WO2000017918A9 - Metal-contact induced crystallization in semiconductor devices - Google Patents

Metal-contact induced crystallization in semiconductor devices

Info

Publication number
WO2000017918A9
WO2000017918A9 PCT/US1999/021649 US9921649W WO0017918A9 WO 2000017918 A9 WO2000017918 A9 WO 2000017918A9 US 9921649 W US9921649 W US 9921649W WO 0017918 A9 WO0017918 A9 WO 0017918A9
Authority
WO
WIPO (PCT)
Prior art keywords
metal
metal layer
layer
recited
amorphous semiconductor
Prior art date
Application number
PCT/US1999/021649
Other languages
French (fr)
Other versions
WO2000017918A1 (en
Inventor
Stephen Fonash
Sanghoon Bae
Original Assignee
Penn State Res Found
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Penn State Res Found filed Critical Penn State Res Found
Priority to AU10938/00A priority Critical patent/AU1093800A/en
Publication of WO2000017918A1 publication Critical patent/WO2000017918A1/en
Publication of WO2000017918A9 publication Critical patent/WO2000017918A9/en

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02367Substrates
    • H01L21/0237Materials
    • H01L21/02422Non-crystalline insulating materials, e.g. glass, polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02436Intermediate layers between substrates and deposited layers
    • H01L21/02439Materials
    • H01L21/02488Insulating materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02518Deposited layers
    • H01L21/02521Materials
    • H01L21/02524Group 14 semiconducting materials
    • H01L21/02532Silicon, silicon germanium, germanium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02518Deposited layers
    • H01L21/02587Structure
    • H01L21/0259Microstructure
    • H01L21/02595Microstructure polycrystalline
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02656Special treatments
    • H01L21/02664Aftertreatments
    • H01L21/02667Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth
    • H01L21/02672Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth using crystallisation enhancing elements

