1. Field of the Invention
The present invention relates to a semiconductor device fabricated by using an SOI (Silicon on Insulator) substrate and a method of fabricating the same. Specifically, the invention relates to a semiconductor device including a thin film transistor (hereinafter referred to as TFT) formed on an SOI substrate.
Incidentally, in the present specification, the semiconductor device indicates any device capable of functioning by using semiconductor characteristics. Thus, the semiconductor device includes not only a TFT but also an electro-optical device typified by a liquid crystal display device or a photoelectric conversion device, a semiconductor circuit in which TFTs are integrated, and an electronic equipment containing such an electro-optical device or a semiconductor circuit as a part.
2. Description of the Related Art
In recent years, VLSI techniques have been remarkably developed, and attention has been paid to an SOI (Silicon on Insulator) structure for realizing low power consumption. This technique is such a technique that an active region (channel formation region) of an FET, which has been conventionally formed of bulk single crystal silicon, is made thin film single crystal silicon.
In an SOI substrate, a buried oxide film made of silicon oxide exists on single crystal silicon, and a single crystal silicon thin film is formed thereon. Various methods of fabricating such SOI substrates are known. As a typical SOI substrate, an SIMOX substrate is known. The term SIMOX is an abbreviation for Separation-by-Implanted Oxygen, and oxygen is ion implanted into a single crystal silicon substrate to form a buried oxide layer. The details of the SIMOX substrate are disclosed in [K. Izumi, M. Docken and H. Ariyoshi: “C.M.O.S. devices fabrication on buried SiO2 layers formed by oxygen implantation into silicon”, Electron. Lett., 14, 593-594 (1978)].
Recently, attention has also been paid to a bonded SOI substrate. The bonded SOI substrate realizes the SOI structure by bonding two silicon substrates as suggested by its name. If this technique is used, a single crystal silicon thin film can be formed also on a ceramic substrate or the like.
Among the bonded SOI substrates, in recent years, attention has been especially paid to a technique called ELTRAN (registered trademark by Canon K.K.). This technique is a method of fabricating an SOI substrate using selective etching of a porous silicon layer. The particular technique of the ELTRAN method is disclosed in, K. Sakaguchi et al., “Current Progress in Epitaxial Layer Transfer (ELTRAN)”, IEICE TRANS. ELECTRON. Vol. E80 C. No. 3 pp. 378-387 March 1997, in detail.
As another SOI technique attracting attention, there is a technique called Smart-Cut (registered trademark of SOITEC Co.). The Smart-Cut method is a technique developed by SOITEC Co. in France in 1996, and is a method of fabricating a bonded SOI substrate using hydrogen embrittlement. The particular technique of the Smart-Cut method is disclosed in “Industrial Research Society (Kogyo Chosa Kai); Electronic Material, August, pp. 83-87, 1977” in detail.
When the foregoing SOI substrate is fabricated, a single crystal silicon substrate having a main surface of a crystal face of a {100} plane (crystal orientation is <100> orientation) has been used in any technique. The reason is that the {100} plane has lowest interface state density (Qss) and is suitable for a field effect transistor that is sensitive to interface characteristics.
However, with respect to the SOI substrate used for a TFT, since a single crystal silicon thin film must be formed on an insulating layer, higher priority must be given to adhesion to the insulating layer than the interface state density. That is, even if the interface state density is low, it is meaningless if the single crystal silicon thin film peels off.
The present invention has been made in view of such problems, and an object thereof is to provide a semiconductor device with high reliability by fabricating an SOI substrate suitable for a TFT and by forming TFTs on the substrate.
The structure of the present invention disclosed in the present specification is characterized by comprising the steps of:
forming a hydrogen-containing layer at a predetermined depth in a single crystal semiconductor substrate having a main surface of a {110} plane;
bonding the single crystal semiconductor substrate and a supporting substrate to each other;
splitting the single crystal semiconductor substrate by a first heat treatment along the hydrogen-containing layer;
carrying out a second heat treatment at a temperature of 900 to 1200° C.;
grinding a single crystal semiconductor layer remaining on the supporting substrate and having a main surface of a {110} plane; and
forming a plurality of TFTs each having an active layer of the single crystal semiconductor layer.
Further, another structure of the present invention is characterized by comprising the steps of:
forming a porous semiconductor layer by anodization of a single crystal semiconductor substrate having a main surface of a {110} plane;
carrying out a heat treatment to the porous semiconductor layer in a reducing atmosphere;
carrying out epitaxial growth of a single crystal semiconductor layer having a main surface of a {110} plane on the porous semiconductor layer;
bonding the single crystal semiconductor substrate and a supporting substrate to each other;
carrying out a heat treatment at a temperature of 900 to 1200° C.;
grinding the single crystal semiconductor substrate until the porous semiconductor layer is exposed;
removing the porous semiconductor layer to expose the single crystal semiconductor layer; and
forming a plurality of TFTs each having an active layer of the single crystal semiconductor layer on the supporting substrate.
Still further, another structure of the present invention is characterized by comprising the steps of:
forming an oxygen-containing layer at a predetermined depth in a single crystal semiconductor substrate having a main surface of a {110} plane;
changing the oxygen-containing layer into a buried insulating layer by a heat treatment; and
forming a plurality of TFTs each having an active layer of a single crystal semiconductor layer having a main surface of a {110} plane on the buried insulating layer.
