US20060065349A1 - Method of fabricating thin dielectric film and thin film capacitor including the dielectric film - Google Patents
Method of fabricating thin dielectric film and thin film capacitor including the dielectric film Download PDFInfo
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- US20060065349A1 US20060065349A1 US10/951,054 US95105404A US2006065349A1 US 20060065349 A1 US20060065349 A1 US 20060065349A1 US 95105404 A US95105404 A US 95105404A US 2006065349 A1 US2006065349 A1 US 2006065349A1
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 239000010408 film Substances 0.000 title claims description 48
- 239000010409 thin film Substances 0.000 title claims description 39
- 239000003990 capacitor Substances 0.000 title claims description 33
- 239000000463 material Substances 0.000 claims abstract description 63
- 239000002243 precursor Substances 0.000 claims abstract description 39
- 238000000034 method Methods 0.000 claims abstract description 34
- 239000000919 ceramic Substances 0.000 claims abstract description 32
- 229910052751 metal Inorganic materials 0.000 claims abstract description 32
- 239000002184 metal Substances 0.000 claims abstract description 32
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- 238000000151 deposition Methods 0.000 claims abstract description 17
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- 239000000203 mixture Substances 0.000 claims abstract description 5
- 238000011049 filling Methods 0.000 claims abstract description 3
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- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052802 copper Inorganic materials 0.000 claims description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- 229910052788 barium Inorganic materials 0.000 claims description 6
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
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- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims description 4
- 238000007598 dipping method Methods 0.000 claims description 3
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- 230000001070 adhesive effect Effects 0.000 claims description 2
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- 238000005507 spraying Methods 0.000 claims description 2
- JVQBUNGVDHSAEJ-UHFFFAOYSA-L strontium;propanoate Chemical class [Sr+2].CCC([O-])=O.CCC([O-])=O JVQBUNGVDHSAEJ-UHFFFAOYSA-L 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims 1
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- 239000010949 copper Substances 0.000 description 5
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- BPJYAXCTOHRFDQ-UHFFFAOYSA-L tetracopper;2,4,6-trioxido-1,3,5,2,4,6-trioxatriarsinane;diacetate Chemical compound [Cu+2].[Cu+2].[Cu+2].[Cu+2].CC([O-])=O.CC([O-])=O.[O-][As]1O[As]([O-])O[As]([O-])O1.[O-][As]1O[As]([O-])O[As]([O-])O1 BPJYAXCTOHRFDQ-UHFFFAOYSA-L 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G4/00—Fixed capacitors; Processes of their manufacture
- H01G4/33—Thin- or thick-film capacitors (thin- or thick-film circuits; capacitors without a potential-jump or surface barrier specially adapted for integrated circuits, details thereof, multistep manufacturing processes therefor)
-
- 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
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1204—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
- C23C18/1208—Oxides, e.g. ceramics
- C23C18/1216—Metal oxides
-
- 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
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1225—Deposition of multilayers of inorganic material
-
- 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
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1229—Composition of the substrate
- C23C18/1241—Metallic substrates
-
- 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
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/125—Process of deposition of the inorganic material
- C23C18/1283—Control of temperature, e.g. gradual temperature increase, modulation of temperature
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G4/00—Fixed capacitors; Processes of their manufacture
- H01G4/002—Details
- H01G4/018—Dielectrics
- H01G4/06—Solid dielectrics
- H01G4/08—Inorganic dielectrics
- H01G4/12—Ceramic dielectrics
Definitions
- Embodiments of the present invention relate to thin film capacitors and to methods of fabricating same.
- Creating thin films having a large capacitance density that is, a capacitance density above about 1 ⁇ F/cm 2 on metal sheets presents a number of challenges.
- One way to achieve large capacitance density would be to achieve a large dielectric constant, given that capacitance density and dielectric constant are directly proportional to one another.
- the dielectric constant of a material is among other things a function of the grain size of that material. In particular, as the grain size of a material increases, generally, so will its dielectric constant.
- growing thin films having large grain sizes that is, thin films having grain sizes above about 50 nm to about 100 nm is a challenge. For example, growing a large grain microstructure requires an optimum combination of nucleation and grain growth.
- a surface roughness of the metal sheet onto which the dielectric film has been deposited tends to present metal peak and valleys into the dielectric film which in turn can lead to a direct shorting between the electrodes of a capacitor that includes the dielectric film.
