US20030089924A1 - Silicon-based PT/PZT/PT sandwich structure and method for manufacturing the same - Google Patents
Silicon-based PT/PZT/PT sandwich structure and method for manufacturing the same Download PDFInfo
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- US20030089924A1 US20030089924A1 US10/291,052 US29105202A US2003089924A1 US 20030089924 A1 US20030089924 A1 US 20030089924A1 US 29105202 A US29105202 A US 29105202A US 2003089924 A1 US2003089924 A1 US 2003089924A1
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- 238000000034 method Methods 0.000 title claims description 29
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title abstract description 12
- 229910052710 silicon Inorganic materials 0.000 title abstract description 12
- 239000010703 silicon Substances 0.000 title abstract description 12
- 238000004519 manufacturing process Methods 0.000 title description 13
- 239000000758 substrate Substances 0.000 claims abstract description 17
- 239000004065 semiconductor Substances 0.000 claims abstract description 11
- 239000000463 material Substances 0.000 claims description 15
- 230000008569 process Effects 0.000 claims description 12
- 238000000137 annealing Methods 0.000 claims description 10
- 238000003980 solgel method Methods 0.000 claims description 7
- 239000003990 capacitor Substances 0.000 claims description 5
- 230000015654 memory Effects 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000377 silicon dioxide Substances 0.000 abstract description 3
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 3
- 239000010408 film Substances 0.000 description 104
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 58
- 230000009466 transformation Effects 0.000 description 12
- 238000010899 nucleation Methods 0.000 description 8
- 230000010287 polarization Effects 0.000 description 8
- 239000010409 thin film Substances 0.000 description 8
- 230000006911 nucleation Effects 0.000 description 7
- 238000000151 deposition Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000004544 sputter deposition Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229940046892 lead acetate Drugs 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000005137 deposition process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000008646 thermal stress Effects 0.000 description 2
- OERNJTNJEZOPIA-UHFFFAOYSA-N zirconium nitrate Chemical compound [Zr+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O OERNJTNJEZOPIA-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D1/00—Resistors, capacitors or inductors
- H10D1/60—Capacitors
- H10D1/68—Capacitors having no potential barriers
- H10D1/682—Capacitors having no potential barriers having dielectrics comprising perovskite structures
- H10D1/684—Capacitors having no potential barriers having dielectrics comprising perovskite structures the dielectrics comprising multiple layers, e.g. comprising buffer layers, seed layers or gradient layers
Definitions
- the present invention relates generally to semiconductors and more specifically to a silicon-based PT/PZT/PT sandwich structure.
- ferroelectric thin films are widely investigated for applications in sensors, actuators, non-volatile memories and photoelectric devices.
- Lead Zirconate titanate (PZT) thin films are especially well known materials because of their remarkable dielectric, peizoelectric, ferroelectric and photoelectric properties. Therefore it would highly desirable to integrate ferroelectric materials in fabrication of semiconductor devices especially in fabricating memory cell capacitor where a high operating speed is highly demanded.
- PZT Lead Zirconate titanate
- sol-gel metalorganic chemical vapor deposition (MOCVD), pulse laser deposition, and sputtering were investigated to fabricate silicon-based PZT thin films as it is highly desirable realize a method of easy operation, low cost, low annealing temperatures and compatibility with semiconductor technology.
- sol-gel method has attracted considerable interest because it can offer several advantages such as simplicity, low cost and easy composition control.
- C. K. Kwok and S. B. Desu presented a novel PZT/PT deposition method to include a PT seeding layer between PZT thin layer and a substrate which can offer nucleation sites and reduce the activation energy for crystallization of PZT thin films.
- the present invention provides a silicon based PT/PZT/PT sandwich structure and a method for fabricating the same for further improving the electrical properties of the device and reducing the manufacturing cost.
- the present invention provides a silicon based PT/PZT/PT sandwich structure having improved ferroelectric properties and a method for manufacturing the same.
- the present invention provides a PT/PZT/PT sandwich structure that can be used for fabricating a memory cell capacitor so that the operating speed of the memory cell can be substantially enhanced.
- the present invention provides a sol-gel process for depositing the ferroelectric thin films for fabricating a silicon-based PT/PZT/PT sandwich structure so that the thermal budget and cost of fabrication are both substantially reduced.
- the electrical properties of the ferroelectric thin films are substantially improved.
- a silicon based PT/PZT/PT structure comprising a silicon semiconductor substrate.
- a dielectric layer is formed over a semiconductor substrate.
- the dielectric layer preferably comprises a silicon dioxide layer.
- a first and the second conductive films are sequentially formed over the dielectric layer.
- the first conductive film preferably comprises a Pt film, and the second conductive film comprises a Ti film.
- a first ferroelectric film is formed over the first and second conductive films.
- the first ferroelectric film preferably comprises a PT film.
- a second ferroelectric film is formed over the first ferroelectric film.
