1. Field of the Invention
Aspects of the present invention relate to an organic light emitting diode (OLED) display device and a method of fabricating the same, and more particularly, to an OLED display device including a capacitor whose capacitance is increased using a method of fabricating a polysilicon layer using a metal catalyst and a method of fabricating the same.
2. Description of the Related Art
In general, polysilicon is widely used as a semiconductor layer of a thin film transistor due to its high field effect mobility and applicability to high-speed operating circuits and complementary metal-oxide-semiconductor (CMOS) circuits. The thin film transistors having a polysilicon layer are generally used as active elements of active matrix liquid crystal displays (AMLCDs), and switching elements and driving elements of organic light emitting diodes (OLEDs).
Here, methods of crystallizing an amorphous silicon layer into the polysilicon layer used for a thin film transistor include a solid phase crystallization (SPC) method, an excimer laser crystallization (ELC) method, a metal induced crystallization (MIC) method, and a metal induced lateral crystallization (MILC) method. In the SPC method, an amorphous silicon layer is annealed at a temperature of about 700° C. or less, i.e., a transition temperature of a glass substrate of a display device for several hours to several tens of hours. In the ELC method, an excimer laser is irradiated on an amorphous silicon layer to locally heat the irradiated portion to a high temperature for a very short time period, so that the amorphous silicon layer is crystallized. In the MIC method, metals such as nickel, palladium, gold, aluminum, etc., are placed in contact with or injected into an amorphous silicon layer, so that the amorphous silicon layer is changed into a polysilicon layer, i.e., a phase change of the amorphous silicon is induced by the metal. In the MILC method, silicide, which is produced by reacting metal with silicon, is laterally and continuously diffused to sequentially induce crystallization of the amorphous silicon layer.
However, the SPC method requires a long time, and the annealing process is performed at a high temperature for a long time, which may deform a substrate. Also, in the ELC method, a high-priced laser device is required, and protrusions may be formed on the polycrystalline surface such that interfacial characteristics between a semiconductor layer and a gate insulating layer may deteriorate.
Currently, research into methods of crystallizing an amorphous silicon layer using a metal is actively progressing because crystallization can be achieved at a lower temperature and with less time than the SPC method. The methods of crystallizing an amorphous silicon layer using a metal include the MIC method, the MILC method, and a super grain silicon crystallization method.
Meanwhile, in an OLED, capacitors are formed, and a capacitor having a high capacitance may be advantageous to the operation of the OLED. Thus, research into increasing the capacitance of the capacitor is required.
Aspects of the present invention provide an organic light emitting diode (OLED) display device in which capacitance of a capacitor is increased by increasing a surface area of the capacitor in a simple manner and a method of fabricating the same.
According to aspects of the present invention, an OLED display device includes: a substrate having a thin film transistor region and a capacitor region; a buffer layer disposed on the substrate; a patterned semiconductor layer disposed on the buffer layer in the thin film transistor region; a gate insulating layer disposed on the substrate to cover the patterned semiconductor layer; a gate electrode disposed on the gate insulating layer and facing a predetermined region of the patterned semiconductor layer; a lower capacitor electrode disposed on the gate insulating layer in the capacitor region; an interlayer insulating layer disposed on the substrate to cover the gate electrode and the lower capacitor electrode; source and drain electrodes disposed on the interlayer insulating layer and electrically connected to the patterned semiconductor layer, and an upper capacitor electrode disposed on the interlayer insulating layer and facing the lower capacitor electrode; a first electrode disposed on the interlayer insulating layer and electrically connected to one of the source and drain electrodes; an organic layer including a light emitting layer, the organic layer being disposed on the first electrode; and a second electrode disposed on the organic layer, wherein regions of each of the buffer layer, the gate insulating layer, the interlayer insulating layer, the lower capacitor electrode, and the upper capacitor electrode that are disposed in the capacitor region of the substrate have surfaces in which protrusions are formed, the protrusions following the shape of grain boundaries of the patterned semiconductor layer.
According to aspects of the present invention, a method of fabricating an organic light emitting diode (OLED) display device includes: forming a substrate having a thin film transistor region and a capacitor region; forming a buffer layer on the substrate; forming an amorphous silicon layer on the buffer layer; forming a metal catalyst layer on the amorphous silicon layer; annealing the substrate to crystallize the amorphous silicon layer into a polysilicon layer; removing the metal catalyst layer; forming protrusions in the buffer layer while patterning the polysilicon layer to form a semiconductor layer in the thin film transistor region; forming a gate insulating layer on the substrate to cover the semiconductor layer; forming a gate electrode on the gate insulating layer and facing a predetermined region of the semiconductor layer; forming a lower capacitor electrode on the gate insulating layer in the capacitor region; forming an interlayer insulating layer on the substrate to cover the gate electrode and the lower capacitor electrode; forming source and drain electrodes on the interlayer insulating layer which are electrically connected to the semiconductor layer; forming an upper capacitor electrode on the interlayer insulating layer and facing the lower electrode; forming a first electrode on the interlayer insulating layer which is electrically connected to one of the source and drain regions of the semiconductor layer; forming an organic layer including a light emitting layer on the first electrode; and forming a second electrode on the organic layer.