- voids typically present in the film will allow metal from at least one of the capacitor electrodes to seep into the voids, leading to shorting and leakage between the electrodes.
- Voids in dielectric layers are disadvantageous for a number of other reasons.
- the dielectric constant of air is very small, the presence of air pockets results in an overall decrease in the dielectric constant of the dielectric layer.
- voids present disadvantages with respect to both the mechanical integrity and the electrical performance of a dielectric layer.
- the prior art proposes solving the problem of voids by exposing the dielectric layer to relatively long periods of sintering in order to densify the layer.
- such a solution disadvantageously increases the thermal budget required for the fabrication of a dielectric film, increasing cost while not necessarily guaranteeing a satisfactory reduction in the number of voids.
- FIGS. 1A-1F various stages of a prior art CSD method for creating a dielectric thin film are depicted.
- the shown CSD method involves the deposition of a CSD precursor film 10 onto a metal sheet or electrode 12 .
- Deposition of the precursor may be achieved using well known spin-on deposition, spraying and dipping techniques.
- FIG. 1B the deposited precursor film 10 is shown as having been subjected to drying, burn-out of organics and annealing through heat treatment.
- FIG. 1A the deposited precursor film 10 is shown as having been subjected to drying, burn-out of organics and annealing through heat treatment.
- FIGS. 1C and 1D and in FIGS. 1E and 1F , fabrication stages similar to those in FIGS. 1A and 1B are respectively depicted.
- the deposition of a precursor film 10 ′ and 10 ′′ as seen in FIGS. 1C and 1E is followed by heat treatment as seen in FIGS. 1D and 1F to yield second and third layers 14 ′ and 14 ′′ of dielectric material, respectively.
- the resulting dielectric film 16 as shown in FIG.
- 1F disadvantageously contains grains of small size, in the order of about 10 nm to about 50 nm, thus exhibiting a low effective dielectric constant, typically in the range from about 100 to about 450.
- voids present in the dielectric film 16 tend to create shorts between the two electrodes of a capacitor formed from assembly 18 of FIG. 1F , as explained above.
- FIG. 1A-1F illustrate stages in the fabrication of a dielectric film on a metal sheet according to the prior art
- FIGS. 2A-2D illustrate stages in the fabrication of a dielectric film on a metal sheet according to an embodiment of the present invention
- FIG. 3 illustrates a thin film capacitor fabricated according to an embodiment of the present invention.
- FIG. 4 illustrates a system comprising a thin film capacitor fabricated according to embodiments of the present invention.
- Embodiments of the present invention pertain to methods of creating a high dielectric constant thin film on a metal sheet, to a thin film capacitor fabricated from a combination of the thin film, the metal sheet, and to a system including the thin film capacitor.
- thin film and “dielectric film” are used interchangeably in the instant description, and refer to a dielectric film adapted to be used in a thin film capacitor.
- metal sheet as used herein refers to a sheet of metal adapted to be used as an electrode in a thin film capacitor.
- FIGS. 2A-2D stages in the fabrication of a combination including a dielectric film on a metal sheet according to an embodiment of the present invention are shown.
- a method according to an embodiment of the present invention includes depositing a ceramic precursor material 100 , such as, for example, a ceramic green sheet onto a metal sheet 110 to obtain a first combination 120 .
- the metal sheet 110 may include, by way of example, Cu or Ni.
- the ceramic precursor material 100 may include a mixture comprising ceramic powder and an organic binder, a plasticizer, or an organic solvent.
- the ceramic powder may have a ceramic particle size between about 0.05 micron to about 0.5 micron.
- Ceramic green sheets are typically used in the multilayer ceramic capacitor art, where multiple layers of green sheets are stacked in between successive multiple layers of metal paste, then fired, singulated, termination metallization added, and surface mounted onto circuit boards, and are thus available on the market for that reason.
- Ceramic green sheets encompassed by embodiments of the present invention may include ceramic green sheets available from ceramic capacitor manufacturers, such as Murata and TDK, which would eventually be used in processing capacitors with temperature ratings, such as, Z5U, X6S, X7R, X7S, etc. Ceramic green sheets according to embodiments of the present invention may be deposited onto the metal sheet by way of roller pressing, by way of a carrier tape adhesive provided on one side of the green sheets, or, in the alternative, they may be laminated onto the metal sheet by a press.