Definitions

  • This invention relates to a method for inducing selective crystallization of an amorphous semiconductor and more particularly, to a method which uses a "metal" printing action to provide crystallization seed sites from which crystallization in a semiconductor layer commences and from which large grains can be produced.
  • Displays, photovoltaics , microelectronics, and MEMS (microelectro-mechanical devices) employ polycrystalline silicon (poly-Si) films. There is a need to be able to fabricate such poly-Si films at low temperatures, using low-cost processing techniques.
  • Poly-Si is used in thin film transistors (TFTs) for the active channel region because of its relatively high mobility and in- solar cells for the same reason; i.e., its high carrier mobility.
  • Low resistance metal/poly-Si suicide materials are also needed for the source and drain contact or contact finger regions of TFTs and for the contact regions of solar cells. Such suicides offer low resistance, chemical stability, and relatively low temperatures of formation. Low resistance metal suicides, formed with poly-Si also are useful as resistors and interconnects in displays, microelectronics, and MEMS, if the metal/poly-Si suicide regions can be readily isolated. Such metal suicide regions can also be subsequently used to initiate electrochemical or electroless deposition of additional metallic layers. In such case, the metal/poly-Si suicide can serve as a foundation for subsequent depositions for further tailoring of resistance .
  • Metal suicides are currently fabricated by reacting co-deposited or sequentially deposited silicon and metal or by a deposited metal film with a silicon substrate or film. This is often done by vacuum depositing the metal, patterning it lithographically, and then reacting the metal with the silicon substrate, using an elevated temperature process.
  • Thin film poly-Si films can be directly deposited or deposited in amorphous silicon (a-Si) form and then crystallized into poly-Si films.
  • crystallization of the a-Si into poly-Si can be achieved by various methods: laser crystallization, solid phase crystallization, and metal induced solid phase crystallization.
  • the metal induced crystallization (MIC) SPC process has been also used to make poly-Si devices in a pre-determined pattern to cause selective crystallization with a low thermal budget.
  • the metals e.g., Pd, Ni, Cr or Mo
  • the metals have been physically deposited in vacuum or from solution. See, for example, US Patents 5,147,826 and 5,275,851.
  • the resulting grain size of the poly-Si film plays a crucial role in determining the performance of a device. Grain size affects critical device parameters such as carrier mobilities in transistors, thin film transistors (TFTs) , solar cells, detectors; on/off ratio of transistors and TFTs ; switching speed of transistors and TFTs; and efficiencies of solar cells.
  • TFTs thin film transistors
  • none of the methods used to produce thin film poly-Si has been able to produce grain sizes larger than on the order of tens of microns (e.g., 10-50 ⁇ m) , i.e., see Lee et al . , Appl. Phys. Lett. 66, 1671 (1995).
  • the invention is a low-cost, pressure-printing method that transfers a metal pattern to an amorphous semiconductor layer.
  • the method further uses the printed metal region (i) to catalyze the MIC process adjacent to the metallized region to produce poly-Si therein and to simultaneously form silicide contacts at the printed region, or ii) to form pre-selected metal silicide regions isolated by non- crystallized and non-silicided a-Si (for resistor and interconnect applications) .
  • the non-silicided regions of silicon can be subsequently oxidized after or during silicidation, thereby forming an ideal isolating medium; i.e., Si0 2 .
  • the printed metal layer plays the key role of inducing crystallization at a low anneal temperature.
  • the method of the invention induces crystallization in an amorphous semiconductor layer, and includes the steps of: a) producing a patterned metal layer on a first substrate, the metal layer exhibiting a weak level of adherence to the first substrate; b) pressing the metal layer into physical contact with the amorphous semiconductor layer; c) applying heat to the metal layer and amorphous semiconductor layer to cause a reaction therebetween and a crystallization of the amorphous semiconductor that is juxtaposed to the metal..
  • the reaction also causes a greater level of adherence to occur between the metal layer and the amorphous semiconductor than the weak level of adherence between the metal layer and the first substrate, allowing the metallization to adhere to the semiconductor when the first substrate is removed .
  • Figs. 1-4 illustrate the steps of the method of the first embodiment of the invention.
  • Fig. 5 is a photomicrograph of a selectively crystallized a-Si film, by Ni patterning, created by a printing action, after a 1 hour anneal at 550°C while pressure is applied to the printing plate.
  • Fig. 6 is a photomicrograph of a selectively crystallized a-Si film, by Ni patterning, created by a printing action, after a 3 hour anneal at 550°C while pressure is applied to the printing plate.
  • Fig. 7 is a plot of Raman Response Shift versus wave number for both Ni-induced poly-Si and non- crystallized poly-Si.
  • Figs. 8-11 illustrate the steps of the method of the second embodiment of the invention.
  • Fig. 12 is a photomicrograph of a selectively crystallized a-Si film that exhibits large Si grains, induced by Ni seeds emplaced by a printing action, after a 3 hour anneal at temperatures not exceeding 650°C, while pressure is applied to the printing plate.
  • Fig. 13 is a photomicrograph of a selectively crystallized a-Si film by Ni patterning created by a printing action, after a 3 hour anneal at temperatures not exceeding 650°C while pressure is applied to the printing plate.
  • Fig. 14 is a plot of the Raman Response from the crystallized Si grain.
  • Figs. 1-4 show the printing process which comprises the first embodiment of the invention.
  • a crystallization-inducing metal catalyst layer produced by sputtering, spraying, evaporating, or dipping into a metal bearing solution to deposit MIC metals (as in the prior art)
  • patterned metal layers are "printed” by pressing a "printing plate” to an amorphous semiconductor layer that needs to be crystallized, or needs to have a low resistance silicide region.
  • Heat is applied during this pressing to transfer metal atoms from metal regions of the printing plate to the a-Si layer.
  • This heat can be applied by conventional furnace annealing or via a rapid thermal anneal (RTA) process.
  • RTA rapid thermal anneal
  • a high current density e.g., >10 5 A/cm 2
  • electrical current can be applied to cause Joule heating, electromigration of the metal, or both, during the pressing to further the metal transfer and formation of metal suicides.
  • a substrate 10 is prepared by depositing on a glass layer 12, an optional barrier layer 14 of, for example, silicon nitride 14, followed by an amorphous layer of silicon 16 , .
  • an optional barrier layer 14 of, for example, silicon nitride 14, followed by an amorphous layer of silicon 16 .
  • a patterned metal printing "plate” see Fig. 2
  • these printing "plates" can be designed for optimum use of RTA so that just the patterned regions are heated.
  • a metal silicide interface is created between metal 18 and a-Si layer 16.
  • the MIC metal pattern is then transferred (all or in part) onto substrate 10 (see Fig. 4) .
  • a-Si film 16 is crystallized in regions 22 at and adjacent to transferred metal regions 18'. The creation of the silicide regions results in a greater level of adherence of the transferred metal regions 18' to substrate 10 than that existing between metal regions 18 and plate 17. Accordingly, when plate 17 is removed from substrate 10, metal regions 18' remain attached to substrate 10.