The gist of the present invention is to use a single crystal semiconductor substrate having a main surface of a {110} plane (crystal face is a {110} plane) as a forming material of a single crystal semiconductor layer finally formed on a supporting substrate when an SOI substrate is fabricated by using an SOI technique such as SIMOX. ELTRAN, or Smart-Cut.
Incidentally, although the semiconductor mentioned here typically indicates silicon, the term also includes other semiconductors such as silicon germanium.
The reason why a single crystal semiconductor substrate having a main surface of a {110} plane is used as a forming material of a single crystal semiconductor layer will be described below. Incidentally, this description will be made using single crystal silicon as an example.
As single crystal silicon, although that formed by an FZ method and that formed by a CZ method exist, in the present invention, it is preferable to use single crystal silicon formed by the FZ method. In the CZ method which is the main stream at present, oxygen of about 2×1018 atoms/cm3 is contained for the purpose of relieving stress, so that there is a fear that an electron or hole mobility is lowered. Particularly, in the case where a minute TFT is formed, this comes to appear remarkably.
However, in the case where single crystal silicon is used for the SOI substrate as in the present invention, since there are many cases where the thickness of a single crystal silicon layer required for an active layer of a TFT is as very thin as 10 to 50 nm, it is not quite necessary to take stress into consideration. Thus, even if the FZ method (oxygen content is 1×1017 atoms/cm3 or less), which can form single crystal silicon more inexpensively than the inexpensive CZ method, is used, satisfactory effects can be obtained.
In a general SOI substrate, a single crystal silicon layer is formed on a silicon oxide film. Thus, adhesion and conformity between the silicon oxide layer and the single crystal silicon layer become important. From such a viewpoint, in the SOI substrate, when the single crystal silicon layer comes in contact with the silicon oxide layer, it is ideal that the contact of the single crystal silicon layer is realized with the most stable plane.
The plane which is in contact with the silicon oxide layer with most stably is a {110} plane. Because, in the case of the {110} plane, the plane is in contact with the silicon oxide layer through three silicon atoms. This state will be explained with reference to photographs shown in
That is, when a single crystal silicon layer having a crystal face of the {110} plane is formed on an insulating layer, it is understood that the number of silicon atoms coming in contact with the insulating layer is three.
Like this, it is understood that three silicon atoms are contained in the {110} plane, and are adjacently arranged in a substantially triangular shape. That is, in such an arrangement state, the single crystal silicon layer is in contact with an insulating layer as an under layer, and forms stable contact which is realized through “surface”. This indicates that the single crystal silicon layer is in contact with the insulating layer as an under layer with very high adhesion.
On the other hand, in the case where the single crystal silicon comes in contact with the silicon oxide layer through another plane, for example, a {100} plane or a {111} plane, the number of silicon atoms coming in contact with the silicon oxide layer is at most two, and unstable contact is formed in which the contact is realized through “line”.
Further, as a great merit of using the single crystal silicon layer having the main surface of the {110} plane, it is possible to mention that a silicon surface is very flat. In the case where the main surface is the {110} plane, a cleavage plane appears lamellary, and it is possible to form a surface with very few asperities.
Like this, in the present invention, first priority is given to adhesion of a single crystal silicon layer to an under layer (silicon oxide layer) in the SOI substrate, and the invention is characterized by using the single crystal silicon substrate having the crystal face of the {110} plane which has not been conventionally used. That is, the invention is characterized in that the single crystal semiconductor substrate having the main surface (crystal face) of the {110} plane is used as a material, and the SOI technique such as SIMOX, ELTRAN, or Smart-Cut is fully used, so that the SOI substrate with high reliability is formed. Incidentally, an oriental flat of the single crystal semiconductor substrate having the main surface of the {110} plane may be made a {111} plane.
Then such an SOI substrate is used, and a plurality of TFTs each having an active layer of a single crystal semiconductor thin film are formed on the same substrate, so that a semiconductor device having high reliability can be realized.
The present invention will next be described in detail with preferred embodiments described below.
In this embodiment, with reference to
First, a single crystal silicon substrate 101 as a forming material of a single crystal silicon layer is prepared. Here, although a P-type substrate having a main surface of a crystal face of a {110} plane is used, an N-type substrate may be used. Of course, a single crystal silicon germanium substrate may be used.
Next, a thermal oxidation treatment is carried out, so that a silicon oxide film 102 is formed on the main surface (corresponding to an element forming surface). Although a film thickness may be suitably determined by a user, the thickness is made 10 to 500 nm (typically 20 to 50 nm). This silicon oxide film 102 functions later as a part of a buried insulating layer of an SOI substrate (
At this time, the adhesion between the single crystal silicon substrate 101 and the silicon oxide film 102 becomes very high. Because, the silicon oxide film 102 is formed on the {110} plane in this invention, so that an interface with very high conformity can be realized. Since this interface is an interface between an active layer and an under film in a final TFT, it is very advantageous that the adhesion (conformity) is high.
The reason why the thickness of the silicon oxide film 102 can be made as thin as 20 to 50 nm is that the crystal face of the single crystal silicon substrate 101 has the {110} plane, so that the silicon oxide film having high adhesion can be formed even though it is thin.
Incidentally, the {110} plane has a problem that when an oxidation reaction proceeds, undulation (asperity) of the silicon surface gradually becomes large. However, in the case where a thin silicon oxide film is provided as in this embodiment, since the amount of oxidation is small, a problem of such undulation can be eliminated to the utmost. This is an advantage that is common to all embodiments disclosed in the present specification.
