.
The structure of the embodiment of the invention one as shown in Figure 2, comprising light source 1, be successively placed on collimator and extender device 2, the polarization spectroscope 10 of light emitted end, be placed on quarter wave plate 11, microcobjective 4 on polarization spectroscope 10 reflected light paths, and be placed on multiple beam generator 12, the collector lens 6 on polarization spectroscope 10 transmitted light paths and be positioned at the pin hole 7 of collector lens 6 focal positions, and press close to the photodetector 8 of pin hole 7 back.Also comprise a detectable signal processing and amplifying system that links to each other with photodetector 8 14, a computer control system 15 and an x-y two-dimentional work bench 13, whole measuring process is controlled and is handled by computer measurement control system 15.
The structure of another embodiment of the present invention two as shown in Figure 3, different with embodiment one is to have added a telescope group 16 between polarization spectroscope 10 and multiple beam generator 12, its angle enlargement factor is M, be used to amplify the incident angle of incident ray, thereby increase the sensitivity of system with respect to parallel flat.
Among above-mentioned two embodiment, the multiple beam generator is selected parallel flat for use.
Major parameter among the embodiment two is as follows:
The reflectivity R=0.9 of parallel flat, thickness d=5mm, it places the pitch angle is 5.7296 °.Microcobjective is selected 40 * 0.7 common flat field achromatic micro objectives for use.The angular magnification M=20 of telescope group.
Below the transverse strength response characteristic of the embodiment of the invention two is carried out emulation, further specify its hyperresolution.
Fig. 4 has provided the horizontal normalized intensity response simulation curve 17,18 and 19 of common confocal microscope, CSIM and present embodiment two.As can be seen from the figure the half-shadow value width (FWHW) of its transverse response center curve is respectively 234nm, 145.6nm and 51nm.
Can be got by theoretical simulation: transmissive multi-beam confocal interference microscope of the present invention has improvement extremely significantly to the transverse resolution of confocal microscope system, reaches tens nanometer.
Below in conjunction with the accompanying drawings the specific embodiment of the present invention and simulated effect are described; but these explanations can not be understood that to have limited scope of the present invention; protection scope of the present invention is limited by the claims of enclosing, and any change of carrying out on claim of the present invention basis all is protection scope of the present invention.

Claims (5)

1. transmissive multi-beam confocal interference microscope with tens nanometer transverse resolution, comprise light source (1), be successively placed on the collimator and extender device (2) of light emitted end, polarization spectroscope (10), be placed on the quarter wave plate (11) on polarization spectroscope (10) reflected light path, microcobjective (4), and the collector lens (6) on polarization spectroscope (10) transmitted light path and be positioned at the pin hole (7) of collector lens (6) focal position, press close to the photodetector (8) of pin hole back, it is characterized in that also comprising the multiple beam generator (12) that is placed between polarization spectroscope (10) and the collector lens (6).
2. according to right 1 described transmissive multi-beam confocal interference microscope, it is characterized in that comprising the telescope group (16) that is placed between polarization spectroscope (10) and multiple beam generator (12), the incident angle that is used to amplify the relative multiple beam generator of incident light (12).
3. according to right 1 described transmissive multi-beam confocal interference microscope, it is characterized in that comprising the x-y two-dimentional work bench (13) that is placed on measurement microcobjective front.
4. according to right 1 described transmissive multi-beam confocal interference microscope, it is characterized in that light source (1) is LASER Light Source or general ordinary light source.
5. according to right 1 described transmissive multi-beam confocal interference microscope, it is characterized in that multiple beam generator (12) is parallel flat or clapboard.
CN 200510123582 2005-11-21 2005-11-21 Transmissive multi-beam confocal interference microscope with tens nanometer transverse resolution Pending CN1763504A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103105142A (en) * 2013-01-29 2013-05-15 哈尔滨工业大学 Long-working-distance skeleton measuring device based on fluorescence excitation of surface to be detected
CN104034268A (en) * 2014-07-01 2014-09-10 西安工业大学 Two-slit interference fringe decoding spectrum confocal displacement sensor and displacement measurement method thereof
CN105319195A (en) * 2015-11-30 2016-02-10 哈尔滨工业大学 Super-resolution structure detection array confocal fluorescence imaging device and imaging method thereof
CN106908012A (en) * 2017-02-24 2017-06-30 哈尔滨工业大学 Horizontal quick scanning confocal measurement apparatus and the optical element surface contour measuring method based on the device
CN107367487A (en) * 2017-06-12 2017-11-21 中国科学院苏州生物医学工程技术研究所 A kind of handheld portable disease of skin auxiliary detection device
CN107850555A (en) * 2015-06-30 2018-03-27 康宁股份有限公司 Roll-offed measurement using the interferometric method of static candy strip
CN112362592A (en) * 2020-10-30 2021-02-12 华中科技大学 Polarization reflection measurement system and detection method thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103105142A (en) * 2013-01-29 2013-05-15 哈尔滨工业大学 Long-working-distance skeleton measuring device based on fluorescence excitation of surface to be detected
CN103105142B (en) * 2013-01-29 2015-09-02 哈尔滨工业大学 Based on the long working distance contour outline measuring set of measured surface fluorescence excitation
CN104034268A (en) * 2014-07-01 2014-09-10 西安工业大学 Two-slit interference fringe decoding spectrum confocal displacement sensor and displacement measurement method thereof
CN107850555A (en) * 2015-06-30 2018-03-27 康宁股份有限公司 Roll-offed measurement using the interferometric method of static candy strip
CN105319195A (en) * 2015-11-30 2016-02-10 哈尔滨工业大学 Super-resolution structure detection array confocal fluorescence imaging device and imaging method thereof
CN106908012A (en) * 2017-02-24 2017-06-30 哈尔滨工业大学 Horizontal quick scanning confocal measurement apparatus and the optical element surface contour measuring method based on the device
CN107367487A (en) * 2017-06-12 2017-11-21 中国科学院苏州生物医学工程技术研究所 A kind of handheld portable disease of skin auxiliary detection device
CN112362592A (en) * 2020-10-30 2021-02-12 华中科技大学 Polarization reflection measurement system and detection method thereof

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