In recent years, various techniques for crystallizing or improving the crystallinity of an amorphous or polycrystalline semiconductor film have been investigated. This technology is used in the manufacture of a variety of devices, such as image sensors and displays, for example, active-matrix liquid-crystal display (AMLCD) devices. In the latter, a regular array of thin-film transistors (TFTs) are fabricated on an appropriate transparent substrate, and each transistor serves as a pixel controller.
Semiconductor films are processed using excimer laser annealing (ELA), also known as line beam ELA, in which a region of the film is irradiated by an excimer laser to partially melt the film and then is crystallized.
Sequential lateral solidification (SLS) using an excimer laser is one method that has been used to form high quality polycrystalline films having large and uniform grains. SLS is a crystallization process that provides elongated grains of a crystallized material in predefined locations on a film.
When polycrystalline material is used to fabricate electronic devices, the total resistance to carrier transport is affected by the combination of barriers that a carrier has to cross as it travels under the influence of a given potential. Due to the additional number of grain boundaries that are crossed when the carrier travels in a direction perpendicular to the long grain axes of the polycrystalline material or when a carrier travels across a larger number of small grains, the carrier will experience higher resistance as compared to the carrier traveling parallel to long grain axes. Therefore, the performance of devices fabricated on polycrystalline films formed using SLS, such as TFTs, will depend upon the crystalline quality and microstructure of the TFT channel relative to the long grain axes, which corresponds to the main growth direction.
To achieve acceptable system performance for devices that utilize a polycrystalline thin film there still remains a need to optimize manufacturing processes that provide a defined, crystallographic orientation of the crystal grains.
In accordance with one aspect, the present invention provides a method for providing polycrystalline films having a controlled microstructure as well as a crystallographic texture. The methods provide elongated grains or single-crystal islands of a specified crystallographic orientation. In particular, a method of processing a film on a substrate includes providing a textured film having crystal grains oriented predominantly in one preferred crystallographic orientation; and then generating a microstructure using sequential lateral solidification crystallization that provides a location-controlled growth of the grains orientated in the preferred crystallographic orientation. One preferred direction of crystallographic orientation is a direction normal to the surface of the film.
The process of sequential lateral solidification (SLS) generally includes generating a plurality of laser beam pulses; directing the plurality of laser beam pulses through a mask to generate a plurality of patterned laser beams; irradiating a portion of a selected region of a film with one of the plurality of patterned beams, the beam having an intensity that is sufficient to melt throughout its entire thickness the irradiated portion of the film, wherein the irradiated portion of the film laterally crystallizes upon cooling. The process includes repositioning the film to irradiate a subsequent portion of the selected region with patterned beams, such that the subsequent position overlaps with the previously irradiated portion permitting the further lateral growth of the crystal grains. In one embodiment, successive portions of the selected region are irradiated such that the film is substantially completely crystallized in a single traversal of the patterned beams over the selected region of the film. By “completely crystallized” it is meant that the selected region of the film possesses the desired microstructure and crystal orientation, so that no further laser scanning of the region is required. The mask includes a dot-patterned mask and has opaque array patterns which include at least one of dot-shaped areas, hexagonal-shaped areas and rectangular shaped areas.
According to one aspect of the invention, the textured film is generated by one of zone melt recrystallization, solid phase recrystallization, direct deposition methods, surface-energy driven secondary grain growth methods or by pulsed laser crystallization methods. The direct deposition methods comprise one of chemical vapor deposition, sputtering and evaporation. The pulsed laser crystallization methods include SLS or multiple-pulse ELA methods. The film can be a metal film or a semiconductor film.
According to another aspect of the present invention, a system for processing a film on a substrate includes at least one, laser for generating a plurality of laser beam pulses; a film support for positioning the film that is capable of movement in at least one direction; a mask support; optics for directing a first set of laser beam pulses through a first mask to generate a textured film; optics for directing a second set of laser beams onto the textured film; and a controller for controlling the movement of the film support and mask support in conjunction with frequency of laser beam pulses.
According to another aspect of the present invention, a device comprising a polycrystalline thin film having periodically located grains in which each of the grains are predominantly of one crystallographic orientation. The predominant crystallographic orientation is a <111> orientation or in another embodiment is a <100> orientation. The periodically located grains form columns of elongated grains.
The foregoing and other features and advantages of the invention will be apparent from the following more particular description of embodiments of the invention, as illustrated in the accompanying drawings.
The processes and systems described herein, defined as hybrid sequential lateral solidification (SLS), provide elongated grains or single-crystal islands of a specified crystallographic orientation. The embodiments of the invention are predicated on the recognition that the crystal orientation of lateral crystal growth during SLS depends on the orientation of the material at the boundary of the irradiated region. Lateral crystal growth of a material from a solidus boundary defined by a textured crystal promotes growth of that crystallographic orientation.
At its most basic, hybrid SLS is a two-step process as illustrated in
In the second step 44 of the hybrid SLS process, SLS is performed. The lateral crystallization results in “location-controlled growth” of grain boundaries and elongated crystals of a desired crystallographic orientation. Location-controlled growth referred to herein is defined as the controlled location of grains and grain boundaries using particular beam patterns and masks such as, for example, dot-patterned masks.
As described briefly herein before, sequential lateral solidification (“SLS”) is a crystallization process that provides elongated grains or single-crystal islands of a crystallized material in predefined locations on a film. However, SLS is not able to fully define the crystallographic orientation of those grains. In an SLS process growth begins with existing grains as it is epitaxial growth and, thus, the process cannot provide for growth in a preferred orientation. Epitaxial growth is referred to as the growth of the crystals of one material on the crystal face of another material, such that the crystalline grains of both materials have the same structural orientation. Sequential lateral solidification produces large grained structures through small-scale translation of a thin film between sequential pulses emitted by a pulsed laser. As the film absorbs the energy of each pulse, a small area of the film melts completely and recrystallizes laterally from the solidus/melt interface to form a crystalline region. By “lateral crystal growth” or “lateral crystallization,” as those terms are used herein, it is meant a growth technique in which a region of a film is melted to the film/surface interface and in which recrystallization occurs in a crystallization front moving laterally across the substrate surface.
The thin film may be a metal or semiconductor film. Exemplary metals include aluminum, copper, nickel, titanium, gold, and molybdenum. Exemplary semiconductor films include conventional semiconductor materials, such as silicon, germanium, and silicon-germanium. Additional layers situated beneath or above the metal or semiconductor film are contemplated. The additional layers can be made of silicon oxide, silicon nitride and/or mixtures of oxide, nitride or other materials that are suitable, for example, for use as a thermal insulator to protect the substrate from overheating or as a diffusion barrier to prevent diffusion of impurities from the substrate to the film. PCT Publication No. WO 2003/084688 describes methods and systems for providing an aluminum thin film with a controlled crystal orientation using pulsed laser induced melting and nucleation-initiated crystallization, the entire teachings of which are incorporated herein by reference.
A thin film is processed into a location-controlled elongated grain polycrystalline thin film using SLS. An exemplary SLS process includes generating a plurality of excimer laser pulses of a predetermined fluence, controllably modulating the fluence of the excimer laser pulses, homogenizing the intensity profile of the laser pulse plane, masking each homogenized laser pulse to define patterned laser beams, irradiating the thin film with the laser beams to effect melting of portions thereof, and controllably and continuously translating the sample to move the patterned beam across the substrate surface. The laser pulse frequency and the movement (speed and direction) of the sample may be adjusted so that the areas of sequential irradiation of the sample overlap from one irradiation/crystallization cycle to the next, so as to provide for the lateral crystal growth that gives rise to large grains. Pulse frequency and stage and mask position may be coordinated and controlled by a computer. Systems and methods for providing continuous motion sequential lateral solidification are provided in U.S. Pat. No. 6,368,945, which is incorporated herein in its entirety by reference. The exemplary SLS processes are described in U.S. Pat. No. 6,555,449, and U.S. patent application Ser. No. 10/944,350 which uses a dot-patterned mask, the entire teachings of which are incorporated herein by reference.