- a method according to an embodiment of the present invention further includes heat treating the ceramic precursor material 100 after its deposition onto metal sheet 110 such that organics in the material are substantially burnt off, and further such that ceramic is sintered (densified) from the ceramic precursor material is densified, such as via sintering.
- the driving force behind the densification of the ceramic is the tendency of the system to reduce its surface area, hence, its surface energy, by joining of the particles and elimination of voids in between.
- Process conditions for the heat treatment of ceramic precursor material 100 may, according to embodiments of the invention, comprise drying, burn-out of organics and annealing through heat treatment.
- the precursor material 100 may be exposed to temperatures between about 200 degrees Centigrade and about 300 degrees Centigrade for about 2 hours to about 5 hours to yield a dried deposit.
- the dried deposit may be exposed to temperatures between about 400 degrees Centigrade and about 600 degrees Centigrade for about 3 hours to about 7 hours to yield an intermediate deposit.
- the intermediate deposit may be exposed to temperatures between about 1000 degrees Centigrade and about 1400 degrees Centigrade for about 6 hours to about 24 hours.
- heat treatment may be performed in a reducing atmosphere.
- Heat treatment of ceramic precursor material 100 as shown in the embodiment of FIG. 2B results in the formation of a heat treated ceramic layer 130 above metal sheet 110 , layer 130 including grains 140 having sizes between about 100 nm and about 500 nm in order to form a ceramic film with a thickness less than or equal to 1 micron.
- a ceramic green sheet tends to shrink by about 20% along its linear dimensions as a result of sintering. The above would suggest that the centers of adjacent ceramic grains would be closer to each other by 20% after heat treatment, as result of the atoms diffusing away from the inter-center bulk regions to voids, resulting in densification and shrinkage.
- layer 130 may have a thickness between about 0.3 micron and about 1 micron, and preferably a thickness of about 0.5 micron.
- layer 130 may define voids 150 (or pinholes) between at least some of the grains 140 .
- voids in the dielectric layer present a number of disadvantages, such as, for example, shorting between the electrodes of a capacitor made from the dielectric layer, leakage within the capacitor, a reduction in the dielectric constant of the dielectric layer, and an increased risk of crack propagation within the dielectric layer. As will be explained further below with respect to FIGS.
- embodiments of the present invention pertain to a method of substantially eliminating voids in the dielectric layer, such as dielectric layer 130 shown in FIG. 2B , advantageously improving the electrical performance and mechanical integrity of a dielectric film made from the dielectric layer.
- a method according to an embodiment of the present invention further includes filling voids 150 present in layer 130 with a CSD precursor material 160 .
- the shown CSD method thus involves the deposition of CSD precursor material 160 onto dielectric layer 130 .
- the CSD precursor material 160 may include an organic liquid solution of organic molecules with embedded metal atoms.
- the precursor material 160 may, by way of example, include either: (1) barium and strontium acetates, dissolved in acetic acid, mixed with titanium tetra-isopropoxide in isopropanol; (2) barium and strontium acetate dissolved in acetic acid mixed with titanium tetra n-butoxide stabilized with acetylacetone and diluted with 2-methoxyethanol; 3) barium and strontium propionates and titanium tetra n-butoxide stabilized with acetylacetone dissolved in a mixture of propionic acid and 1-butanol.
- Deposition of the CSD precursor material may be achieved using well known spin-on, spray or dipping techniques. The CSD precursor material thus deposited will substantially fill voids 150 by flowing through cracks in dielectric layer 130 .
- the deposited CSD precursor material 160 may be subjected to heat treatment including drying, organic burn-out and annealing.
- the precursor film 10 may be exposed to temperatures between about 100 degrees Centigrade and about 200 degrees Centigrade for about 15 minutes to about 30 minutes to yield a dried CSD deposit.
- the dried deposit may be exposed to temperatures between about 300 degrees Centigrade to about 500 degrees Centigrade for about 1 hour and about 3 hours to yield an intermediate CSD deposit.
- the intermediate deposit may be exposed to temperatures between about 500 degrees Centigrade to about 1000 degrees Centigrade, preferably for about 0.5 hour and about 3 hours, although longer exposure times would be possible.
- Heat treatment results in the burning out of residual organics in the precursor 160 and further in the growth of small-sized CSD grains 165 in CSD medium 170 .
- Grains 165 could, by way of example, include barium strontium titanate. Heat treatment will allow better densification of the CSD grains.
- Grains 165 of medium 170 contribute to substantially fill voids between grains 180 .
