US20140131835A1 - Semiconductor device with rutile titanium oxide dielectric film - Google Patents
Semiconductor device with rutile titanium oxide dielectric film Download PDFInfo
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- US20140131835A1 US20140131835A1 US13/674,929 US201213674929A US2014131835A1 US 20140131835 A1 US20140131835 A1 US 20140131835A1 US 201213674929 A US201213674929 A US 201213674929A US 2014131835 A1 US2014131835 A1 US 2014131835A1
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- tio2
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- electrode
- dielectric layer
- titanium oxide
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 72
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000004065 semiconductor Substances 0.000 title description 3
- 239000003990 capacitor Substances 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 12
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 claims description 8
- HTXDPTMKBJXEOW-UHFFFAOYSA-N iridium(IV) oxide Inorganic materials O=[Ir]=O HTXDPTMKBJXEOW-UHFFFAOYSA-N 0.000 claims description 4
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910004166 TaN Inorganic materials 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 238000000231 atomic layer deposition Methods 0.000 description 27
- 238000000034 method Methods 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 238000010926 purge Methods 0.000 description 9
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- 238000002441 X-ray diffraction Methods 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 238000000151 deposition Methods 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000003989 dielectric material Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
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- H01L29/92—
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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
- H10D1/692—Electrodes
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/40—Oxides
- C23C16/405—Oxides of refractory metals or yttrium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
- C23C16/45523—Pulsed gas flow or change of composition over time
- C23C16/45525—Atomic layer deposition [ALD]
- C23C16/45527—Atomic layer deposition [ALD] characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02172—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing at least one metal element, e.g. metal oxides, metal nitrides, metal oxynitrides or metal carbides
- H01L21/02175—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing at least one metal element, e.g. metal oxides, metal nitrides, metal oxynitrides or metal carbides characterised by the metal
- H01L21/02186—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing at least one metal element, e.g. metal oxides, metal nitrides, metal oxynitrides or metal carbides characterised by the metal the material containing titanium, e.g. TiO2
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H01L21/0228—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition deposition by cyclic CVD, e.g. ALD, ALE, pulsed CVD
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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
Definitions
- the present invention relates to semiconductor devices and more particularly, to an improved high-k dielectric layer, a capacitor structure using the same, and an exemplary fabrication method thereof.
- titanium oxide TiO2
- rutile TiO2 It is often desirable to increase rutile TiO2 in the capacitor dielectric film because it has a much higher dielectric constant (k>90) than anatase TiO2.
- TiO2 dielectric layer is deposited by using an atomic layer deposition (ALD) method.
- ALD atomic layer deposition
- TiO2 is inherently formed in the anatase phase during the ALD process.
- methods such as impurity doping, post annealing (600° C. or higher) and/or ozone-based ALD in combination with template layers are employed.
- the impurity doping method has problems such as high cost, low throughput and is hard to control.
- the drawback of the post annealing method is the additional thermal budget and mechanical stress, which may seriously degrade the MOS devices.
- the problems of the ozone-based ALD/template layer method include low deposition rate ( ⁇ 0.4 ⁇ per ALD cycle) and the risk of etching or oxidizing the underlying layer.
- Water-based ALD method which uses water vapor as oxidant in the ALD cycles, is also employed to deposit the TiO2 dielectric layer.
- the water-based ALD method has a much higher deposition rate than the ozone-based ALD method, meaning higher throughput.
- TiO2 deposited using the water-based ALD method is inherently in the anatase phase.
- rutile TiO2 in the water-based ALD process a 10 nm thick TiO2 film or a relatively higher process temperature is typically required.
- the invention provides a capacitor structure including a first electrode on a substrate; a template layer on the first electrode; a titanium oxide (TiO2) dielectric layer on the template layer, wherein the TiO2 dielectric layer has substantially only rutile phase; and a second electrode on the TiO2 dielectric layer.
- TiO2 dielectric layer is formed by using a modified water-based ALD process.