According to aspects of the present invention, an OLED display device includes: a substrate having a thin film transistor region and a capacitor region; a buffer layer disposed on the substrate, the buffer layer having protrusions in the capacitor region that extend therefrom away from the substrate; and a capacitor disposed on the buffer layer in the capacitor region, wherein the capacitor follows the shape of the protrusions of the buffer layer.
According to aspects of the present invention, a method of manufacturing an organic light emitting diode (OLED) display device includes: forming a substrate having a thin film transistor region and a capacitor region; forming a buffer layer on the substrate; forming an amorphous silicon layer on the buffer layer; crystallizing the amorphous silicon layer to form a polysilicon layer having grain boundaries; forming protrusions in portions of the buffer layer adjacent to the grain boundaries of the polysilicon layer while patterning the polysilicon layer to form a semiconductor layer, the semiconductor layer being disposed in the thin film transistor region; forming a lower capacitor electrode on the gate insulating layer in the capacitor region, the lower capacitor electrode having protrusions corresponding to the protrusions of the buffer layer; forming an interlayer insulating layer on the substrate to cover at least the lower capacitor electrode, the interlayer insulating layer having protrusions corresponding to the protrusions of the lower capacitor electrode; and forming an upper capacitor electrode on the interlayer insulating layer and facing the lower electrode, the upper capacitor electrode having protrusions corresponding to the protrusions of the interlayer insulating layer.
According to aspects of the present invention: a method of manufacturing an organic light emitting diode (OLED) display device includes: forming a buffer layer on a substrate; forming protrusions in portions of the buffer layer; forming a lower capacitor electrode on the gate insulating layer, the lower capacitor electrode having protrusions corresponding to the protrusions of the buffer layer; forming an interlayer insulating layer on the substrate to cover at least the lower capacitor electrode, the interlayer insulating layer having protrusions corresponding to the protrusions of the lower capacitor electrode; and forming an upper capacitor electrode on the interlayer insulating layer and facing the lower electrode, the upper capacitor electrode having protrusions corresponding to the protrusions of the interlayer insulating layer.
Additional aspects and/or advantages of the invention will be set forth in part in the description which follows and, in part, will be obvious from the description, or may be learned by practice of the invention.
These and/or other aspects and advantages of the invention will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
Reference will now be made in detail to the present embodiments of the present invention, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to the like elements throughout. The embodiments are described below in order to explain the present invention by referring to the figures. In the drawings, the sizes and proportions of layers/regions may be exaggerated, and like reference numerals refer to like elements. It will be understood that when an element such as a layer, film, region, or substrate is referred to as being “formed on” or “disposed on” another element, it can be disposed directly on the other element, or intervening elements may also be present. In contrast, when an element is referred to as being “formed directly on” or “disposed directly on” another element, there are no intervening elements present.
Next, referring to
A metal catalyst is deposited on the diffusion layer 123 to form the metal catalyst layer 125. Here, one selected from the group consisting of Ni, Pd, Ag, Au, Al, Sn, Sb, Cu, Tb, and Cd. For example, nickel (Ni) may be used as the metal catalyst. Here, the metal catalyst layer 125 may be formed with an areal density of 1011 atoms/cm2 to 1015 atoms/cm2 on the diffusion layer 123. When the metal catalyst is formed with an areal density less than 1011 atoms/cm2, the amount of seeds that are crystallization nuclei is small, and thus the amorphous silicon layer may not be crystallized into a polysilicon layer using a super grain silicon (SGS) method. Alternatively, when the metal catalyst is formed with an areal density greater than 1015 atoms/cm2, the amount of metal catalyst diffused into the amorphous silicon layer is great, and thus grains of a resultant polysilicon layer are small. Furthermore, as the amount of remaining metal catalyst increases in the resultant polysilicon layer, characteristics of a semiconductor layer formed by patterning the polysilicon layer deteriorate.