- the resulting dielectric film 175 as shown in FIG. 2D advantageously contains grains 180 of large size, in the order of about 100 nm and about 500 nm.
- voids between grains 180 are substantially filled by the resulting CSD grains 165 which have a smaller size, that is, a size in the range from about 0.02 to about 0.04 microns.
- the resulting dielectric film 175 thus has large capacitance density, for example, between about 500 to about 4000 with minimal voids.
- An alternate embodiment of the present invention would involve the deposition of the CSD precursor material 160 directly onto the ceramic precursor material 100 before heat treatment of the ceramic precursor material. Heat treatment of both CSD precursor material and of the ceramic precursor material would then take place simultaneously, yielding the structure shown in FIG. 2D .
- a thin film capacitor 190 according to an embodiment of the present invention is shown as having been formed from the combination of FIG. 2D .
- a second metal sheet 200 is provided above dielectric film 175 by any of well known techniques, such as, for example, sputtering copper followed by copper plating, or copper vacuum evaporation, etc.
- Thin film capacitor 190 may be embedded into an organic substrate according to any of the well known methods, as would be readily recognized by one skilled in the art.
- embodiments of the present invention yield thicker and hence more mechanically and electrically reliable dielectric films for thin film capacitors.
- Dielectric films according to embodiments of the present invention have higher dielectric constants (typically in the range between 700 and 4000) than dielectric films of the prior art (typically in the range between 100 and 450).
- the higher dielectric constants are a result of the dominant presence of large grain high k material, in this way potentially yielding large capacitance densities, despite a greater thickness of the dielectric films.
- the greater thickness of the dielectric films according to embodiments of the present invention further contributes to a minimization in shorting and/or leakage issues of the prior art.
- embodiments of the present invention advantageously avoid the need to grow large grains starting from CSD precursor materials, and the problems associated therewith, since large grains would already be present in the ceramic precursor material for the dielectric film. Moreover, embodiments of the present invention would advantageously reduce manufacturing costs for thin films to the extent that they make possible the use of high volume manufacturing powder green sheets as opposed to the use of CSD precursor chemicals.
- a system 900 including an electronic assembly 1000 which may include a thin film capacitor 190 similar to thin film capacitor 190 of FIG. 3 , capacitor 190 having been embedded onto an organic substrate and packaged along with a die 210 .
- Electronic assembly 1000 may also include a microprocessor, or an application specific IC (ASIC).
- ASIC application specific IC
- Integrated circuits found in chipsets e.g., graphics, sound, and control chipsets
- the system 900 may also include a main memory 1002 , a graphics processor 1004 , a mass storage device 1006 , and/or an input/output module 1008 coupled to each other by way of a bus 1010 , as shown.
- the memory 1002 include but are not limited to static random access memory (SRAM) and dynamic random access memory (DRAM).
- SRAM static random access memory
- DRAM dynamic random access memory
- the mass storage device 106 include but are not limited to a hard disk drive, a compact disk drive (CD), a digital versatile disk drive (DVD), and so forth.
- Examples of the input/output module 1008 include but are not limited to a keyboard, cursor control arrangements, a display, a network interface, and so forth.
- the bus 1010 examples include but are not limited to a peripheral control interface (PCI) bus, and Industry Standard Architecture (ISA) bus, and so forth.
- the system 900 may be a wireless mobile phone, a personal digital assistant, a pocket PC, a tablet PC, a notebook PC, a desktop computer, a set-top box, a media-center PC, a DVD player, and a server.
- PCI peripheral control interface
- ISA Industry Standard Architecture
- the system 900 may be a wireless mobile phone, a personal digital assistant, a pocket PC, a tablet PC, a notebook PC, a desktop computer, a set-top box, a media-center PC, a DVD player, and a server.
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- Chemical Kinetics & Catalysis (AREA)
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Abstract
Description
- Embodiments of the present invention relate to thin film capacitors and to methods of fabricating same.