- FIG. 1 is a cross-sectional diagram showing a portion of a capacitor structure according to one embodiment of this invention
- FIG. 2 is a flow chart illustrating an exemplary process of forming the capacitor structure as set forth in FIG. 1 according to this invention
- FIG. 3 is a flow chart illustrating an exemplary modified water-based ALD process
- FIG. 5 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer formed by using O3 pulse/purge ratio of 20:1 and different duration of O3 pulse.
- FIG. 1 is a cross-sectional diagram showing a portion of a capacitor structure according to one embodiment of this invention.
- the capacitor structure 20 is disposed on a substrate 10 such as a silicon-based substrate.
- the substrate 10 may be any appropriate semiconductor substrate.
- the capacitor structure 20 comprises a a first electrode 22 on the substrate, a template layer 23 on the first electrode 22 , a high-k dielectric layer 24 on the template layer 23 , and a second electrode 26 on the high-k dielectric layer 24 .
- the first electrode 22 may be a noble material such as ruthenium (Ru).
- the template layer 23 may comprise Ru, RuO2, Ir, or IrO2.
- the first electrode 22 may be deposited using any appropriate techniques such as chemical vapor deposition (CVD), ALD, physical vapor deposition (PVD), or sputtering.
- the second electrode 26 may be a novel metal or any suitable conductive material such as metal oxide or metal nitride.
- the second electrode 26 may be Ru, Pt or Ir, RuO2, IrO2, TiN, TaN, WN or the like.
- the high-k dielectric layer 24 that is directly deposited onto the template layer 23 is rutile TiO2.
- substantially, the high-k dielectric layer 24 has only one single phase: rutile. That is, the high-k dielectric layer 24 has substantially no x-ray diffraction peak associated with anatase TiO2.
- the thickness of the high-k dielectric layer 24 is about 8 nm or thinner.
- no impurity such as aluminum (Al) is doped into the high-k dielectric layer 24 .
- FIG. 2 is a flow chart illustrating an exemplary process of forming the capacitor structure 20 as set forth in FIG. 1 according to this invention
- FIG. 3 is a flow chart illustrating an exemplary modified water-based ALD process.
- the process flow 100 includes four sequential major steps 102 ⁇ 108 .
- the first electrode 22 such as Ru is deposited onto the substrate 10 .
- the template layer 23 is formed on the first electrode 22 .
- a modified water-based ALD process is performed to deposit a rutile TiO2 layer 24 on the template layer 23 .
- the thickness of the rutile TiO2 layer 24 may be about 8 nm or thinner.
- the second electrode 26 is formed on the rutile TiO2 layer 24 . No post anneal or post thermal treatment is required between Step 10
- the aforesaid modified water-based ALD process comprises a plurality of Ti ALD cycles, and each ALD cycle comprises, in the order of: (1) supplying a Ti precursor into a reaction chamber (Ti pulse); (2) purging the reaction chamber with inert gas; (3) supplying water vapor into the reaction chamber (H2O pulse); and (4) purging the reaction chamber with inert gas.
- the process temperature may range between 150° C. and 450° C., for example, 285° C. .
- the Ti precursor such as TiCl4
- a portion of the Ti precursor is adsorbed to an exposed surface of the substrate 10 .
- the purge gas such as argon or nitrogen then removes the rest of the Ti precursor that is not adsorbed.
- the water vapor that acts as an oxidant supplied to the substrate 10 then reacts with the adsorbed Ti precursor to form a single atomic TiO2 layer on the substrate 10 .
- the aforesaid modified water-based ALD process may comprise multiple stages according to one embodiment.
- the aforesaid ALD cycle may be repeated n times to initially deposit a first TiO2 layer on the template layer 23 .
- n is an integer ranging between 5 and 80 inclusive.
- the initially deposited first TiO2 layer on the template layer 23 may be anatase TiO2.