  • poly-Si layers are created as are metal/poly-Si low resistance layers that can both be utilized during subsequent semiconductor processing.
  • Figs. 5 and 6 display photomicrographs of selectively crystallized a-Si films, produced by the "printing" process of Figs.1-4, wherein Ni was the MIC metal.
  • a 1000 A silicon nitride layer and a 1000 A a-Si layer were consecutively PECVD deposited at 320°C on Corning 7059 glass.
  • a printing plate was prepared by evaporating a 500 A Ni layer onto a Corning 1737 glass substrate. The Ni film was then patterned into a thin film isolation pattern.
  • a 1 hour anneal at 550°C was performed during the pressing, and in the case of Fig. 6, a 3 hour anneal at 550°C was performed during pressing.
  • poly-Si films surround the Ni patterns that have induced the crystallization of the a-Si films.
  • metal silicide patterns that are surrounded by crystallized poly ⁇ Si films; i.e., the areas surrounding the silicide patterns are poly-Si which can visually be distinguished due to the absorption difference between the crystallized poly-Si and the non-crystallized a-Si.
  • Figs. 5 there are clearly defined metal silicide patterns that are surrounded by crystallized poly ⁇ Si films; i.e., the areas surrounding the silicide patterns are poly-Si which can visually be distinguished due to the absorption difference between the crystallized poly-Si and the non-crystallized a-Si.
  • the poly-Si area surrounding the metal pattern grows proportionally with annealing time; i.e., the widths of poly-Si areas in Fig. 5 and 6 are about 8 and 25 ⁇ m, respectively, giving a lateral crystallization rate of 8 ⁇ m/hr. It is to be noted that selective printing of the metal pattern can be used for device contact isolation since the crystallization is seen to occur selectively around the printed metal pattern.
  • the incident laser beam was focused to 3 ⁇ m diameter spot on the surface of the samples.
  • Raman spectra for printed Ni induced poly-Si and non-crystallized a-Si areas are shown in Fig. 7 for the 3 hr. annealed sample.
  • the crystallized Si transverse optical (TO) phonon peak at 519cm "1 which is the hallmark of crystalline Si, is clearly present, whereas no optical phonon peak is present around 519 cm "1 for the non-crystallized a-Si region.
  • the printed metal patterns of Fig. 5 and 6 were examined using a surface profiler and conductivity measurements According to the surface profile measurement, 400-450 A of Ni was moved from the printing plate to the a-Si film substrate for the 3 hr transfer / crystallization sample. These printed Ni patterns adhered to the substrate during both 10 min ultrasonic cleanings with alcohol and with deionizd water.
  • the poly-Si area surrounding the metal silicide pattern is widened, as shown in Fig. 6. Since crystallization is selectively induced around the metal pattern, the printed metal pattern induced-crystallization can be used for a device isolation step in poly-Si device fabrication processes. Measurements indicated that the conductivity of the metal silicide region of the illustrated pattern was in the range of 10 5 ⁇ 10 6 S/cm. This is conductive enough to be used for electrical metal contacts, interconnects, and tailored resistors.
  • the conductivity of the suicided areas can be adjusted down from this high conductivity range for resistor applications by control of the thermal budget (temperature vs. time) and the pressure during the printing step.
  • the silicide regions can then be used to drive selective electrochemical deposition or electroless deposition onto the printed regions .
  • the metal (e.g., Ni , Pd, Cr, Cu or Mo) printing method described above can be used for producing poly-Si regions and for producing metal/poly-Si silicide, resistors, or interconnect regions.
  • the technique replaces metal deposition, lithography, and etching steps with a simple printing step.
  • the annealing during the pressing seen in Figs. 1-4 can be furnace annealing or a rapid thermal anneal. The latter allows the use of lower temperatures in the regions not to be crystallized. This can be assured if the printing plate is designed to absorb the light of RTA only in the metallized regions. Further, depending upon the source used to accomplish the anneal action (i.e., heat or light or both), a 6 hour or less exposure time should be sufficient to accomplish the printing action.
  • the printing method of the invention can be modified to provide a low-cost, metal-induced solid phase large grain growth in thin film poly-Si semiconductor devices.
  • the modified method is capable of achieving large grain sizes (> L 100 ⁇ m) .
  • the crystallization of the a-Si into poly-Si films consists of two stages; i.e., nucleation and grain growth. Since the nucleation stage has a higher activation energy than the grain growth stage, employing heterogeneous nuclei can lower crystallization temperatures. Some metals (e.g., Ni , Cr, Ti, Co, Fe, or In), or these metals' suicides that have good lattice match with crystalline Si, can act as heterogeneous nuclei and enhance solid phase, large-grain growth.
  • Figs. 8-11 depict a method for obtaining metal - induced solid phase large grain growth from an a-Si precursor film 50 (Fig. 8) , using patterned metal seeds 52 (Fig. 9) .
  • metal patterns or seeds 52 are "printed" onto a-Si film 50 by pressing during the application of heat or light.
  • a-Si film 50 can be crystallized into large grains (Fig. 11) or one large grain.
  • lithographic processes and etching can be used to define metal patterns or seeds 52 on "plate" 56.
  • patterned metal plate 56 can be used not only to induce crystallization but also to supply n or p type dopants for semiconductor devices; i.e., metal printing plate 56 and seeds 52 can act as a dopant supplier from which n or p type dopant diffuses into semiconductor or a-Si surfaces during annealing for crystallization.
  • n or p type dopants on the surface of metal patterns/seeds 52 ion implantation, sputtering, electroless plating, spraying, or other dopant incoporation approaches can be employed.
  • FIGs. 12 and 13 are photomicrographs that show large crystalline Si grains (>100 ⁇ m) which have been induced by Ni seeds printed on the a-Si precursor film, using a patterned Ni block or printing plate.
  • the samples were annealed for 3 hour at 550 °C and 1.5 hour at a temperature not exceeding 650 °C during the printing process; i.e., during the pressing of metal seed patterns 52 onto the a-Si films.
  • crystalline Si i.e., large grain Si
  • the sizes of these metal induced large grains can thus be controlled by controlling when impingement occurs .
  • Fig. 14 shows Raman scattering from the sample shown in Fig. 13.
  • the Raman pattern seen in Fig. 14 displays a strong peak at 519 cm "1 which corresponds to the TO mode of crystalline Si while it does not show any broad shoulder at ⁇ 480 cm "1 which is present when there is amorphous content in the film.
  • a fluctuating temperature anneal procedure can speed the creation of the large grain growth. To be specific, if the temperature is cycled a number of times between about 350°C to about 750°C and maintained at the higher temperature for a short enough period that the elevated temperature does not significantly affect the support for the semiconductor layer, more rapid creation of the larger grains is seen.
  • the maximum anneal temperature in such a fluctuating temperature exposure is dependent upon the softening temperature of the substrate .
  • CMOS circuitry for microelectronics can be fabricated inside a grain; TFTs can located intra-granularly; and large area devices such as solar cells and detectors can be made with very large grains.