- Creating thin films having a large capacitance density, that is, a capacitance density above about 1 μF/cm2 on metal sheets presents a number of challenges. One way to achieve large capacitance density would be to achieve a large dielectric constant, given that capacitance density and dielectric constant are directly proportional to one another. It is well known that the dielectric constant of a material is among other things a function of the grain size of that material. In particular, as the grain size of a material increases, generally, so will its dielectric constant. However, growing thin films having large grain sizes, that is, thin films having grain sizes above about 50 nm to about 100 nm is a challenge. For example, growing a large grain microstructure requires an optimum combination of nucleation and grain growth. This is hard to achieve on a polycrystalline metal sheet. Typically, the multitude of random sites on the rough polycrystalline metal sheet acts as nucleation sites, resulting in a microstructure with very small grain size (about 10 nm to about 50 nm). Once the film microstructure is composed of a large number of small grains, further heating will not result in a large grain microstructure, because larger grains would grow at the expense of the smaller grains. However, a large number of similar-sized grains cannot grow into each other to form larger grains.
- As a result of the above, attempts at creating thin films having a large capacitance density has shifted toward reducing a thickness of the deposited thin film dielectric, while avoiding the problems noted above with respect to creating dielectrics of large grain size. Thus, the prior art typically focuses on small grain sized thin film technology (that is dielectric thin films having grain sizes in the range from about 10 nm to about 50 nm, with dielectric constants ranging from about 100 to about 450. To the extent that the capacitance density of a material is known to be inversely proportional to its thickness, the prior art has aimed at keeping the thickness of such dielectric films in the order of about 0.1 microns. However, disadvantageously, such films have tended to present serious shorting issues. First, a surface roughness of the metal sheet onto which the dielectric film has been deposited, to the extent that it is usually significant with respect to a thickness of the dielectric film, tends to present metal peak and valleys into the dielectric film which in turn can lead to a direct shorting between the electrodes of a capacitor that includes the dielectric film. In addition, again, since a thickness of the dielectric film is small, voids typically present in the film will allow metal from at least one of the capacitor electrodes to seep into the voids, leading to shorting and leakage between the electrodes.
- Voids in dielectric layers are disadvantageous for a number of other reasons. First, because of the presence of air pockets brought about as a result of the presence of voids, stress concentration points are typically created in the dielectric film, thus increasing the risk of crack propagation therein. In addition, to the extent that the dielectric constant of air is very small, the presence of air pockets results in an overall decrease in the dielectric constant of the dielectric layer. Thus, voids present disadvantages with respect to both the mechanical integrity and the electrical performance of a dielectric layer. The prior art proposes solving the problem of voids by exposing the dielectric layer to relatively long periods of sintering in order to densify the layer. However, such a solution disadvantageously increases the thermal budget required for the fabrication of a dielectric film, increasing cost while not necessarily guaranteeing a satisfactory reduction in the number of voids.
- With respect to fabricating thin film capacitors, as noted above, a predominant prior art method involves chemical solution deposition (CSD). Referring to
FIGS. 1A-1F , various stages of a prior art CSD method for creating a dielectric thin film are depicted. As seen inFIG. 1A , the shown CSD method involves the deposition of aCSD precursor film 10 onto a metal sheet orelectrode 12. Deposition of the precursor may be achieved using well known spin-on deposition, spraying and dipping techniques. Thereafter, atFIG. 1B , the depositedprecursor film 10 is shown as having been subjected to drying, burn-out of organics and annealing through heat treatment. As seen inFIG. 1B , heat treatment results in the decomposition of residual organics in the precursor and further in the growth of small-sized grains, which together contribute to form afirst layer 14 of dielectric material. InFIGS. 1C and 1D , and inFIGS. 1E and 1F , fabrication stages similar to those inFIGS. 1A and 1B are respectively depicted. Thus, the deposition of aprecursor film 10′ and 10″ as seen inFIGS. 1C and 1E is followed by heat treatment as seen inFIGS. 1D and 1F to yield second andthird layers 14′ and 14″ of dielectric material, respectively. The resultingdielectric film 16 as shown inFIG. 1F disadvantageously contains grains of small size, in the order of about 10 nm to about 50 nm, thus exhibiting a low effective dielectric constant, typically in the range from about 100 to about 450. In addition, voids present in thedielectric film 16 tend to create shorts between the two electrodes of a capacitor formed from assembly 18 ofFIG. 1F , as explained above. - Conventional thin film dielectric fabrication methods thus do not allow the formation of a dielectric film that both exhibits a high capacitance density and substantially avoids shorting and/or leakage issues between electrodes in a capacitor including the film.
