WO2004013915A1 - Detecteur optique, procede de fabrication et d'actionnement du detecteur optique, et procede de mesure de l'intensite lumineuse - Google Patents

Detecteur optique, procede de fabrication et d'actionnement du detecteur optique, et procede de mesure de l'intensite lumineuse Download PDF

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Publication number
WO2004013915A1
WO2004013915A1 PCT/JP2003/009577 JP0309577W WO2004013915A1 WO 2004013915 A1 WO2004013915 A1 WO 2004013915A1 JP 0309577 W JP0309577 W JP 0309577W WO 2004013915 A1 WO2004013915 A1 WO 2004013915A1
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Prior art keywords
optical sensor
layer
carbon nanotube
drain electrode
source electrode
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PCT/JP2003/009577
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English (en)
Japanese (ja)
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Yukihiro Sugiyama
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Sanyo Electric Co.,Ltd.
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Priority to JP2004525794A priority Critical patent/JP3933664B2/ja
Priority to AU2003252283A priority patent/AU2003252283A1/en
Publication of WO2004013915A1 publication Critical patent/WO2004013915A1/fr
Priority to US11/003,355 priority patent/US20050093425A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/60Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation in which radiation controls flow of current through the devices, e.g. photoresistors
    • H10K30/65Light-sensitive field-effect devices, e.g. phototransistors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K39/00Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group H10K30/00
    • H10K39/30Devices controlled by radiation
    • H10K39/32Organic image sensors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/20Carbon compounds, e.g. carbon nanotubes or fullerenes
    • H10K85/221Carbon nanotubes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

Definitions

  • the present invention relates to an optical sensor, a method for manufacturing and driving the optical sensor, and a method for detecting light intensity.
  • the present inventor has proceeded with the development of a sensor that uses a molecule that is polarized by light irradiation (hereinafter appropriately referred to as a photosensitive molecule) as a photodetection substance. If such photosensitive molecules can be used as the light detection part of an optical sensor, it is expected that optical information can be detected with high sensitivity and high accuracy.
  • a photosensitive molecule a molecule that is polarized by light irradiation
  • Bacteriorhodopsin a protein that constitutes the purple membrane (Purpiemmembrane) of halophilic bacteria together with lipids, is a photoreceptor protein and shows a differential response to light irradiation (Fig. 1).
  • the image recognition device described in Patent Document 1 uses the response of bacteriococcal dopsin for an image sensor that extracts the contour of a moving object, etc. It detects the induced current induced in the electrode. According to this image recognition device, since the induced current is detected, the noise is smaller than that of the image recognition device that detects the induced voltage. Thus, a signal can be detected even when the electrode is miniaturized. In addition, by using an alignment film of bacteriorhodopsin, it is possible to make the photodetector ultra-thin. it can.
  • Patent Literature 1 Japanese Patent Application Laid-Open No. 2000-002 6 7 2 2 3
  • Non-Patent Document 1 M e t o o d s i n En z y m o 1 o g y, 31, A, p p. 6 6 7-6 7 8 (1 9 7 4)
  • the signal due to the electric polarization of photosensitive molecules such as bacteriophage dopsin is small, and even when detecting the induced current, a sufficient induced current value is not necessarily obtained. Therefore, when using this signal as an optical sensor, amplification to obtain a sufficient current value may be necessary. Conventionally, since this amplification system requires a large-scale device, it was necessary to incorporate an optical sensor into a large-scale device.
  • an object of the present invention is to provide a small and highly sensitive optical sensor, a method for manufacturing and driving the optical sensor, and a method for detecting light intensity.
  • a substrate a source electrode and a drain electrode formed on the substrate; a carbon nanotube electrically connecting the source electrode and the drain electrode; and a carbon nanotube provided on the carbon nanotube.
  • polarization occurs in a layer in which polarization is generated by light reception, and an induced charge is generated.
  • the carbon nanotube has the property that the conductance changes depending on the strength of the electric field, and thus the induced charge triggers the change in the conductance of the carbon nanotube, and the current flowing between the source and drain electrodes. The value changes. By detecting the change in the current value, the intensity of the received light can be detected.
  • the electrode is minute.
  • a sufficient current value can be obtained.
  • the size of the optical sensor can be reduced. This makes it possible to increase the number of source and drain electrodes per unit area, that is, the number of pixels.
  • a step of forming a source electrode and a drain electrode on a surface of a substrate a step of connecting the source electrode and the drain electrode with a force-pont nanotube, Forming a layer in which polarization occurs, and a method for manufacturing an optical sensor.
  • the source electrode and the drain electrode are connected by the carbon nanotube, and a layer in which polarization occurs due to light reception is formed on the carbon nanotube. Therefore, it is possible to stably manufacture a high-precision, small-sized optical sensor having a large number of pixels.
  • a predetermined current is caused to flow between the source electrode and the drain electrode, and a change in the current value is detected.
  • the method for driving an optical sensor according to the present invention is characterized in that a predetermined current is flowing between a source electrode and a drain electrode, and the conductance of a carbon nanotube is changed according to the degree of polarization generated by light reception. It detects the change in the current value accompanying the current. The intensity of the received light is detected based on the magnitude of the change in the current value. Since the change in the current value is larger than when the polarization of the photosensitive molecule is directly detected, measurement with high sensitivity and high accuracy is possible.
  • a method for detecting light intensity using a layer including a layer polarized by light reception and a carbon nanotube provided in the vicinity of the layer comprising applying a voltage to the carbon nanotube, A light intensity detection method is provided, wherein a change in a current value in the carbon nanotube caused by light reception of the layer is detected, and a light intensity is detected from the change in the current value.
  • the layer that is polarized by light reception by light irradiation is separated. And induces induced charge. Triggered by this induced charge, the conductance of the carbon nanotube changes, and the current flowing through the carbon nanotube changes.
  • the light intensity can be detected by detecting the change in the current value. According to the method of the present invention, a relatively large change in current value can be obtained from a relatively small polarization signal, and the light intensity can be measured with high accuracy and sensitivity.
  • the layer polarized by the light reception may be configured to include pateriorhodopsin. This makes it possible to stably and reliably generate polarization in the layer that is polarized by light reception. Therefore, a light detection method with high accuracy and sensitivity can be provided.
  • an insulating layer may be provided on a surface of the carbon nanotube.
  • the insulating layer may be a polymer layer.
  • the polymer layer can be, for example, an organic polymer layer.
  • the insulating layer may be a layer in which a polymer is wound around a side surface of the carbon nanotube.
  • the coating layer can be a strong and stable layer. Therefore, the operation stability of the optical sensor can be improved, and the reliability can be improved.
  • the thickness of the coating layer can be reduced. For this reason, the conductance of the carbon nanotube can be more reliably changed.
  • the “polymer” refers to a molecule having a skeleton chain length sufficient to be wound around a carbon nanotube. Also, the polymer is carbon "Wound" on the side surface of the nanotube means that the molecular chain of the polymer wraps around the side surface of the tube and wraps around the surface of the carbon nanotube.
  • the step of forming an alignment film of carbon nanotubes may include a step of forming an insulating layer containing the coating molecules on a surface of the carbon nanotubes. By doing so, it is possible to reliably insulate the carbon nanotube from the layer polarized by light reception.
  • a polymer may be used as the coating molecule, and a polymer layer may be formed on the surface of the carbon nanotube. In this case, the coverage of the insulating layer can be improved. Therefore, the surface of the carbon nanotube can be more stably insulated.
  • the protein is modified by spreading the dispersion in which the protein is dispersed as the coating molecule on a liquid surface, and the modified protein is wound around a side surface of the carbon nanotube. May be.
  • a polymer can be wound on the surface of a carbon nanotube by a simple method. Therefore, the surface of the carbon nanotube can be coated by a simple method. Therefore, the insulating property of the surface of the carbon nanotube can be further ensured. .
  • the polymer can be a polypeptide.
  • the skeleton chain can be stably coated on the carbon nanotube.
  • the polypeptide may be a denatured protein.
  • the protein is denatured by using a protein as the polymer, and the dispersion is spread on a liquid surface to denature the protein.