- the first stage is ended by performing an ozone pulse and purge step that substantially transfer the entire thickness of the initially deposited first TiO2 layer on the template layer 23 into rutile TiO2.
- the duration of the ozone pulse may be greater than 5 seconds.
- the aforesaid ALD cycle may be repeated m times to initially deposit a second TiO2 layer on the rutile TiO2.
- m is an integer ranging between 5 and 80 inclusive, and wherein n may be not equal to m.
- the second stage is also ended by performing an ozone pulse and purge step that substantially transfer the entire thickness of the second TiO2 layer into rutile TiO2.
- the Ti ALD cycle to O3 pulse/purge ratio may range between 80:1 and 5:1.
- FIG. 4 also shows the result of without adding O3 pulse wherein the 8 nm water-based ALD TiO2 layer is amorphous.
- FIG. 5 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer formed by using O3 pulse/purge ratio of 20:1 and different duration of O3 pulse (10 seconds, 20 seconds and 40 seconds).
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Abstract
A capacitor structure includes a first electrode on a substrate; a template layer on the first electrode; a titanium oxide (TiO2) dielectric layer on the template layer, wherein the TiO2 dielectric layer has substantially only rutile phase; and a second electrode on the TiO2 dielectric layer. The titanium oxide dielectric layer is an undoped titanium oxide dielectric layer.
Description
- 1. Field of the Invention
- The present invention relates to semiconductor devices and more particularly, to an improved high-k dielectric layer, a capacitor structure using the same, and an exemplary fabrication method thereof.
- 2. Description of the Prior Art
- As known in the art, downscaling of the metal-insulator-metal capacitor for dynamic random access memory (DRAM) devices has required the introduction of high permittivity dielectrics, for example, titanium oxide (TiO2). It is well known that titanium oxide has multiple phases which have different dielectric constants. Two known phases of titanium oxide are anatase and rutile. It is often desirable to increase rutile TiO2 in the capacitor dielectric film because it has a much higher dielectric constant (k>90) than anatase TiO2.
- Typically, TiO2 dielectric layer is deposited by using an atomic layer deposition (ALD) method. However, TiO2 is inherently formed in the anatase phase during the ALD process. To form a TiO2 dielectric layer with the rutile phase and low leakage as well, methods such as impurity doping, post annealing (600° C. or higher) and/or ozone-based ALD in combination with template layers are employed. However, the impurity doping method has problems such as high cost, low throughput and is hard to control. The drawback of the post annealing method is the additional thermal budget and mechanical stress, which may seriously degrade the MOS devices. The problems of the ozone-based ALD/template layer method include low deposition rate (˜0.4 Å per ALD cycle) and the risk of etching or oxidizing the underlying layer.
- Water-based ALD method, which uses water vapor as oxidant in the ALD cycles, is also employed to deposit the TiO2 dielectric layer. The water-based ALD method has a much higher deposition rate than the ozone-based ALD method, meaning higher throughput. However, TiO2 deposited using the water-based ALD method is inherently in the anatase phase. To form rutile TiO2 in the water-based ALD process, a 10 nm thick TiO2 film or a relatively higher process temperature is typically required.
- There is a need in this industry to provide an improved method for depositing a high-k dielectric material such as rutile TiO2 with a higher deposition/growth rate and a low leakage and without introducing the aforesaid prior art shortcomings.
- According to one aspect, the invention provides a capacitor structure including a first electrode on a substrate; a template layer on the first electrode; a titanium oxide (TiO2) dielectric layer on the template layer, wherein the TiO2 dielectric layer has substantially only rutile phase; and a second electrode on the TiO2 dielectric layer. The TiO2 dielectric layer is formed by using a modified water-based ALD process.
- These and other objectives of the present invention will no doubt become obvious to those of ordinary skill in the art after reading the following detailed description of the preferred embodiment that is illustrated in the various figures and drawings.