- the second ferroelectric film preferably comprises a PZT film.
- a third ferroelectric film is formed over the second ferroelectric film.
- the third ferroelectric film preferably comprises a PT film.
- the resulting structure is annealed.
- a third and fourth conductive films are sequentially formed over the third ferroelectric layer.
- the third and fourth conductive films preferably comprises a Pt and Ti films respectively.
- the third and fourth conductive films are patterned.
- the first ferroelectric film comprises a PT film
- the PT film has a similar lattice constant and crystallographic symmetry as those of the second ferroelectric film which comprises a PZT film, therefore PZT film of high quality can be grown on the PT film. Since the nucleation barriers of PT film is lower compared to PZT film, PT film can offer excellent nucleation sites for facilitating complete crystallization of PZT film.
- PT film can also effectively facilitate the pervoskite transformation at a comparatively lower temperature.
- a typical perovskite transformation process or an annealing process require high temperature, for example for PZT film, a temperature of about 900° C. is required to effect the perovskite transformation.
- the perovskite transformation temperature can be effectively reduced from 900° C. to 700° C. Therefore, PT can effectively reduce the fabrication thermal budget thus, the fabrication cost can be substantially reduced. Since the perovskite transformation can be achieved at a lower temperature, there is no risk of adverse effect on the device due to thermal stress, therefore the reliability of the device can be increased.
- FIGS. 1 through 8 are schematic, cross sectional views showing the progression of manufacturing steps for fabricating a silicon based PT/PZT/PT sandwich structure according to the preferred embodiment of the present invention.
- FIGS. 1 through 7 are schematic, cross sectional views showing the progression of manufacturing steps for fabricating a silicon based PT/PZT/PT sandwich structure according to the preferred embodiment of the present invention.
- a semiconductor substrate 100 is provided.
- the semiconductor substrate 100 is preferably made of silicon material.
- a dielectric layer 102 is formed over a semiconductor substrate 100 .
- the dielectric layer 102 is preferably made of silicon dioxide material formed by performing a conventional deposition technique such as a thermal oxidation.
- the thickness of the dielectric layer 102 is preferably within a range of about 0.5-2.0 ⁇ m.
- a thin first conductive film 104 is formed over the second support layer 102 .
- the first conductive film 104 preferably comprises a Ti material.
- the first conductive film 104 is preferably formed by performing a sputtering process.
- the thickness of the first conductive film 104 is preferably within a range of 1000-2000 ⁇ .
- a thin second conductive film 106 is formed over the first conductive layer 104 .
- the second conductive film 106 preferably comprises a Pt material.
- the second conductive film 106 is preferably formed by performing a sputtering process.
- the thickness of the second conductive film 106 is preferably within a range of 50 to 100 ⁇ .
- the first and the second conductive films forms the lower electrode of the capacitor.
- a first thin ferroelectric film 108 is spin coated over the second conductive film 106 .
- the first ferroelectric film 108 preferably comprises a PT film.
- the first ferroelectric film 108 is preferably formed by performing a sol-gel deposition process.
- a PT precursor solution is prepared by dissolving proper quantities of lead acetate [Pb(CH 3 COO) 2 .3H 2 O] and tetra titanate [Ti(OC 4 H 9 ) 4 ] in 2-methoxy ethanol to form a PT solution.
- the composition of lead acetate is preferably within a range of 0.9-1.1% w/v.
- the first ferroelectric film 108 dried by heating the substrate at 200° C. over a hot plate for 1 minute. Then the substrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the first ferroelectric film 108 can be improved.
- the thickness of the first ferroelectric film 108 is preferably within a range of 0.01-0.1 ⁇ m.
- a second ferroelectric film 110 is coated over the first ferroelectric film 108 .
- the second ferroelectric film 110 is preferably formed by performing a sol-gel deposition process.
- a PZT precursor solution is prepared by dissolving proper quantities of lead acetate [Pb(CH 3 COO) 2 .3H 2 O] zirconium nitrate (Zr(NO 3 ) 4 .5H 2 O)] and tetra butyl titanate [Ti(OC 4 H 9 ) 4 ] in 2-methoxy ethanol to form a PZT solution.
- the above PZT solution is used for forming the second ferroelectric film 110 by a sol-gel process.
- the second ferroelectric film 110 is dried by heating the substrate 100 at 200° C. over a hot plate for 1 minute. Then the substrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the second ferroelectric film 110 can be improved.
- the thickness of the ferroelectric film 112 is preferably within a range of 0.15-2.0 ⁇ m.
- a third ferroelectric film 112 is spin coated over the second ferroelectric film 110 .
- the third ferroelectric film 112 preferably comprises a PT film.
- the third ferroelectric film 112 is preferably formed by performing a sol-gel process by using a PT precursor solution of similar composition as described above.