  • the denatured protein is wound around a side surface of the carbon nanotube. Can be made.
  • the polypeptide may be a membrane protein. Since the membrane protein often has a region with high hydrophobicity, by using this, the protein can be efficiently adsorbed on the side surface of the carbon nanotube and can be stably wound.
  • the optical sensor of the present invention comprises: a substrate; a source electrode and a drain electrode formed on the substrate; a carbon nanotube for electrically connecting the source electrode and the drain electrode; And a layer in which polarization is generated by light reception. For this reason, a small signal due to polarization in the layer where polarization occurs due to light reception is used as a trigger, and a large electrical signal, that is, a change in the current value between the source and drain electrodes is obtained, and this change in the current value is detected. As a result, an optical sensor capable of detecting light with high accuracy and sensitivity and a driving method thereof are realized.
  • an optical sensor capable of stably manufacturing an optical sensor having high accuracy, sensitivity, small size, and a large number of pixels.
  • a voltage is applied to the carbon nanotube, a change in a current value in the carbon nanotube caused by light reception of the layer where polarization occurs due to light reception is detected, and the light intensity is determined from the change in the current value.
  • a relatively large change in the current value can be obtained from a relatively small polarization signal, and a light intensity detection method capable of measuring light intensity with high accuracy and sensitivity is realized.
  • Fig. 1 is a diagram showing light irradiation to pateriorhodopsin and its electrical response.
  • FIG. 2 is a sectional view showing an example of the optical sensor according to the embodiment.
  • FIG. 3 is a schematic diagram showing an example of the optical sensor according to the embodiment.
  • FIG. 4 is a cross-sectional view schematically showing a manufacturing process of the optical sensor according to the embodiment.
  • FIG. 5 is a perspective view schematically showing a part of the structure of the optical sensor according to the embodiment.
  • FIG. 6 is a diagram showing a method for producing an alignment film of carbon nanotubes.
  • FIG. 7 is a top view schematically showing a method of connecting a source electrode and a drain electrode using a carbon nanotube.
  • FIG. 8 is a cross-sectional view schematically illustrating a method of connecting a source electrode and a drain electrode using carbon nanotubes.
  • FIG. 9 is a cross-sectional view showing a method for producing a protein monolayer and a method for laminating the same.
  • FIG. 10 is a cross-sectional view showing a method for producing a denatured protein monolayer and a method for laminating the same.
  • FIG. 11 is a sectional view showing an example of the image recognition element according to the embodiment.
  • Fig. 12 is a diagram showing the electric polarization characteristics of bacteriorhodopsin by light irradiation.
  • FIG. 13 is a diagram schematically showing an output image of the image recognition element according to the embodiment.
  • Fig. 14 is a diagram showing a A-A plot of the LB film of the purple film.
  • FIG. 15 is a cross-sectional view schematically showing a connection method using a carbon nanotube for a source electrode and a drain electrode.
  • FIG. 16 is a diagram showing an example of the configuration of the electrode according to the embodiment.
  • Fig. 17 is a diagram showing an AFM image of an alignment film of carbon nanotubes using a purple film as a support.
  • Fig. 18 is a diagram showing an AFM image of an alignment film of carbon nanotubes produced without using a support.
  • FIG. 19 is a view illustrating a method of manufacturing a carbon nanotube structure according to an example.
  • FIG. 20 is a diagram showing a TEM image of the carbon nanotube structure according to the example.
  • FIG. 21 is a sectional view showing an example of the optical sensor according to the embodiment.
  • FIG. 22 is a cross-sectional view schematically showing a manufacturing process of the optical sensor according to the embodiment.
  • FIG. 23 is a top view schematically showing a method of connecting a source electrode and a drain electrode using carbon nanotubes.
  • FIG. 24 is a cross-sectional view schematically illustrating a method of connecting a source electrode and a drain electrode using a force-feed nanotube.
  • FIG. 25 is a cross-sectional view schematically illustrating a method of connecting a source electrode and a drain electrode using a carbon nanotube.
  • FIG. 26 is a sectional view showing an example of the image recognition element according to the embodiment. BEST MODE FOR CARRYING OUT THE INVENTION
  • FIG. 2 is a diagram showing an example of the configuration of the optical sensor according to the present invention.
  • a substrate 3 a source electrode 5 a and a drain electrode 5 b provided on the substrate 3, a carbon nanotube 7 connecting them, and an insulation formed on the carbon nanotube 7 It includes a layer 11 and a layer 13 which is formed on the insulating layer 11 and is polarized by light reception.
  • photosensitive molecules molecules that are polarized by light reception
  • the induced charge changes the conductance of the carbon nanotube 7, so that the current flowing between the source electrode 5a and the drain electrode 5b The value changes.
  • FIG. 3 is a diagram schematically showing how the conductance of the carbon nanotube 7 changes.
  • the electric charge generated by the photoelectric polarization of the photosensitive molecule changes the 7T electron field of the carbon nanotube 7, so that the conductance of the force tube 11 changes. Due to the change in the conductance of the carbon nanotube, the value of the current flowing through the carbon nanotube 7 changes.
  • the carbon nanotubes 7 are used to connect the source electrode 5 a and the drain electrode 5 b, and the carbon nanotubes 7 have a layer 13 on the upper side of which the polarization is generated by receiving light. The value of the current flowing between the source electrode 5a and the drain electrode 5b via the gate electrode changes.
  • a small signal by the photoelectric polarization of photosensitive molecules can be detected as a current value changes in the order of nano amperes (1 0 _ 9 A). Therefore, a high-sensitivity optical sensor that converts an optical signal into an electric signal can be provided.
  • the source electrode and the drain electrode are two-dimensionally arranged on the surface of the substrate.
  • the source and drain electrodes can be arranged as shown in FIG.
  • FIG. 16 is a diagram showing another example of the arrangement of the source electrode and the drain electrode.
  • the arrangement of FIG. 16 includes a first electrode 101 and a second electrode 102 provided to be spaced from the first electrode 101 and to surround the periphery of the first electrode 101. And.
  • One of the first electrode 101 and the second electrode 102 is a source electrode, and the other is a drain electrode. With such an electrode arrangement, it is relatively easy to connect the source electrode and the drain electrode with carbon nanotubes, and the productivity is improved.
  • an insulating layer may be provided between the carbon nanotube and a layer in which polarization is generated by light reception.
  • the insulating layer can mainly contain proteins. By doing so, the thickness of the insulating layer can be reduced, so that the polarization generated in the layer where polarization occurs due to light reception can effectively lead to a change in the conductance of the carbon nanotube.
  • the insulating layer may mainly contain denatured proteins.
  • the isolated layer contains modified bacteriorhodopsin.
  • a layer in which polarization is generated by light reception may be configured to mainly include molecules that are polarized by light reception.
  • a layer in which polarization is generated by receiving light may include a molecular alignment film that is polarized by receiving light.
  • the layer in which polarization is generated by light reception may be a layer containing oriented Bacterio-mouth dopsin.
  • Bacterial oral dopsin is a photosensitive molecule, has high structural stability among proteins, and accurately polarizes optical signals. Therefore, the accuracy and sensitivity of the optical sensor can be further improved. Further, the durability of the optical sensor can be improved.
  • an oriented purple membrane can be exemplified.
  • FIG. 3 is a schematic configuration diagram of an optical sensor using a purple film.
  • the layer 13 in which polarization occurs upon light reception is made of a purple membrane, and is composed of a photosensitive molecule, bacteriorhodopsin 41, and a lipid bilayer.
  • the protein monomolecular film 51 and the layer 13 where polarization is generated by light reception are appropriately illustrated in FIG. 2 including the case where the photosensitive molecule and other components are contained as described above. It is to be expressed in a way.
  • the layer in which the polarization is generated by the light reception is formed by the oriented pateriorhodopsi. 03009577
  • the sensitivity of the optical sensor can be improved.
  • the photosensitive molecule for example, a synthetic polymer having a photoelectric conversion function or a biological substance can be used.
  • a biological substance for example, a molecule having a porphyrin ring such as chlorophyll a can be used.