- The accompanying drawings are included to provide a further understanding of the embodiments, and are incorporated in and constitute a part of this specification. The drawings illustrate some of the embodiments and, together with the description, serve to explain their principles. In the drawings:
-
FIG. 1 is a cross-sectional diagram showing a portion of a capacitor structure according to one embodiment of this invention; -
FIG. 2 is a flow chart illustrating an exemplary process of forming the capacitor structure as set forth inFIG. 1 according to this invention; -
FIG. 3 is a flow chart illustrating an exemplary modified water-based ALD process; -
FIG. 4 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer (relative intensity as a function of 2 theta) in the spectral region between 2 theta=20 and 2 theta=60; and -
FIG. 5 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer formed by using O3 pulse/purge ratio of 20:1 and different duration of O3 pulse. - It should be noted that all the figures are diagrammatic. Relative dimensions and proportions of parts of the drawings have been shown exaggerated or reduced in size, for the sake of clarity and convenience in the drawings. The same reference signs are generally used to refer to corresponding or similar features in modified and different embodiments.
- In the following detailed description, reference is made to the accompanying drawings, which form a part hereof, and in which is shown by way of illustration specific examples in which the embodiments may be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to practice them, and it is to be understood that other embodiments may be utilized and that structural, logical and electrical changes may be made without departing from the described embodiments. The following detailed description is, therefore, not to be taken in a limiting sense, and the included embodiments are defined by the appended claims.
-
FIG. 1 is a cross-sectional diagram showing a portion of a capacitor structure according to one embodiment of this invention. As shown inFIG. 1 , thecapacitor structure 20 is disposed on asubstrate 10 such as a silicon-based substrate. However, it is understood that thesubstrate 10 may be any appropriate semiconductor substrate. Thecapacitor structure 20 comprises a afirst electrode 22 on the substrate, atemplate layer 23 on thefirst electrode 22, a high-kdielectric layer 24 on thetemplate layer 23, and asecond electrode 26 on the high-kdielectric layer 24. Thefirst electrode 22 may be a noble material such as ruthenium (Ru). Thetemplate layer 23 may comprise Ru, RuO2, Ir, or IrO2. Thefirst electrode 22 may be deposited using any appropriate techniques such as chemical vapor deposition (CVD), ALD, physical vapor deposition (PVD), or sputtering. Thesecond electrode 26 may be a novel metal or any suitable conductive material such as metal oxide or metal nitride. For example, thesecond electrode 26 may be Ru, Pt or Ir, RuO2, IrO2, TiN, TaN, WN or the like. - According to this embodiment, the high-k
dielectric layer 24 that is directly deposited onto thetemplate layer 23 is rutile TiO2. According to this embodiment, substantially, the high-kdielectric layer 24 has only one single phase: rutile. That is, the high-kdielectric layer 24 has substantially no x-ray diffraction peak associated with anatase TiO2. According to this embodiment, the thickness of the high-kdielectric layer 24 is about 8 nm or thinner. According to this embodiment, no impurity such as aluminum (Al) is doped into the high-kdielectric layer 24. - Referring now to