- the third ferroelectric film 112 is dried by heating the substrate at 200° C. over a hot plate for 1 minute. Then the substrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the third ferroelectric film 112 can be improved.
- the thickness of the third ferroelectric film 112 is preferably within a range of 0.01-0.10 ⁇ m.
- the resulting multilayered films are subjected to an annealing process 113 to obtain a well crystallized thin films.
- the annealing process 113 is preferably carried out at a temperature of about 650-750° C. for a duration of about 30-45 minutes.
- the first, the second and the third ferroelectric films 108 , 110 and 112 are transformed from an amorphous state to a stable well crystallized perovskite state.
- a thin third conductive film 114 is formed over the second ferroelectric film 112 .
- the third conductive film 114 preferably comprises a Ti material.
- the third conductive film 114 is preferably formed by performing a sputtering process.
- the thickness of the third conductive film 116 is preferably within a range of 1000-2000 521 .
- a thin fourth conductive film 116 is formed over the third conductive film 114 .
- the fourth conductive film 116 preferably comprises a Pt material.
- the fourth conductive film 116 is preferably formed by performing a sputtering process.
- the thickness of the fourth conductive film 116 is preferably within a range of 50-100 ⁇ .
- the third and the fourth conductive films forms the upper electrode of the capacitor.
- the third and the fourth conductive films 114 and 116 are patterned as shown by numeral 114 ′ and 116 ′ respectively.
- the coercive field is about 30-50 kV/cm
- the leakage current is about 1 ⁇ 10 ⁇ 6 to 1 ⁇ 10 ⁇ 8 A/cm2
- the remnant polarization is about 3-15 ⁇ C/cm 2
- the coercive filed is measured to be 24 KV/cm
- the leakage current is 5 ⁇ 10 ⁇ 9 A/cm 2
- the remnant polarization is 17 ⁇ C/cm 2 . Therefore the operating speed of the device can be substantially increased.
- a second ferroelectric film 110 which is made of a PZT film, is formed on the first ferroelectric film 108 which is made of a PT film, it is to be understood that since the PT film has a similar lattice constant and crystallographic symmetry as those of a PZT film, the PT film can offer excellent nucleation sites for high quality PZT crystal growth.
- the ferroelectric films must be annealed to effect perovskite transformation from an amorphous state to a stable well crystallized perovskite state in order to function effectively. Since the PT film has lower nucleation barriers, and since the perovskite transformation is nucleation reaction, it can effectively reduce the perovskite transformation temperature of the PZT film. Thus, the thermal budget can be effectively decreased.
- the perovskite transformation temperature of PZT only and PZT/PT structures is about 900° C. and 750° C. respectively. While the perovskite transformation temperature of the PT/PZT/PT sandwich structure is only 600-700° C. Since the perovskite transformation can be achieved at a lower temperature, there is no risk of adverse effect on the device due to thermal stress, therefore the reliability of the device can be increased.
- the present invention provides a simple, compliant and cost effective process for fabricating a silicon-based PT/PZT/PT sandwich structure having improved electrical properties.
- the PT/PZT/PT sandwich structures were simulated theoretically to show the effect of the improved PT/PZT/PT sandwich structures.
- the simulation results of three PT/PZT/PT sandwich structures examples according to the present invention are listed below.
- the dielectric constant is measured to be 920
- the coercive filed is measured to be 24 KV/cm
- the remnant polarization is 17 micro-C/cm 2
- the leakage current is 5 ⁇ 10 ⁇ 9 A/cm 2 .
- the dielectric constant is measured to be 915
- the coercive filed is measured to be 20 KV/cm
- the remnant polarization is 19 micro-C/cm 2
- the leakage current is 2 ⁇ 10 ⁇ 9 A/cm 2 .
- the dielectric constant is measured to be 900
- the coercive filed is measured to be 18 KV/cm
- the remnant polarization is 23 micro-C/cm 2
- the leakage current is 1 ⁇ 10 ⁇ 9 A/cm 2 .
- CONCLUSION Compared to the electrical properties of the PZT/PT and PZT only structures, the coercive field and the leakage current of the sandwich structure are decreased substantially, while the remnant polarization is increased.
- each layer in the PT/PZT/PT sandwich structure is designed based on the analysis of the coercive field, the leakage current and the remnant polarization values.
- the aim of the design is to further improve the electrical properties of the structure without affecting the structure firmness.
- the design parameters of each layer is as below.
- the thickness of the first PT film is about 0.01-0.1 ⁇ m.
- the thickness of the second PT film is about 0.01-0.1 ⁇ m.
- the present invention provides a simple, compliant design parameters. Because the present invention shows a sol-gel process for forming the thin ferroelectric film, and the advantage of using the PT films for lowering the annealing temperature, the manufacturing process can be simplified and the cost of fabrication is substantially reduced.