An alternate SLS method is used in different embodiments and is referred to herein as the dot-patterned SLS process.
Embodiments of the present invention provide uniformly oriented material in epitaxy by performing SLS on a textured precursor. A laterally grown grain adapts the orientation of the seed. The polycrystalline film varies widely from grain to grain in the prior art. By selecting seed crystals of similar crystallographic orientation (texture), it is possible to grow large location-controlled (microstructure) grains of similar crystallographic orientation. The embodiments of this invention are directed at particular combinations of a texture-developing technology and the SLS process.
Conventional methods of obtaining a precursor textured film are used in the first step, including zone melt recrystallization (ZMR), solid phase recrystallization, direct deposition techniques (chemical vapor deposition (CVD), sputtering, evaporation), surface-energy-driven secondary grain growth (SEDSGG) and pulsed laser crystallization (SLS, multiple-pulse ELA) methods. It is envisioned that other texture-inducing methods may also be used in a similar way to generate the textured precursors. Even though the methods of obtaining a precursor textured film are applicable to a large variety of metal and/or semiconductor films, the following methods are described with respect to a silicon film due to the importance of the silicon in semiconductor industry and the level of understanding of silicon in the industry due to all the studies performed to date using silicon.
The following methods are used in different embodiments to provide textured polycrystalline films that can then be used in a hybrid SLS process to create microstructure-controlled and crystallographic-orientation controlled poly-Si films. These methods describe the use of non-patterned planar samples. Methods using patterning, such as graphoepitaxy are often suggested as a means to also reach some control of the microstructure. SLS, however, is not always tolerant of non-planar or patterned films and, in addition, it is most likely superior in controlling the microstructure.
As-Deposited CVD poly-Silicon films can be used to provide (110) or (100) texture in crystalline films. As-deposited poly-silicon films sometimes show texture, depending on the details of the deposition process, such as pressure and temperature. Typically, texture in these films develops throughout the deposition process, that is initial growth at the SiO2 interface is randomly oriented. As the lateral growth in SLS starts at the very edge of the unmolten portion, which is located at the SiO2 interface, crystallographic orientation may still be random (which has been observed for <110> oriented poly-Si films). It is, however, possible that methods are developed that yield texture throughout the thickness of the film or that a post-treatment is performed to establish the same goal through grain growth (i.e., preferred grains growing at the expense of others).
Seed Selection through Ion Channeling (SSIC) can be used to provide (110) texture in crystalline films. Non-textured (or mildly (110)-textured) as-deposited poly-silicon (Si) films can be converted into strongly (110) textured films by silicon “self implantation” at a specific dose close to the complete amorphization threshold followed by solid-phase crystallization. Due to the effect of ion channeling along the <110> directions in Si grains, only those grains that have this direction parallel to the direction of the implantation survive. When the implantation is perpendicular to the surface of the Si film, this means that <110> surface oriented grains survive. During the subsequent recrystallization, a large-grain <110> oriented poly-Si film is obtained.
Surface-Energy-Driven Grain Growth (SEDGG) can be used to generate (111) texture in crystalline film. SEDGG is a particular secondary grain growth mechanism and is commonly also called surface-energy-driven secondary grain growth (SEDSGG). Primary, or normal, grain growth is observed upon heating (>1000° C.) of a material and is driven by a reduction of the grain boundary area. In the case of thin films, this process is halted when the grain diameter reaches values comparable to the film thickness. Beyond that point, secondary, or abnormal, grain growth can occur. This process is driven by free energy anisotropies at the surface and the interface of the secondary grains. Since the magnitude of the surface free energy is almost certainly larger than that of the Si—SiO2 interface free energy, it is expected that minimization thereof dominates the process. The energy of a free surface of Si is minimized with (111) texture and indeed it is observed that secondary grains are predominantly <111>.
Analysis on SEDGG predominantly discusses results obtained with Si films doped with phosphorous (P) or arsenic (As). These dopants are known to enhance the rate of secondary grain growth, through an increase of the grain boundary mobility. Intrinsic films still show secondary grain growth; order to get reasonable growth rates, the driving force and/or increase the grain boundary mobility is increased in alternative ways. Respective examples hereof are decreasing the film thickness or increasing the annealing temperature.
Metal-Induced Lateral Crystallization (MILC) can be used to provide crystalline films having (110) texture. In metal-induced crystallization, metal, the most popular being nickel (Ni), is brought in contact with the Si film and subsequent heating causes the film to crystallize rapidly. When the Ni—Si contacting is done only locally (for example, by having a windowed buffer layer between the Si and metal films), a laterally crystallized poly-Si film is obtained with a lower Ni residue and with a high degree of (110) texture.
In this process, NiSi2 precipitates are formed by Ni diffusion through the Si film. NiSi2 has a cubic lattice and the lattice mismatch with c-Si is only 0.4%. Due to this small mismatch, a few nm of c-Si will grow after which the Ni migrates/diffuses to its surface and the process is repeated. As the process continues, long needle-like crystals are formed and high degree of crystallization can be reached if some additional solid-phase crystallization is allowed to happen sideways from these needle-like crystals. Growth on the NiSi2 precipitates occurs on a single {111} plane only and as such it is one dimensional. Occasionally, however, a different {111} plane is chosen and the needle-like crystal makes a 109° or 71° turn. This process can be sustained when the needles remain in the plane of the film (i.e., they do not hit surface of interface) and this can be achieved when the surface orientation of the grains is <110>.
Partial Melting ZMR can be used to provide crystalline films having (100) texture. Zone-melting recrystallization (ZMR) of Si films results in the formation of large grained polycrystalline Si films having a preferential <100> surface orientation of the crystals. An embodiment of the present invention uses these orientated polycrystalline films as a precursor for crystallization using SLS. The embodiment includes the use of oriented seed grains to promote the formation of large directionally grown oriented crystals. Thus, ZMR of polycrystalline films is used to obtain (100) textured large-grain poly-Si films. Growth of long (100) textured grains starts on grains formed in the “transition region” between the unmelted and the completely melted areas of the film. This is the regime of partial melting (i.e., coexistence of solid and liquid), which only exists in radiatively heated Si films as a result of a significant increase in reflectivity of Si upon melting (a semiconductor—metal transition). In this partial melting regime, <100> grains have been observed to dominate, a phenomenon that is linked to a crystallographic anisotropy in the SiO2—Si interfacial energy.
The above results have typically been obtained at scanning velocities of a few mm/s to less than 1 mm/s. For higher velocities (i.e., for “rapid-ZMR”), (100) textured growth is no longer stable and a random orientation is obtained. It is observed that the crystallographic orientation of laterally growing grains “rolls off” into random orientations. The “transition region”, however, exhibits a strong (100) texture, even though the degree decreases with increasing velocity. One way to maximize the degree of texture in partial melting rapid-ZMR is to create a precursor with a maximized number of seeds for <100> growth. One way to do so includes depositing a (100)-textured poly-Si films. It may also work to precrystallize the Si film into very small-grain material that, provided orientation is random, ensures a high density of texture (100) grains, for example, through complete-melting crystallization (CMC) to create nucleated grains.
Zone melt irradiation using a continuous laser produces silicon films having <100> orientation as described by M. W. Geis et. al., “Zone-Melting recrystallization of Si films with a moveable-strip-heater oven”, J. Electro-Chem. Soc. 129, 2812 (1982), the entire teachings of which are incorporated hereby by reference.
Near-Complete-Melting ELA can be used to generate crystalline films having (111) texture. Multiple-pulse excimer-laser crystallization in the partial melting regime is used to create uniform poly-Si films having grains that are predominantly <111> surface-oriented. Maximum grain size uniformity can be obtained due to interference effects at the roughened surface of the poly-Si film. This leads to poly-Si films with a grain size that is roughly equal to the wavelength, for example, using a XeCl laser ˜300 nm. At slightly higher energy densities, but still below the complete-melting threshold, grain diameter is no longer stabilized by the interference effects and much larger predominantly <111> surface-oriented grains are obtained.