As described above, an annealing process is performed on the substrate 100 on which the buffer layer 110, the amorphous silicon layer 120a, the diffusion layer 123, and the metal catalyst layer 125 are formed to move at least a portion of the metal catalyst of the metal catalyst layer 125 to a surface of the amorphous silicon layer 120a. That is, only a small amount of metal catalyst diffuses through the diffusion layer 123 to the surface of the amorphous silicon layer 120a, and most of the metal catalyst does not reach the amorphous silicon layer 120a or pass through the diffusion layer 123.
Therefore, the amount of metal catalyst reaching the surface of the amorphous silicon layer 120a is determined depending on a diffusion blocking ability of the diffusion layer 123, and the diffusion blocking ability of the diffusion layer 123 is closely related to the thickness of the diffusion layer 123. For example, as the diffusion layer 123 becomes thicker, the amount of metal catalyst to be diffused is reduced, and thus the grain size is increased. Moreover, as the diffusion layer becomes thinner, the amount of metal catalyst to be diffused is increased, and thus the grain size is reduced.
Here, the annealing process may be performed at a temperature of 200° C. to 900° C., for example, 350° C. to 500° C. for several seconds to several hours to diffuse the metal catalyst of the metal catalyst layer 125 to the amorphous silicon layer 120a. When the annealing process is performed at such a temperature for such a time period, deformation of a substrate caused by an excessive annealing process can be prevented to increase manufacturing yield and to reduce manufacturing costs. The annealing process may be performed using one of a furnace process, a rapid thermal annealing (RTA) process, an UV process, and a laser process (i.e., any of these processes).
After the amorphous silicon layer 120a is crystallized into the polysilicon layer, the diffusion layer 123 and the metal catalyst layer 125 are removed. Referring to
When the polysilicon layer is patterned into the semiconductor layer 120 using dry etching, grain boundaries on which metal silicides of the polysilicon layer crystallized by the metal catalyst gather and a seed region are not completely removed from the surface of the etched buffer layer and remain as a protrusion A. Therefore, the protrusion A remaining on the buffer layer 110 is formed in the same shape as a grain boundary that is formed by crystallizing the amorphous silicon layer into the polysilicon layer. In addition, when the grain size of the semiconductor layer 120 formed of the polysilicon layer is great, the frequency of the protrusions A on the buffer layer is reduced, and when the grain size is small, the frequency of the protrusions A is increased.
Referring to
Afterwards, a single layer of aluminum (Al) or an aluminum alloy, such as aluminum-neodymium (Al—Nd), or a multilayer in which an aluminum alloy is stacked on a chromium (Cr) or molybdenum (Mo) alloy is used to form a metal layer for a gate electrode (not shown). Then, the metal layer for a gate electrode is etched using photolithography and etching to form a gate electrode 140 facing the semiconductor layer 120 in the thin film transistor region a at a predetermined region of the semiconductor layer 120, i.e., a channel region thereof, and a lower capacitor electrode 145 in the capacitor region b.
Therefore, the protrusions are formed on the lower capacitor electrode 145, and thus a surface area of the electrode is increased. As a result, the increased surface area causes a capacitance of the capacitor to be increased when the capacitor is completely formed.
Referring to
The interlayer insulating layer 150 may be formed of a silicon nitride layer, a silicon oxide layer, or a combination thereof. Also, the source and drain electrodes 160a and 160b and the upper capacitor electrode 163 may be formed of one selected from the group consisting of molybdenum (Mo), chromium (Cr), tungsten (W), molybdenum-tungsten (MoW), aluminum (Al), aluminum-neodymium (Al—Nd), titanium (Ti), titanium nitride (TiN), copper (Cu), a Mo alloy, an Al alloy, and a Cu alloy.
Afterwards, referring to
The first electrode 180 may be formed as an anode or a cathode. When the first electrode 180 is formed as an anode, the anode may be formed of a transparent conductive layer made of ITO, IZO or ITZO; and when the first electrode 180 is formed as a cathode, the cathode may be formed of Mg, Ca, Al, Ag, Ba, or alloys thereof.
Referring to
While a polysilicon layer crystallized using a SGS method is described, MILC and MIC methods in which crystallization is performed using a metal catalyst can be used as the method of crystallizing the amorphous silicon layer, and the methods may be used alone or in combination.
According to aspects of the present invention, an amorphous silicon layer is crystallized using a metal catalyst to form a semiconductor layer formed of a polysilicon layer. Further, protrusions that are formed by residual metals remaining in the silicon layer upon crystallization on a buffer layer in the form of metal silicides cause a surface area of the buffer layer to be increased. As a result, an OLED display device may have a capacitor formed on the buffer layer whose capacitance is increased.