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Abstract
A silicon based PT/PZT/PT sandwich structure is disclosed. A dielectric layer is formed over a semiconductor substrate. The dielectric layer preferably comprises a silicon dioxide layer. A first and the second conductive films are sequentially formed over the dielectric layer. A first ferroelectric film is formed over the first and second conductive films. A second ferroelectric film is formed over the first ferroelectric film. A third ferroelectric film is formed over the second ferroelectric film. The resulting structure is annealed. A third and fourth conductive films are sequentially formed over the third ferroelectric layer. The third and fourth conductive films are patterned.
Description
- 1. Filed of Invention
- The present invention relates generally to semiconductors and more specifically to a silicon-based PT/PZT/PT sandwich structure.
- 2. Description of Related Art
- Recently, ferroelectric thin films are widely investigated for applications in sensors, actuators, non-volatile memories and photoelectric devices. Lead Zirconate titanate (PZT) thin films are especially well known materials because of their remarkable dielectric, peizoelectric, ferroelectric and photoelectric properties. Therefore it would highly desirable to integrate ferroelectric materials in fabrication of semiconductor devices especially in fabricating memory cell capacitor where a high operating speed is highly demanded. One problem is even though such a design rule is well known, given the complexity integrating these materials and their manufacturing process, and even their use becomes less attractive when cost and size are critical.
- Therefore, various deposition methods, such as sol-gel, metalorganic chemical vapor deposition (MOCVD), pulse laser deposition, and sputtering were investigated to fabricate silicon-based PZT thin films as it is highly desirable realize a method of easy operation, low cost, low annealing temperatures and compatibility with semiconductor technology. Among various fabrication techniques, sol-gel method has attracted considerable interest because it can offer several advantages such as simplicity, low cost and easy composition control. In 1993, C. K. Kwok and S. B. Desu presented a novel PZT/PT deposition method to include a PT seeding layer between PZT thin layer and a substrate which can offer nucleation sites and reduce the activation energy for crystallization of PZT thin films.
- The present invention provides a silicon based PT/PZT/PT sandwich structure and a method for fabricating the same for further improving the electrical properties of the device and reducing the manufacturing cost.
- The present invention provides a silicon based PT/PZT/PT sandwich structure having improved ferroelectric properties and a method for manufacturing the same.
- The present invention provides a PT/PZT/PT sandwich structure that can be used for fabricating a memory cell capacitor so that the operating speed of the memory cell can be substantially enhanced.
- The present invention provides a sol-gel process for depositing the ferroelectric thin films for fabricating a silicon-based PT/PZT/PT sandwich structure so that the thermal budget and cost of fabrication are both substantially reduced. The electrical properties of the ferroelectric thin films are substantially improved.
- According to the preferred embodiment of the present invention, a silicon based PT/PZT/PT structure comprising a silicon semiconductor substrate. A dielectric layer is formed over a semiconductor substrate. The dielectric layer preferably comprises a silicon dioxide layer. A first and the second conductive films are sequentially formed over the dielectric layer. The first conductive film preferably comprises a Pt film, and the second conductive film comprises a Ti film. A first ferroelectric film is formed over the first and second conductive films. The first ferroelectric film preferably comprises a PT film. A second ferroelectric film is formed over the first ferroelectric film. The second ferroelectric film preferably comprises a PZT film. A third ferroelectric film is formed over the second ferroelectric film. The third ferroelectric film preferably comprises a PT film. The resulting structure is annealed. A third and fourth conductive films are sequentially formed over the third ferroelectric layer. The third and fourth conductive films preferably comprises a Pt and Ti films respectively. The third and fourth conductive films are patterned.
- It is to be further understood by those skilled in the art that since the dielectric constant of PT film is smaller compared to PZT film, therefore by placing a PZT film in between two PT thin films, the electrical properties can be substantially improved. Therefore the operating speed of the device can be substantially increased.
- It is to be understood by those skilled in the art that the first ferroelectric film comprises a PT film, since the PT film has a similar lattice constant and crystallographic symmetry as those of the second ferroelectric film which comprises a PZT film, therefore PZT film of high quality can be grown on the PT film. Since the nucleation barriers of PT film is lower compared to PZT film, PT film can offer excellent nucleation sites for facilitating complete crystallization of PZT film.
- It is to be further understood by those skilled in the art that since the perovskite transformation is also a nucleation reaction, PT film can also effectively facilitate the pervoskite transformation at a comparatively lower temperature. A typical perovskite transformation process or an annealing process require high temperature, for example for PZT film, a temperature of about 900° C. is required to effect the perovskite transformation. By forming a PZT film on the PT film, the perovskite transformation temperature can be effectively reduced from 900° C. to 700° C. Therefore, PT can effectively reduce the fabrication thermal budget thus, the fabrication cost can be substantially reduced. Since the perovskite transformation can be achieved at a lower temperature, there is no risk of adverse effect on the device due to thermal stress, therefore the reliability of the device can be increased.