FIG. 2 andFIG. 3 , and briefly toFIG. 1 , whereinFIG. 2 is a flow chart illustrating an exemplary process of forming thecapacitor structure 20 as set forth inFIG. 1 according to this invention, andFIG. 3 is a flow chart illustrating an exemplary modified water-based ALD process. As shown inFIG. 2 , theprocess flow 100 includes four sequentialmajor steps 102˜108. InStep 102, thefirst electrode 22 such as Ru is deposited onto thesubstrate 10. InStep 104, thetemplate layer 23 is formed on thefirst electrode 22. Subsequently, inStep 106, a modified water-based ALD process is performed to deposit arutile TiO2 layer 24 on thetemplate layer 23. According to this embodiment, the thickness of therutile TiO2 layer 24 may be about 8 nm or thinner. Finally, inStep 108, thesecond electrode 26 is formed on therutile TiO2 layer 24. No post anneal or post thermal treatment is required betweenStep 10 - According to this embodiment, the aforesaid modified water-based ALD process comprises a plurality of Ti ALD cycles, and each ALD cycle comprises, in the order of: (1) supplying a Ti precursor into a reaction chamber (Ti pulse); (2) purging the reaction chamber with inert gas; (3) supplying water vapor into the reaction chamber (H2O pulse); and (4) purging the reaction chamber with inert gas. According to this embodiment, the process temperature may range between 150° C. and 450° C., for example, 285° C. . When the Ti precursor such as TiCl4 is supplied into the reaction chamber, a portion of the Ti precursor is adsorbed to an exposed surface of the
substrate 10. The purge gas such as argon or nitrogen then removes the rest of the Ti precursor that is not adsorbed. The water vapor that acts as an oxidant supplied to thesubstrate 10 then reacts with the adsorbed Ti precursor to form a single atomic TiO2 layer on thesubstrate 10. - As shown in
FIG. 3 , the aforesaid modified water-based ALD process may comprise multiple stages according to one embodiment. In the first stage, for example, the aforesaid ALD cycle may be repeated n times to initially deposit a first TiO2 layer on thetemplate layer 23. For example, n is an integer ranging between 5 and 80 inclusive. The initially deposited first TiO2 layer on thetemplate layer 23 may be anatase TiO2. The first stage is ended by performing an ozone pulse and purge step that substantially transfer the entire thickness of the initially deposited first TiO2 layer on thetemplate layer 23 into rutile TiO2. The duration of the ozone pulse may be greater than 5 seconds. In the second stage, for example, the aforesaid ALD cycle may be repeated m times to initially deposit a second TiO2 layer on the rutile TiO2. For example, m is an integer ranging between 5 and 80 inclusive, and wherein n may be not equal to m. The second stage is also ended by performing an ozone pulse and purge step that substantially transfer the entire thickness of the second TiO2 layer into rutile TiO2. According to one embodiment, the Ti ALD cycle to O3 pulse/purge ratio may range between 80:1 and 5:1. -
FIG. 4 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer (relative intensity as a function of 2 theta) in the spectral region between 2 theta=20 and 2 theta=60. As shown inFIG. 4 , the TiO2 layers formed by using various O3 pulse/purge ratio ranging between 50:1 and 10:1 have obvious peak at 2 theta=27 and this indicate that the intervening O3 pulse helps rutile TiO2 crystallization.FIG. 4 also shows the result of without adding O3 pulse wherein the 8 nm water-based ALD TiO2 layer is amorphous.FIG. 5 shows the X-ray diffraction spectrum of the modified water-based ALD TiO2 layer formed by using O3 pulse/purge ratio of 20:1 and different duration of O3 pulse (10 seconds, 20 seconds and 40 seconds). - Those skilled in the art will readily observe that numerous modifications and alterations of the device and method may be made while retaining the teachings of the invention. Accordingly, the above disclosure should be construed as limited only by the metes and bounds of the appended claims.
Claims (4)
1. A capacitor structure comprising:
a first electrode on a substrate;
a template layer on the first electrode;
an undoped titanium oxide (TiO2) dielectric layer on the template layer, wherein the undoped TiO2 dielectric layer has substantially only rutile phase; and
a second electrode on the undoped TiO2 dielectric layer.
2. The capacitor structure according to claim 1 wherein the first electrode comprises Ru.
3. The capacitor structure according to claim 1 wherein the template layer comprises Ru, RuO2, Ir, or IrO2.
4. The capacitor structure according to claim 1 wherein the second electrode comprises Ru, Pt or Ir, RuO2, IrO2, TiN, TaN, or WN.