Thus, the single crystal silicon layer formed by using this invention has a very flat surface. For example, a distance between the top and top of the undulation is 10 times or less (preferably 20 times or less) as long as a distance between adjacent atoms of the three atoms contained in the {110} plane. That is, it is about 5 nm or less (preferably 10 nm or less).
Next, hydrogen is added through the silicon oxide film 102 from the side of the main surface of the single crystal silicon substrate 101. In this case, the hydrogen addition may be carried out as the form of hydrogen ions using an ion implantation method. Of course, the addition step of hydrogen may be carried out by other means. In this way, a hydrogen-containing layer 103 is formed. In this embodiment, a hydrogen ion with a dosage of 1×1016 to 1×1017 atom/cm2 is added (
Since the depth where the hydrogen-containing layer is formed determines the thickness of the single crystal silicon layer later, precise control is required. In this embodiment, control of a hydrogen addition profile in the depth direction is made so that the single crystal silicon layer with a thickness of 50 nm remains between the main surface of the single crystal silicon substrate 101 and the hydrogen-containing layer 103.
Since the {110} plane is a plane which has the lowest atomic density, even if hydrogen ions are added, a probability of collision with silicon atoms is lowest. That is, it is possible to suppress damage at the time of ion addition to the minimum.
Next, the single crystal silicon substrate 101 and a supporting substrate are bonded to each other. In this embodiment, a silicon substrate 104 is used as the supporting substrate, and a silicon oxide film 105 for bonding is provided on its surface. As the silicon substrate 104, it is satisfactory if an inexpensive silicon substrate formed by the FZ method is prepared. Of course, it does not matter if a polycrystal silicon substrate is used. Besides, if only flatness can be assured, a highly refractory substrate such as a quartz substrate, a ceramic substrate, or a crystallized glass substrate may be used (
At this time, since a bonding interface is formed of highly hydrophilic silicon oxide films, they are adhered to each other with hydrogen bonds by reaction of moisture contained in both the surfaces.
Next, a heat treatment (first heat treatment) at 400 to 600° C. (typically 500° C.) is carried out. By this heat treatment, in the hydrogen-containing layer 103, a volume change of a minute vacancy occurs, and a broken surface is produced along the hydrogen-containing layer 103. By this, the single crystal silicon substrate 101 is split, so that the silicon oxide film 102 and a single crystal silicon layer 106 are made to remain on the supporting substrate (
Next, as a second heat treatment, a furnace annealing step is carried out in a temperature range of 1050 to 1150° C. In this step, at the bonded interface, stress relaxation of Si—O—Si bonds occurs, so that the bonded interface becomes stable. That is, this becomes a step of completely bonding the single crystal silicon layer 106 to the supporting substrate. In this embodiment, this step is carried out at 1100° C. for 2 hours.
The bonded interface is stabilized in this way, so that a buried insulating layer 107 is defined. In
Next, the surface of the single crystal silicon layer 106 is flattened. For flattening, a polishing step called CMP (Chemical Mechanical Polishing) or a furnace annealing treatment at high temperature (about 900 to 1200° C.) in a reducing atmosphere may be carried out.
The final thickness of the single crystal silicon layer 106 may be made 10 to 200 nm (preferably 20 to 100 nm).
Next, the single crystal silicon layer 106 is patterned to form an island-like silicon layer 108 which becomes an active layer of a TFT. In this embodiment, although only one island-like silicon layer is shown, a plurality of layers are formed on the same substrate (
In the manner as described above, the island-like silicon layer 108 having the main surface of the {110} plane is obtained. The present invention is characterized in that the island-like silicon layer obtained in this way is used as an active layer of a TFT, and a plurality of TFTs are formed on the same substrate.
Next, a method of forming a TFT will be described with reference to
Next, a thermal oxidation step is carried out so that a silicon oxide film 203 with a thickness of 10 nm is formed on the surface of the island-like silicon layer 202. This silicon oxide film 203 functions as a gate insulating film. After the gate insulating film 203 is formed, a polysilicon film having conductivity is formed thereon, and a gate wiring line 204 is formed by patterning (
Incidentally, in this embodiment, although the polysilicon film having N-type conductivity is used as the gate wiring line, the material is not limited to this. Particularly, for the purpose of decreasing the resistance of the gate wiring line, it is also effective to use a metal material such as tantalum, tantalum alloy, or a laminate film of tantalum and tantalum nitride. Moreover, for the purpose of obtaining the gate wiring line with further low resistance, it is also effective to use copper or copper alloy.
After the state of
Next, a thin silicon oxide film 206 with a thickness of about 5 to 10 nm is formed on the surface of the gate wiring line. This may be formed by using a thermal oxidation method or a plasma oxidation method. The formation of the silicon oxide film 206 has an object to make it function as an etching stopper in a next side wall forming step.
After the silicon oxide film 206 as an etching stopper is formed, a silicon nitride film is formed and etch back is carried out, so that a side wall 207 is formed. In this way, the state of
In this embodiment, although the silicon nitride film is used as the side wall 207, a polysilicon film or an amorphous silicon film may be used. Of course, it is needless to say that if the material of the gate wiring line is changed, room for choice of a material which can be used as the side wall is widened.