  • the carbon nanotube may be any of a single-walled carbon nanotube (SWCNT) and a multi-walled carbon nanotube (MWCNT).
  • SWCNT single-walled carbon nanotube
  • MWCNT multi-walled carbon nanotube
  • SWCNT having metallic properties has a property that conductance is easily changed by the surrounding electronic environment, and thus can be suitably used as a wiring member for electrically connecting a source electrode and a drain electrode.
  • FIGS. 2 and 3 show the optical sensor according to the present embodiment.
  • a source electrode 5a and a drain electrode 5b connected by a carbon nanotube 7 are provided on the substrate 3, and an insulating layer 11 is formed on the surface of the source electrode 5a and the drain electrode 5b connected by the carbon nanotube 7. Is formed.
  • the carbon nanotube 7 is SWCNT.
  • a protein monomolecular film 51 is provided as a layer 13 where polarization is generated by light reception.
  • a protective layer 15 is provided on the upper part of the layer 13 where polarization is generated by light reception.
  • the transparent conductive layer 17 and the transparent substrate 19 are provided on the protective layer 15. They are provided in order.
  • an offset voltage may be applied to the transparent conductive layer 17. In this case, for example, the substrate 3 can be grounded.
  • the optical sensor according to the present embodiment operates as follows. That is,
  • a current is not applied while a voltage is applied between the source electrode 5a and the drain electrode 5b.
  • the trigger signal in step II) may be used as a switch so that a current flows between the source electrode 5a and the drain electrode 5b. That is, it is assumed that no current flows when light is not received, and the current is turned on when light is received. By measuring this current value, the light intensity is detected.
  • the photoinduced charge of the photosensitive molecule is not taken out as it is as a detection signal, but is used as a trigger signal for changing the source-drain current. That is, the photo-induced charge of the photosensitive molecule is used as a trigger signal for a change in the conductance of the carbon nanotube disposed between the source and the drain, and the source electrode 5a and the drain electrode 5b changed by the trigger signal. It is configured so that the current value between them is detected.
  • the carbon nanotubes 7 used in the optical sensor of the present embodiment are single-walled carbon nanotubes (SWCNTs).
  • SWCNTs single-walled carbon nanotubes
  • the conductance significantly changes according to the surrounding electronic state. Accordingly, in the optical sensor of the present embodiment, more to connect the source electrode 5 a and the drain electrode 5 b by SWCNT, a signal by photoelectric polarization of photosensitive molecule, nanoampere (1 0- 9 A) current of about It can be detected as a change.
  • the sensitivity of the optical sensor can be improved as compared with the case where the photoelectron polarization of the photosensitive molecule is directly detected. Monkey,
  • the polarization speed (reciprocal of the delay time) of bacteriorhodopsin monotonically increases in accordance with the increase in the intensity of light applied to the optical sensor. . Also, as the intensity of the irradiated light increases, the drain current flowing through the carbon nanotube increases due to the polarization of bacteriorhodopsin.
  • multi-walled carbon nanotubes can be used as the carbon nanotubes 7.
  • MW CN T multi-walled carbon nanotubes
  • the substrate and the source electrode 5a and the drain electrode 5b can be composed of a semiconductor.
  • the optical sensor according to the present embodiment is manufactured by the following steps.
  • Step of forming source electrode 5 a and drain electrode 5 b on substrate 3 As shown in FIG. 4 (a), an electrode pair serving as source electrode 5 a and drain electrode 5 b is formed on one surface of substrate 3. To form When the source electrode 5 a and the drain electrode 5 b are two-dimensionally arranged on the surface of the substrate 3, for example, the configuration shown in FIG. 5 can be used.
  • the substrate 3 for example, an insulating material such as silicon, SiC, MgO, or quartz or a semiconductor material can be used.
  • Photolithography and dry etching or ⁇ A mask is formed by, for example, etching.
  • the source electrode 5a and the drain electrode 5b are formed by a method of bonding a thin metal plate on the substrate 3 provided with the mask, a method of depositing a metal on the substrate 3, a sputtering method, or the like.
  • the metal constituting the source electrode 5a and the drain electrode 5b include metals that can form carbides such as Ti and Cr, low-resistance metals such as Au, Pt, and Cu, and alloys thereof.
  • an Au—Cr alloy can be used.
  • a metal capable of forming a carbide since the contact resistance between the source electrode 5a and the drain electrode 5b and the carbon nanotube 7 can be reduced.
  • Au is preferable because it is a noble metal and has a low specific electric resistance.
  • the source electrode 5 a When a noble metal such as Au or Pt or a metal having a low affinity for carbon is used for the source electrode 5 a and the drain electrode 5 b, the source electrode 5 a Preferably, an adhesive layer containing a metal capable of forming a carbide such as Ti or Cr is provided on the surfaces of a and the drain electrode 5b.
  • a metal capable of forming a carbide such as Ti or Cr
  • an electrode in which a Ti layer is formed on Au can be used. By doing so, it is possible to reduce the contact resistance between the carbon nanotubes 7 and the source electrode 5a and the drain electrode 5b.
  • a method of forming the adhesive layer a method of depositing a metal capable of forming a carbide on the surfaces of the source electrode 5a and the drain electrode 5b can be cited.
  • the thickness of the source electrode 5a and the drain electrode 5b can be, for example, 0.5 nm or more and 100 nm or less.
  • the distance between the source electrode and the drain electrode of the source electrode 5 a and the drain electrode 5 b is appropriately designed according to the length of the carbon nanotube 7. For example, it is 50 nm or more and 10 tm or less.
  • the source electrode 5a and the drain electrode 5b provided on the surface of the substrate 3 are connected to the current detecting means via wiring from the back side of the substrate 3 as described later in the fifth embodiment. can do. By doing so, the current value flowing between each source electrode 5a and the drain electrode 5b can be detected. Can be
  • the source electrode 5a and the drain electrode 5b formed on the surface of the substrate are electrically connected by a carbon nanotube 7, as shown in FIG. 4B.
  • the carbon nanotubes 7, for example, those having a length of 50 nm or more and 10 nm or less can be used. Also, SWCNT or MWCNT can be used.
  • Examples of a method of connecting the source electrode 5a and the drain electrode 5b with the carbon nanotubes 7 include a method of attaching a carbon nanotube alignment film to the surface of the substrate 3 and a method of AFM (atomic force microscope). There is a method of moving the carbon nanotube 7 using a probe or the like, and a method of growing the carbon nanotube 7 horizontally on the substrate 3 from the side surfaces of the source electrode 5a and the drain electrode 5b.
  • a method for attaching an alignment film of carbon nanotubes to the surface of the substrate 3 will be described. Other methods will be described later in the third embodiment and the fourth embodiment.
  • the step of connecting the source electrode 5a and the drain electrode 5b with the carbon nanotubes 7 includes the step of forming an alignment film of the carbon nanotubes 7, and the step of connecting the alignment film of the carbon nanotubes 7 to the source electrodes 5a and 5b. Attaching to the surface of the substrate on which the drain electrode 5 is provided. After that, a step of selectively removing the carbon nanotubes 7 attached to regions other than the source electrode 5a, the drain electrode 5b, and the region between the source electrode 5a and the drain electrode 5b is performed.
  • the alignment film of the carbon nanotubes 7 can be manufactured as follows. First, carbon nanotubes 7 and proteins are dispersed in a dispersion medium. As the dispersion medium, an aqueous solution of an organic solvent or the like can be used. For example, a 33 v / VDMF (dimethylformamide) aqueous solution can be used.
  • the protein is a support that keeps the carbon nanotubes 7 oriented. You. As such a support, for example, purple membrane or doptic bacterium contained in purple membrane is used. Purple membranes can be isolated from halophilic bacteria such as Halobacterium salinar urn.
  • the method described in Methodsin Enzymo 1 ogy, 31, A, pp. 667-678 (1974) can be used.
  • An excessive amount of carbon nanotubes 7 is added to the dispersion of the support, and dispersed using an ultrasonic disperser or the like. Aggregates of carbon nanotubes 7 remaining in the dispersion are removed.
  • the dispersion of the carbon nanotubes 7 and the support obtained above is gently spread using a syringe or the like on the liquid surface of the lower layer liquid stretched in the water tank.