Priority Applications (4)
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US13/674,929 US20140131835A1 (en) | 2012-11-12 | 2012-11-12 | Semiconductor device with rutile titanium oxide dielectric film |
TW102108659A TWI553812B (en) | 2012-11-12 | 2013-03-12 | Semiconductor component having rutile crystalline phase titanium dioxide dielectric film |
CN201310356172.8A CN103811481B (en) | 2012-11-12 | 2013-08-15 | Semiconductor device with rutile crystalline phase titania dielectric film |
US14/147,603 US9202860B2 (en) | 2012-11-12 | 2014-01-06 | Method for fabricating capacitor having rutile titanium oxide dielectric film |
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US13/674,929 US20140131835A1 (en) | 2012-11-12 | 2012-11-12 | Semiconductor device with rutile titanium oxide dielectric film |
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US14/147,603 Continuation US9202860B2 (en) | 2012-11-12 | 2014-01-06 | Method for fabricating capacitor having rutile titanium oxide dielectric film |
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US14/147,603 Active US9202860B2 (en) | 2012-11-12 | 2014-01-06 | Method for fabricating capacitor having rutile titanium oxide dielectric film |
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US20140185182A1 (en) * | 2013-01-02 | 2014-07-03 | Nanya Technology Corp. | Semiconductor device with rutile titanium oxide dielectric film |
Citations (2)
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US20090065896A1 (en) * | 2007-09-07 | 2009-03-12 | Seoul National University Industry Foundation | CAPACITOR HAVING Ru ELECTRODE AND TiO2 DIELECTRIC LAYER FOR SEMICONDUCTOR DEVICE AND METHOD OF FABRICATING THE SAME |
US20090134445A1 (en) * | 2005-08-30 | 2009-05-28 | Hynix Semiconductor Inc. | Semiconductor device with dielectric structure and method for fabricating the same |
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CN1153732C (en) * | 2000-10-16 | 2004-06-16 | 南京大学 | Ordinary-temp hydrolysis process for synthesizing nm-class rutile-type TiO2 with high specific surface area from TiCl4 |
CN1988078A (en) * | 2005-12-22 | 2007-06-27 | 财团法人工业技术研究院 | Metal-insulator-metal capacitor |
JP2010192520A (en) * | 2009-02-16 | 2010-09-02 | Elpida Memory Inc | Method for manufacturing semiconductor device |
JP5647792B2 (en) * | 2009-04-01 | 2015-01-07 | ピーエスフォー ルクスコ エスエイアールエルPS4 Luxco S.a.r.l. | Method for manufacturing capacitor insulating film for capacitor |
CN101859645A (en) * | 2009-04-09 | 2010-10-13 | 王永军 | Large power super capacitor power battery |
US7968452B2 (en) * | 2009-06-30 | 2011-06-28 | Intermolecular, Inc. | Titanium-based high-K dielectric films |
EP2434529B1 (en) * | 2010-09-28 | 2020-02-12 | IMEC vzw | Metal-insulator-metal capacitor for use in semiconductor devices and manufacuring method therfor |
US8609553B2 (en) * | 2011-02-07 | 2013-12-17 | Micron Technology, Inc. | Methods of forming rutile titanium dioxide and associated methods of forming semiconductor structures |
-
2012
- 2012-11-12 US US13/674,929 patent/US20140131835A1/en not_active Abandoned
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2013
- 2013-03-12 TW TW102108659A patent/TWI553812B/en active
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US20090134445A1 (en) * | 2005-08-30 | 2009-05-28 | Hynix Semiconductor Inc. | Semiconductor device with dielectric structure and method for fabricating the same |
US20090065896A1 (en) * | 2007-09-07 | 2009-03-12 | Seoul National University Industry Foundation | CAPACITOR HAVING Ru ELECTRODE AND TiO2 DIELECTRIC LAYER FOR SEMICONDUCTOR DEVICE AND METHOD OF FABRICATING THE SAME |
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US9202860B2 (en) | 2015-12-01 |
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CN103811481B (en) | 2016-12-28 |
US20140134821A1 (en) | 2014-05-15 |
TWI553812B (en) | 2016-10-11 |
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