- FIGS. 1 through 8 are schematic, cross sectional views showing the progression of manufacturing steps for fabricating a silicon based PT/PZT/PT sandwich structure according to the preferred embodiment of the present invention.
- Reference will be made in detail to the present preferred embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers are used in the drawings and the description to refer to the same or like parts.
- FIGS. 1 through 7 are schematic, cross sectional views showing the progression of manufacturing steps for fabricating a silicon based PT/PZT/PT sandwich structure according to the preferred embodiment of the present invention.
- Referring to FIG. 1, a
semiconductor substrate 100 is provided. Thesemiconductor substrate 100 is preferably made of silicon material. Adielectric layer 102 is formed over asemiconductor substrate 100. Thedielectric layer 102 is preferably made of silicon dioxide material formed by performing a conventional deposition technique such as a thermal oxidation. The thickness of thedielectric layer 102 is preferably within a range of about 0.5-2.0 μm. - Referring to FIG. 2, a thin first
conductive film 104 is formed over thesecond support layer 102. The firstconductive film 104 preferably comprises a Ti material. The firstconductive film 104 is preferably formed by performing a sputtering process. The thickness of the firstconductive film 104 is preferably within a range of 1000-2000 Å. A thin secondconductive film 106 is formed over the firstconductive layer 104. The secondconductive film 106 preferably comprises a Pt material. The secondconductive film 106 is preferably formed by performing a sputtering process. The thickness of the secondconductive film 106 is preferably within a range of 50 to 100 Å. The first and the second conductive films forms the lower electrode of the capacitor. - Referring to FIG. 2, a first thin
ferroelectric film 108 is spin coated over the secondconductive film 106. The firstferroelectric film 108 preferably comprises a PT film. The firstferroelectric film 108 is preferably formed by performing a sol-gel deposition process. A PT precursor solution is prepared by dissolving proper quantities of lead acetate [Pb(CH3COO)2.3H2O] and tetra titanate [Ti(OC4H9)4] in 2-methoxy ethanol to form a PT solution. The composition of lead acetate is preferably within a range of 0.9-1.1% w/v. Since the formation of the above PT solution is simple, the composition and the density of the solution can be easily controlled. Since the density of the above PT solution is low, it is possible to control the spin-speed for forming very thin PT films of desired thickness. The firstferroelectric film 108 dried by heating the substrate at 200° C. over a hot plate for 1 minute. Then thesubstrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the firstferroelectric film 108 can be improved. The thickness of the firstferroelectric film 108 is preferably within a range of 0.01-0.1 μm. - Referring to FIG. 4, a second
ferroelectric film 110 is coated over the firstferroelectric film 108. The PZT material preferably having a composition of Pbx(ZryTi1−y)O3 wherein x=0.9-1.1, y=0.4-0.6. The secondferroelectric film 110 is preferably formed by performing a sol-gel deposition process. A PZT precursor solution is prepared by dissolving proper quantities of lead acetate [Pb(CH3COO)2.3H2O] zirconium nitrate (Zr(NO3)4.5H2O)] and tetra butyl titanate [Ti(OC4H9)4] in 2-methoxy ethanol to form a PZT solution. The composition of the PZT in PZT solution is preferably of [Pbx(ZryTi1−y)O3] where x=0.9-1.1 and y=0.4-0.6. The above PZT solution is used for forming the secondferroelectric film 110 by a sol-gel process. The secondferroelectric film 110 is dried by heating thesubstrate 100 at 200° C. over a hot plate for 1 minute. Then thesubstrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the secondferroelectric film 110 can be improved. The thickness of theferroelectric film 112 is preferably within a range of 0.15-2.0 μm. - Referring to FIG. 5, a third
ferroelectric film 112 is spin coated over the secondferroelectric film 110. The thirdferroelectric film 112 preferably comprises a PT film. The thirdferroelectric film 112 is preferably formed by performing a sol-gel process by using a PT precursor solution of similar composition as described above. The thirdferroelectric film 112 is dried by heating the substrate at 200° C. over a hot plate for 1 minute. Then thesubstrate 100 is heated at 600° C. for 2 minutes in a tube oven to remove impurities such as organic residues so that the ferroelectric property of the thirdferroelectric film 112 can be improved. The thickness of the thirdferroelectric film 112 is preferably within a range of 0.01-0.10 μm. - Referring to FIG. 6, the resulting multilayered films are subjected to an
annealing process 113 to obtain a well crystallized thin films. Theannealing process 113 is preferably carried out at a temperature of about 650-750° C. for a duration of about 30-45 minutes. During theannealing process 113, the first, the second and the third 108, 110 and 112 are transformed from an amorphous state to a stable well crystallized perovskite state.ferroelectric films - Referring to FIG. 7, a thin third