- Embodiments of the present invention are illustrated by way of example and not by way of limitation in the figures of the accompanying drawings, in which the like references indicate similar elements and in which:
-
FIG. 1A-1F illustrate stages in the fabrication of a dielectric film on a metal sheet according to the prior art; -
FIGS. 2A-2D illustrate stages in the fabrication of a dielectric film on a metal sheet according to an embodiment of the present invention; -
FIG. 3 illustrates a thin film capacitor fabricated according to an embodiment of the present invention; and -
FIG. 4 illustrates a system comprising a thin film capacitor fabricated according to embodiments of the present invention. - Embodiments of the present invention pertain to methods of creating a high dielectric constant thin film on a metal sheet, to a thin film capacitor fabricated from a combination of the thin film, the metal sheet, and to a system including the thin film capacitor.
- Various aspects of the illustrative embodiments will be described using terms commonly employed by those skilled in the art to convey the substance of their work to others skilled in the art. However, it will be apparent to those skilled in the art that the present invention may be practiced with only some of the described aspects. For purposes of explanation, specific numbers, materials and configurations are set forth in order to provide a thorough understanding of the illustrative embodiments. However, it will be apparent to one skilled in the art that the present invention may be practiced without the specific details. In other instances, well-known features are omitted or simplified in order not to obscure the illustrative embodiments.
- Various operations will be described as multiple discrete operations, in turn, in a manner that is most helpful in understanding the present invention; however, the order of description should not be construed as to imply that these operations are necessarily order dependent. In particular, these operations need not be performed in the order of presentation.
- The word “embodiment” is used repeatedly. The word generally does not refer to the same embodiment, however, it may. The terms “comprising”, “having” and “including” are synonymous, unless the context dictates otherwise.
- The phrases “thin film” and “dielectric film” are used interchangeably in the instant description, and refer to a dielectric film adapted to be used in a thin film capacitor. In addition, “metal sheet” as used herein refers to a sheet of metal adapted to be used as an electrode in a thin film capacitor.
- Referring now to
FIGS. 2A-2D , stages in the fabrication of a combination including a dielectric film on a metal sheet according to an embodiment of the present invention are shown. - As seen in
FIG. 2A , a method according to an embodiment of the present invention includes depositing aceramic precursor material 100, such as, for example, a ceramic green sheet onto ametal sheet 110 to obtain afirst combination 120. Themetal sheet 110 may include, by way of example, Cu or Ni. Theceramic precursor material 100 may include a mixture comprising ceramic powder and an organic binder, a plasticizer, or an organic solvent. According to embodiments of the present invention, the ceramic powder may have a ceramic particle size between about 0.05 micron to about 0.5 micron. Ceramic green sheets are typically used in the multilayer ceramic capacitor art, where multiple layers of green sheets are stacked in between successive multiple layers of metal paste, then fired, singulated, termination metallization added, and surface mounted onto circuit boards, and are thus available on the market for that reason. Examples of ceramic green sheets encompassed by embodiments of the present invention may include ceramic green sheets available from ceramic capacitor manufacturers, such as Murata and TDK, which would eventually be used in processing capacitors with temperature ratings, such as, Z5U, X6S, X7R, X7S, etc. Ceramic green sheets according to embodiments of the present invention may be deposited onto the metal sheet by way of roller pressing, by way of a carrier tape adhesive provided on one side of the green sheets, or, in the alternative, they may be laminated onto the metal sheet by a press. - Referring next to
FIG. 2B , a method according to an embodiment of the present invention further includes heat treating theceramic precursor material 100 after its deposition ontometal sheet 110 such that organics in the material are substantially burnt off, and further such that ceramic is sintered (densified) from the ceramic precursor material is densified, such as via sintering. During the sintering process, the driving force behind the densification of the ceramic is the tendency of the system to reduce its surface area, hence, its surface energy, by joining of the particles and elimination of voids in between. Process conditions for the heat treatment ofceramic precursor material 100 may, according to embodiments of the invention, comprise drying, burn-out of organics and annealing through heat treatment. During drying, theprecursor material 100 may be exposed to temperatures between about 200 degrees Centigrade and about 300 degrees Centigrade for about 2 hours to about 5 hours to yield a dried deposit. During the subsequent burn-out stage, the dried deposit may be exposed to temperatures between about 400 degrees Centigrade and about 600 degrees Centigrade for about 3 hours to about 7 hours to yield an intermediate deposit. During annealing stage, the intermediate deposit may be exposed to temperatures between about 1000 degrees Centigrade and about 1400 degrees Centigrade for about 6 hours to about 24 hours. In order to avoid oxidizing themetal sheet 110 during heat treatment of theceramic precursor material 100, such as, for example, when themetal sheet 110 is made of Cu or Ni, heat treatment may be performed in a reducing atmosphere. Heat treatment ofceramic precursor material 100 as shown in the embodiment ofFIG. 