Even though the energy density at which these processes are performed is in the partial melting regime, some complete melting must locally occur in order to allow for the cumulative growth of grains larger than the film thickness. It is suggested that preferential melting can occur at grain boundaries due to a locally enhanced absorption and/or reduced melting temperature. During melting and regrowth of the grain-boundary area, there apparently is a preference for <111> oriented grains either in their resistance to melting or their lateral growing velocity. As a result, <111> oriented grains grow at the expense of differently oriented grains.
With respect to Si precursor films, multiple-pulse irradiation from an excimer laser in the near-melting regime provides Si films having <111> orientation as described by H. J. Kim and James S. Im in Mat. Res. Soc. Sym. Proc., 321, 665-670 (1994) the entire teachings of which are incorporated herein by reference.
SLS can be used to generate crystalline films having (110) texture. The hybrid SLS process in certain embodiments can use an SLS process in the first step of generating a textured precursor. The SLS process used in the first step is a texture inducing SLS process. Analysis of directional poly-Si obtained through excimer-laser based SLS (see
One method to obtain a particular (100) texture includes a particular SLS process to create a certain in-plane texture twice, perpendicular with respect to each other. The details of this process are described in U.S. Patent Application No. 60/503,419, J. S. Im, entitled “Method and system for producing crystalline thin films with a uniform crystalline orientation,” the entire teachings of which are incorporated herein by reference. This can lead to formation of surface oriented material: if the orientation is controlled in both x and y directions, the orientation in the z direction per definition is controlled as well.
SLS can be used to generate crystalline films having (111) texture. Analysis of SLS using a pulsed solid-state laser (frequency-doubled Nd:YVO4), are described by M. Nerding et. al., in, “Tailoring texture in laser crystallization of silicon thin-films on glass,” Solid State Phenom. 93, 173 (2003), the entire contents of which are incorporated herein by reference. Although fundamentally the same process as with an excimer laser, there are some differences that can influence the orientation of the grains. The most prominent of these is the wavelength (532 nm), but it is possible that the spatial profile (Gaussian) and the pulse duration (20 ns) also play a role in the process. When SiNx buffer layers are used, however, a strong (111) surface orientation is obtained for a film thickness of at least approximately 150 nm.
In an embodiment, epitaxial growth of III-V semiconductors, such as Gallium arsenide (GaAs), on a Silicon (Si) carrier enables products that combine the benefits of both materials: for example, light emitting diodes (LEDs) made in GaAs combined with electrical circuitry made in Si. If, in addition, the Si is a deposited film on top of a non-semiconducting substrate, such as glass, one is able to have these benefits on large-area and/or transparent substrates for a low price.
Proper epitaxy, however, requires both high-quality (i.e., defect free) as well as a uniformly oriented material. High quality can be achieved with the sequential lateral solidification (SLS) method, most importantly, with processes that can be used to create location-controlled single-crystal islands. In particular, the embodiments described herein of the hybrid SLS process are useful in the thin film transistor (TFT) industry as they leverage epitaxial growth, provide for TFT uniformity though anisotropy of performance level both through mobility and through interfacial defect density and TFT uniformity through quality of the material. Details of the effects of uniformity of TFTs, being field effect devices, are described by T. Sato, Y. Takeishi, H. Hara and Y. Okamoto, “Mobility anisotropy of electrons in inversion layers on oxidized silicon surfaces,” in Physical Review B (Solid State) 4, 1950 (1971) and by M. H. White and J. R. Cricchi, “Characterization of thin-oxide MNOS memory transistors,” in IEEE Trans. Electron Devices ED-19, 1280 (1972), the entire teachings of both are incorporated herein by reference.
In an embodiment, a higher energy-density ELA process as described herein before is used as a result of which a larger average grain size film is obtained. These films can either have a strong (111) or (100) texture depending upon the conditions of the ELA process selected; a process that is likely to be related to anisotropies in melting and solidification of differently oriented grains. A very high degree of texture is obtained with commercially available line-beam ELA systems. These precursor textured films are not used in production of TFTs or for epitaxial processes due to the randomness of the microstructure.
The experimental conditions for the embodiment [(111) texture, SLS (150 nm Si)] include scanning a 500×500 μm2 with a 4 μm between-pulse translation leading to 125 pulses per unit area, performed with the SLS system described with respect to
Combining the ELA pretreatment with the SLS process as described in U.S. patent application Ser. No. 10/944,350, the entire contents of which are incorporated herein by reference, leads to location-controlled single-crystal islands with a <111> orientation that may be useful for epitaxial growth of III-V semiconductors or even for uniform TFT on low-cost large-area transparent substrates.
In
In particular embodiments using the dot-SLS (process dot-patterned mask) the <111> and <100> islands can be obtained island having the <100> orientation have the lowest density of defects, followed by <111>. These two observations indicate a preference for especially <100> and to a lesser degree <111> orientation. These observations are valid when working at typical conditions (i.e., 50-250 nm Si films, 30-300 ns pulse duration, room temperature, etc.). Alternate embodiments that include working at different conditions, can suppress the formation of Sigma3 boundaries, meaning that defect free islands of any orientation can be obtained.
In view of the wide variety of embodiments to which the principles of the present invention can be applied, it should be understood that the illustrated embodiments are exemplary only, and should not be taken as limiting the scope of the present invention. For example, the steps of the diagrams may be taken in sequences other than those described, and more or fewer elements may be used in the diagrams. While various elements of the embodiments have been described as being implemented in software, other embodiments in hardware or firmware implementations may alternatively be used, and vice-versa.
It will be apparent to those of ordinary skill in the art that methods involved in creating crystallographic orientation controlled poly-silicon films may be embodied in a computer program product that includes a computer usable medium. For example, such a computer usable medium can include a readable memory device, such as, a hard drive device, a CD-ROM, a DVD-ROM, or a computer diskette, having computer readable program code segments stored thereon. The computer readable medium can also include a communications or transmission medium, such as, a bus or a communications link, either optical, wired, or wireless having program code segments carried thereon as digital or analog data signals.
Other aspects, modifications, and embodiments are within the scope of the following claims.
This application is a divisional of and claims priority under 35 U.S.C., §121 to U.S. patent application Ser. No. 10/994,205, filed on Nov. 18, 2004 and entitled Systems and Methods for Creating Crystallographic-Orientation Controlled poly-Silicon Films, the entire contents of which are incorporated hereby by reference.