conductive film 114 is formed over the secondferroelectric film 112. The thirdconductive film 114 preferably comprises a Ti material. The thirdconductive film 114 is preferably formed by performing a sputtering process. The thickness of the thirdconductive film 116 is preferably within a range of 1000-2000 521 . A thin fourthconductive film 116 is formed over the thirdconductive film 114. The fourthconductive film 116 preferably comprises a Pt material. The fourthconductive film 116 is preferably formed by performing a sputtering process. The thickness of the fourthconductive film 116 is preferably within a range of 50-100 Å. The third and the fourth conductive films forms the upper electrode of the capacitor. - Referring to FIG. 8, the third and the fourth
114 and 116 are patterned as shown by numeral 114′ and 116′ respectively.conductive films - It is to be understood by those skilled in the art that since the dielectric constant of the
108 and 112 is smaller compared to PZT material, therefore by placing thePT films PZT film 110 in between two 108 and 112, the electrical properties of the resulting structure can be of more superior compared to PT/PZT or PZT structures. The electrical properties such as the coercive field and the leakage current can be substantially reduced and the remnant polarization can be effectively increased. For example, for a PZT film of thickness 0.1-0.5 μm, the coercive field is about 30-50 kV/cm, the leakage current is about 1×10−6 to 1×10−8 A/cm2 and the remnant polarization is about 3-15 μC/cm2. Whereas for thickness of the layers in the PT/PZT/PT sandwich structure of 0.02/0.2-0.5/0.02 μm, the coercive filed is measured to be 24 KV/cm, the leakage current is 5×10−9 A/cm2 and the remnant polarization is 17 μC/cm2. Therefore the operating speed of the device can be substantially increased.PT films - With the approach of the present invention, a second
ferroelectric film 110 which is made of a PZT film, is formed on the firstferroelectric film 108 which is made of a PT film, it is to be understood that since the PT film has a similar lattice constant and crystallographic symmetry as those of a PZT film, the PT film can offer excellent nucleation sites for high quality PZT crystal growth. - It is to be further understood by those skilled in the art that the ferroelectric films must be annealed to effect perovskite transformation from an amorphous state to a stable well crystallized perovskite state in order to function effectively. Since the PT film has lower nucleation barriers, and since the perovskite transformation is nucleation reaction, it can effectively reduce the perovskite transformation temperature of the PZT film. Thus, the thermal budget can be effectively decreased. For example, the perovskite transformation temperature of PZT only and PZT/PT structures is about 900° C. and 750° C. respectively. While the perovskite transformation temperature of the PT/PZT/PT sandwich structure is only 600-700° C. Since the perovskite transformation can be achieved at a lower temperature, there is no risk of adverse effect on the device due to thermal stress, therefore the reliability of the device can be increased.
- It is to be further understood by those skilled in the art that the present invention provides a simple, compliant and cost effective process for fabricating a silicon-based PT/PZT/PT sandwich structure having improved electrical properties.
- The PT/PZT/PT sandwich structures were simulated theoretically to show the effect of the improved PT/PZT/PT sandwich structures. The simulation results of three PT/PZT/PT sandwich structures examples according to the present invention are listed below.
- For the thickness of the layers in the PT/PZT/PT sandwich structure of 0.02/0.2/0.02 micron, the dielectric constant is measured to be 920, the coercive filed is measured to be 24 KV/cm and the remnant polarization is 17 micro-C/cm 2 and the leakage current is 5×10−9 A/cm2.
- For the thickness of the layers in the PT/PZT/PT sandwich structure of 0.04/1/0.02 micron, the dielectric constant is measured to be 915, the coercive filed is measured to be 20 KV/cm and the remnant polarization is 19 micro-C/cm 2 and the leakage current is 2×10−9 A/cm2.
- For the thickness of the layers in the PT/PZT/PT sandwich structure of 0.1/1.5/0.1 micron, the dielectric constant is measured to be 900, the coercive filed is measured to be 18 KV/cm and the remnant polarization is 23 micro-C/cm 2 and the leakage current is 1×10−9 A/cm2.
- CONCLUSION: Compared to the electrical properties of the PZT/PT and PZT only structures, the coercive field and the leakage current of the sandwich structure are decreased substantially, while the remnant polarization is increased.
- While the best mode utilizes the above specific thickness PT/PZT/PT sandwich structure, however it should be understood that the present invention is applicable to PT/PZT/PT sandwich structures with PT/PZT/PT layers of different thickness and different composition of PZT and PT material thereof, may be used to practice the present invention.