Next, an impurity having the same conductivity as the former step is added again. The concentration of the impurity added at this time is made higher than that at the former step. In this embodiment, arsenic is used as the impurity, and the concentration is made 1×1021 atoms/cm3. However, it is not necessary to make limitation to this. By the addition step of the impurity, a source region 208, a drain region 209, an LDD region 210, and a channel formation region 211 are defined (
In this way, after the respective impurity regions are formed, activation of the impurity is carried out by furnace annealing, laser annealing, lamp annealing, or the like.
Next, silicon oxide films formed on the surfaces of the gate wiring line 204, the source region 208, and the drain region 209 are removed to expose their surfaces. Then a cobalt film 212 with a thickness of about 5 nm is formed and a thermal treatment step is carried out. By this heat treatment, a reaction of cobalt and silicon occurs, so that a silicide layer (cobalt silicide layer) 213 is formed (
This technique is a well-known silicide technique. Thus, it does not matter if titanium or tungsten is used instead of cobalt, and a heat treatment condition and the like may be referred to the well-known technique. In this embodiment, the heat treatment step is carried out by using lamp annealing.
After the silicide layer 213 is formed in this way, the cobalt film 212 is removed. Thereafter, an interlayer insulating film 214 with a thickness of 1 μm is formed. As the interlayer insulating film 214, a silicon oxide film, a silicon nitride film, a silicon nitride oxide film, or a resin film, such as polyamide, polyimide, acryl, etc., may be used. Alternatively, these insulating films may be laminated.
Next, contact holes are formed in the interlayer insulating film 214, and a source wiring line 215 and a drain wiring line 216 made of a material containing aluminum as its main ingredient are formed. Finally, the entire component is subjected to furnace annealing at 300° C. for 2 hours in a hydrogen atmosphere, and hydrogenating is completed.
In this way, a TFT as shown in
Besides, in this embodiment, although the description has been made with the N-channel TFT as an example, it is also easy to fabricate a P-channel TFT. Further, it is also possible to form a CMOS circuit by forming an N-channel TFT and a P-channel TFT on the same substrate and by complementarily combining them.
Further, in the structure of
That is, the invention is also a very effective technique as a method of fabricating an electro-optical device typified by a liquid crystal display device, an EL (electroluminescence) display device, an EC (electrochromic) display device, a photoelectric conversion device (optical sensor), and the like.
In this embodiment, a description will be made of an example in which an SOI substrate different from that of embodiment 1 is fabricated by using a single crystal silicon substrate having a main surface of a {110} plane, and a semiconductor device is fabricated by using the SOI substrate using
First, a single crystal silicon substrate 301 having a main surface (crystal face) of a {110} plane is prepared. Next, the main surface is subjected to anodization to form a porous silicon layer 302. The anodization step may be carried out in a mixed solution of hydrofluoric acid and ethanol. The porous silicon layer 302 is regarded as a single crystal silicon layer provided with columnar surface holes at a surface density of about 1011 holes/cm3, and succeeds to the crystal state (orientation, etc.) of the single crystal silicon substrate 301 as it is. Incidentally, since the ELTRAN method itself is well known, the detailed description will be omitted here.
After the porous silicon layer 302 is formed, it is preferable to carry out a heat treatment step in a reducing atmosphere and within a temperature range of 900 to 1200° C. (preferably 1000 to 1150° C.). In this embodiment, a heat treatment at 1050° C. for 2 hours is carried out in a hydrogen atmosphere.
As the reducing atmosphere, although a hydrogen atmosphere, an ammonia atmosphere, or an inert gas atmosphere containing hydrogen or ammonia (mixed atmosphere of hydrogen and nitrogen, or hydrogen and argon, etc.) is preferable, flattening of the surface of the crystalline silicon film can be made even in an inert gas atmosphere. However, when a reduction of a natural oxidation film is carried out by using a reducing action, many silicon atoms with high energy are generated and the flattening effect is resultantly increased. Thus, use of the reducing atmosphere is preferable.
However, attention needs to be especially paid to the point that the concentration of oxygen or an oxygen compound (for example, OH radical) contained in the atmosphere must be 10 ppm or less (preferably 1 ppm or less). Otherwise, the reducing reaction by hydrogen comes not to occur.
At this time, in the vicinity of the surface of the porous silicon layer 302, the surface holes are filled up by movement of silicon atoms, so that a very flat silicon surface can be obtained.
Next, a single crystal silicon layer 303 is epitaxially grown on the porous silicon layer 302. At this time, since the epitaxially grown single crystal silicon layer 303 reflects the crystal structure of the single crystal silicon substrate 301 as it is, its main surface becomes a {110} plane. The film thickness may be 10 to 200 nm (preferably 20 to 100 nm) (
Next, the single crystal silicon layer 303 is oxidized to form a silicon oxide layer 304. As a forming method, it is possible to use thermal oxidation, plasma oxidation, laser oxidation, or the like. At this time, a single crystal silicon layer 305 remains (
Next, as a supporting substrate, a polycrystal silicon substrate 306 provided with a silicon oxide layer on its surface is prepared. Of course, a ceramic substrate, a quartz substrate, or a glass ceramic substrate each provided with an insulating film on its surface may be used.