Abstract

The method of the invention induces crystallization in an amorphous semiconductor layer (16), and includes the steps of: a) producing a patterned metal layer (18) on a first substrate (17), the metal layer (18) exhibiting a weak level of adherence to the first substrate; b) pressing the metal layer (18) into physical contact with the amorphous semiconductor layer (16); c) applying heat, light or both to the metal layer (18) and amorphous semiconductor layer (16) to cause a reaction therebetween and a crystallization of the amorphous semiconductor that is juxtaposed to the metal.

Description

Metal - Contact Induced Crystallization in Semiconductor
Devices
This Application claims priority from U. S. Provisional Applications: Serial No. 60/101,259, filed September 21, 1998 and Serial No. 60/106,897, filed November 3, 1998.
FTKT..D OF THE INVENTION
This invention relates to a method for inducing selective crystallization of an amorphous semiconductor and more particularly, to a method which uses a "metal" printing action to provide crystallization seed sites from which crystallization in a semiconductor layer commences and from which large grains can be produced.
BACKGROUND OF THE INVENTION
Displays, photovoltaics , microelectronics, and MEMS (microelectro-mechanical devices) employ polycrystalline silicon (poly-Si) films. There is a need to be able to fabricate such poly-Si films at low temperatures, using low-cost processing techniques. Poly-Si is used in thin film transistors (TFTs) for the active channel region because of its relatively high mobility and in- solar cells for the same reason; i.e., its high carrier mobility.
Low resistance metal/poly-Si suicide materials are also needed for the source and drain contact or contact finger regions of TFTs and for the contact regions of solar cells. Such suicides offer low resistance, chemical stability, and relatively low temperatures of formation. Low resistance metal suicides, formed with poly-Si also are useful as resistors and interconnects in displays, microelectronics, and MEMS, if the metal/poly-Si suicide regions can be readily isolated. Such metal suicide regions can also be subsequently used to initiate electrochemical or electroless deposition of additional metallic layers. In such case, the metal/poly-Si suicide can serve as a foundation for subsequent depositions for further tailoring of resistance .
Metal suicides are currently fabricated by reacting co-deposited or sequentially deposited silicon and metal or by a deposited metal film with a silicon substrate or film. This is often done by vacuum depositing the metal, patterning it lithographically, and then reacting the metal with the silicon substrate, using an elevated temperature process.
Thin film poly-Si films can be directly deposited or deposited in amorphous silicon (a-Si) form and then crystallized into poly-Si films. In the latter approach, crystallization of the a-Si into poly-Si can be achieved by various methods: laser crystallization, solid phase crystallization, and metal induced solid phase crystallization. The metal induced crystallization (MIC) SPC process has been also used to make poly-Si devices in a pre-determined pattern to cause selective crystallization with a low thermal budget. For poly-Si films produced by MICSPC, the metals (e.g., Pd, Ni, Cr or Mo) have been physically deposited in vacuum or from solution. See, for example, US Patents 5,147,826 and 5,275,851.
Regardless of the method used to fabricate poly-Si films, the resulting grain size of the poly-Si film plays a crucial role in determining the performance of a device. Grain size affects critical device parameters such as carrier mobilities in transistors, thin film transistors (TFTs) , solar cells, detectors; on/off ratio of transistors and TFTs ; switching speed of transistors and TFTs; and efficiencies of solar cells. However, none of the methods used to produce thin film poly-Si (including the as-deposited approach) , has been able to produce grain sizes larger than on the order of tens of microns (e.g., 10-50 μm) , i.e., see Lee et al . , Appl. Phys. Lett. 66, 1671 (1995).
There is a need for a low cost, low temperature method for inducing crystallization in amorphous semiconductors. Also there is a need to produce large crystals during such a crystallization procedure.
SUMMARY OF THE INVENTION
The invention is a low-cost, pressure-printing method that transfers a metal pattern to an amorphous semiconductor layer. Application of the metal pattern, using heat and applied pressure, results in a patterned poly-crystalline semiconductor region, or in the event that the semiconductor is silicon and the metal is a silicide-former, the application results in a patterned metal/poly-crystalline silicide region. The method further uses the printed metal region (i) to catalyze the MIC process adjacent to the metallized region to produce poly-Si therein and to simultaneously form silicide contacts at the printed region, or ii) to form pre-selected metal silicide regions isolated by non- crystallized and non-silicided a-Si (for resistor and interconnect applications) . In the latter case, the non-silicided regions of silicon can be subsequently oxidized after or during silicidation, thereby forming an ideal isolating medium; i.e., Si02. In either case, the printed metal layer plays the key role of inducing crystallization at a low anneal temperature.
The method of the invention induces crystallization in an amorphous semiconductor layer, and includes the steps of: a) producing a patterned metal layer on a first substrate, the metal layer exhibiting a weak level of adherence to the first substrate; b) pressing the metal layer into physical contact with the amorphous semiconductor layer; c) applying heat to the metal layer and amorphous semiconductor layer to cause a reaction therebetween and a crystallization of the amorphous semiconductor that is juxtaposed to the metal.. The reaction also causes a greater level of adherence to occur between the metal layer and the amorphous semiconductor than the weak level of adherence between the metal layer and the first substrate, allowing the metallization to adhere to the semiconductor when the first substrate is removed .
BRIEF DESCRIPTION OF THE DRAWINGS
Figs. 1-4 illustrate the steps of the method of the first embodiment of the invention.
Fig. 5 is a photomicrograph of a selectively crystallized a-Si film, by Ni patterning, created by a printing action, after a 1 hour anneal at 550°C while pressure is applied to the printing plate.