- It is to be understood by those skilled in the art that the thickness of each layer in the PT/PZT/PT sandwich structure is designed based on the analysis of the coercive field, the leakage current and the remnant polarization values. The aim of the design is to further improve the electrical properties of the structure without affecting the structure firmness. The design parameters of each layer is as below. The thickness of the first PT film is about 0.01-0.1 μm. The thickness of PZT layer is about 0.15-2.0 μm and the composition of PZT is Pb x(ZryTi1−y)O3 wherein x=0.9-1.1, y=0.4-0.6. The thickness of the second PT film is about 0.01-0.1 μm. Therefore the present invention provides a simple, compliant design parameters. Because the present invention shows a sol-gel process for forming the thin ferroelectric film, and the advantage of using the PT films for lowering the annealing temperature, the manufacturing process can be simplified and the cost of fabrication is substantially reduced.
- While the invention has been described in conjunction with a specific best mode, it is to be understood that many alternatives, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alternatives, modifications, and variations which fall within the spirit and scope of the included claims. All matters set forth herein or shown in the accompanying drawings are to be interpreted in an illustrative and non-limiting sense.
- It is to be understood that the foregoing general description and the following detailed description are exemplary, and are intended to provide further explanation of the invention as claimed.
Claims (22)
1. A PT/PZT/PT sandwich structure for integrated circuit device, the structure comprising:
a semiconductor substrate;
a dielectric layer formed over the substrate;
a first conductive film formed over the dielectric layer;
a second conductive film formed over the first conductive film;
a first ferroelectric film formed over the second conductive film;
a second ferroelectric film formed over the first ferroelectric film;
a third ferroelectric film formed over the second ferroelectric film, wherein the dielectric constant of the first and the third ferroelectric films is lower than the second ferroelectric film, wherein the material of the first and the third ferroelectric films are made of same material;
a third conductive film formed over the second ferroelectric film; and
a fourth conductive film formed over the third conductive film.
2. The structure according to claim 1 , wherein the first and the third ferroelectric films comprises a PT film, wherein the lead content in the PT film is within a range of 0.9-1.1% w/v.
3. The structure according to claim 1 , the thickness of the first and third ferroelectric films is within a range between 0.01 to 0.10 μm.
4. The structure according to claim 1 , wherein the second ferroelectric film is formed in between the first and the third ferroelectric films, wherein the second ferroelectric film comprises a PZT film, and the first, the third ferroelectric films comprises a PT film.
5. The structure according to claim 4 , wherein the composition of the PZT film comprises of Pbx(ZryTi1−y)O3 wherein x=0.9-1.1, y=0.4-0.6.
6. The structure according to claim 1 , wherein the thickness of the second ferroelectric film are within a range of 0.15 to 2.0 μm.
7. The structure according to claim 1 , wherein the first, the second and the third ferroelectric films is formed by performing a sol-gel process.
8. The structure according to claim 1 , wherein after the third ferroelectric layer is formed, an annealing process is performed.
9. The structure according to claim 8 , wherein the annealing step is carried out at a temperature of 650-700° C. for a duration of 30-45 minutes, wherein the first, the second and the third ferroelectric films are transformed from an amorphous form to a stable well crystallized perovskite form.
10. The structure according to claim 1 , wherein the first and the third conductive films comprises a Ti film, wherein the thickness of the first and the third conductive films is within a range of 1000-2000 Å.
11. The structure according to claim 1 , wherein the second and the fourth conductive films comprises a Pt film, wherein the thickness of the second and the fourth conductive films is within a range of 50-100 Å.
12. A method for fabricating a PT/PZT/PT sandwich structure for fabricating a memory cell capacitor of integrated circuit device, the method comprising:
providing a semiconductor substrate;
forming a dielectric layer over the substrate;
forming a first conductive film over the dielectric layer;
forming a second conductive film over the first conductive film;
forming a first ferroelectric film over the second conductive film;
forming a second ferroelectric film over the first ferroelectric film;
forming a third ferroelectric film over the second ferroelectric film, wherein the dielectric constant of the first and the third ferroelectric films is lower than the second ferroelectric film, wherein the material of the first and the third ferroelectric films are made of same material;
forming a third conductive film over the third ferroelectric film; and
forming a fourth conductive film over the third conductive film.
13. The method according to claim 12 , wherein the first and the third ferroelectric films comprises a PT film, wherein the lead content in the PT film is within a range of 0.9-1.1% w/v.
14. The method according to claim 12 , the thickness of the first and third ferroelectric films is within a range between 0.01 to 0.10 μm.
15. The method according to claim 12 , wherein the second ferroelectric film is formed in between the first and the third ferroelectric films, wherein the second ferroelectric film comprises a PZT film, and the first, the third ferroelectric films comprises a PT film.
16. The method according to claim 15 , wherein the composition of the PZT film comprises of Pbx(ZryTi1−y)O3 wherein x=0.9-1.1, y=0.4-0.6.
17. The method according to claim 12 , wherein the thickness of the second ferroelectric film is within a range of 0.15 to 2.0 μm.
18. The method according to claim 12 , wherein the first, the second and the third ferroelectric films are formed by performing a sol-gel process.
19. The method according to claim 1 , wherein after the step of forming the third ferroelectric layer, an annealing process is performed.