  • a monomolecular film of the carbon nanotube 7 is obtained.
  • Langmuir trough 61 is used as the water tank, and pure water adjusted to pH 3.5 with HC 1 is used as the lower layer liquid.
  • the monomolecular film of the carbon nanotube 7 is allowed to stand, and the protein is interfacially denatured by the interfacial tension of the lower layer solution.
  • the protein is interfacially denatured by the interfacial tension of the lower layer solution.
  • the bacteriorhodopsin in the purple membrane it is preferable to allow the bacteriorhodopsin in the purple membrane to stand at room temperature for 5 hours or more until the interface is denatured.
  • the aggregate of the denatured protein becomes a support for the carbon nanotubes 7, and the carbon nanotubes 7 can be maintained in an oriented state.
  • the monomolecular film in which the carbon nanotubes 7 are arranged substantially in parallel is obtained by compressing using a movable barrier 63 of Langmuir Trough as a partition plate.
  • FIG. 6 is an AFM photograph of the alignment film of carbon nanotubes 7, and each carbon nanotube 7 is shown in a white circle.
  • FIG. 17 is a diagram showing an AFM image of a carbon nanotube oriented film produced using a purple film as a support.
  • FIG. 18 is a diagram showing an AFM image when an alignment film of carbon nanotubes was similarly prepared without using a support.
  • a biomolecule visualization / measurement apparatus B MVM-X1 (Nano Scope IIIa manufactured by Digital Instruments) was used for AFM observation. Silicon single crystal (NCH) was used as a probe, and the measurement mode was tapping AFM. The measurement range was 4 mX 4 m (Z 10 nm).
  • the alignment film of the carbon nanotubes 7 thus obtained is attached to the electrode surface obtained in the step (i) by a horizontal attachment method.
  • the horizontal deposition method is a method in which the substrate is brought into contact with the liquid surface so that the substrate surface is horizontal to the alignment film on the water surface, and the substrate is pulled up, so that the alignment film on the water surface is attached to the surface of the substrate.
  • an alignment film of carbon nanotubes 7 is formed on the surface of the substrate 3 provided with the source electrode 5a and the drain electrode 5b.
  • FIGS. 7 (a) to 7 (f) correspond to the steps in FIGS. 8 (a) to 8 (f).
  • a source electrode 5a and a drain electrode 5b are formed on the surface of the substrate 3.
  • an insulating film 21 is formed on the surface of the carbon nanotube alignment film by using a plasma CVD method or the like.
  • the insulating film 2 for example, it can be used as S I_ ⁇ 2.
  • the thickness of the insulating film 21 can be, for example, not less than l nm and not more than 1 m.
  • a resist film 25 is formed on the substrate.
  • the insulating film 21 and the carbon nanotubes 7 where the resist film 25 is not applied are removed by a method such as dry etching or wet etching. .
  • the resist film 25 is removed using a solution that dissolves the resist film 25 without dissolving the insulating film 21.
  • the carbon nanotube 7 is provided between the source electrode 5a and the drain electrode 5b as shown in FIGS. 7 (f) and 8 (f), and unnecessary portions of the carbon nanotube 7 are removed.
  • the obtained substrate 3 is obtained.
  • the process (iii) can be performed without removing the insulating film 21, and a mask other than the insulator is applied.
  • the manufacturing method can be simplified as compared with the case in which it is performed.
  • annealing is performed as appropriate in the steps after FIG. 7 (b) and FIG. 8 (b).
  • carbide is formed at the interface between the carbon nanotubes 7 and the source electrode 5a and the drain electrode 5b, and electrical contact can be increased.
  • a mask is formed on the surface of the substrate 3 so that only the upper part of the electrode is used as an opening, and a metal layer serving as an electrode is further formed on each of the source electrode 5a and the drain electrode 5b.
  • the formation of the metal layer is gold
  • the method can be performed in the same manner as (i), such as a metal deposition method or a sputtering method. By doing so, the carbon nanotubes 7 connecting the source electrode 5a and the drain electrode 5b are sandwiched between the upper and lower metal layers, so that better electrical contact can be obtained. it can.
  • the source electrode 5a and the drain electrode 5b can be easily and efficiently connected by using the oriented monomolecular film of the carbon nanotubes 7. Then, as shown in FIG. 5, a set of the source electrode 5 a and the drain electrode 5 b is used as a pixel 9 to detect a current flowing between the pixels 9. Therefore, the pixel 9 can be miniaturized. For example, 100 million pixels Z cm 2 can be obtained.
  • Step of forming insulating layer 11 on carbon nanotubes 7 As shown in FIG. 4 (c), the carbon nanotubes formed on the source electrode 5a and the drain electrode 5b in the step (ii) An insulating layer 11 is formed on the surface of 7.
  • the insulating layer 11 As a method for forming the insulating layer 11, for example, there is a method in which a polymer such as polyimide is spin-coated on the surface of the substrate 3 on which the carbon nanotubes 7 are provided.
  • a film made of denatured protein is formed, and the film is attached to the surface of the substrate 3 provided with the source electrode 5a, the drain electrode 5b, and the carbon nanotube 7 on the surface by a horizontal attachment method or the like, and is insulated. It can also be used as layer 11.
  • An example of a membrane composed of denatured protein is a denatured membrane of bacteriorhodopsin.
  • a purple membrane containing bacteriorhodopsin can be used. The purple membrane can be isolated from a halophilic bacterium such as Halobacterium salinarum (Halobabacterium salinarum) as in the step (ii).
  • the purple membrane containing rhodopsin 341 is dispersed in a dispersion medium 342 to prepare a protein developing solution 350.
  • a dispersion medium 342 In a water tank filled with lower layer liquid 360? On the surface, spread it gently using a syringe 362 or the like. In the present embodiment, a Langmuir trough 361 is used as the water tank.
  • a 33 v / v% aqueous solution of dimethylformamide (DMF) can be used as the dispersion medium 342.
  • the lower layer solution 360 for example, pure water adjusted to pH 3.5 with HC1 can be used.
  • the protein monolayer obtained above the lower layer solution 360 By allowing the protein monolayer obtained above the lower layer solution 360 to stand for a predetermined time, the protein is interface-denatured by interfacial tension, and a denatured protein monolayer 352 is obtained. In the case of bacteriorhodopsin 341, it is better to leave it at room temperature for at least 5 hours.
  • the monomolecular film formed on the liquid surface of the lower layer liquid 360 is compressed until a predetermined surface pressure is reached.
  • bacteriorhodopsin 341 it is compressed, for example, to a surface pressure of 15 mNZm.
  • the surface pressure is a one-dimensional pressure and is expressed as the force per unit length.
  • the monomolecular film is formed in a sheet shape on the liquid surface of the lower layer liquid, and when compressed from the side, a one-dimensional force acts from the side of the film. At this time, the value obtained by dividing the force by the one-dimensional length in the lateral direction of the monolayer to which the force is applied is the surface pressure.
  • the modified protein monomolecular film 352 is attached to the surface of the substrate 3 obtained in the step (ii) by the horizontal attachment method. Further, by repeating the horizontal attachment method, the denatured protein monolayer 352 can be accumulated. By changing the number of accumulated layers, the thickness of the insulating layer 11 can be changed. For example, since the thickness of one layer of the denatured protein monolayer 352 is about 1.5 nm, the thickness of the insulating layer 11 can be set to a predetermined thickness in units of 1.5 nm.
  • (iv) Form a layer 13 on the insulating layer 11 where polarization occurs due to light reception.
  • a layer 13 in which polarization is generated by receiving light is formed on the surface of the insulating layer 11 obtained in the step (iii).
  • the layer 13 in which polarization is generated by light reception can be a monomolecular film or a stacked film of molecules in which polarization is generated by light reception.
  • the layer 13 in which polarization is generated by light reception can be, for example, a bacteriorhodopsin orientation film.
  • the bacteriorhodopsin alignment film is preferably used because it causes stable polarization upon receiving light.
  • purple membrane contains bacteriorhodopsin, which has relatively excellent durability, and is preferably used.