Fig. 6 is a photomicrograph of a selectively crystallized a-Si film, by Ni patterning, created by a printing action, after a 3 hour anneal at 550°C while pressure is applied to the printing plate.
Fig. 7 is a plot of Raman Response Shift versus wave number for both Ni-induced poly-Si and non- crystallized poly-Si.
Figs. 8-11 illustrate the steps of the method of the second embodiment of the invention.
Fig. 12 is a photomicrograph of a selectively crystallized a-Si film that exhibits large Si grains, induced by Ni seeds emplaced by a printing action, after a 3 hour anneal at temperatures not exceeding 650°C, while pressure is applied to the printing plate.
Fig. 13 is a photomicrograph of a selectively crystallized a-Si film by Ni patterning created by a printing action, after a 3 hour anneal at temperatures not exceeding 650°C while pressure is applied to the printing plate.
Fig. 14 is a plot of the Raman Response from the crystallized Si grain.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Figs. 1-4 show the printing process which comprises the first embodiment of the invention. Instead of using a crystallization-inducing metal catalyst layer produced by sputtering, spraying, evaporating, or dipping into a metal bearing solution to deposit MIC metals (as in the prior art) , patterned metal layers are "printed" by pressing a "printing plate" to an amorphous semiconductor layer that needs to be crystallized, or needs to have a low resistance silicide region.
Heat is applied during this pressing to transfer metal atoms from metal regions of the printing plate to the a-Si layer. This heat can be applied by conventional furnace annealing or via a rapid thermal anneal (RTA) process. In addition to the heat produced by the furnace anneal or RTA, to assure the formation of metal suicides, a high current density (e.g., >105 A/cm2) electrical current can be applied to cause Joule heating, electromigration of the metal, or both, during the pressing to further the metal transfer and formation of metal suicides.
With reference to Fig. 1, a substrate 10 is prepared by depositing on a glass layer 12, an optional barrier layer 14 of, for example, silicon nitride 14, followed by an amorphous layer of silicon 16 , . To prepare a patterned metal printing "plate" (see Fig. 2) , lithographic processes and etching, commonly used in semiconductor processing, are employed to define MIC metal patterns 18 (e.g., Pd, Ni, Cr or Mo) on "plate" 17. It is preferred that the MIC metal pattern 18 be loosely adherent to plate 17 (e.g. a glass) . Through the use of anti-reflection and reflection coatings, these printing "plates" can be designed for optimum use of RTA so that just the patterned regions are heated.
As shown in Fig. 3, plate 17 is pressed against substrate 10 so that MIC metal 18 is pressed against a- Si film 16. At the same time, the structure of Fig. 3 is subjected to an anneal treatment (i.e., thermal or light exposure) . As a result, a metal silicide interface is created between metal 18 and a-Si layer 16. The MIC metal pattern is then transferred (all or in part) onto substrate 10 (see Fig. 4) . Further a-Si film 16 is crystallized in regions 22 at and adjacent to transferred metal regions 18'. The creation of the silicide regions results in a greater level of adherence of the transferred metal regions 18' to substrate 10 than that existing between metal regions 18 and plate 17. Accordingly, when plate 17 is removed from substrate 10, metal regions 18' remain attached to substrate 10.
As a result of the above procedure, poly-Si layers are created as are metal/poly-Si low resistance layers that can both be utilized during subsequent semiconductor processing..
Figs. 5 and 6 display photomicrographs of selectively crystallized a-Si films, produced by the "printing" process of Figs.1-4, wherein Ni was the MIC metal. A 1000 A silicon nitride layer and a 1000 A a-Si layer were consecutively PECVD deposited at 320°C on Corning 7059 glass. A printing plate was prepared by evaporating a 500 A Ni layer onto a Corning 1737 glass substrate. The Ni film was then patterned into a thin film isolation pattern.
In Fig. 5, a 1 hour anneal at 550°C was performed during the pressing, and in the case of Fig. 6, a 3 hour anneal at 550°C was performed during pressing. As seen in Figs. 5 and 6, poly-Si films surround the Ni patterns that have induced the crystallization of the a-Si films. As also seen in Figs. 5 and 6, there are clearly defined metal silicide patterns that are surrounded by crystallized poly~Si films; i.e., the areas surrounding the silicide patterns are poly-Si which can visually be distinguished due to the absorption difference between the crystallized poly-Si and the non-crystallized a-Si. As shown in Figs. 5 and 6, the poly-Si area surrounding the metal pattern grows proportionally with annealing time; i.e., the widths of poly-Si areas in Fig. 5 and 6 are about 8 and 25 μm, respectively, giving a lateral crystallization rate of 8 μm/hr. It is to be noted that selective printing of the metal pattern can be used for device contact isolation since the crystallization is seen to occur selectively around the printed metal pattern.
To assess further the poly-Si film produced by the printing process of the invention, a Raman spectrometer was employed with an Ar laser (wavelength=514 nm) . The incident laser beam was focused to 3 μm diameter spot on the surface of the samples. Raman spectra for printed Ni induced poly-Si and non-crystallized a-Si areas are shown in Fig. 7 for the 3 hr. annealed sample. As seen in the crystallized area, the crystallized Si transverse optical (TO) phonon peak at 519cm"1 , which is the hallmark of crystalline Si, is clearly present, whereas no optical phonon peak is present around 519 cm"1 for the non-crystallized a-Si region.
The printed metal patterns of Fig. 5 and 6 were examined using a surface profiler and conductivity measurements According to the surface profile measurement, 400-450 A of Ni was moved from the printing plate to the a-Si film substrate for the 3 hr transfer / crystallization sample. These printed Ni patterns adhered to the substrate during both 10 min ultrasonic cleanings with alcohol and with deionizd water.