After the preparation of the single crystal silicon substrate 301 and the supporting substrate (polycrystal silicon substrate 306) is completed in this way, both of the substrates are bonded to each other in such a manner that the respective main surfaces are opposite to each other. In this case, the silicon oxide layer provided on each of the substrates functions as an adhesive (
After bonding is ended, a heat treatment step at a temperature of 1050 to 1150° C. is next carried out, and the bonded interface made of both the silicon oxide layers is stabilized. In this embodiment, this heat treatment step is carried out at 1100° C. for 2 hours. Incidentally, a portion indicated by a dotted line in
Next, the single crystal silicon substrate 301 is ground from the rear surface side by mechanical polishing such as CMP, and the grinding step is ended when the porous silicon layer 302 is exposed. In this way, the state shown in
Next, the porous silicon layer 302 is subjected to wet etching and is selectively removed. As an etchant to be used, a mixed solution of a hydrofluoric acid solution and a hydrogen peroxide solution is preferable. It is reported that a solution of a mixture of 49% HF and 30% H2O2 at a ratio of 1:5 has a selecting ratio of a hundred thousand times or more between a single crystal silicon layer and a porous silicon layer.
The state shown in
Although the SOI substrate is completed at this time, since minute asperities exist on the surface of the single crystal silicon layer 308, it is desirable to carry out a heat treatment step in a hydrogen atmosphere to perform flattening. This flattening phenomenon occurs due to speed-increasing surface diffusion of silicon atoms by reduction of a natural oxidation film.
At this time, since there is also an effect that boron contained in the single crystal silicon layer 308 (that contained in a P-type silicon substrate) is released into a vapor phase by hydrogen atoms, the heat treatment step is also effective in decrease of impurities.
Next, the obtained single crystal silicon layer 308 is patterned to form an island-like silicon layer 309. Although only one layer is shown in the drawings, it is needless to say that a plurality of island-like silicon layers may be formed.
Thereafter, a TFT can be fabricated in accordance with the same steps as those described in embodiment 1 with reference to
In this embodiment, a description will be made on an example in which a single crystal silicon substrate having a main surface of a {110} plane is used to fabricate an SOI substrate different from that of embodiment 1 or embodiment 2, and a semiconductor device is fabricated by using the substrate using
In
At this time, since the {110} plane has small atomic density, a probability of collision of the oxygen ion and silicon atom becomes lower. That is, it is possible to suppress damage of the silicon surface due to the addition of oxygen to the minimum. Of course, if the substrate temperature is raised at 400 to 600° C. during the ion addition, the damage can be further decreased.
Next, a heat treatment at a temperature of 800 to 1200° C. is carried out, so that the oxygen-containing layer 402 is changed into a buried insulating layer 403. The width of the oxygen-containing layer 402 in the depth direction is determined by a distribution of the oxygen ion at the ion addition, and has a distribution with a gentle tail. However, by this heat treatment, the interface between the single crystal silicon substrate 401 and the buried insulating layer 403 becomes very steep (
The thickness of this buried insulating layer 403 is 10 to 500 nm (typically 20 to 50 nm). The reason why the buried insulating layer as thin as 20 to 50 nm can be realized is that the interface between the single crystal silicon substrate 401 and the buried insulating layer 403 is stably coupled, which is the very result of the fact that the single crystal silicon substrate having the main surface of the {110} plane is used as the material of the single crystal silicon layer.
When the buried insulating layer 403 is formed in this way, a single crystal silicon layer 404 remains on the buried insulating layer 403. That is, in this embodiment, since the single crystal silicon substrate having the main surface of the {110} plane is used, the main surface (crystal face) of the single crystal silicon layer 404 obtained after the buried insulating layer is formed comes to have the {110} plane as well. Incidentally, adjustment may be made so that the thickness of the single crystal silicon layer 404 becomes 10 to 200 nm (preferably 20 to 100 nm).
After the single crystal silicon layer 404 is obtained in this way, patterning is carried out to obtain an island-like silicon layer 405. A plurality of island-like silicon layers may be formed.
Thereafter, a plurality of TFTs may be completed in accordance with the steps described in embodiment 1 using
In this embodiment, an example of a reflection type liquid crystal display device as a semiconductor device of the present invention will be shown in
In
Further, although the description in this embodiment has been made on the liquid crystal display device as an example, it is needless to say that the present invention can be applied to an EL (electroluminescence) display device or an EC (electrochromic) display device as long as the display device is an active matrix type display device. Here, an example of a circuit constituting the driver circuits 13 and 14 of
In
A part of circuits constituting the pixel matrix circuit 12 of
The insulating layer 504 is provided thereon, and the titanium wiring line 505 is provided thereon. At this time, a recess portion is formed in a part of the insulating layer 504, and only silicon nitride and silicon oxide of the lowermost layer are made to remain. By this, auxiliary capacitance is formed between the drain wiring line 508 and the titanium wiring line 505.
Besides, the titanium wiring line 505 provided in the pixel matrix circuit has an electric field shielding effect between the source/drain wiring line and a subsequent pixel electrode. Further, it also functions as a black mask at gaps between a plurality of pixel electrodes provided.
Then, the insulating layer 506 is provided to cover the titanium wiring line 505, and a pixel electrode 509 made of a reflective conductive film is formed thereon. Of course, it does not matter if contrivance to raise reflectivity may be made on the surface of the pixel electrode 509.
Actually, although an orientation film or a liquid crystal layer is provided on the pixel electrode 509, the description will be omitted here.