2B results in the formation of a heat treatedceramic layer 130 abovemetal sheet 110,layer 130 includinggrains 140 having sizes between about 100 nm and about 500 nm in order to form a ceramic film with a thickness less than or equal to 1 micron. Typically, a ceramic green sheet tends to shrink by about 20% along its linear dimensions as a result of sintering. The above would suggest that the centers of adjacent ceramic grains would be closer to each other by 20% after heat treatment, as result of the atoms diffusing away from the inter-center bulk regions to voids, resulting in densification and shrinkage. Preferably, according to one embodiment,layer 130 may have a thickness between about 0.3 micron and about 1 micron, and preferably a thickness of about 0.5 micron. As seen inFIG. 2B ,layer 130 may define voids 150 (or pinholes) between at least some of thegrains 140. As noted above, voids in the dielectric layer present a number of disadvantages, such as, for example, shorting between the electrodes of a capacitor made from the dielectric layer, leakage within the capacitor, a reduction in the dielectric constant of the dielectric layer, and an increased risk of crack propagation within the dielectric layer. As will be explained further below with respect toFIGS. 2C and 2D , embodiments of the present invention pertain to a method of substantially eliminating voids in the dielectric layer, such asdielectric layer 130 shown inFIG. 2B , advantageously improving the electrical performance and mechanical integrity of a dielectric film made from the dielectric layer. - Referring next to
FIG. 2C , a method according to an embodiment of the present invention further includes fillingvoids 150 present inlayer 130 with aCSD precursor material 160. As seen inFIG. 2C , the shown CSD method thus involves the deposition ofCSD precursor material 160 ontodielectric layer 130. TheCSD precursor material 160 may include an organic liquid solution of organic molecules with embedded metal atoms. Theprecursor material 160 may, by way of example, include either: (1) barium and strontium acetates, dissolved in acetic acid, mixed with titanium tetra-isopropoxide in isopropanol; (2) barium and strontium acetate dissolved in acetic acid mixed with titanium tetra n-butoxide stabilized with acetylacetone and diluted with 2-methoxyethanol; 3) barium and strontium propionates and titanium tetra n-butoxide stabilized with acetylacetone dissolved in a mixture of propionic acid and 1-butanol. Deposition of the CSD precursor material may be achieved using well known spin-on, spray or dipping techniques. The CSD precursor material thus deposited will substantially fillvoids 150 by flowing through cracks indielectric layer 130. - Thereafter, at
FIG. 2D , the depositedCSD precursor material 160 may be subjected to heat treatment including drying, organic burn-out and annealing. During drying, theprecursor film 10 may be exposed to temperatures between about 100 degrees Centigrade and about 200 degrees Centigrade for about 15 minutes to about 30 minutes to yield a dried CSD deposit. During the subsequent burn-out stage, the dried deposit may be exposed to temperatures between about 300 degrees Centigrade to about 500 degrees Centigrade for about 1 hour and about 3 hours to yield an intermediate CSD deposit. During annealing, the intermediate deposit may be exposed to temperatures between about 500 degrees Centigrade to about 1000 degrees Centigrade, preferably for about 0.5 hour and about 3 hours, although longer exposure times would be possible. Heat treatment results in the burning out of residual organics in theprecursor 160 and further in the growth of small-sized CSD grains 165 inCSD medium 170.Grains 165 could, by way of example, include barium strontium titanate. Heat treatment will allow better densification of the CSD grains.Grains 165 ofmedium 170 contribute to substantially fill voids betweengrains 180. The resultingdielectric film 175 as shown inFIG. 2D advantageously containsgrains 180 of large size, in the order of about 100 nm and about 500 nm. In addition, as a result of the CSD deposition described above, voids betweengrains 180 are substantially filled by the resultingCSD grains 165 which have a smaller size, that is, a size in the range from about 0.02 to about 0.04 microns. The resultingdielectric film 175 thus has large capacitance density, for example, between about 500 to about 4000 with minimal voids. - An alternate embodiment of the present invention would involve the deposition of the