20. The method according to claim 19 , wherein the annealing step is carried out at a temperature of 650-700° C. for a duration of 30-45 minutes, wherein the first, the second and the third ferroelectric films are transformed from an amorphous form to a stable well crystallized perovskite form.
21. The method according to claim 12 , wherein the first and the third conductive films comprises a Ti film, wherein the thickness of the first and the third conductive films is within a range of 1000-2000 Å.
22. The method according to claim 12 , wherein the second and the fourth conductive films comprises a Pt film, wherein the thickness of the second and the fourth conductive films is within a range of 50-100 Å.
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| US10/291,052 US20030089924A1 (en) | 2001-05-23 | 2002-11-08 | Silicon-based PT/PZT/PT sandwich structure and method for manufacturing the same |
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| US09/863,950 US6507060B2 (en) | 2001-05-23 | 2001-05-23 | Silicon-based PT/PZT/PT sandwich structure and method for manufacturing the same |
| US10/291,052 US20030089924A1 (en) | 2001-05-23 | 2002-11-08 | Silicon-based PT/PZT/PT sandwich structure and method for manufacturing the same |
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| US6943392B2 (en) * | 1999-08-30 | 2005-09-13 | Micron Technology, Inc. | Capacitors having a capacitor dielectric layer comprising a metal oxide having multiple different metals bonded with oxygen |
| US6558517B2 (en) * | 2000-05-26 | 2003-05-06 | Micron Technology, Inc. | Physical vapor deposition methods |
| US6838122B2 (en) * | 2001-07-13 | 2005-01-04 | Micron Technology, Inc. | Chemical vapor deposition methods of forming barium strontium titanate comprising dielectric layers |
| US20030017266A1 (en) * | 2001-07-13 | 2003-01-23 | Cem Basceri | Chemical vapor deposition methods of forming barium strontium titanate comprising dielectric layers, including such layers having a varied concentration of barium and strontium within the layer |
| US7011978B2 (en) * | 2001-08-17 | 2006-03-14 | Micron Technology, Inc. | Methods of forming capacitor constructions comprising perovskite-type dielectric materials with different amount of crystallinity regions |
| JP3971598B2 (en) * | 2001-11-01 | 2007-09-05 | 富士通株式会社 | Ferroelectric capacitor and semiconductor device |
| US20050145908A1 (en) * | 2003-12-30 | 2005-07-07 | Moise Theodore S.Iv | High polarization ferroelectric capacitors for integrated circuits |
| WO2005074032A1 (en) * | 2004-01-28 | 2005-08-11 | Fujitsu Limited | Semiconductor device and its manufacturing method |
| US7298018B2 (en) * | 2004-12-02 | 2007-11-20 | Agency For Science, Technology And Research | PLT/PZT ferroelectric structure |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US5548475A (en) * | 1993-11-15 | 1996-08-20 | Sharp Kabushiki Kaisha | Dielectric thin film device |
| US5426075A (en) * | 1994-06-15 | 1995-06-20 | Ramtron International Corporation | Method of manufacturing ferroelectric bismuth layered oxides |
| JP3279453B2 (en) * | 1995-03-20 | 2002-04-30 | シャープ株式会社 | Non-volatile random access memory |
| KR100360468B1 (en) * | 1995-03-20 | 2003-01-24 | 삼성전자 주식회사 | manufacturing method of ferroelectric film, capacator adopting the film and menufacturing method of the capacator |
| JP3022328B2 (en) * | 1996-06-19 | 2000-03-21 | 日本電気株式会社 | Thin film formation method |
| JP3193302B2 (en) * | 1996-06-26 | 2001-07-30 | ティーディーケイ株式会社 | Film structure, electronic device, recording medium, and method of manufacturing ferroelectric thin film |
| TW468253B (en) * | 1997-01-13 | 2001-12-11 | Hitachi Ltd | Semiconductor memory device |
| US6115281A (en) * | 1997-06-09 | 2000-09-05 | Telcordia Technologies, Inc. | Methods and structures to cure the effects of hydrogen annealing on ferroelectric capacitors |
| JPH11195768A (en) * | 1997-10-22 | 1999-07-21 | Fujitsu Ltd | Electronic device including perovskite oxide film, method of manufacturing the same, and ferroelectric capacitor |
| US6297085B1 (en) * | 1997-12-11 | 2001-10-02 | Texas Instruments Incorporated | Method for manufacturing ferroelectric capacitor and method for manufacturing ferroelectric memory |
| KR100275726B1 (en) * | 1997-12-31 | 2000-12-15 | 윤종용 | Ferroelectric memory device and fabrication method thereof |
| KR100292819B1 (en) * | 1998-07-07 | 2001-09-17 | 윤종용 | Capacitor and manufacturing method thereof |
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2001
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| US6507060B2 (en) | 2003-01-14 |
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