The reflection type liquid crystal display device having the structure as described above can be fabricated by using the present invention. Of course, when combined with a well-known technique, it is also possible to easily fabricate a transmission type liquid crystal display device. Further, when combined with a well-known technique, it is also possible to easily fabricate an active matrix type EL display device.
The present invention can be applied to all conventional IC techniques. That is, the present invention can be applied to all semiconductor circuits presently available on the market. For example, the present invention may be applied to a microprocessor such as a RISC processor integrated on one chip or an ASIC processor, and may be applied to circuits from a signal processing circuit such as a D/A converter to a high frequency circuit for a portable equipment (portable telephone, PHS, mobile computer).
Of course, the microprocessor shown in
However, in any microprocessor with any function, it is an IC (Integrated Circuit) 28 that functions as a central part. The IC 28 is a functional circuit in which an integrated circuit formed on a semiconductor chip 29 is protected with ceramic or the like.
An N-channel TFT 30 and a P-channel TFT 31 having the structure of this invention constitute the integrated circuit formed on the semiconductor chip 29. Note that when a basic circuit is constituted by a CMOS circuit as a minimum unit, power consumption can be suppressed.
Besides, the microprocessor shown in this embodiment is mounted on various electronic equipments and functions as a central circuit. As typical electronic equipments, a personal computer, a portable information terminal equipment, and other all household electric appliances can be enumerated. Besides, a computer for controlling a vehicle (automobile, electric train, etc.) can also be enumerated.
A CMOS circuit and a pixel matrix circuit formed through carrying out the present invention may be applied to various electro-optical devices (active matrix type liquid crystal display devices, active matrix type EL display devices, active matrix type EC display devices). Namely, the present invention may be embodied in all the electronic equipments that incorporate those electro-optical devices as display media.
As such an electronic equipment, a video camera, a digital camera, a projector (rear-type projector or front-type projector), a head mount display (goggle-type display), a navigation system for vehicles, a personal computer, and a portable information terminal (a mobile computer, a cellular phone, or an electronic book) may be enumerated. Examples of those are shown in
The light source optical system shown in
Further, on discretion of a person who carries out the invention, the light source optical system may be provided with an optical system such as an optical lens, a film having a polarization function, a film for adjusting the phase difference, and an IR film.
As described above, the scope of application of the present invention is very wide, and the invention can be applied to electronic equipments of any fields. The electronic equipment of this embodiment can be realized even if any combination of embodiments 1 to 5 is used.
Number | Date | Country | Kind |
---|---|---|---|
10-251635 | Sep 1998 | JP | national |
This application is a continuation of copending U.S. application Ser. No. 11/731,415, filed on Mar. 30, 2007 which is a continuation of U.S. application Ser. No. 10/9 14,357, filed on Aug. 9, 2004 which is a continuation of U.S. application Ser. No. 09/808,162, filed on Mar. 13, 2001 (now U.S. Pat. No. 6,803,264 issued Oct. 12, 2004) which is a divisional of U.S. application Ser. No. 09/386,782, filed on Aug. 31, 1999 (now U.S. Pat. No. 6,335,231 issued Jan. 1, 2002).
Number | Name | Date | Kind |
---|---|---|---|
3964941 | Wang | Jun 1976 | A |
4217153 | Fukunaga et al. | Aug 1980 | A |
4583122 | Ohwada et al. | Apr 1986 | A |
4665419 | Sasaki | May 1987 | A |
4733947 | Ota et al. | Mar 1988 | A |
4753896 | Matloubian | Jun 1988 | A |
4768076 | Aoki et al. | Aug 1988 | A |