As anneal time is increased, the poly-Si area surrounding the metal silicide pattern is widened, as shown in Fig. 6. Since crystallization is selectively induced around the metal pattern, the printed metal pattern induced-crystallization can be used for a device isolation step in poly-Si device fabrication processes. Measurements indicated that the conductivity of the metal silicide region of the illustrated pattern was in the range of 105~106 S/cm. This is conductive enough to be used for electrical metal contacts, interconnects, and tailored resistors.
The conductivity of the suicided areas can be adjusted down from this high conductivity range for resistor applications by control of the thermal budget (temperature vs. time) and the pressure during the printing step. In addition, the silicide regions can then be used to drive selective electrochemical deposition or electroless deposition onto the printed regions .
As can thus be seen, the metal (e.g., Ni , Pd, Cr, Cu or Mo) printing method described above can be used for producing poly-Si regions and for producing metal/poly-Si silicide, resistors, or interconnect regions. The technique replaces metal deposition, lithography, and etching steps with a simple printing step. The annealing during the pressing seen in Figs. 1-4 can be furnace annealing or a rapid thermal anneal. The latter allows the use of lower temperatures in the regions not to be crystallized. This can be assured if the printing plate is designed to absorb the light of RTA only in the metallized regions. Further, depending upon the source used to accomplish the anneal action (i.e., heat or light or both), a 6 hour or less exposure time should be sufficient to accomplish the printing action.
It has been further discovered that the printing method of the invention can be modified to provide a low-cost, metal-induced solid phase large grain growth in thin film poly-Si semiconductor devices. The modified method is capable of achieving large grain sizes (>L100 μm) .
In solid phase crystallization, the crystallization of the a-Si into poly-Si films consists of two stages; i.e., nucleation and grain growth. Since the nucleation stage has a higher activation energy than the grain growth stage, employing heterogeneous nuclei can lower crystallization temperatures. Some metals (e.g., Ni , Cr, Ti, Co, Fe, or In), or these metals' suicides that have good lattice match with crystalline Si, can act as heterogeneous nuclei and enhance solid phase, large-grain growth.
Figs. 8-11 depict a method for obtaining metal - induced solid phase large grain growth from an a-Si precursor film 50 (Fig. 8) , using patterned metal seeds 52 (Fig. 9) . As shown in Fig. 10, metal patterns or seeds 52 are "printed" onto a-Si film 50 by pressing during the application of heat or light. By proper choice of the printed pattern, a-Si film 50 can be crystallized into large grains (Fig. 11) or one large grain.
To prepare the patterned printing plate of Fig.9, lithographic processes and etching can be used to define metal patterns or seeds 52 on "plate" 56. In an extension of printing approach, patterned metal plate 56 can be used not only to induce crystallization but also to supply n or p type dopants for semiconductor devices; i.e., metal printing plate 56 and seeds 52 can act as a dopant supplier from which n or p type dopant diffuses into semiconductor or a-Si surfaces during annealing for crystallization. To incorporate n or p type dopants on the surface of metal patterns/seeds 52, ion implantation, sputtering, electroless plating, spraying, or other dopant incoporation approaches can be employed.
A Ni printing block and Ni seeds were chosen to demonstrate metal -induced, solid phase, large grain growth from amorphous silicon precursors. Figs. 12 and 13 are photomicrographs that show large crystalline Si grains (>100 μm) which have been induced by Ni seeds printed on the a-Si precursor film, using a patterned Ni block or printing plate. The samples were annealed for 3 hour at 550 °C and 1.5 hour at a temperature not exceeding 650 °C during the printing process; i.e., during the pressing of metal seed patterns 52 onto the a-Si films.
To observe grain structures, the crystallized films in Figs. 12 and 13 were etched by a Secco etchant. In both cases, crystalline Si (i.e., large grain Si) is seen to be laterally growing until the grains impinge on another. Depending on how the metal pattern is designed or how the metal seeds are distributed, the sizes of these metal induced large grains can thus be controlled by controlling when impingement occurs .
Raman spectroscopy was used to measure the crystallinity of thin films Si samples. In the Raman spectrum, the peaks at ~ 520 cm"1 and ~ 480 cm"1 originate from transverse optical (TO) modes of crystalline Si and a-Si, respectively. Fig. 14 shows Raman scattering from the sample shown in Fig. 13. The Raman pattern seen in Fig. 14 displays a strong peak at 519 cm"1 which corresponds to the TO mode of crystalline Si while it does not show any broad shoulder at ~ 480 cm"1 which is present when there is amorphous content in the film.
It has been determined that a fluctuating temperature anneal procedure can speed the creation of the large grain growth. To be specific, if the temperature is cycled a number of times between about 350°C to about 750°C and maintained at the higher temperature for a short enough period that the elevated temperature does not significantly affect the support for the semiconductor layer, more rapid creation of the larger grains is seen. The maximum anneal temperature in such a fluctuating temperature exposure is dependent upon the softening temperature of the substrate .
The approach of using the printing of metal seed patterns to induce large grain growth can be used for producing large grain poly-Si films for TFTs, solar cells, or microelectronic devices. Having such large grains of controlled size and location means CMOS circuitry for microelectronics can be fabricated inside a grain; TFTs can located intra-granularly; and large area devices such as solar cells and detectors can be made with very large grains. By employing this solid phase large grain growth method, high quality thin film devices can be made and the number of processing steps can be reduced.
It should be understood that the foregoing description is only illustrative of the invention. Various alternatives and modifications can be devised by those skilled in the art without departing from the invention. Accordingly, the present invention is intended to embrace all such alternatives, modifications and variances which fall within the scope of the appended claims .