  • the purple membrane can be isolated from a halophilic bacterium such as Halobacterium salinarum (Ha1 ob ct ter i urn sa lin a urn) in the same manner as in the step (ii).
  • the step of forming the layer 13 in which polarization is generated by light reception includes the steps of: spreading a dispersion liquid containing molecules that are polarized by light reception on a liquid surface to form an alignment film of molecules that are polarized by light reception; and polarizing by light reception.
  • the step of attaching an alignment film of molecules that are polarized by light reception to the surface of the transparent substrate 19 will be described later in step (V).
  • a purple membrane containing bacteriorhodopsin 41 as a protein component is dispersed in a dispersion medium 42 to prepare a protein developing solution 50.
  • the obtained protein developing solution 50 is gently developed using a syringe 62 or the like on the liquid surface of a water tank filled with the lower layer solution 60.
  • a Langmuir trough 61 is used as a water tank.
  • bacteriorhodopsin 41 for example, a 33 vZv% dimethylformamide (DMF) aqueous solution is used as the dispersion medium 42. Can be.
  • DMF dimethylformamide
  • the lower layer solution 60 for example, an acidic solution such as an aqueous solution of hydrochloric acid having a pH of 3.5 can be used.
  • an acidic solution such as an aqueous solution of hydrochloric acid having a pH of 3.5
  • a protein monolayer 51 is obtained above the lower layer solution 60.
  • the orientation of the molecules forming the protein monolayer 51 becomes almost the same due to the effect of the interfacial tension of the lower layer solution 60.
  • the dispersion medium 42 is quiescent to volatilize. If a protein is used as the photosensitive molecule, set the standing time so that interface denaturation does not occur. For example, when using bacteriorhodopsin 41, the standing time is about 10 minutes.
  • the protein monomolecular film 51 formed on the liquid surface of the lower layer solution 60 is compressed until it reaches a predetermined surface pressure.
  • bacteriorhodopsin 41 for example, compress at a compression rate of 20 cm 2 / min until the surface pressure reaches 15 in NZm.
  • a monomolecular film is attached to the surface of the insulating layer 11 by a horizontal attachment method.
  • a horizontal attachment method For example, when bacteriorhodopsin is used, the thickness of one monolayer is about 5 nm.
  • a monomolecular film can be laminated on the surface of the insulating layer 11.
  • each time one layer is laminated rinse with pure water and dry under N 2 gas atmosphere.
  • the thickness of the layer 13 where polarization occurs due to light reception can be changed, so that the sensitivity of the optical sensor can be adjusted.
  • C i is an index relating to the initial concentration of bacteriophage dopsin in the protein monolayer 51
  • 11.5 nm 2 is the area per one molecule of bacteriophage dopsin obtained by X-ray diffraction.
  • a transparent conductive layer 17 and a protective layer 15 are provided in this order on one surface of the transparent substrate 19.
  • a transparent material such as resin or glass can be used.
  • a light-transmitting conductive layer such as indium tin oxide (ITO) can be used.
  • ITO indium tin oxide
  • the protective layer 15 for example, a transparent insulating material such as glass, resin, or a denatured protein film same as the insulating layer 11 can be used.
  • the conductance of the carbon nanotube 7 changes due to the polarization due to the light reception of the protein molecule, and the current flowing between the source electrode 5a and the drain electrode 5b changes. . By detecting this change, the presence / absence and intensity of light reception can be detected.
  • the value of the current flowing between the source electrode 5a and the drain electrode 5b is larger than that of the signal due to the polarization due to the light reception of the protein molecule, which is necessary for the conventional optical sensor. It is not necessary to connect to the large-sized amplifying device.
  • the layer 13 in which polarization is generated by receiving light is a thin film of a photosensitive molecule, and therefore, is thin and has high sensitivity. Since a pair of the source electrode 5a and the drain electrode 5b connected by the carbon nanotubes 7 are used as the pixels 9, the number of pixels per unit area is high (FIG. 5). Further, the optical sensor according to the present embodiment is an element that converts an optical signal into an electric signal, and can change a current value between the source electrode and the drain electrode by light irradiation.
  • the source electrode and the drain electrode are formed two-dimensionally on the substrate surface as shown in FIG. 5, but they may be formed so as to be arranged in a line.
  • Such a one-dimensional optical sensor can be used, for example, for non-contact dimension measurement, position measurement, facsimile pattern reading, and the like.
  • step of connecting the source electrode 5a and the drain electrode 5b with the carbon nanotubes 7 may be performed by the following method.
  • a force is applied to the substrate 3 on which the source electrode 5a and the drain electrode 5b are provided.
  • the alignment film of the carbon nanotube 7 is adsorbed.
  • a resist film 25 having openings above the source electrode 5a and the drain electrode 5b is formed.
  • the resist film 25 can be formed by, for example, a photoresist method.
  • a metal layer 27 is formed on the entire substrate on which the resist film 25 is provided.
  • the metal layer 27 is appropriately selected from metals or alloys used for the source electrode 5a and the drain electrode 5b.
  • the metal layer 27, the source electrode 5a, and the drain electrode 5b may use the same metal or different metals.
  • the formation of the metal layer can be performed in the same manner as (i) production of the source electrode 5a and the drain electrode 5b on the substrate 3, such as a metal vapor deposition method and a sputtering method.
  • the resist film 25 is removed with a stripper.
  • the metal layer 27 provided on the surface of the resist film 25 other than the upper portions of the source electrode 5a and the drain electrode 5b is removed.
  • the source electrode 5a or the drain electrode 5b and the metal layer 27 are provided on the upper and lower portions of the carbon nanotube 7, respectively.
  • the contact between the carbon nanotubes 7 and the metal constituting each electrode can be further improved. Therefore, the contact resistance between the carbon nanotube 7 and the source electrode 5a and the drain electrode 5b can be reduced, and the value of the current flowing between the source electrode 5a and the drain electrode 5b can be increased.
  • step of connecting the source electrode 5a and the drain electrode 5b with the carbon nanotubes 7 may be performed by the following method.
  • a dispersion of the carbon nanotube 7 is applied to the substrate 3 provided with the source electrode 5a and the drain electrode 5b.
  • a method in which the carbon nanotube 7 is moved to a predetermined position using an AFM probe or the like may be used.
  • the carbon nanotube 7 can be more precisely arranged between the source electrode and the drain electrode.
  • step of connecting the source electrode 5a and the drain electrode 5b by the carbon nanotube 7 may be performed by the following method.
  • the catalyst metal is not particularly limited as long as it serves as a catalyst for the growth of carbon nanotubes.
  • a metal containing at least one of Fe, Co, and Ni is preferably used.
  • An alloy such as Fe—Ni alloy or Ni—Co alloy may be used.
  • vapor deposition, lithography, sputtering, patterning using a solution of the catalyst metal, or the like can be performed. At this time, it is effective to appropriately adjust the deposition temperature, the substrate material, the method of depositing the catalyst metal, and the like. Further, the catalyst metal can be patterned by, for example, a lift-off method.
  • a film formed by a chemical vapor deposition method is preferably used as a method for growing carbon nanotubes in a horizontal direction on a substrate with a catalyst metal as a growth starting point.
  • CVD method a plasma CVD method, a thermal CVD method, or the like can be used.
  • a plasma CVD method capable of growing carbon nanotubes at a relatively low temperature is preferably used.
  • Source gases used for growth by the CVD method include saturated hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, and cyclohexane; and unreacted gases such as ethylene, acetylene, propylene, benzene, and toluene.
  • saturated hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, and cyclohexane
  • unreacted gases such as ethylene, acetylene, propylene, benzene, and toluene.
  • Saturated hydrocarbons; raw materials containing oxygen such as acetone, methanol, ethanol, carbon monoxide, or carbon dioxide; raw materials containing nitrogen such as benzonitrile; these may be used alone or in combination of two or more. it can.
  • the carrier gas flowing into the reactor together with the raw material gas for example, hydrogen or helium can be used, but its use is not essential.