4786955 | Plus et al. | Nov 1988 | A |
4822752 | Sugahara et al. | Apr 1989 | A |
4857986 | Kinugawa | Aug 1989 | A |
4899202 | Blake et al. | Feb 1990 | A |
4933298 | Hasegawa | Jun 1990 | A |
4943837 | Konishi et al. | Jul 1990 | A |
5002630 | Kermani et al. | Mar 1991 | A |
5059304 | Field | Oct 1991 | A |
5130770 | Blanc et al. | Jul 1992 | A |
5215931 | Houston | Jun 1993 | A |
5243213 | Miyazawa et al. | Sep 1993 | A |
5258323 | Sarma et al. | Nov 1993 | A |
5261999 | Pinker et al. | Nov 1993 | A |
5317236 | Zavracky et al. | May 1994 | A |
5341028 | Yamaguchi et al. | Aug 1994 | A |
5371037 | Yonehara | Dec 1994 | A |
5374564 | Bruel | Dec 1994 | A |
5387555 | Linn et al. | Feb 1995 | A |
5403759 | Havemann | Apr 1995 | A |
5424230 | Wakai | Jun 1995 | A |
5426062 | Hwang | Jun 1995 | A |
5444282 | Yamaguchi et al. | Aug 1995 | A |
5508209 | Zhang et al. | Apr 1996 | A |
5550070 | Funai et al. | Aug 1996 | A |
5569620 | Linn et al. | Oct 1996 | A |
5573961 | Hsu et al. | Nov 1996 | A |
5574292 | Takahashi et al. | Nov 1996 | A |
5576556 | Takemura et al. | Nov 1996 | A |
5581092 | Takemura | Dec 1996 | A |
5612230 | Yuzurihara et al. | Mar 1997 | A |
5640033 | Matsuoka | Jun 1997 | A |
5643826 | Ohtani et al. | Jul 1997 | A |
5648277 | Zhang et al. | Jul 1997 | A |
5693959 | Inoue et al. | Dec 1997 | A |
5698869 | Yoshimi et al. | Dec 1997 | A |
5710057 | Kenney | Jan 1998 | A |
5714395 | Bruel | Feb 1998 | A |
5719065 | Takemura et al. | Feb 1998 | A |
5750000 | Yonehara et al. | May 1998 | A |
5778237 | Yamamoto et al. | Jul 1998 | A |
5784132 | Hashimoto | Jul 1998 | A |
5793073 | Kaminishi et al. | Aug 1998 | A |
5818076 | Zhang et al. | Oct 1998 | A |
5821138 | Yamazaki et al. | Oct 1998 | A |
5837569 | Makita et al. | Nov 1998 | A |
5840616 | Sakaguchi et al. | Nov 1998 | A |
5841173 | Yamashita | Nov 1998 | A |
5849627 | Linn et al. | Dec 1998 | A |
5854123 | Sato et al. | Dec 1998 | A |
5854509 | Kunikiyo | Dec 1998 | A |
5877070 | Goesele et al. | Mar 1999 | A |
5882987 | Srikrishnan | Mar 1999 | A |
5886385 | Arisumi et al. | Mar 1999 | A |
5893730 | Yamazaki et al. | Apr 1999 | A |
5899711 | Smith | May 1999 | A |
5904528 | Lin et al. | May 1999 | A |
5913111 | Kataoka et al. | Jun 1999 | A |
5923962 | Ohtani et al. | Jul 1999 | A |
5926430 | Noda et al. | Jul 1999 | A |
5943105 | Fujikawa et al. | Aug 1999 | A |
5949107 | Zhang | Sep 1999 | A |
5953622 | Lee et al. | Sep 1999 | A |
5962897 | Takemura et al. | Oct 1999 | A |
5965918 | Ono | Oct 1999 | A |
5966594 | Adachi et al. | Oct 1999 | A |
5966620 | Sakaguchi et al. | Oct 1999 | A |
5982002 | Takasu et al. | Nov 1999 | A |
5985681 | Hamajima et al. | Nov 1999 | A |
5985740 | Yamazaki et al. | Nov 1999 | A |
6020252 | Aspar et al. | Feb 2000 | A |
6027988 | Cheung et al. | Feb 2000 | A |
6031249 | Yamazaki et al. | Feb 2000 | A |
6044474 | Klein | Mar 2000 | A |
6049092 | Konuma et al. | Apr 2000 | A |
6051453 | Takemura | Apr 2000 | A |
6054363 | Sakaguchi et al. | Apr 2000 | A |
6063706 | Wu | May 2000 | A |
6077731 | Yamazaki et al. | Jun 2000 | A |
6093937 | Yamazaki et al. | Jul 2000 | A |
6096582 | Inoue et al. | Aug 2000 | A |
6107639 | Yamazaki et al. | Aug 2000 | A |
6107654 | Yamazaki | Aug 2000 | A |
6118148 | Yamazaki | Sep 2000 | A |
6124613 | Kokubun | Sep 2000 | A |
6127702 | Yamazaki et al. | Oct 2000 | A |
6133073 | Yamazaki et al. | Oct 2000 | A |
6140667 | Yamazaki et al. | Oct 2000 | A |
6157421 | Ishii | Dec 2000 | A |
6165880 | Yaung et al. | Dec 2000 | A |
6171982 | Sato | Jan 2001 | B1 |
6184556 | Yamazaki et al. | Feb 2001 | B1 |
6191007 | Matsui et al. | Feb 2001 | B1 |
6191476 | Takahashi et al. | Feb 2001 | B1 |
6207969 | Yamazaki | Mar 2001 | B1 |
6211041 | Ogura | Apr 2001 | B1 |
6218678 | Zhang et al. | Apr 2001 | B1 |
6262438 | Yamazaki et al. | Jul 2001 | B1 |
6268842 | Yamazaki et al. | Jul 2001 | B1 |
6271101 | Fukunaga | Aug 2001 | B1 |
6287900 | Yamazaki et al. | Sep 2001 | B1 |
6291275 | Yamazaki et al. | Sep 2001 | B1 |
6294478 | Sakaguchi et al. | Sep 2001 | B1 |
6307220 | Yamazaki | Oct 2001 | B1 |
6326249 | Yamazaki et al. | Dec 2001 | B1 |
6331208 | Nishida et al. | Dec 2001 | B1 |