Number | Name | Date | Kind |
---|---|---|---|
3632205 | Marcy et al. | Jan 1972 | A |
4234358 | Celler et al. | Nov 1980 | A |
4309225 | Fan et al. | Jan 1982 | A |
4382658 | Shields et al. | May 1983 | A |
4456371 | Lin | Jun 1984 | A |
4639277 | Hawkins | Jan 1987 | A |
4691983 | Kobayashi et al. | Sep 1987 | A |
4727047 | Bozler et al. | Feb 1988 | A |
4758533 | Magee et al. | Jul 1988 | A |
4793694 | Liu | Dec 1988 | A |
4800179 | Mukai et al. | Jan 1989 | A |
4855014 | Kakimoto et al. | Aug 1989 | A |
4870031 | Sugahara et al. | Sep 1989 | A |
4940505 | Schachameyer et al. | Jul 1990 | A |
4970546 | Suzuki et al. | Nov 1990 | A |
4977104 | Sawada et al. | Dec 1990 | A |
5032233 | Yu et al. | Jul 1991 | A |
5061655 | Ipposhi et al. | Oct 1991 | A |
5076667 | Stewart et al. | Dec 1991 | A |
RE33836 | Resor, III et al. | Mar 1992 | E |
5145808 | Sameshima et al. | Sep 1992 | A |
5173441 | Yu et al. | Dec 1992 | A |
5204659 | Sarma | Apr 1993 | A |
5233207 | Anzai et al. | Aug 1993 | A |
5247375 | Mochizuki et al. | Sep 1993 | A |
5281840 | Sarma | Jan 1994 | A |
5285236 | Jain | Feb 1994 | A |
5291240 | Jain | Mar 1994 | A |
5294811 | Aoyama et al. | Mar 1994 | A |
5304357 | Sato et al. | Apr 1994 | A |
5338959 | Kim et al. | Aug 1994 | A |
5373803 | Noguchi et al. | Dec 1994 | A |
5395481 | McCarthy | Mar 1995 | A |
5409867 | Asano et al. | Apr 1995 | A |
5453594 | Konecny | Sep 1995 | A |
5456763 | Kaschmitter et al. | Oct 1995 | A |
5496768 | Kudo et al. | Mar 1996 | A |
5512494 | Tanabe et al. | Apr 1996 | A |
5523193 | Nelson | Jun 1996 | A |
5529951 | Noguchi et al. | Jun 1996 | A |
5571430 | Kawasaki et al. | Nov 1996 | A |
5591668 | Maegawa et al. | Jan 1997 | A |
5663579 | Noguchi | Sep 1997 | A |
5683935 | Miyamato | Nov 1997 | A |
5710050 | Makita et al. | Jan 1998 | A |
5721606 | Jain | Feb 1998 | A |
5742426 | York | Apr 1998 | A |
5756364 | Tanaka et al. | May 1998 | A |
5766989 | Maegawa et al. | Jun 1998 | A |
5767003 | Noguchi | Jun 1998 | A |
5817548 | Noguchi et al. | Oct 1998 | A |
5844588 | Anderson | Dec 1998 | A |
5858807 | Kawamura | Jan 1999 | A |
5861991 | Fork | Jan 1999 | A |
5893990 | Tanaka et al. | Apr 1999 | A |
5948291 | Neylan et al. | Sep 1999 | A |
5960323 | Wakita et al. | Sep 1999 | A |
5986807 | Fork | Nov 1999 | A |
6002523 | Tanaka | Dec 1999 | A |
6014944 | Aklufi et al. | Jan 2000 | A |
6020224 | Shimogaichi et al. | Feb 2000 | A |
6020244 | Thompson et al. | Feb 2000 | A |
6045980 | Edelkind et al. | Apr 2000 | A |
6072631 | Guenther et al. | Jun 2000 | A |
6081381 | Shalapenok et al. | Jun 2000 | A |
6117752 | Suzuki et al. | Sep 2000 | A |
6120976 | Treadwell et al. | Sep 2000 | A |
6130009 | Smith et al. | Oct 2000 | A |
6130455 | Yoshinouchi et al. | Oct 2000 | A |
6135632 | Flint | Oct 2000 | A |
6136632 | Higashi | Oct 2000 | A |
6156997 | Yamazaki et al. | Dec 2000 | A |
6162711 | Ma et al. | Dec 2000 | A |
6169014 | McCulloch et al. | Jan 2001 | B1 |
6172820 | Kuwahara et al. | Jan 2001 | B1 |
6176922 | Aklufi et al. | Jan 2001 | B1 |
6177301 | Jung et al. | Jan 2001 | B1 |
6184490 | Schweizer | Feb 2001 | B1 |
6187088 | Okumura et al. | Feb 2001 | B1 |
6190985 | Buynoski | Feb 2001 | B1 |
6193796 | Yang et al. | Feb 2001 | B1 |
6203952 | O'Brien et al. | Mar 2001 | B1 |
6235614 | Yang et al. | May 2001 | B1 |
6242291 | Kusumoto et al. | Jun 2001 | B1 |
6274488 | Talwar et al. | Aug 2001 | B1 |
6285001 | Fleming et al. | Sep 2001 | B1 |
6300175 | Moon et al. | Oct 2001 | B1 |
6313435 | Shoemaker et al. | Nov 2001 | B1 |
6316338 | Jung et al. | Nov 2001 | B1 |
6320227 | Lee et al. | Nov 2001 | B1 |
6322625 | Im | Nov 2001 | B2 |
6326186 | Kirk et al. | Dec 2001 | B1 |
6326215 | Keen | Dec 2001 | B1 |
6326286 | Park et al. | Dec 2001 | B1 |
6333232 | Kunikiyo et al. | Dec 2001 | B1 |
6341042 | Matsunaka et al. | Jan 2002 | B1 |
6348990 | Igasaki et al. | Feb 2002 | B1 |
6353218 | Yamazaki et al. | Mar 2002 | B1 |
6358784 | Zhang et al. | Mar 2002 | B1 |
6368945 | Im | Apr 2002 | B1 |
6388146 | Onishi et al. | May 2002 | B1 |
6388386 | Kunii et al. | May 2002 | B1 |
6392810 | Tanaka et al. | May 2002 | B1 |
6393042 | Tanaka et al. | May 2002 | B1 |
6407012 | Miyasaka et al. | Jun 2002 | B1 |
6410373 | Chang et al. | Jun 2002 | B1 |
6429100 | Yoneda et al. | Aug 2002 | B2 |
6432758 | Cheng et al. | Aug 2002 | B1 |
6437284 | Okamoto et al. | Aug 2002 | B1 |
6444506 | Kusumoto et al. | Sep 2002 | B1 |
6445359 | Ho | Sep 2002 | B1 |
6448612 | Miyazaki et al. | Sep 2002 | B1 |
6451631 | Grigoropoulos et al. | Sep 2002 | B1 |
6455359 | Yamazaki et al. | Sep 2002 | B1 |
6468845 | Nakajima et al. | Oct 2002 | B1 |
6471772 | Tanaka et al. | Oct 2002 | B1 |
6472684 | Yamazaki et al. | Oct 2002 | B1 |
6476447 | Yamazaki et al. | Nov 2002 | B1 |
6479837 | Ogawa et al. | Nov 2002 | B1 |
6482722 | Kunii et al. | Nov 2002 | B2 |
6493042 | Bozdagi et al. | Dec 2002 | B1 |
6495067 | Ono et al. | Dec 2002 | B1 |
6495405 | Voutsas et al. | Dec 2002 | B2 |
6501095 | Yamaguchi et al. | Dec 2002 | B2 |
6504175 | Mei et al. | Jan 2003 | B1 |
6506636 | Yamazaki et al. | Jan 2003 | B2 |
6511718 | Paz de Araujo et al. | Jan 2003 | B1 |
6512634 | Tanaka et al. | Jan 2003 | B2 |
6516009 | Tanaka et al. | Feb 2003 | B1 |
6521492 | Miyasaka et al. | Feb 2003 | B2 |
6526585 | Hill | Mar 2003 | B1 |
6528359 | Kusumoto et al. | Mar 2003 | B2 |
6531681 | Markle et al. | Mar 2003 | B1 |
6535535 | Yamazaki et al. | Mar 2003 | B1 |
6555422 | Yamazaki et al. | Apr 2003 | B1 |
6555449 | Im et al. | Apr 2003 | B1 |
6563077 | Im | May 2003 | B2 |
6573163 | Voutsas et al. | Jun 2003 | B2 |
6573531 | Im et al. | Jun 2003 | B1 |
6577380 | Sposili et al. | Jun 2003 | B1 |
6582827 | Im | Jun 2003 | B1 |
6590228 | Voutsas et al. | Jul 2003 | B2 |
6608326 | Shinagawa et al. | Aug 2003 | B1 |
6621044 | Jain et al. | Sep 2003 | B2 |
6635554 | Im et al. | Oct 2003 | B1 |
6635932 | Grigoropoulos et al. | Oct 2003 | B2 |
6667198 | Shimoto et al. | Dec 2003 | B2 |
6693258 | Sugano et al. | Feb 2004 | B2 |
6734635 | Kunii et al. | May 2004 | B2 |
6741621 | Asano | May 2004 | B2 |
6750424 | Tanaka | Jun 2004 | B2 |