  • the source electrode and the drain electrode can be connected by the carbon nanotube. Thereafter, an electrode can be formed on the carbon nanotubes by appropriately bonding a metal plate to the electrode surface or vapor-depositing a metal. By doing so, the carbon nanotube and the source electrode and the drain electrode are more appropriately bonded, so that the contact resistance can be reduced.
  • an alignment film of carbon nanotubes is formed, and the source electrode 5a and the drain electrode 5b are connected by a carbon nanotube.
  • the support component is wound around the surface of the carbon nanotube to have a uniform thickness. It was found that a coating was formed.
  • FIG. 21 is a diagram showing a configuration of the optical sensor of the present embodiment.
  • the basic configuration of the optical sensor of FIG. 21 is the same as that of the sensor of the first embodiment (FIG. 2).
  • the same components as those of the nanocarbon manufacturing apparatus 125 described in the first embodiment are denoted by the same reference numerals, and description thereof will be omitted as appropriate.
  • the optical sensor of FIG. 21 has a carbon nanotube structure composed of a carbon nanotube 105 whose surface is coated with a modifying molecule 125 instead of the carbon nanotube 7 of the optical sensor described in the first embodiment.
  • the optical sensor of FIG. 2 is different from the optical sensor of FIG. 2 in that it has a body 131, and does not have an insulating layer 11 between the force-feeding nanotube 7 and a layer 13 in which polarization is generated by light reception.
  • the optical sensor shown in FIG. 21 schematically shows a state in which the modifying molecule 1229 is wound around the surface of the carbon nanotube 105 to form an insulating layer. Covers the surface of the carbon nanotubes 105 uniformly. Further, the insulating layer only needs to uniformly cover the surface of the carbon nanotube 105, and is not limited to a mode wound around the carbon nanotube 105.
  • FIG. 22 is a cross-sectional view showing a manufacturing process of the optical sensor of FIG.
  • the source electrode 5a and the drain electrode 5b are formed on the substrate 3 (FIG. 22 (a)).
  • the source electrode 5a and the drain electrode 5b are connected by the carbon nanotube structure 13 1 (FIG. 22 (b)), and a layer 13 on which polarization occurs due to light reception is formed thereon (FIG. 22 (b)).
  • Figure 22 (c) a laminate is formed by joining the substrate 3 and the transparent substrate 19 (FIG. 22 (e)).
  • a transparent conductive layer 17 and a protective layer 15 are provided in this order (FIG. 22 (d)).
  • the optical sensor shown in FIG. 21 is obtained.
  • the method described in the first embodiment can be used for forming the source electrode 5a and the drain electrode 5b on the substrate 3 (FIG. 22A).
  • connection of the source electrode 5a and the drain electrode 5b by the carbon nanotube structure 13 1 was obtained by forming an alignment film of the carbon nanotube structure 13 1. After the alignment film is attached to the surface of the substrate 3 and unnecessary portions of the carbon nanotube structure 131 are removed, the modifying molecules 129 on the source electrode 5a and the drain electrode 5b are removed. This method will be described later.
  • the alignment film of the carbon nanotube structure 13 1 is manufactured by using the method described in the first embodiment (FIG. 6).
  • the thickness of the insulating layer covering the carbon nanotube 105 is For example, it can be 0.1 nm or more and 100 nm or less, and preferably 10 nm or less. By doing so, the thickness of the insulating layer can be reduced. For this reason, the conductance change of the carbon nanotube 105 due to the induced charge generated by the polarization of the layer 13 where the polarization is generated by the light reception can be increased. Therefore, an optical sensor with higher sensitivity can be obtained.
  • the alignment film is attached to the surface of the substrate 3 by a method such as a horizontal attachment method.
  • FIGS. 23 (a) to 23 (e) are top views of the respective steps, and the corresponding sectional views are FIGS. 24 (a) to 24 (e).
  • FIGS. 23 (b) and 24 (b) show the structure of the carbon nanotube structure 1 on the substrate 3 (FIGS. 23 (a) and 24 (a)) on which the source electrode 5a and the drain electrode 5b are formed.
  • FIG. 3 is a diagram showing a state in which an alignment film of No. 31 is adsorbed.
  • Patterning was performed to remove only the carbon nanotube structure 131 adsorbed to unnecessary portions, leaving only the carbon nanotube structure 131 adsorbed above the source electrode 5a and the drain electrode 5b and between the electrodes.
  • a resist film 25 is formed (FIGS. 23C and 24C).
  • the carbon nanotube structure 131 in a region not having the resist film 25 on the upper portion is removed (FIGS. 23D and 24D).
  • the resist film 25 is removed using a solution that dissolves the resist film 25 without dissolving the modifying molecules 129 and the carbon nanotubes 105 (FIGS. 23 (e) and 24 (e)).
  • FIG. 25 is a cross-sectional view showing a step of removing the modifying molecule 129 on the electrode.
  • the source electrode 5a and the drain electrode are formed on the entire surface of the substrate 3 (Fig. 25 (a)) from which the unnecessary carbon nanotube A resist film 31 having an opening at the top of the electrode 5b is formed (FIG. 25 (b)). As a result, both ends of the carbon nanotube structure 13 1 are exposed.
  • the carbon nanotubes 105 have no coating only on the electrodes.
  • Oxygen plasma can be used for atshing.
  • a plasma of nitrogen or a nitrogen-containing gas can be used.
  • the resist film 31 is removed using a solution that dissolves the resist film 31 without dissolving the carbon nanotubes 105 (FIG. 25 (d)).
  • the modifying molecule 129 on the electrode is removed.
  • the electrical connection between the carbon nanotube 105 and the electrode can be improved by removing the modifying molecule 125 on the electrode.
  • annealing is performed as appropriate in the steps after FIG. 23 (b) and FIG. 24 (b), for example, under vacuum.
  • a carbide is formed at the interface between the source electrode 5a and the drain electrode 5b and the carbon nanotube 105, thereby increasing electrical contact.
  • a mask is formed on the surface of the substrate 3 so that only the upper part of the electrode is an opening, and a metal layer to be an electrode is further formed on each of the source electrode 5a and the drain electrode 5b. You can also. By doing so, a structure in which the source nanotube 105 connecting the source electrode 5a and the drain electrode 5b is sandwiched between the upper and lower metal layers is obtained. Therefore, the electrical contact can be further improved.
  • a thin insulating film may be formed on the source electrode 5a and the drain electrode 5b by applying a mask on the surface of the substrate 3 so that only the upper part of the electrode is an opening. This can prevent direct contact between the source electrode 5a, the drain electrode 5b, and the carbon nanotube 105 exposed on these electrodes and the layer 13 where polarization occurs due to light reception. Also, as mentioned above, Even if a metal layer serving as an electrode is further formed on each of the source electrode 5a and the drain electrode 5b, the metal layer and the layer 13 where polarization occurs due to light reception should not be in direct contact. it can. Therefore, the accuracy of the optical sensor can be further improved.
  • the modifying molecule 129 is wound around the outer periphery of the side surface of the carbon nanotube 105, the modifying molecule 129 is evenly distributed on the surface of the carbon nanotube structure 131. Insulating film is formed. Therefore, without forming an insulating film on the carbon nanotube 105, it is possible to attach the layer 13 where polarization is generated by direct light reception on the carbon nanotube structure 131. . Therefore, it is possible to stably supply an optical sensor having a simpler configuration.
  • the insulating layer on the surface of the carbon nanotube 105 that is, the layer of the modifying molecule 125 is uniform on the surface of the carbon nanotube 105 as a thin film having a thickness of, for example, about 0.1 nm or more and 100 nm or less. Is formed. For this reason, the polarization in the layer 13 where the polarization occurs due to the light reception is ensured while the insulation between the layer 13 where the polarization occurs due to the light reception and the carbon nanotube 105 is ensured. It can be accurately converted to a change in conductance.
  • the periphery of the carbon nanotube 105 is covered with the modifier molecule 129 with a uniform thickness, the operation stability of the optical sensor is improved.
  • such a coating of the modifying molecule 129 suppresses the influence of the surrounding water from affecting the conductivity of the carbon nanotube 105. Therefore, the accuracy and sensitivity of the optical sensor can be further improved.