Although a few embodiments of the present invention have been shown and described, it would be appreciated by those skilled in the art that changes may be made in this embodiment without departing from the principles and spirit of the invention, the scope of which is defined in the claims and their equivalents.
Number | Date | Country | Kind |
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10-2009-0018200 | Mar 2009 | KR | national |
This application is a divisional of U.S. patent application Ser. No. 12/713,846, filed on Feb. 26, 2010, and claims priority from and the benefit of Korean Patent Application No. 10-2009-0018200, filed on Mar. 3, 2009, the disclosures of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
5517037 | Yamamoto | May 1996 | A |
5814540 | Takemura et al. | Sep 1998 | A |
5818083 | Ito | Oct 1998 | A |
6198133 | Yamazaki et al. | Mar 2001 | B1 |
6294442 | Kamal | Sep 2001 | B1 |
6294815 | Yamazaki et al. | Sep 2001 | B1 |
6703266 | Chen et al. | Mar 2004 | B1 |
6806099 | Takeda et al. | Oct 2004 | B2 |
6812473 | Amemiya | Nov 2004 | B1 |
6927107 | Makita et al. | Aug 2005 | B1 |
7015501 | Redecker et al. | Mar 2006 | B2 |
7091519 | Yamazaki et al. | Aug 2006 | B2 |
7341907 | Li et al. | Mar 2008 | B2 |
7615421 | Lee et al. | Nov 2009 | B2 |
7618852 | Jang et al. | Nov 2009 | B2 |
20010003659 | Aya et al. | Jun 2001 | A1 |
20020063261 | Zhang | May 2002 | A1 |
20030080337 | Yudasaka et al. | May 2003 | A1 |
20040004597 | Kung et al. | Jan 2004 | A1 |
20040115906 | Makita et al. | Jun 2004 | A1 |
20040173796 | Miyasaka | Sep 2004 | A1 |
20050023531 | Shoji et al. | Feb 2005 | A1 |
20050161742 | Isobe et al. | Jul 2005 | A1 |
20050184290 | Ohnuma | Aug 2005 | A1 |
20050275019 | Seo et al. | Dec 2005 | A1 |
20060040429 | Park et al. | Feb 2006 | A1 |
20060051914 | Kakehata et al. | Mar 2006 | A1 |
20060061266 | Kang et al. | Mar 2006 | A1 |
20060121651 | Park et al. | Jun 2006 | A1 |
20060130939 | Jang et al. | Jun 2006 | A1 |
20070238229 | Chang et al. | Oct 2007 | A1 |
20080111135 | Choi et al. | May 2008 | A1 |
20080157083 | Park et al. | Jul 2008 | A1 |
20080211024 | Kato et al. | Sep 2008 | A1 |
20080258186 | Surdeanu et al. | Oct 2008 | A1 |
20090050894 | Park et al. | Feb 2009 | A1 |
20090239352 | Kitagawa et al. | Sep 2009 | A1 |
20100224882 | Lee et al. | Sep 2010 | A1 |
Number | Date | Country |
---|---|---|
1779985 | May 2006 | CN |
0763765 | Mar 1997 | EP |
1 903 604 | Mar 2008 | EP |
2 226 833 | Sep 2010 | EP |
63-033868 | Feb 1988 | JP |
63-304668 | Dec 1988 | JP |
01-102525 | Apr 1989 | JP |
05-173177 | Jul 1993 | JP |
06-067203 | Mar 1994 | JP |
06-260651 | Sep 1994 | JP |
07-013196 | Jan 1995 | JP |
08-045850 | Feb 1996 | JP |
09-107100 | Apr 1997 | JP |
2001-189275 | Jul 2001 | JP |
2001-337348 | Dec 2001 | JP |
2003-060209 | Feb 2003 | JP |
2003-100629 | Apr 2003 | JP |
2003-115457 | Apr 2003 | JP |
2003-188098 | Jul 2003 | JP |
2004-207298 | Jul 2004 | JP |
2005-064487 | Mar 2005 | JP |
2005-229096 | Aug 2005 | JP |
2005-354028 | Dec 2005 | JP |
2006-019682 | Jan 2006 | JP |
2006-024881 | Jan 2006 | JP |
2006-330736 | Dec 2006 | JP |
2007-013145 | Jan 2007 | JP |
2007-027202 | Feb 2007 | JP |
2007-035812 | Feb 2007 | JP |
2007-073953 | Mar 2007 | JP |
2007-193313 | Aug 2007 | JP |
2007-311767 | Nov 2007 | JP |
2008-166698 | Jul 2008 | JP |
2008-166703 | Jul 2008 | JP |
2008-166785 | Jul 2008 | JP |