6755909 | Jung | Jun 2004 | B2 |
6784455 | Maekawa et al. | Aug 2004 | B2 |
6830993 | Im et al. | Dec 2004 | B1 |
6858477 | Deane et al. | Feb 2005 | B2 |
6908835 | Sposili et al. | Jun 2005 | B2 |
6916690 | Chang | Jul 2005 | B2 |
6961117 | Im | Nov 2005 | B2 |
6962860 | Yamazaki et al. | Nov 2005 | B2 |
6984573 | Yamazaki et al. | Jan 2006 | B2 |
7029996 | Im et al. | Apr 2006 | B2 |
7078281 | Tanaka et al. | Jul 2006 | B2 |
7078793 | Ruckerbauer et al. | Jul 2006 | B2 |
7091411 | Falk et al. | Aug 2006 | B2 |
7115503 | Im | Oct 2006 | B2 |
7119365 | Takafuji et al. | Oct 2006 | B2 |
7132204 | Jung | Nov 2006 | B2 |
7144793 | Gosain et al. | Dec 2006 | B2 |
7160763 | Im et al. | Jan 2007 | B2 |
7164152 | Im | Jan 2007 | B2 |
7172952 | Chung | Feb 2007 | B2 |
7183229 | Yamanaka | Feb 2007 | B2 |
7187016 | Arima | Mar 2007 | B2 |
7189624 | Ito | Mar 2007 | B2 |
7192479 | Mitani et al. | Mar 2007 | B2 |
7192818 | Lee et al. | Mar 2007 | B1 |
7199397 | Huang et al. | Apr 2007 | B2 |
7217605 | Kawasaki et al. | May 2007 | B2 |
7220660 | Im et al. | May 2007 | B2 |
7297982 | Suzuki et al. | Nov 2007 | B2 |
7311778 | Im et al. | Dec 2007 | B2 |
7318866 | Im | Jan 2008 | B2 |
7323368 | Takayama et al. | Jan 2008 | B2 |
7326876 | Jung | Feb 2008 | B2 |
7364952 | Im | Apr 2008 | B2 |
7399359 | Im et al. | Jul 2008 | B2 |
7622370 | Im | Nov 2009 | B2 |
7629234 | Bruland | Dec 2009 | B2 |
7645337 | Im et al. | Jan 2010 | B2 |
7679028 | Im et al. | Mar 2010 | B2 |
7691687 | Im | Apr 2010 | B2 |
7700462 | Tanaka et al. | Apr 2010 | B2 |
7709378 | Im | May 2010 | B2 |
7804647 | Mitani et al. | Sep 2010 | B2 |
7964480 | Im et al. | Jun 2011 | B2 |
20010001745 | Im et al. | May 2001 | A1 |
20010029089 | Tanaka | Oct 2001 | A1 |
20010030292 | Brotherton | Oct 2001 | A1 |
20010041426 | Im | Nov 2001 | A1 |
20020083557 | Jung | Jul 2002 | A1 |
20020104750 | Ito | Aug 2002 | A1 |
20020119609 | Hatano et al. | Aug 2002 | A1 |
20020151115 | Nakajima et al. | Oct 2002 | A1 |
20020197778 | Kasahara et al. | Dec 2002 | A1 |
20030006221 | Hong et al. | Jan 2003 | A1 |
20030013278 | Jang et al. | Jan 2003 | A1 |
20030013280 | Yamanaka | Jan 2003 | A1 |
20030022471 | Taketomi et al. | Jan 2003 | A1 |
20030029212 | Im | Feb 2003 | A1 |
20030057418 | Asano | Mar 2003 | A1 |
20030060026 | Yamazaki et al. | Mar 2003 | A1 |
20030068836 | Hongo et al. | Apr 2003 | A1 |
20030088848 | Crowder | May 2003 | A1 |
20030096489 | Im et al. | May 2003 | A1 |
20030104682 | Hara | Jun 2003 | A1 |
20030119286 | Im et al. | Jun 2003 | A1 |
20030148565 | Yamanaka | Aug 2003 | A1 |
20030148594 | Yamazaki et al. | Aug 2003 | A1 |
20030183270 | Falk et al. | Oct 2003 | A1 |
20030194613 | Voutsas et al. | Oct 2003 | A1 |
20030196589 | Mitani et al. | Oct 2003 | A1 |
20030218171 | Isobe et al. | Nov 2003 | A1 |
20040041158 | Hongo et al. | Mar 2004 | A1 |
20040053450 | Sposili et al. | Mar 2004 | A1 |
20040061843 | Im | Apr 2004 | A1 |
20040127066 | Jung | Jul 2004 | A1 |
20040140470 | Kawasaki et al. | Jul 2004 | A1 |
20040169176 | Peterson et al. | Sep 2004 | A1 |
20040182838 | Das et al. | Sep 2004 | A1 |
20040209447 | Gosain et al. | Oct 2004 | A1 |
20040222187 | Lin | Nov 2004 | A1 |
20040224487 | Yang | Nov 2004 | A1 |
20050003591 | Takaoka et al. | Jan 2005 | A1 |
20050032249 | Im et al. | Feb 2005 | A1 |
20050034653 | Im et al. | Feb 2005 | A1 |
20050059222 | You | Mar 2005 | A1 |
20050059223 | Im | Mar 2005 | A1 |
20050059224 | Im | Mar 2005 | A1 |
20050059265 | Im | Mar 2005 | A1 |
20050112906 | Maekawa et al. | May 2005 | A1 |
20050139830 | Takeda et al. | Jun 2005 | A1 |
20050141580 | Partlo et al. | Jun 2005 | A1 |
20050142450 | Jung | Jun 2005 | A1 |
20050142451 | You | Jun 2005 | A1 |
20050202654 | Im | Sep 2005 | A1 |
20050235903 | Im et al. | Oct 2005 | A1 |
20050236908 | Rivin | Oct 2005 | A1 |
20050255640 | Im et al. | Nov 2005 | A1 |
20050282319 | Bruland et al. | Dec 2005 | A1 |
20060030164 | Im | Feb 2006 | A1 |
20060035478 | You | Feb 2006 | A1 |
20060040512 | Im | Feb 2006 | A1 |
20060060130 | Im | Mar 2006 | A1 |
20060102901 | Im et al. | May 2006 | A1 |
20060125741 | Tanaka et al. | Jun 2006 | A1 |
20060134890 | Im | Jun 2006 | A1 |
20060211183 | Duan et al. | Sep 2006 | A1 |
20060254500 | Im et al. | Nov 2006 | A1 |
20070007242 | Im | Jan 2007 | A1 |
20070010074 | Im | Jan 2007 | A1 |
20070010104 | Im et al. | Jan 2007 | A1 |
20070012664 | Im | Jan 2007 | A1 |
20070020942 | Im | Jan 2007 | A1 |
20070032096 | Im | Feb 2007 | A1 |
20070051302 | Gosain et al. | Mar 2007 | A1 |
20070054477 | Kim et al. | Mar 2007 | A1 |
20070108472 | Jeong et al. | May 2007 | A1 |
20070111349 | Im | May 2007 | A1 |
20070145017 | Im et al. | Jun 2007 | A1 |
20070184638 | Kang et al. | Aug 2007 | A1 |
20070215877 | Kato et al. | Sep 2007 | A1 |
20070215942 | Chen et al. | Sep 2007 | A1 |
20080035863 | Im et al. | Feb 2008 | A1 |
20080124526 | Im | May 2008 | A1 |
20080176414 | Im | Jul 2008 | A1 |
20090001523 | Im | Jan 2009 | A1 |
20090137105 | Im | May 2009 | A1 |
20090140173 | Im | Jun 2009 | A1 |
20090218577 | Im | Sep 2009 | A1 |
20090242805 | Im | Oct 2009 | A1 |
20090309104 | Im et al. | Dec 2009 | A1 |
20100024865 | Shah et al. | Feb 2010 | A1 |
20100187529 | Im | Jul 2010 | A1 |
20110248278 | Im et al. | Oct 2011 | A1 |
20110309370 | Im | Dec 2011 | A1 |
Number | Date | Country |
---|---|---|
1495848 | May 2004 | CN |
101111925 | Jan 2008 | CN |
198 39 718 | Mar 2000 | DE |
101 03 670 | Aug 2002 | DE |
655774 | May 1995 | EP |
681316 | Nov 1995 | EP |
1067593 | Jan 2001 | EP |
2338342 | Dec 1999 | GB |
2338343 | Dec 1999 | GB |
2338597 | Dec 1999 | GB |
S57-027035 | Feb 1982 | JP |
62160781 | Jul 1987 | JP |
62181419 | Aug 1987 | JP |
62216320 | Sep 1987 | JP |
H01-256114 | Oct 1989 | JP |
2081422 | Mar 1990 | JP |
2283036 | Nov 1990 | JP |
04033327 | Feb 1992 | JP |
04-279064 | Oct 1992 | JP |
5041519 | Feb 1993 | JP |
5048190 | Feb 1993 | JP |
06-011729 | Jan 1994 | JP |
6252048 | Sep 1994 | JP |
H06-260502 | Sep 1994 | JP |
6283422 | Oct 1994 | JP |
7176757 | Jul 1995 | JP |
H08-078330 | Mar 1996 | JP |
H09-007968 | Jan 1997 | JP |
9171971 | Jun 1997 | JP |