  • the optical sensor according to the present embodiment has a configuration in which a plurality of electrode pairs including a source electrode and a drain electrode are two-dimensionally arranged on a substrate surface.
  • the structure of each sensor unit is the same as in the first embodiment.
  • the optical sensor of the present embodiment can be suitably applied to an image recognition element, an image sensor of a television camera, and the like.
  • an example in which the optical sensor according to the present embodiment is used as an image recognition element will be described. I will tell.
  • FIG. 11 shows an image recognition element 100 according to the present embodiment.
  • the image recognition device 100 shown in FIG. 11 is manufactured in the same manner as in the first embodiment.
  • single crystal silicon is used for the substrate 3.
  • a purple film is used for the layer 13 where polarization is generated by light reception.
  • a protein monomolecular film 51 containing bacteriorhodopsin 41 and lipid is obtained, and this is laminated to form a layer 13 in which polarization is generated by light reception.
  • a purple film is used for the insulating layer 11.
  • the current value flowing through the source electrode 5a and the drain electrode 5b of each pixel 9 is detected by the current detecting means 23. Therefore, the resolution is high and the sensitivity is high.
  • a difference image obtained by calculating a temporary difference between consecutive frame images of an image acquired by an input device such as a CCD is used.
  • This method is hereinafter referred to as the “de-one-time difference method”.
  • the overnight difference method takes advantage of the fact that the difference between two consecutive frame images is generally due to the portion of the image that corresponds to the contour of the moving object.
  • the contour data of the moving object extracted by the data difference method depends on the background image data of the moving object. In other words, even if the light intensity of the moving object is constant, if the light intensity of the background around the moving object changes, the contour data, which is the difference value, will not be constant. For this reason, it was difficult to detect the contour with high accuracy under the condition where the light intensity of the background image changes.
  • the image recognition element 100 according to the present embodiment can extract the outline of the moving object without taking a data difference, as described below.
  • FIG. 13 shows an output image obtained by the image recognition element when a moving image including a moving object is irradiated on the image recognition element 100 in FIG.
  • 1 1 1 is the input image at time t
  • 1 13 is the straight line ⁇ of the output image for the input image at t.
  • the output current value of each is shown.
  • the output current values on the straight line A ⁇ in the image are shown.
  • the induced current value corresponding to the contour on the front side in the moving direction is a predetermined constant value (+8 in Figs. 13 (a) and 13 (b)) corresponding to the light intensity of the moving object.
  • the induced current value corresponding to the portion of the moving object that is no longer irradiated with light, that is, the contour on the rear side in the moving direction of the moving object is a predetermined constant value according to the light intensity of the moving object (see FIG. In 1 3 (b), it is 1 5).
  • the induced current value of the contour is constant. Further, the induced current value corresponding to the portion of the moving object that has been continuously irradiated with light and the portion that has been no longer irradiated becomes zero with the passage of time.
  • the in-contour image of the moving object extracted by the image recognition element 100 of the present embodiment is a real image. For this reason, even if the background of the input moving image is a complicated image with a pattern or the like, only the outline of the moving object in the moving image can be extracted and does not depend on the background image. Further, by searching for the contour of the moving object, the moving direction of the object can be extracted.
  • the image recognition element 100 of the present embodiment since the pixels 9 are minute, the number of pixels per unit area can be increased to about 100 million. Therefore, the contour of the moving object can be extracted more precisely.
  • the pixel 9 constituting the image recognition element 100 of the present embodiment has a current value flowing between the source electrode 5a and the drain electrode 5b due to a change in the conductance of the carbon nanotube 7 due to the polarization of the bacterial rhodopsin 41. Therefore, the change in the current value is relatively large, and the contour of the moving object can be detected with high sensitivity.
  • FIG. 26 is a diagram showing the image recognition element 29.
  • the same components as those of the image recognition element 100 described in the first embodiment are denoted by the same reference numerals, and the description will be appropriately omitted.
  • the modification molecule 1 29 is coated around the carbon nanotube 105 in a similar manner.
  • a thin insulating layer of a modified molecule 129 is formed around the carbon nanotube structure 13 1. Therefore, polarization can be generated accurately and stably in the protein monomolecular film 51 without providing the insulating layer 11 between the layer 13 where polarization is generated by light reception and the carbon nanotube 105. .
  • a purple film can be used for the layer 13 in which polarization is generated by light reception.
  • the method described in the fifth and sixth embodiments can be used for manufacturing the image recognition element 29.
  • FIG. 19 is a diagram showing a method for manufacturing such a carbon nanotube structure 1 17.
  • a purple membrane containing pacteriorhodopsin 102 was dispersed in a dispersion medium (FIG. 19 (a)).
  • a purple membrane or a bacteriococcal dopsin 102 contained in the purple membrane can be used.
  • Purple membranes can be isolated from halophilic bacteria, such as Halobacterium um salinar um.
  • the method described in Methodsin Enzymology, 31, A, p. 667-678 (1974) was used.
  • As the dispersion medium 103 a 33 vZv% DMF (dimethylformamide) aqueous solution was used.
  • 33 vZv% DMF dimethyl Formamide
  • pacteriorhodopsin 102 To the dispersion of pacteriorhodopsin 102 was added an excess amount of force-pon nanotube 105, and the dispersion was performed for at least 1 hour using an ultrasonic disperser (Fig. 19 (b)). After the dispersion, remaining aggregates of carbon nanotubes 105 were removed.
  • As the carbon nanotube a multi-layer carbon nanotube manufactured by MTR Ltd. (Closeddendtpepe, diameter: 10 to 200 nm, purification purity: about 95%) was used.
  • the thus obtained dispersion liquid 107 (FIG. 19 (c)) was gently spread on the liquid surface of the lower liquid liquid 111 set in the water tank using the syringe 109 (FIG. 19 (d)). As a result, a monomolecular film of carbon nanotube 105 was obtained.
  • Langmuir Trough 113 was used as the water tank, and pure water adjusted to pH 3.5 with HC1 was used as the lower layer liquid 111.
  • the monomolecular film of the carbon nanotube 105 was allowed to stand still, and the bacteriorhodopsin 102 was interfacially denatured by the interfacial tension of the lower solution 111.
  • the membrane In the case of using purple membrane, it is preferable to leave the membrane at room temperature for 5 hours or more until bacteriorhodopsin in the purple membrane is interface-denatured. . In this way, the modified bacteriorhodopsin 115 is wound around the side surface of the force-feeding nanotube 105 (Fig. 19 (f)).
  • FIG. 20 is a view showing a TEM image of the carbon nanotube structure 1 17.
  • a layer of denatured bacterial mouth dopsin 115 was uniformly formed on the surface of carbon nanotube 105.
  • the layer thickness was about 3 nm.
  • bacteriorhodopsin 102 and carbon nanotubes 105 were dispersed and developed on a liquid surface by a simple method.
  • a carbon nanotube structure 1 17 was successfully produced.
  • An optical sensor can be stably manufactured by attaching the obtained carbon nanotube structure 117 on a substrate.

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Abstract

L'invention concerne un détecteur optique utilisant des molécules polarisées lors de la réception de lumière, une paire d'électrode source (5a) et d'électrode de drain (5b) disposées sur un substrat étant électriquement connectées l'une à l'autre au moyen d'un nanotube de carbone (7). Lorsque des molécules photosensibles constituant une couche (13) pouvant être polarisée par la lumière reçue sont polarisées par cette dernière, la conductance du nanotube de carbone (7) se modifie. Cette modification de la conductance permet de changer la valeur du courant circulant entre l'électrode source (5a) et l'électrode de drain (5b), ce qui permet de détecter le changement du courant. La fabrication d'un film orienté du nanotube de carbone (7) permet de rendre la connexion entre l'électrode source (5a) et l'électrode de drain (5b) facile et excellente. L'invention porte aussi sur un détecteur optique petit et présentant une précision et une sensibilité élevées, sur des procédés de fabrication et d'actionnement d'un détecteur optique, et sur un procédé de mesure de l'intensité lumineuse.