6335231 | Yamazaki et al. | Jan 2002 | B1 |
6335716 | Yamazaki et al. | Jan 2002 | B1 |
6342433 | Ohmi et al. | Jan 2002 | B1 |
6365933 | Yamazaki et al. | Apr 2002 | B1 |
6369410 | Yamazaki et al. | Apr 2002 | B1 |
6380046 | Yamazaki | Apr 2002 | B1 |
6380560 | Yamazaki et al. | Apr 2002 | B1 |
6388291 | Zhang et al. | May 2002 | B1 |
6388652 | Yamazaki et al. | May 2002 | B1 |
6420759 | Yamazaki et al. | Jul 2002 | B2 |
6421754 | Kau et al. | Jul 2002 | B1 |
6424011 | Assaderaghi et al. | Jul 2002 | B1 |
6433361 | Zhang et al. | Aug 2002 | B1 |
6452211 | Ohtani et al. | Sep 2002 | B1 |
6455401 | Zhang et al. | Sep 2002 | B1 |
6458637 | Yamazaki et al. | Oct 2002 | B1 |
6465287 | Yamazaki et al. | Oct 2002 | B1 |
6528820 | Yamazaki et al. | Mar 2003 | B1 |
6549184 | Koyama et al. | Apr 2003 | B1 |
6583474 | Yamazaki et al. | Jun 2003 | B2 |
6590230 | Yamazaki et al. | Jul 2003 | B1 |
6602761 | Fukunaga | Aug 2003 | B2 |
6617612 | Zhang et al. | Sep 2003 | B2 |
6667494 | Yamazaki et al. | Dec 2003 | B1 |
6686623 | Yamazaki | Feb 2004 | B2 |
6787806 | Yamazaki et al. | Sep 2004 | B1 |
6803264 | Yamazaki et al. | Oct 2004 | B2 |
6849872 | Yamazaki et al. | Feb 2005 | B1 |
6867431 | Konuma et al. | Mar 2005 | B2 |
6875633 | Fukunaga | Apr 2005 | B2 |
6882018 | Ohtani et al. | Apr 2005 | B2 |
7023052 | Yamazaki et al. | Apr 2006 | B2 |
7138658 | Yamazaki et al. | Nov 2006 | B2 |
RE39484 | Bruel | Feb 2007 | E |
7172929 | Yamazaki et al. | Feb 2007 | B2 |
7176525 | Fukunaga | Feb 2007 | B2 |
7199024 | Yamazaki | Apr 2007 | B2 |
7223666 | Ohtani et al. | May 2007 | B2 |
7381599 | Konuma et al. | Jun 2008 | B2 |
7473592 | Yamazaki et al. | Jan 2009 | B2 |
7473971 | Yamazaki et al. | Jan 2009 | B2 |
7476576 | Yamazaki et al. | Jan 2009 | B2 |
20020109144 | Yamazaki | Aug 2002 | A1 |
20040104435 | Ohtani et al. | Jun 2004 | A1 |
20040256621 | Konuma et al. | Dec 2004 | A1 |
20050009252 | Yamazaki et al. | Jan 2005 | A1 |
20050142705 | Konuma et al. | Jun 2005 | A1 |
20050153489 | Konuma et al. | Jul 2005 | A1 |
20070007529 | Takemura et al. | Jan 2007 | A1 |
20070020888 | Yamazaki et al. | Jan 2007 | A1 |
20070108510 | Fukunaga | May 2007 | A1 |
20070173000 | Yamazaki | Jul 2007 | A1 |
20070184632 | Yamazaki et al. | Aug 2007 | A1 |
20070210451 | Ohtani et al. | Sep 2007 | A1 |
20070252206 | Yamazaki et al. | Nov 2007 | A1 |
20080054269 | Yamazaki et al. | Mar 2008 | A1 |
20080061301 | Yamazaki | Mar 2008 | A1 |
20080067529 | Yamazaki | Mar 2008 | A1 |
20080067596 | Yamazaki et al. | Mar 2008 | A1 |
20080067597 | Yamazaki | Mar 2008 | A1 |
20080070335 | Yamazaki et al. | Mar 2008 | A1 |
20080083953 | Yamazaki | Apr 2008 | A1 |
20080113488 | Yamazaki et al. | May 2008 | A1 |
20080213953 | Yamazaki | Sep 2008 | A1 |
20080286941 | Yamazaki | Nov 2008 | A1 |
20080286942 | Yamazaki | Nov 2008 | A1 |
20080286956 | Yamazaki | Nov 2008 | A1 |
Number | Date | Country |
---|---|---|
0 485 233 | May 1992 | EP |
63-318779 | Dec 1988 | JP |
1-264254 | Oct 1989 | JP |
2-42725 | Feb 1990 | JP |
3-79035 | Apr 1991 | JP |
04-206766 | Jul 1992 | JP |
04-348532 | Dec 1992 | JP |
05-211128 | Aug 1993 | JP |
05-226620 | Sep 1993 | JP |
7-249749 | Sep 1995 | JP |
09-008124 | Jan 1997 | JP |
09-045882 | Feb 1997 | JP |
09-213916 | Aug 1997 | JP |
09-260682 | Oct 1997 | JP |
09-289166 | Nov 1997 | JP |
09-289167 | Nov 1997 | JP |
9-289323 | Nov 1997 | JP |
9-293876 | Nov 1997 | JP |
10-12889 | Jan 1998 | JP |
10-64817 | Mar 1998 | JP |
10-093100 | Apr 1998 | JP |
10-125881 | May 1998 | JP |
10-125926 | May 1998 | JP |
10-125927 | May 1998 | JP |
10-133233 | May 1998 | JP |
10-135350 | May 1998 | JP |
10-135468 | May 1998 | JP |
10-135475 | May 1998 | JP |
11-163363 | Jun 1999 | JP |
2000-012864 | Jan 2000 | JP |
Number | Date | Country | |
---|---|---|---|
20080113487 A1 | May 2008 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 09386782 | Aug 1999 | US |
Child | 09808162 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 11731415 | Mar 2007 | US |
Child | 11926552 | US | |
Parent | 10914357 | Aug 2004 | US |
Child | 11731415 | US | |
Parent | 09808162 | Mar 2001 | US |
Child | 10914357 | US |