2009-059940 | Mar 2009 | JP |
10-1997-0063763 | Sep 1997 | KR |
10-1997-0072491 | Nov 1997 | KR |
10-2000-0055877 | Sep 2000 | KR |
10-0285865 | Mar 2001 | KR |
10-2001-0078788 | Aug 2001 | KR |
10-0317638 | Dec 2001 | KR |
10-2002-0021546 | Mar 2002 | KR |
10-2003-0028696 | Apr 2003 | KR |
10-2004-0035409 | Apr 2004 | KR |
10-2004-0036761 | May 2004 | KR |
10-2004-0040762 | May 2004 | KR |
10-2004-0098958 | Nov 2004 | KR |
10-0470274 | Feb 2005 | KR |
10-2006-0018533 | Mar 2006 | KR |
10-2006-0058934 | Jun 2006 | KR |
10-0623228 | Sep 2006 | KR |
10-0628989 | Sep 2006 | KR |
10-0772347 | Oct 2007 | KR |
10-2007-0107142 | Nov 2007 | KR |
10-2007-0107168 | Nov 2007 | KR |
10-0778781 | Nov 2007 | KR |
10-0839735 | Jun 2008 | KR |
10-2008-0086967 | Sep 2008 | KR |
361694 | Jun 1999 | TW |
I296855 | May 2008 | TW |
I305681 | Jan 2009 | TW |
I307961 | Mar 2009 | TW |
Entry |
---|
Final Office Action for related U.S. Appl. No. 12/714,201 dated Jan. 17, 2013. |
Non-Final Office Action for related U.S. Appl. No. 12/714,201 dated Sep. 27, 2012. |
Final Office Action for related U.S. Appl. No. 12/713,928 dated Sep. 20, 2012. |
Non-Final Office Action for related U.S. Appl. No. 12/713,928 dated Mar. 28, 2012. |
Final Office Action for related U.S. Appl. No. 12/714,154 dated Apr. 10, 2012. |
Final Office Action for related U.S. Appl. No. 12/714,137 dated Mar. 22, 2012. |
Ex Parte Quayle Action for related U.S. Appl. No. 12/714,252 dated May 9, 2011. |
Final Office Action for related U.S. Appl. No. 12/714,201 dated Apr. 24, 2012. |
Non-Final Office Action for related U.S. Appl. No. 12/714,154 dated Dec. 23, 2011. |
Non-Final Office Action for related U.S. Appl. No. 12/714,137 dated Dec. 19, 2011. |
Final Office Action for related U.S. Appl. No. 12/713,928 dated Jul. 10, 2012. |
Soo Young Yoon et al., “Metal-induced crystallization of amorphous silicon,” Thin Solid Films 383 (2001), pp. 34-38. |
Notice of Allowance and Fee(s) Due for related U.S. Appl. No. 12/714,252 dated Aug. 30, 2011. |
Non-Final Office Action for related U.S. Appl. No. 12/714,201 dated Jan. 13, 2012. |
S. L. Gras et al., “Intelligent Control of Surface Hydrophobicity,” ChemphyChem, vol. 8, Oct. 2007, Wiley-VCH, Germany, pp. 2036-2050. |
Non-Final Office Action for related U.S. Appl. No. 12/713,846 dated Aug. 27, 2012. |
Notice of Allowance and Fee(s) Due for related U.S. Appl. No. 12/713,846 dated Dec. 14, 2012. |
Non-Final Office Action for related U.S. Appl. No. 12/712,591 dated Feb. 28, 2013. |
Non-Final Office Action issued on Feb. 26, 2014 in U.S. Appl. No. 12/714,154. |
Final Office Action issued on Oct. 17, 2013 in U.S. Appl. No. 12/714,154. |
Final Office Action issued on Jul. 24, 2013 in U.S. Appl. No. 12/712,591. |
Final Office Action issued on Mar. 12, 2014 in U.S. Appl. No. 12/714,201. |
European Extended Search Report issued on Mar. 4, 2014 in European Application No. 10154502.8. |
Notice of Allowance issued on May 24, 2013 in U.S. Appl. No. 13/177,936. |
Non-Final Office Action issued on Jul. 5, 2013 in U.S. Appl. No. 12/714,154. |
Non-Final Office Action dated Dec. 3, 2013 in U.S. Appl. No. 12/714,201. |
Number | Date | Country | |
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20130228760 A1 | Sep 2013 | US |
Number | Date | Country | |
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Parent | 12713846 | Feb 2010 | US |
Child | 13841121 | US |