PCT/JP2003/009577 2002-08-01 2003-07-29 Detecteur optique, procede de fabrication et d'actionnement du detecteur optique, et procede de mesure de l'intensite lumineuse WO2004013915A1 (fr)

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JP2004525794A JP3933664B2 (ja) 2002-08-01 2003-07-29 光センサ、光センサの製造方法および駆動方法、ならびに光強度検出方法
AU2003252283A AU2003252283A1 (en) 2002-08-01 2003-07-29 Optical sensor, method for manufacturing and driving optical sensor, and method for measuring light intensity
US11/003,355 US20050093425A1 (en) 2002-08-01 2004-12-06 Optical sensor, method of manufacturing and driving an optical sensor, method of detecting light intensity

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005008787A1 (fr) * 2003-07-18 2005-01-27 Japan Science And Technology Agency Capteur optique
JP2005229019A (ja) * 2004-02-16 2005-08-25 Univ Nagoya カーボンナノチューブに対する電極の形成方法及びそれを用いたカーボンナノチューブfet
WO2005117251A1 (fr) * 2004-05-25 2005-12-08 Gennady Mikhailovich Mikheev Dispositif optoelectronique
JP2007022873A (ja) * 2005-07-20 2007-02-01 National Institute Of Advanced Industrial & Technology 水分散性蛋白質−カーボンナノチューブ複合体、その製造方法及びその用途
JP2007043150A (ja) * 2005-07-29 2007-02-15 Interuniv Micro Electronica Centrum Vzw 細長いナノ構造体を有する波長センシティブ検出器
WO2008023373A2 (fr) * 2006-08-22 2008-02-28 Ramot At Tel Aviv University Ltd. Dispositif optoélectronique et son procédé de fabrication
US7524929B2 (en) 2005-02-22 2009-04-28 Ramot At Tel Aviv University Ltd. Optoelectronic device and method of fabricating the same
JP2010040783A (ja) * 2008-08-05 2010-02-18 Sony Corp 光電変換装置及び光電変換素子
JP2010232683A (ja) * 2010-07-05 2010-10-14 Sony Corp 光電変換装置及び光電変換素子
WO2011052781A1 (fr) * 2009-11-02 2011-05-05 株式会社村田製作所 Élément de conversion photoélectrique et dispositif de conversion photoélectrique
CN101656298B (zh) * 2008-08-19 2012-06-13 鸿富锦精密工业(深圳)有限公司 红外探测器
KR101216124B1 (ko) 2004-02-20 2012-12-27 유니버시티 오브 플로리다 리서치 파운데이션, 인크. 반도체 장치 및 나노튜브 접촉부 이용 방법
US8624227B2 (en) 2005-02-22 2014-01-07 Ramot At Tel-Aviv University Ltd. Optoelectronic device and method of fabricating the same
TWI427277B (zh) * 2008-08-29 2014-02-21 Hon Hai Prec Ind Co Ltd 紅外探測器
KR101439407B1 (ko) * 2013-05-20 2014-09-15 한국과학기술연구원 광수용체 단백질 기반 분광광도계, 이의 제조 방법 및 이를 이용한 광 검출 방법

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06294682A (ja) * 1993-04-12 1994-10-21 Fuji Photo Film Co Ltd 光電変換素子
US5438192A (en) * 1993-12-09 1995-08-01 The United States Of America As Represented By The Secretary Of The Army Photodynamic protein-based photodetector and photodetector system for image detection and processing
JP2000156423A (ja) * 1998-11-18 2000-06-06 Internatl Business Mach Corp <Ibm> 電界効果トランジスタを含む超小型電子素子
JP2000267223A (ja) * 1999-03-17 2000-09-29 Sanyo Electric Co Ltd 光情報処理素子
WO2002054505A2 (fr) * 2001-01-03 2002-07-11 International Business Machines Corporation Systeme et procede de fragmentation par induction electrique de nanostructures
JP2002334986A (ja) * 2001-03-08 2002-11-22 Sanyo Electric Co Ltd 光透過型画像認識素子および画像認識センサ

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06294682A (ja) * 1993-04-12 1994-10-21 Fuji Photo Film Co Ltd 光電変換素子
US5438192A (en) * 1993-12-09 1995-08-01 The United States Of America As Represented By The Secretary Of The Army Photodynamic protein-based photodetector and photodetector system for image detection and processing
JP2000156423A (ja) * 1998-11-18 2000-06-06 Internatl Business Mach Corp <Ibm> 電界効果トランジスタを含む超小型電子素子
JP2000267223A (ja) * 1999-03-17 2000-09-29 Sanyo Electric Co Ltd 光情報処理素子
WO2002054505A2 (fr) * 2001-01-03 2002-07-11 International Business Machines Corporation Systeme et procede de fragmentation par induction electrique de nanostructures
JP2002334986A (ja) * 2001-03-08 2002-11-22 Sanyo Electric Co Ltd 光透過型画像認識素子および画像認識センサ

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
MARTEL R. ET AL.: "Single- and multi-wall carbon nanotube field-effect transistors", APPLIED PHYSICS LETTERS, vol. 73, no. 17, 26 October 2000 (2000-10-26), pages 2447 - 2449, XP000996900 *

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005008787A1 (fr) * 2003-07-18 2005-01-27 Japan Science And Technology Agency Capteur optique
JP2005229019A (ja) * 2004-02-16 2005-08-25 Univ Nagoya カーボンナノチューブに対する電極の形成方法及びそれを用いたカーボンナノチューブfet
KR101216124B1 (ko) 2004-02-20 2012-12-27 유니버시티 오브 플로리다 리서치 파운데이션, 인크. 반도체 장치 및 나노튜브 접촉부 이용 방법
WO2005117251A1 (fr) * 2004-05-25 2005-12-08 Gennady Mikhailovich Mikheev Dispositif optoelectronique
US8212005B2 (en) 2005-02-22 2012-07-03 Ramot At Tel-Aviv University Ltd. Optoelectronic device and method of fabricating the same
US7524929B2 (en) 2005-02-22 2009-04-28 Ramot At Tel Aviv University Ltd. Optoelectronic device and method of fabricating the same
US8624227B2 (en) 2005-02-22 2014-01-07 Ramot At Tel-Aviv University Ltd. Optoelectronic device and method of fabricating the same
JP2007022873A (ja) * 2005-07-20 2007-02-01 National Institute Of Advanced Industrial & Technology 水分散性蛋白質−カーボンナノチューブ複合体、その製造方法及びその用途
JP2007043150A (ja) * 2005-07-29 2007-02-15 Interuniv Micro Electronica Centrum Vzw 細長いナノ構造体を有する波長センシティブ検出器
WO2008023373A2 (fr) * 2006-08-22 2008-02-28 Ramot At Tel Aviv University Ltd. Dispositif optoélectronique et son procédé de fabrication
WO2008023373A3 (fr) * 2006-08-22 2008-06-26 Univ Ramot Dispositif optoélectronique et son procédé de fabrication
TWI400809B (zh) * 2008-08-05 2013-07-01 Sony Corp 光電轉換器及光電轉換元件
US8212201B2 (en) 2008-08-05 2012-07-03 Sony Corporation Photoelectric converter and photoelectric conversion element
JP2010040783A (ja) * 2008-08-05 2010-02-18 Sony Corp 光電変換装置及び光電変換素子
CN101656298B (zh) * 2008-08-19 2012-06-13 鸿富锦精密工业(深圳)有限公司 红外探测器
TWI427277B (zh) * 2008-08-29 2014-02-21 Hon Hai Prec Ind Co Ltd 紅外探測器
WO2011052781A1 (fr) * 2009-11-02 2011-05-05 株式会社村田製作所 Élément de conversion photoélectrique et dispositif de conversion photoélectrique
JP2010232683A (ja) * 2010-07-05 2010-10-14 Sony Corp 光電変換装置及び光電変換素子
KR101439407B1 (ko) * 2013-05-20 2014-09-15 한국과학기술연구원 광수용체 단백질 기반 분광광도계, 이의 제조 방법 및 이를 이용한 광 검출 방법
US9903761B2 (en) 2013-05-20 2018-02-27 Korea Institute Of Science And Technology Photoreceptor protein-based spectrophotometer, method for manufacturing the same and method for light detection using the same

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