H09-270393 | Sep 1997 | JP |
9260681 | Oct 1997 | JP |
9321210 | Dec 1997 | JP |
10189998 | Jul 1998 | JP |
H10-244390 | Sep 1998 | JP |
11025064 | Jan 1999 | JP |
11064883 | Mar 1999 | JP |
11-281997 | Oct 1999 | JP |
H11-297852 | Oct 1999 | JP |
11330000 | Nov 1999 | JP |
2000505241 | Apr 2000 | JP |
2000-315652 | Nov 2000 | JP |
2000346618 | Dec 2000 | JP |
2001023920 | Jan 2001 | JP |
2002-203809 | Jul 2002 | JP |
2000223425 | Aug 2002 | JP |
2002-353142 | Dec 2002 | JP |
2002353159 | Dec 2002 | JP |
2003-031496 | Jan 2003 | JP |
2004031809 | Jan 2003 | JP |
2003-509844 | Mar 2003 | JP |
20003100653 | Apr 2003 | JP |
2004-311935 | Nov 2004 | JP |
457553 | Oct 2001 | TW |
464960 | Nov 2001 | TW |
564465 | Dec 2003 | TW |
569350 | Jan 2004 | TW |
WO-9745827 | Dec 1997 | WO |
WO-9824118 | Jun 1998 | WO |
WO-9931719 | Jun 1999 | WO |
WO-0014784 | Mar 2000 | WO |
WO-0118854 | Mar 2000 | WO |
WO-0118855 | Mar 2001 | WO |
WO-0171786 | Sep 2001 | WO |
WO-0171791 | Sep 2001 | WO |
WO-0173769 | Oct 2001 | WO |
WO-0231869 | Apr 2002 | WO |
WO-0242847 | May 2002 | WO |
WO-0286954 | May 2002 | WO |
WO-02086955 | Oct 2002 | WO |
WO-03018882 | Mar 2003 | WO |
WO-03046965 | Jun 2003 | WO |
WO-03084688 | Oct 2003 | WO |
WO-2004017379 | Feb 2004 | WO |
WO-2004017380 | Feb 2004 | WO |
WO-2004017381 | Feb 2004 | WO |
WO-2004017382 | Feb 2004 | WO |
WO-2004075263 | Sep 2004 | WO |
WO-2005029546 | Mar 2005 | WO |
WO-2005029548 | Mar 2005 | WO |
WO-2005029550 | Mar 2005 | WO |
WO-2005029551 | Mar 2005 | WO |
WO-2006055003 | May 2006 | WO |
Entry |
---|
Bergmann, R. et al., Nucleation and Growth of Crystalline Silicon Films on Glass for Solar Cells, Phys. Stat. Sol., 1998, pp. 587-602, vol. 166, Germany. |
Biegelsen, D.K., L.E. Fennell and J.C. Zesch, Origin of oriented crystal growth of radiantly melted silicon on SiO/sub 2, Appl. Phys. Lett. 45, 546 (1984). |
Boyd, I. W., “Laser Processing of Thin Films and Microstructures, Oxidation, Deposition and Etching of Insulators,” (Springer—Verlag Berlin Heidelber, 1987. |
Broadbent et al., “Excimer Laser Processing of Al-1%Cu/TiW Interconnect Layers,” Proceedings, Sixth International IEEE VLSI Multilevel Interconnection Conference, Santa Clara, CA, Jun. 12-13, pp. 336-345 (1989). |
Brotherton et al., “Influence of Melt Depth in Laser Crystallized Poly-Si Thin Film Transistors,” Journal of Appl. Phys., 82:4086 (1997). |
Brotherton, “Polycrystalline Silicon Thin Film Transistors,” Semicond. Sci. Tech., 10:721-738 (1995). |
Brotherton, S.D., et al., Characterisation of poly-Si TFTs in Directionally Solidified SLS Si, Asia Display/IDW'01, p. 387-390. |
Crowder et al., “Low-Temperature Single-Crystal Si TFT's Fabricated on Si Films Processed via Sequential Lateral Solidification,” IEEE Electron Device Letter, 19 (8): 306 (1998). |
Crowder et al., “Parametric Investigation of SLS-processed Poly-silicon Thin Films for TFT Applications,” Preparations and Characterization, Elsevier, Sequoia, NL, vol. 427, No. 1-2, Mar. 3, 2003, pp. 101-107, XP004417451. |
Crowder et al., “Sequential Lateral Solidification of PECVD and Sputter Deposited a-Si Films”, Mat. Res. Soc. Symp. Proc. 621:Q.9.7.1-9.7.6, 2000. |
Dassow, R. et al. Laser-Crystallized Polycrystalline Silicon on Glass for Photovoltaic Applications, Solid State Phenomena, pp. 193-198, vols. 67-68, Scitec Publications, Switzerland. |
Dassow, R. et al. Nd:YVO4 Laser Crystallization for Thin Film Transistors with a High Mobility, Mat. Res. Soc. Symp. Proc., 2000, Q9.3.1-Q9.3.6, vol. 621, Materials Research Society. |
Dassow, R. et al., Laser crystallization of silicon for high-performance thin-film transistors, Semicond. Sci. Technol., 2000, pp. L31-L34, vol. 15, UK. |
Dimitriadis, C.A., J. Stoemenos, P.A. Coxon, S. Friligkos, J. Antonopoulos and N.A. Economou, Effect of pressure on the growth of crystallites of low-pressure chemical-vapor-deposited polycrystalline silicon films and the effective electron mobility under high normal field in thin-film transistors, J. Appl. Phys. 73, 8402 (1993). |
Endert et al., “Excimer Laser: A New Tool for Precision Micromachining,” Optical and Quantum Electronics, 27:1319 (1995). |
Fogarassy et al., “Pulsed Laser Crystallization of Hydrogen-Free a-Si Thin Films for High-Mobility Poly-Si TFT Fabrication,” Applied Physics A—Solids and Surfaces, 56:365-373 (1993). |
Geis et al., “Crystallographic orientation of silicon on an amorphous substrate using an artificial surface-relief grating and laser crystallization,” Appl. Phys. Lett. 35(1) Jul. 1, 1979, 71-74. |
Geis et al., “Silicon graphoepitaxy using a strip-heater oven,” Appl. Phys. Lett. 37(5), Sep. 1, 1980, 454-456. |
Geis et al., “Zone-Melting recrystallization of SI Films with a moveable-strip heater oven,” J. Electro-Chem. Soc., 129: 2812 (1982). |
Gosain et al., “Formation of (100)-Textured Si Film Using an Excimer Laser on a Glass Substrate,” Jpn. J. Appl. Phys., vol. 42 (2003) pp. L135-L137. |
Gupta et al., “Numerical Analysis of Excimer-laser induced melting and solidification of Si Thin Films”, Applied Phys. Lett., 71:99, 1997. |
Hau-Riege et al., “The Effects Microstructural Transitions at Width Transitions on interconnect reliability,” Journal of Applied Physics, 87(12): 8467-8472. |
Hawkins, W.G. et al., “Origin of lamellae in radiatively melted silicon flims,” Appl. Phys. Lett. 42(4), Feb. 15, 1983. |
Hayzelden, C. and J.L. Batstone, Silicide formation and silicide-mediated crystallization of nickel-implanted amorphous silicon thin films, J. Appl. Phys. 73, 8279 (1993). |
Im et al., “Controlled Super-Lateral Growth of Si Films for Microstructural Manipulation and Optimization,” Phys. Stat. Sol. (a), 166:603 (1998). |
Im et al., “Crystalline Si Films for Integrated Active-Matrix Liquid-Crystals Displays,” MRS Bulletin, 21:39 (1996). |
Im et al., “On the Super Lateral Growth Phenomenon Observed in Excimer Laser-Induced Crystallization of Thin Si Films,” Appl. Phys. Lett., 64 (17): 2303 (1994). |
Im et al., “Phase Transformation Mechanisms Involved in Excimer Laser Crystallization of Amorphous Silicon Films,” Appl. Phys. Lett., 63 (14): 1969 (1993). |
Im et al., “Single-Crystal Si Films for Thin-Film Transistor Devices,” Appl. Phys. Lett., 70(25): 3434 (1997). |
Im et al., U.S. Appl. No. 11/141,815. |
Im et al., U.S. Appl. No. 11/293,655. |
Im, J.S., Method and system for producing crystalline thin films with a uniform crystalline orientation, U.S. Appl. No. 60/503,419; ref. file # 36013(BB); Columbia ref. M02-063. |
Ishida et al., “Ultra-shallow boxlike profiles fabricated by pulsed ultraviolet-laser doping process,” J. Vac. Sci. Technol. B 12(1): 399-403, (1994). |
Ishihara et al., “A Novel Double-Pulse Excimer-Laser Crystallization Method of Silicon Thin-Films,” Publication Office, Japanese Journal of Applied Physics, Tokyo, Japan, 34(8A): 3976-3981 (1995). |
Jeon et al., “Two-step laser recrystallization of poly-Si for effective control of grain boundaries,” Journal of Non Crystalline Solids, 266-269: 645-649 (2000). |
Jung, Y.H., et al., Low Temperature Polycrystalline Si TFTs Fabricated with Directionally Crystallized Si Film, Mat. Res. Soc. Symp. Proc. vol. 621, Z8.3.1-6, 2000. |
Jung, Y.H., et al., The Dependence of Poly-Si TFT Characteristics on the Relative Misorientation Between Grain Boundaries and the Active Channel, Mat. Res. Soc. Symp. Proc. vol. 621, Q9.14.1-6, 2000. |
Kahlert, H., “Creating Crystals,” OE Magazine, Nov. 2001, 33-35. |
Kim et al., “Grain Boundary Location-Controlled Poly-Si Films for TFT Devices Obtained Via Novel Excimer Laser Process,” Mat. Res. Soc. Symp. Proc., vol. 358, 1995. |
Kim et al., “Multiple Pulse Irradiation Effects in Excimer Laser-Induced Crystallization of Amorphous Si Films,” Mat. Res. Soc. Sym. Proc., 321:665-670 (1994). |
Kim, “Excimer-Laser-Induced Crystallization of Amorphous Silicon Thin Films,” Ph. D. Dissertation Abstract, Columbia University, 1996. |
Kim, C. et al., “Development of SLS-Based SOG Display,” IDMC 2005, pp. 252-255. |
Kim, H. J. et al., “Excimer Laser Induced Crystallization of Thin Amorphous Si Films on SiO2: Implications of Crystallized Microstructures for Phase Transformation Mechanisms,” Mat. Res. Soc. Symp. Proc., vol. 283, 1993. |
Kim, H.-J., et al., “The effects of dopants on surface-energy-driven secondary grain growth in silicon films,” J. Appl. Phys. 67 (2), Jan. 15, 1990. |
Kim, H.J. et al., “Multiple Pulse Irradiation Effects in Excimer Laser—Induced Crystallization of Amorphous Si Films,” Materials Research Society Symposium Proceedings, vol. 321, pp. 665-670, 1994. |
Kim, H.J. et al., “New Excimer-laser-crystallization method for producing large-grained and grain boundary-location-controlled Si Films for Thin Film Transistors”, Applied Phys. Lett., 68: 1513. |
Kimura, M. and K. Egami, Influence of as-deposited film structure on (100) texture in laser-recrystallized silicon on fused quartz, Appl. Phys. Lett. 44, 420 (1984). |
Knowles, D.S. et al., “P-59: Thin Beam Crystallization Method: a New Laser Annealing Tool with Lower Cost and Higher Yield for LTPS Panels,” SID 00 Digest, pp. 1-3. |
Kohler, J.R. et al., Large-grained polycrystalline silicon on glass by copper vapor laser annealing. Thin Solid Films, 1999, pp. 129-132, vol. 337, Elsevier. |
Kung, K.T.Y. and R. Reif, Implant-dose dependence of grain size and (110) texture enhancements in polycrystalline Si films by seed selection through ion channeling, J. Appl. Phys. 59, 2422 (1986). |
Kung, K.T.Y., R.B. Iverson and R. Reif, Seed selection through ion channeling to modify crystallographic orientations of polycrystalline Si films on SiO/sub 2/:Implant angle dependence, Appl. Phys. Lett. 46, 683 (1985). |
Kuriyama, H., T. Nohda, S. Ishida, T. Kuwahara, S. Noguchi, S. Kiyama, S. Tsuda and S. Nakano, Lateral grain growth of poly-Si films with a specific orientation by an excimer laser annealing method, Jpn. J. Appl. Phys. 32, 6190 (1993). |
Kuriyama, H., T. Nohda, Y. Aya, T. Kuwahara, K. Wakisaka, S. Kiyama and S. Tsuda, Comprehensive study of lateral grain growth in poly-Si films by excimer laser annealing and its application to thin film transistors, Jpn. J. Appl. Phys. 33, 5657 (1994). |
Lee, S.-W. and S.-K. Joo, Low temperature poly-Si thin-film transistor fabrication by metal-induced lateral crystallization, IEEE Electron Device Letters 17, 160 (1996). |
Lee, S.-W., Y.-C. Jeon and S.-K. Joo, Pd induced lateral crystallization of amorphous Si thin films, Appl. Phys. Lett. 66, 1671 (1995). |
Leonard, J.P. et al, “Stochastic modeling of solid nucleation in supercooled liquids”, Appl. Phys. Lett. 78:22, May 28, 2001, 3454-3456. |
Limanov, A. et al., Single-Axis Projection Scheme for Conducting Sequential Lateral Solidification of Si Films for Large-Area Electronics, Mat. Res. Soc. Symp. Proc., 2001, D10.1.1-D10.1.7, vol. 685E, Materials Research Society. |
Limanov, A. et al., The Study of Silicon Films Obtained by Sequential Lateral Solidification by Means of a 3-k-Hz Excimer Laser with a Sheetlike Beam, Russian Microelectronics, 1999, pp. 30-39, vol. 28, No. 1, Russia. |
Limanov, A.B., et al., Development of Linear Sequential Lateral Solidification Technique to Fabricate Quasi-Single-Cyrstal Super-thin Si Films for High-Performance Thin Film Transistor Devices, Perspectives, Science, and Technologies for Novel Silicon on Insulator Devices, Eds. P.L.F. Hemment, Kluwer Academic Publishers 2000, pp. 55-61. |
Mariucci et al., “Grain boundary location control by patterned metal film in excimer laser crystallized polysilicon,” Proceedings of the Fifth International Conference on Polycrystalline Semiconductors, Schwabisch Gmund, Germany, 67-68: 175-180 (1998). |
McWilliams et al., “Wafer-Scale Laser Pantography: Fabrication of N-Metal-Oxide-Semiconductor Transistors and Small-Scale Integrated Circuits by Direct-Write Laser-Induced Pyrolytic Reactions,” Applied Physics Letters, American Institute of Physics, New York, US, 43(10): 946-948 (1983). |
Micro/Las Lasersystem GMBH, “Overview of Beam Delivery Systems for Excimer Lasers,” (1999). |
Micro/Las Lasersystem GMBH, “UV Optics Systems for Excimer Laser Based Micromachining and Marking,” (1999). |
Miyasaka, M., K. Makihira, T. Asano, E. Polychroniadis and J. Stoemenos, In situ observation of nickel metal-induced lateral crystallization of amorphous silicon thin films, Appl. Phys. Lett. 80, 944 (2002). |
Miyata et al, “Low-Temperature Polycrystalline Silicon Thin-Film Transistors for Large-Area Liquid Crystal Display,” Japanese J. of Applied Physics, Part 1—Regular Papers Short Notes & Review Papers, 31:4559-62 (1992). |
Nebel, “Laser Interference Structuring of A-Si:h” Amorphous Silicon Technology—1996, San Francisco, CA Apr. 8-12, Materials Research Society Symposium Proceedings, vol. 420, Pittsburgh, PA (1996). |
Nerding, M., S. Christiansen, R. Dassow, K. Taretto, J.R. Kohler and H.P. Strunk, Tailoring texture in laser crystallization of silicon thin-films on glass, Solid State Phenom. 93, 173 (2003). |
Noguchi, “Appearance of Single-Crystalline Properties in Fine-Patterned Si Thin Film Transistors (TFTs) by Solid Phase Crystallization (SPC),” Jpn. J. Appl. Phys., 32:L1584-L1587 (1993). |
Ozawa et al., “Two-Dimensionally Position-Controlled Excimer-Laser-Crystallization of Silicon Thin Films on Glassy Substrate,” Jpn. J. Appl. Phys. 38(10):5700-5705 (1999). |
Sato et al., “Mobility anisotropy of electrons in inversion layers on oxidized silicon surfaces,” Physical Review B (State) 4, 1950 (1971). |
Smith, H.I. et al, “The Mechanism of Orientation in Si Graphoepitaxy by Laser Strip Heater Recrystallization,” J. Electrochem. Soc.: Solid-State Science and Technology, vol. 130, No. 10, Oct. 1983, pp. 2050-2053. |
Song et al., “Single Crystal Si Islands on SiO2 Obtained Via Excimer Laser Irradiation of a Patterned Si Film”, Applied Phys. Lett., 68:3165, 1996. |
Sposili et al., “Line-scan sequential lateral solidification of Si thin films”, Appl. Phys. A67, 273-6, 1998. |
Sposili et al., “Sequential Lateral Solidification of Thin Silicon Films on SiO2,” Appl. Phys. Lett., 69(19): 2864 (1996). |
Sposili et al., “Single-Crystal Si Films via a Low-Substrate-Temperature Excimer-Laser Crystallization Method,” Mat. Res. Soc. Symp. Proc., 452: 953-958 (1997). |
Thompson, C.V. and H.I. Smith, Surface-energy-driven secondary grain growth in ultrathin (<100 nm) films of silicon, Appl. Phys. Lett. 44, 603 (1984). |
van der Wilt, P.C. et al., “State-of-the-Art Laser Crystallization of Si for Flat Panel Displays,” PhAST, May 18, 2004, pp. 1-34. |
van der Wilt, P.C. et al., “The Commercialization of the SLS Technology,” Taiwan FPD, Jun. 11, 2004, pp. 1-12. |
van der Wilt, P.C., “Textured poly-Si films for hybrid SLS,” Jul. 2004, pp. 1-5. |
Voutsas, A. T., “Assessment of the Performance of Laser-Based Lateral-Crystallization Technology via Analysis and Modeling of Polysilicon Thin-Film-Transistor Mobility,” IEEE Transactions on Electronic Devices, vol. 50, No. 6, Jun. 2003. |
Voutsas, A.T. et al.: “Effect of process parameters on the structural characteristics of laterallyy grown, laser-annealed polycrystalline silicon films,” Journal of applicaed Physics, vol. 94, No. 12, Dec. 15, 2003. |
Voutsas, A.T., A new era of crystallization: advances in polysilicon crystallization and crystal engineering, Applied Surface Science 250-262, 2003. |
Voutsas, A.T., et al., Effect of process parameters on the structural characteristics of laterally grown, laser-annealed polycrystalline silicon films, Journal of Applied Physics, vol. 94, No. 12, p. 7445-7452, Dec. 15, 2003. |
Watanabe et al., “Crystallization Process of Polycrystalline Silicon by KrF Excimer Laser Annealing,” Japanese J. of Applied Physics, Part 1—Regular Papers Short Notes & Review Papers, 33:4491-98 (1994). |
Weiner, K. H. et al. “Laser-assisted, Self-aligned Silicide Formation,” A Verdant Technologies technical brief, Aug. 7, 1997, 1-9. |
Weiner, K. H. et al., “Ultrashallow Junction Formation Using Projection Gas Immersion Laser Doping (PGILD),” A Verdant Technologies Technical Brief, Aug. 20, 1997. |
Werner, J.H., et al. From polycrystalline to single crystalline silicon on glass, Thin Solid Films 383, 95-100, 2001. |
White et al., “Characterization of thin-oxide MNOS memory transistors,” IEEE Trans. Electron Devices ED-19, 1280 (1972). |
Yamamuchi et al., “Polycrystalline silicon thin films processed with silicon ion implantation and subsequent solid-phase crystallization: Theory, experiments, and thin-film transistor applications,” Journal of Applied Physics, 75(7):3235-3257 (1994). |
Yoshimoto et al., “Excimer-Laser-Produced and Two-Dimensionally Position-Controlled Giant Si Grains on Organic SOG Underlayer,” p. 285-286, AM-LCD (2000). |
Bergmann, R.B. et al., “The future of crystalline silicon films on foreign substrates,” Thin Solid Films 403-404 (2002) 162-169. |
Jeon et al., “New-Excimer Laser Recrystallization of Poly-Si for Effective Grain Growth and Grain Boundary Arrangement”, Jpn. J. Appl. Phys., Apr. 2000, vol. 39, Part 1, No. 4B, pp. 2012-2014. |
International Search Report for corresponding International Patent Application No. PCT/US2010/033565, mailed Jul. 1, 2010, 1 page. |
International Search Report for corresponding International Patent Application No. PCT/US2010/055106, mailed Jan. 4, 2011, 1 page. |
Andrä et al., “A new technology for crystalline silicon thin film solar cells on glass based on the laser crystallization,” IEEE, pp. 217-220 (2000). |
Andrä et al., “Multicrystalline LLC-SI thin film solar cells on low temperature glass,” Poster, 3rd world Conference on Photovoltaic Energy Conversion, Osaka, Japan, pp. 1174-1177, May 11-18, 2003. |
Sinke et al., “Explosive crystallization of amorphous silicon: Triggering and propagation,” Applied Surface Science, vol. 43, pp. 128-135 (1989). |
Van Der Wilt, “A hybrid approach for obtaining orientation-controlled single-crystal Si regions on glass substrates,” Proc. of SPIE vol. 6106, 61060B-1 to B-15, (2006). |
Jeon et al., “New Excimer Laser Recrystalization of Poly-Si for Effective Grain Growth and Grain Boundary Arrangement,” Jpn. J. Appl. Phys. vol. 39 (2000) pp. 2012-2014, Part 1, No. 4B, Apr. 2000. |
Number | Date | Country | |
---|---|---|---|
20090309104 A1 | Dec 2009 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10994205 | Nov 2004 | US |
Child | 12544695 | US |