Claims

1. A method for inducing crystallization in an amorphous semiconductor layer, said method comprising the steps of:
producing a patterned metal layer on a first substrate;
pressing said patterned metal layer into physical contact with said amorphous semiconductor layer;
applying heat, light or both to said metal layer and amorphous semiconductor layer to cause a crystallization of regions of said amorphous semiconductor that are in juxtaposition to said metal region.
2. The method as recited in claim 1, wherein said metal layer exhibits a weak level of adherence to said first substrate and said applying of heat, light or both causes a reaction between said metal layer and amorphous layer, said reaction causing a greater level of adherence than said weak level of adherence between said metal layer and amorphous semiconductor, so as to allow said metal layer to adhere to said semiconductor layer when said first substrate is removed therefrom.
3. The method as recited in claim 1, wherein said metal layer is selected from the group consisting of: Pd, Ni, Cr, Cu or Mo.
4. The method as recited in claim 1, wherein said semiconductor is silicon.
5. The method as recited in claim 4, wherein said metal is a silicide forming metal.
6. The method as recited in claim 1, wherein said applying step causes said patterned metal layer and amorphous semiconductor to be subjected to temperature range of about 350°C to 750°C for a period of about six hours or less .
7. The method as recited in claim 6, wherein said applying step causes the temperature to be repeatedly cycled between lower and upper limits of said temperature range .
8. The method as recited in claim 1, wherein said patterned metal layer comprises a plurality metal particles .
9.. The method as recited in claim 1 wherein said patterned metal layer further includes a dopant material that is caused to penetrate said semiconductor during said applying step.
10. The method as recited in claim 1, wherein said applying step further causes application of a current between said patterned metal layer and said amorphous semiconductor layer to aid in formation of a metal silicide therebetween.
PCT/US1999/021649 1998-09-21 1999-09-21 Metal-contact induced crystallization in semiconductor devices WO2000017918A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU10938/00A AU1093800A (en) 1998-09-21 1999-09-21 Metal-contact induced crystallization in semiconductor devices

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US10125998P 1998-09-21 1998-09-21
US60/101,259 1998-09-21
US10689798P 1998-11-03 1998-11-03
US60/106,897 1998-11-03

Publications (2)

Publication Number Publication Date
WO2000017918A1 WO2000017918A1 (en) 2000-03-30
WO2000017918A9 true WO2000017918A9 (en) 2000-08-10

Family

ID=26798076

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/021649 WO2000017918A1 (en) 1998-09-21 1999-09-21 Metal-contact induced crystallization in semiconductor devices

Country Status (3)