CSD precursor material 160 directly onto theceramic precursor material 100 before heat treatment of the ceramic precursor material. Heat treatment of both CSD precursor material and of the ceramic precursor material would then take place simultaneously, yielding the structure shown inFIG. 2D . - Referring next to
FIG. 3 , athin film capacitor 190 according to an embodiment of the present invention is shown as having been formed from the combination ofFIG. 2D . As seen inFIG. 3 , asecond metal sheet 200 is provided abovedielectric film 175 by any of well known techniques, such as, for example, sputtering copper followed by copper plating, or copper vacuum evaporation, etc.Thin film capacitor 190 may be embedded into an organic substrate according to any of the well known methods, as would be readily recognized by one skilled in the art. - Advantageously, embodiments of the present invention yield thicker and hence more mechanically and electrically reliable dielectric films for thin film capacitors. Dielectric films according to embodiments of the present invention have higher dielectric constants (typically in the range between 700 and 4000) than dielectric films of the prior art (typically in the range between 100 and 450). The higher dielectric constants are a result of the dominant presence of large grain high k material, in this way potentially yielding large capacitance densities, despite a greater thickness of the dielectric films. The greater thickness of the dielectric films according to embodiments of the present invention further contributes to a minimization in shorting and/or leakage issues of the prior art. In addition, embodiments of the present invention advantageously avoid the need to grow large grains starting from CSD precursor materials, and the problems associated therewith, since large grains would already be present in the ceramic precursor material for the dielectric film. Moreover, embodiments of the present invention would advantageously reduce manufacturing costs for thin films to the extent that they make possible the use of high volume manufacturing powder green sheets as opposed to the use of CSD precursor chemicals.
- Referring to
FIG. 4 , there is illustrated one of many possible systems in which embodiments of the present invention may be used. There is shown asystem 900 including anelectronic assembly 1000 which may include athin film capacitor 190 similar tothin film capacitor 190 ofFIG. 3 ,capacitor 190 having been embedded onto an organic substrate and packaged along with adie 210.Electronic assembly 1000 may also include a microprocessor, or an application specific IC (ASIC). Integrated circuits found in chipsets (e.g., graphics, sound, and control chipsets) may also be packaged inassembly 1000 accordance with embodiments of this invention. - For the embodiment depicted by
FIG. 4 , thesystem 900 may also include amain memory 1002, agraphics processor 1004, amass storage device 1006, and/or an input/output module 1008 coupled to each other by way of a bus 1010, as shown. Examples of thememory 1002 include but are not limited to static random access memory (SRAM) and dynamic random access memory (DRAM). Examples of the mass storage device 106 include but are not limited to a hard disk drive, a compact disk drive (CD), a digital versatile disk drive (DVD), and so forth. Examples of the input/output module 1008 include but are not limited to a keyboard, cursor control arrangements, a display, a network interface, and so forth. Examples of the bus 1010 include but are not limited to a peripheral control interface (PCI) bus, and Industry Standard Architecture (ISA) bus, and so forth. In various embodiments, thesystem 900 may be a wireless mobile phone, a personal digital assistant, a pocket PC, a tablet PC, a notebook PC, a desktop computer, a set-top box, a media-center PC, a DVD player, and a server. - Although specific embodiments have been illustrated and described herein for purposes of description of the preferred embodiment, it will be appreciated by those of ordinary skill in the art that a wide variety of alternate and/or equivalent implementations calculated to achieve the same purposes may be substituted for the specific embodiment shown and described without departing from the scope of the present invention. Those with skill in the art will readily appreciate that the present invention may be implemented in a very wide variety of embodiments. This application is intended to cover any adaptations or variations of the embodiments discussed herein. Therefore, it is manifestly intended that this invention be limited only by the claims and the equivalents thereof.
Claims (26)
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US20090238955A1 (en) * | 2008-03-20 | 2009-09-24 | E. I. Du Pont De Nemours And Company | Processes for the manufacture of barium titanate capacitors on nickel foils |
US8875363B2 (en) * | 2008-09-25 | 2014-11-04 | Cda Processing Limited Liability Company | Thin film capacitors on metal foils and methods of manufacturing same |
CN101429047B (en) * | 2008-12-12 | 2011-08-03 | 北京创导工业陶瓷有限公司 | Process for producing large-scale sheet |
CN103526337B (en) * | 2013-09-30 | 2015-07-29 | 同济大学 | A kind of method of synthesizing barium strontium titanate nanotube |
CN112038122A (en) * | 2020-10-06 | 2020-12-04 | 许华清 | Dielectric film processing device of capacitor |
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