Country Link
US (1) US6277714B1 (en)
AU (1) AU1093800A (en)
WO (1) WO2000017918A1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6521492B2 (en) * 2000-06-12 2003-02-18 Seiko Epson Corporation Thin-film semiconductor device fabrication method
TWI226660B (en) * 2003-04-01 2005-01-11 Univ Nat Taiwan Method of fabricating polysilicon film by Nickel/Copper induced lateral crystallization
US7202143B1 (en) 2003-10-23 2007-04-10 The Board Of Trustees Of The University Of Arkansas Low temperature production of large-grain polycrystalline semiconductors
WO2007025062A2 (en) * 2005-08-25 2007-03-01 Wakonda Technologies, Inc. Photovoltaic template
KR20080065460A (en) * 2007-01-09 2008-07-14 엘지전자 주식회사 Manufacturing method of poly-crystal silicon photovoltaic device having low-temperature using horizontally metal induced crystallization method
US20080241356A1 (en) * 2007-04-02 2008-10-02 Jianming Fu Photovoltaic devices manufactured using crystalline silicon thin films on glass
US8927392B2 (en) * 2007-11-02 2015-01-06 Siva Power, Inc. Methods for forming crystalline thin-film photovoltaic structures
TWI359460B (en) * 2007-11-26 2012-03-01 Tatung Co A method of fabricating a polycrystalline semicond
US8236603B1 (en) 2008-09-04 2012-08-07 Solexant Corp. Polycrystalline semiconductor layers and methods for forming the same
US8415187B2 (en) * 2009-01-28 2013-04-09 Solexant Corporation Large-grain crystalline thin-film structures and devices and methods for forming the same
US9099411B2 (en) 2011-08-24 2015-08-04 The Board Of Trustees Of The Leland Stanford Junior University Metal-induced crystallization of continuous semiconductor thin films controlled by a diffusion barrier
KR101351856B1 (en) 2012-06-22 2014-01-22 희성전자 주식회사 Bonding Method for Hetero-Type Substrate
CN117542764A (en) * 2023-12-28 2024-02-09 长鑫集电(北京)存储技术有限公司 Semiconductor heat treatment apparatus and heat treatment method for semiconductor

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5264072A (en) * 1985-12-04 1993-11-23 Fujitsu Limited Method for recrystallizing conductive films by an indirect-heating with a thermal-conduction-controlling layer
US4914500A (en) * 1987-12-04 1990-04-03 At&T Bell Laboratories Method for fabricating semiconductor devices which include sources and drains having metal-containing material regions, and the resulting devices
US5698451A (en) * 1988-06-10 1997-12-16 Mobil Solar Energy Corporation Method of fabricating contacts for solar cells
US5147826A (en) * 1990-08-06 1992-09-15 The Pennsylvania Research Corporation Low temperature crystallization and pattering of amorphous silicon films
DE4035842A1 (en) 1990-11-10 1992-05-14 Telefunken Electronic Gmbh METHOD FOR RECRISTALLIZING PREAMORPHIZED SEMICONDUCTOR SURFACE ZONES
US5275851A (en) 1993-03-03 1994-01-04 The Penn State Research Foundation Low temperature crystallization and patterning of amorphous silicon films on electrically insulating substrates
US5529937A (en) * 1993-07-27 1996-06-25 Semiconductor Energy Laboratory Co., Ltd. Process for fabricating thin film transistor
US5843811A (en) * 1996-04-10 1998-12-01 University Of Florida Method of fabricating a crystalline thin film on an amorphous substrate

Also Published As

Publication number Publication date
AU1093800A (en) 2000-04-10
WO2000017918A1 (en) 2000-03-30
US6277714B1 (en) 2001-08-21

Similar Documents

Publication Publication Date Title
US5147826A (en) Low temperature crystallization and pattering of amorphous silicon films
US5773329A (en) Polysilicon grown by pulsed rapid thermal annealing
EP0526779B1 (en) Pulsed gas plasma-enhanced chemical vapor deposition of silicon
Liu et al. Selective area crystallization of amorphous silicon films by low‐temperature rapid thermal annealing
KR100473996B1 (en) Cystallization method of amorphous silicon
JP3580473B2 (en) Crystallizing method of amorphous film and thin film transistor
JP3558200B2 (en) Method for forming polycrystalline film by crystallization of microcrystalline film, method for forming thin film transistor, thin film transistor, and liquid crystal display
US6277714B1 (en) Metal-contact induced crystallization in semiconductor devices
US6620719B1 (en) Method of forming ohmic contacts using a self doping layer for thin-film transistors
JP4291539B2 (en) Semiconductor device and manufacturing method thereof
JP2000036465A (en) Single-crystal thin-film transistor manufactured through transition metal continuous transfer method
JPH07321339A (en) Semiconductor device and manufacture thereof
KR100392120B1 (en) Method for forming polycrystalline silicon film
JP2010206201A (en) Method of manufacturing polycrystal silicon layer
JP2001094109A (en) Semiconductor device and manufacturing method therefor
JP3041177B2 (en) Method for manufacturing semiconductor device
US7659185B2 (en) Method for forming silicon thin-film on flexible metal substrate
JP2004158850A (en) Forming method for polycrystalline silicon film and manufacturing method for thin-film transistor using same
KR100623693B1 (en) Method for fabricating thin film transistor
Bae et al. Defined crystallization of amorphous-silicon films using contact printing
JP2006013425A (en) Thin film transistor and its manufacturing method
JP3190512B2 (en) Semiconductor fabrication method
KR100470021B1 (en) Method for crystallizing of silicon and method for fabricating of Thin film transistor
WO2000001004A1 (en) Method of forming single-crystal silicon layer and method of manufacturing semiconductor device
JP3705733B2 (en) Manufacturing method of semiconductor device

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref country code: AU

Ref document number: 2000 10938

Kind code of ref document: A

Format of ref document f/p: F

AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
AK Designated states

Kind code of ref document: C2

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: C2

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

COP Corrected version of pamphlet

Free format text: PAGES 1/6-6/6, DRAWINGS, REPLACED BY NEW PAGES 1/6-6/6; DUE TO LATE TRANSMITTAL BY THE RECEIVING OFFICE

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase